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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="research-article"><?properties manuscript?><front><journal-meta><journal-id journal-id-type="nlm-journal-id">0322116</journal-id><journal-id journal-id-type="pubmed-jr-id">6595</journal-id><journal-id journal-id-type="nlm-ta">Prev Med</journal-id><journal-id journal-id-type="iso-abbrev">Prev Med</journal-id><journal-title-group><journal-title>Preventive medicine</journal-title></journal-title-group><issn pub-type="ppub">0091-7435</issn><issn pub-type="epub">1096-0260</issn></journal-meta><article-meta><article-id pub-id-type="pmid">31679842</article-id><article-id pub-id-type="pmc">7393609</article-id><article-id pub-id-type="doi">10.1016/j.ypmed.2019.105849</article-id><article-id pub-id-type="manuscript">HHSPA1566286</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Mortality-to-incidence ratios by US Congressional District: Implications for epidemiologic, dissemination and implementation research, and public health policy</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Eberth</surname><given-names>Jan M.</given-names></name><xref ref-type="aff" rid="A1">a</xref></contrib><contrib contrib-type="author"><name><surname>Zahnd</surname><given-names>Whitney E.</given-names></name><xref ref-type="aff" rid="A2">b</xref></contrib><contrib contrib-type="author"><name><surname>Adams</surname><given-names>Swann Arp</given-names></name><xref ref-type="aff" rid="A3">c</xref></contrib><contrib contrib-type="author"><name><surname>Friedman</surname><given-names>Daniela B.</given-names></name><xref ref-type="aff" rid="A4">d</xref></contrib><contrib contrib-type="author"><name><surname>Wheeler</surname><given-names>Stephanie B.</given-names></name><xref ref-type="aff" rid="A5">e</xref></contrib><contrib contrib-type="author"><name><surname>H&#x000e9;bert</surname><given-names>James R.</given-names></name><xref ref-type="aff" rid="A6">f</xref><xref rid="CR1" ref-type="corresp">*</xref></contrib></contrib-group><aff id="A1"><label>a</label>University of South Carolina, Cancer Prevention and Control Program, Rural and Minority Health Research Center, Department of Epidemiology and Biostatistics, United States of America</aff><aff id="A2"><label>b</label>University of South Carolina, Rural and Minority Health Research Center, United States of America</aff><aff id="A3"><label>c</label>University of South Carolina, Cancer Prevention and Control Program, Department of Epidemiology and Biostatistics and College of Nursing, United States of America</aff><aff id="A4"><label>d</label>University of South Carolina, Cancer Prevention and Control Program, Department of Health Promotion, Education, and Behavior, United States of America</aff><aff id="A5"><label>e</label>University of North Carolina, Chapel Hill, Department of Health Policy and Management, Gillings School of Global Public Health, CPCRN Coordinating Center, United States of America</aff><aff id="A6"><label>f</label>University of South Carolina, Cancer Prevention and Control Program, Department of Epidemiology and Biostatistics, United States of America</aff><author-notes><corresp id="CR1"><label>*</label> Corresponding author. <email>jhebert@sc.edu</email> (J.R. H&#x000e9;bert).</corresp></author-notes><pub-date pub-type="nihms-submitted"><day>12</day><month>7</month><year>2020</year></pub-date><pub-date pub-type="epub"><day>01</day><month>11</month><year>2019</year></pub-date><pub-date pub-type="ppub"><month>12</month><year>2019</year></pub-date><pub-date pub-type="pmc-release"><day>31</day><month>7</month><year>2020</year></pub-date><volume>129 Suppl</volume><fpage>105849</fpage><lpage>105849</lpage><!--elocation-id from pubmed: 10.1016/j.ypmed.2019.105849--><abstract id="ABS1"><p id="P1">The mortality-to-incidence ratio (MIR) can be computed from readily accessible, public-use data on cancer incidence and mortality, and a high MIR value is an indicator of poor survival relative to incidence. Newly available data on congressional district-specific cancer incidence and mortality from the U.S. Cancer Statistics (USCS) database from 2011 to 2015 were used to compute MIR values for overall (all types combined), breast, cervix, colorectal, esophagus, lung, oral, pancreas, and prostate cancer. Congressional districts in the South and Midwest, including MS, AL, and KY, had higher (worse) MIR values for all cancer types combined than for the U.S. as a whole. For all cancers combined, there was a positive correlation between each district&#x02019;s percent of rural residents and the MIR (r = 0.47; p &#x0003c; .001). The MIR for all cancer types combined was lower in districts within states that expanded Medicaid vs. those states that did not expand Medicaid (0.36 vs. 0.38; p &#x0003c; .001). A positive correlation was seen between the proportion of non-Hispanic Black residents and MIR (r = 0.15; p &#x0003c; .01 for all cancers). Lower MIRs were observed in districts in New England and in states that expanded Medicaid. However, there also were some interesting departures from this rule (e.g., Wyoming, South Dakota, parts of Wisconsin and Florida). Rural congressional districts have generally higher MIRs than more urban districts. There is some concern that poorer, more rural states that did not expand Medicaid may experience greater disparities in MIRs relative to Medicaid expansion states in the future.</p></abstract><kwd-group><kwd>Neoplasms</kwd><kwd>Cancer incidence</kwd><kwd>Cancer mortality</kwd><kwd>Mortality-to-incidence ratio</kwd><kwd>Racial</kwd><kwd>disparities, Congressional Districts, Rurality</kwd></kwd-group></article-meta></front><body><sec id="S1"><label>1.</label><title>Introduction</title><p id="P2">The mortality-to-incidence ratio (MIR) is an indicator of how well a population does after receiving a cancer diagnosis. High MIR values for a region are an indicator of poor cancer outcomes relative to incidence, thereby indicating areas for targeting interventions related to access to screening, treatment and improved survivorship care. The MIR can be computed from readily accessible, public-use data on cancer incidence and mortality for the entire country&#x02013;i.e., without costly and cumbersome data linkage&#x02013;while survival data (considered to be superior to the MIR) is publicly available only for the SEER (Surveillance, Epidemiology, and End Results) database covering a minimal 9 regions or states since 1975 in our nation, or about 9.4% of the entire U.S. population, to slightly over &#x02153; (34.6%) in SEER 18 <ext-link ext-link-type="uri" xlink:href="https://seer.cancer.gov/registries/data.html">https://seer.cancer.gov/registries/data.html</ext-link> (2019). Prior studies have used the MIR to portray disease severity across geographic regions (e.g., county) and by key demographic subgroups such as race/ethnicity (<xref rid="R5" ref-type="bibr">Adams et al., 2015a</xref>, <xref rid="R6" ref-type="bibr">2015b</xref>; <xref rid="R10" ref-type="bibr">Babatunde et al., 2016</xref>; <xref rid="R31" ref-type="bibr">Hebert et al., 2009</xref>; <xref rid="R40" ref-type="bibr">Odahowski et al., 2018</xref>; <xref rid="R47" ref-type="bibr">Sunkara and Hebert, 2015</xref>, <xref rid="R49" ref-type="bibr">2016b</xref>; <xref rid="R53" ref-type="bibr">Wagner et al., 2012</xref>). The recent availability of U.S. congressional district-specific cancer incidence and mortality data from the Centers for Disease Control and Prevention (CDC) United States Cancer Statistics (USCS) visualization tool provides a unique opportunity to calculate and depict the MIR using a fairly consistent denominator across districts (e.g., congressional districts are designed with an average population size of around 711,000), and to contribute to data-driven decision-making at the legislative level.</p><p id="P3">This project was designed to display maps of MIRs by congressional district with the goal of discerning regional patterns. We also compare MIRs in congressional districts nested within states that expanded Medicaid vs. those that did not; which expands on our team&#x02019;s previous work (<xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>), and examine MIR differences by race (i.e., comparing Black vs. non-Hispanic White residents) in expansion and non-expansion states.</p></sec><sec id="S2"><label>2.</label><title>Methods</title><p id="P4">We obtained overall and race-specific 2011&#x02013;2015 age-adjusted incidence and mortality rates for all cancers combined and for the following cancers: [female] breast, cervix, colorectal, esophagus, lung, oral, pancreas, and prostate for each congressional district in the U.S. We then calculated the MIR, by dividing the mortality rate by the incidence rate for each congressional district and cancer type, respectively. Because incidence data were suppressed for Illinois, Kansas, and Minnesota, we were unable to calculate MIRs for congressional districts in these states.</p><p id="P5">We then mapped these MIR values by congressional district for the entire U.S. A color-coded classification method called &#x0201c;natural breaks&#x0201d; was used to distinguish districts with similar values. This method categorizes MIR values according to the data&#x02019;s inherent natural groupings (e.g., minimizes within-group and maximizes between-group differences for each cancer type). Because the data distribution and subsequent groupings differ across cancer types, the maps for each cancer type should be interpreted independently and not compared to each other. The method decreases the likelihood of falsely grouping dissimilar districts together by empirically determining the best-fitting groupings. All of the maps use the same color scheme. US congressional districts with the lowest MIRs are depicted in yellow. Those with the next lowest MIRs are depicted in light green. Those congressional districts with intermediate (i.e. around the median) MIRs are shown in dark green. Those congressional districts with the 2nd to the highest MIRs are depicted by light blue, while those with the highest MIRs are depicted by dark blue. Areas of the country with no data or suppressed data (including all of Illinois, Kansas, and Minnesota) are indicated by crosshatching. All maps were developed using ArcGIS&#x000ae; 10.1 software.</p><p id="P6">We also examined the MIRs by U.S. Census Divisions (n = 9, nested within 4 regions), Medicaid expansion status, and sociodemographic composition. Medicaid expansion status was obtained from the Kaiser Family Foundation and is indicative of the expansion status at the time of this analysis (<xref rid="R34" ref-type="bibr">Kaiser Family Foundation, 2019</xref>). We obtained congressional district-level sociodemographic data (% of residents living in rural areas, % non-Hispanic Black, and % Hispanic) from the U.S. Census Bureau (<xref rid="R52" ref-type="bibr">US Census Bureau, 2019</xref>). We examined race-specific MIRs overall for cancer types where &#x0003c;33% of congressional districts&#x02019; data were suppressed due to too few cases or deaths (i.e., &#x0003c;16 cases/deaths within a congressional district). We performed Analysis of Variance (ANOVA) to examine mean MIRs by Census Division, calculated <italic>t</italic>-tests to examine mean MIR by race and by Medicaid expansion status, and calculated Pearson&#x02019;s correlation coefficients to examine the association between MIR and sociodemographic characteristics. We also performed a <italic>post-hoc</italic> analysis using Tukey&#x02019;s test to examine which mean MIRs by census division were significantly different than one another. All analyses were performed in SAS&#x000ae; 9.4. Data from the CDC are suppressed when small numbers could lead to unstable estimation of incidence or mortality rates, which occurred for some race-specific rates. Thus, race-specific analyses were performed only for cancer types in which the data were suppressed for &#x0003c;33% of congressional districts.</p></sec><sec id="S3"><label>3.</label><title>Results</title><p id="P7"><xref rid="F1" ref-type="fig">Fig. 1</xref> presents the MIR for all cancers combined. Maps revealed that congressional districts in the South and Midwest, particularly the East South Central Census Division including MS, AL, and KY, had higher MIR values (where dark and light blue indicate worst survival) for all cancer types combined, indicating that individuals in these districts died at a higher rate given a cancer diagnosis than those for the country as a whole. Districts within CT, NY, NJ, CA, NV, and the upper Midwest had the lowest MIR values (where yellow to light green indicate best survival); i.e., had better survival given cancer diagnosis. Those areas that have the highest MIRs tend to be in the South and Appalachia and a band west of the Rocky Mountains.</p><p id="P8"><xref rid="F2" ref-type="fig">Fig. 2</xref>, showing female breast cancer MIRs, reveals a similar pattern, where the higher MIRs are concentrated in the South, including the Mississippi Valley, Appalachia, and the southern portion west of the Rocky Mountains. <xref rid="F3" ref-type="fig">Fig. 3</xref>, showing cervical cancer MIRs, reveals high MIRs in the South and Appalachia, Southern Missouri, Western New York, Arizona, Northern California and Western Oregon. <xref rid="F4" ref-type="fig">Fig. 4</xref>, depicting colorectal cancer MIRs, shows a more scattered pattern, with the worst (dark blue) MIRs in Western Oregon, Southern Nevada, New Mexico, Eastern Oklahoma, North Central South Carolina, Eastern Maryland, Southeastern Michigan, Eastern Arkansas, Eastern Virginia and Southeastern Texas. <xref rid="F5" ref-type="fig">Fig. 5</xref> shows that the highest esophageal cancer MIRs are located in areas not previously observed, within a band extending from Northeastern North Carolina through the Great Lakes, the Western Rockies, Northeastern California, Wyoming and South Dakota. <xref rid="F6" ref-type="fig">Fig. 6</xref>, depicting MIRs for lung cancer, also reveals the lowest rates on the East Coast and high rates in Wyoming, Nevada, Southeastern California, Western Oregon, Southern New Mexico, Oklahoma Northern Michigan, Alabama and the Gulf Coast. <xref rid="F7" ref-type="fig">Fig. 7</xref>, depicting oral cancer, shows a pattern similar to less virulent cancers, with the highest MIRs in the South and Appalachia; but high rates also are seen in the Western Rockies, New Mexico, and portions of Southern California and the Pacific Northwest. <xref rid="F8" ref-type="fig">Fig 8</xref>, depicting pancreatic cancer, shows pockets of high MIRs in the West, South, Appalachia and Michigan and Ohio. <xref rid="F9" ref-type="fig">Fig 9</xref> shows that prostate cancer MIRs tend to be higher in the West in general; although there is considerable variability in rates across the country, with high MIRs in parts of the South, Appalachia, Maine, and parts of the Midwest.</p><p id="P9"><xref rid="T1" ref-type="table">Table 1</xref>, showing the mean MIR by U.S. Census Division, parallels the data presented in <xref rid="F1" ref-type="fig">Figs. 1</xref>&#x02013;<xref rid="F9" ref-type="fig">9</xref> within each congressional district. Specifically, districts within New England and the Middle Atlantic states had fairly consistently lower MIRs for all cancer types combined and for all of the individual cancer sites, including the most deadly among these cancers. <italic>Post-hoc</italic> analysis shows that the East South Central Division had significantly higher MIRs than six of the other division, with the highest magnitude difference being with the New England congressional districts. Similar patterns were seen for cervical and lung cancers. For colorectal and prostate cancers MIRs tended to be elevated in the Mountain Census Division relative to other Divisions. Female breast cancer and oral cancer MIRs were higher in congressional districts in the West South Central Division compared to other Divisions. For pancreas cancer, there was less variability in MIRs across Census Divisions, though the Middle Atlantic Division had lower MIRs than other Divisions.</p><p id="P10">Looking at simple racial comparisons (<xref rid="T2" ref-type="table">Table 2</xref>) we found that MIRs were higher for Black [female] breast cancers [0.23 Black vs. 0.16 White; p &#x0003c; .001 based on independent <italic>t</italic>-test]. However, we found that Black individuals had lower MIRs for all cancer types combined [0.41 Black vs. 0.43 White; p &#x0003c; .001] and for lung cancer [0.73 Black vs. 0.85 White; p &#x0003c; .001]. All other cancer sites had &#x02265;33% data suppressed (esophagus, cervix, prostate or pancreas) or there was no significant difference by race (colorectal cancer). We performed a <italic>post-hoc</italic> analysis to examine racial differences in MIRs in the South Census Region, comprised of the South Atlantic, East South Central, and West South Central Divisions, where data are more complete for most cancers across racial groups (i.e. where there are higher proportions of Black residents). We found that MIRs were higher among Black residents than White residents for breast, cervical, prostate, and oral cancers; MIRs were marginally higher among White residents for all cancers combined as well as colorectal and lung cancers. Further, there was no significant difference in esophagus or pancreas cancer MIRs between Black and White residents in the South Census Region.</p><p id="P11"><xref rid="T3" ref-type="table">Table 3</xref> compares MIRs in states that have not expanded Medicaid versus those that have. In general, MIRs are lower in states that expanded Medicaid, consistent with our previous investigation (<xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>). However, cancers of the esophagus and pancreas, the two most deadly cancers of those that we considered, have MIRs that are higher in Medicaid expansion states than in non-expansion states. There were no differences for oral or prostate cancer.</p><p id="P12"><xref rid="T4" ref-type="table">Table 4</xref> provides the correlation coefficients between district-level MIRs and the percent rural, percent non-Hispanic Black, and percent Hispanic. A moderate, statistically significant correlation between the MIR for all cancer types combined and rurality was observed (r = 0.47). For individual cancer types, the highest and lowest correlation for rurality was for lung cancer (0.31) and oral cancer (0.04), respectively. We also observed a positive, significant correlation between the MIR for all cancer types combined and percent non-Hispanic Black residents in the district. The correlations with percent non-Hispanic Black were highest for cervical and breast cancer. Correlations with percent Hispanic residents in the district were highly variable (i.e., with no consistent patterns observed).</p></sec><sec id="S4"><label>4.</label><title>Discussion</title><p id="P13">The availability of cancer incidence and mortality data by U.S congressional district allowed us to examine MIRs stratified by this policy-relevant geopolitical unit for the first time. Generally speaking, there were striking differences in MIRs across the country, with higher MIRs in the South and in other pockets such as Appalachia and the region just west of the Rocky Mountains, not including most of the West Coast. These data provide important information for policy makers about opportunities to further examine the determinants of these mortality (relative to incidence) differentials and to explore potential interventions to reduce cancer burden in areas with high relative mortality, given the underlying incidence of disease.</p><p id="P14">While we cannot infer causality from these analysis, we note that the strongest correlation identified in our study was between the % of the congressional district that lives in a rural area and MIR. Recent studies have shown that rural populations have both higher mortality and incidence rates compared to their urban counterparts (<xref rid="R12" ref-type="bibr">Blake et al., 2017</xref>; <xref rid="R32" ref-type="bibr">Henley et al., 2017</xref>; <xref rid="R61" ref-type="bibr">Zahnd et al., 2018</xref>). So, high MIRs are particularly concerning given that these populations often start out with higher incidence. Further, additional studies have shown that higher mortality rates cluster in the South, which has a large population of rural minorities (<xref rid="R39" ref-type="bibr">Mokdad et al., 2017</xref>; <xref rid="R60" ref-type="bibr">Zahnd et al., 2017</xref>). Results of these descriptive analyses are consistent with those we have seen previously; i.e., elevated county- and state-level MIRs in the South and in more rural areas (<xref rid="R5" ref-type="bibr">Adams et al., 2015a</xref>, <xref rid="R6" ref-type="bibr">2015b</xref>; <xref rid="R10" ref-type="bibr">Babatunde et al., 2016</xref>; <xref rid="R31" ref-type="bibr">Hebert et al., 2009</xref>; <xref rid="R40" ref-type="bibr">Odahowski et al., 2018</xref>; <xref rid="R53" ref-type="bibr">Wagner et al., 2012</xref>). In addition to the high cancer burden, rural areas have low access to cancer screening and cancer specialists (<xref rid="R1" ref-type="bibr">Aboagye et al., 2014</xref>; <xref rid="R21" ref-type="bibr">Eberth et al., 2018</xref>). Congressional district-level maps may help inform public policies and related funding to improve access to early cancer detection, with concomitant downstaging of disease (i.e., detection earlier in disease course), and timely treatment in vulnerable populations. For some cancers such as colorectal (<xref rid="R58" ref-type="bibr">Xirasagar et al., 2015</xref>) and oral (<xref rid="R27" ref-type="bibr">Gupta et al., 1999</xref>), screening allows for removal of precancerous lesions. With ratios of 50 to 200 precancerous lesions for every cancer detected these screening modalities are powerful methods of primary prevention. Further research also can provide additional important information to help identify areas of greatest need for expansion of health care services including for different kinds of cancer screening and related programming (e.g., recruitment of providers for the National Breast and Cervical Cancer Early Detection Program).</p><p id="P15">Results based on Medicaid expansion also are consistent with what we have observed previously with respect to availability of services and probability of dying of a particular cancer (S. A. <xref rid="R7" ref-type="bibr">Adams et al., 2016</xref>; <xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>). Based on that prior work, we know that disparities in cancer screening already disfavor states with high cancer rates (<xref rid="R7" ref-type="bibr">Adams et al., 2016</xref>; <xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>). These disparities in states that have refused Medicaid expansion threaten to widen unless significant efforts are mounted to ensure their residents obtain preventive health care and, subsequently, high-quality cancer treatment. Primary prevention, including via screening modalities such as colonoscopy, is important because it will lower overall burden of disease by reducing the total number of incident cases. Reducing incidence, as opposed to downstaging (detecting earlier in disease course), will have little influence on the MIR. Of course, this is complicated by the fact that some cancers, such as prostate, tend to be indolent &#x02013; with the consequence that early detection would result in lead-time bias.</p><p id="P16">The MIR is dependent on factors that influence the probability of dying once individuals have a cancer, including poor access to and receipt of appropriate and timely cancer treatment. Because the MIR is dependent on incidence it is influenced by factors that allow for detecting the cancer earlier in the disease course and increase effectiveness of care including, but not exclusively, due to downstaging. Experience from Massachusetts, which instituted the Massachusetts Healthcare Reform Law in 2006 shows a significant decrease in mortality among vascular surgery patients (<xref rid="R23" ref-type="bibr">Eslami et al., 2018</xref>). This kind of specialist care also could improve survivorship among cancer patients. Indeed, we have seen similar results for surgical care for cancer after Medicaid expansion, with specific improvements in disparities. (<xref rid="R57" ref-type="bibr">Xiao et al., 2018</xref>) Besides specialist care, there are indications that insurance expansion also will improve community cancer care (<xref rid="R9" ref-type="bibr">Angier et al., 2017</xref>). Effects observed further upstream in terms of improved cancer screening and concomitant downstaging of disease may improve the MIR if fewer patients are diagnosed at later stages of disease when prognosis is generally poor (<xref rid="R25" ref-type="bibr">Gan et al., 2019</xref>; <xref rid="R46" ref-type="bibr">Soni et al., 2018</xref>; <xref rid="R62" ref-type="bibr">Zerhouni et al., 2019</xref>). States rejecting Medicaid expansion tend to suffer from both lower-quality/less-intensive screening and less specialist care (<xref rid="R62" ref-type="bibr">Zerhouni et al., 2019</xref>).</p><p id="P17">Results showing a positive correlation between the MIR and percent of Black residents in the district underline the importance of race as a possible social determinant of cancer survival. Although we cannot infer a causal association due to the ecologic nature of the data, our findings lay the groundwork for future research on the association between race, place, and health outcomes using more rigorous methods. We and others have documented striking racial disparities in cancer rates that especially disproportionately burden Black residents in the South (<xref rid="R2" ref-type="bibr">Adams et al., 2006</xref>, <xref rid="R3" ref-type="bibr">2009</xref>, <xref rid="R4" ref-type="bibr">2012</xref>; <xref rid="R8" ref-type="bibr">Alberg et al., 2006</xref>; <xref rid="R10" ref-type="bibr">Babatunde et al., 2016</xref>; <xref rid="R13" ref-type="bibr">Brandt et al., 2006</xref>; <xref rid="R14" ref-type="bibr">Cavicchia et al., 2012</xref>; <xref rid="R18" ref-type="bibr">Daguise et al., 2006</xref>; <xref rid="R19" ref-type="bibr">Drake et al., 2006</xref>; <xref rid="R24" ref-type="bibr">Esnaola and Ford, 2012</xref>; <xref rid="R29" ref-type="bibr">Hebert et al., 2006a</xref>, <xref rid="R30" ref-type="bibr">2006b</xref>, <xref rid="R31" ref-type="bibr">2009</xref>; <xref rid="R41" ref-type="bibr">Peres et al., 2017</xref>; <xref rid="R42" ref-type="bibr">Samson et al., 2016</xref>; <xref rid="R45" ref-type="bibr">Smith et al., 2008</xref>; <xref rid="R51" ref-type="bibr">Tong et al., 2015</xref>; <xref rid="R53" ref-type="bibr">Wagner et al., 2012</xref>; <xref rid="R59" ref-type="bibr">Yen et al., 2006</xref>). Looking at the pattern of MIRs nationally, however, we observed departures from the pattern observed in the South. Most striking was that there were an inverse correlations between % Non-Hispanic Black population composition and MIRs for the two most fatal of all cancer sites &#x02013; esophagus and pancreas.</p><p id="P18">Future work should focus on differences in grade and stage of disease by race across different geographic regions, especially in light of the observation that Blacks often present with more virulent disease (<xref rid="R35" ref-type="bibr">Krok-Schoen et al., 2016</xref>; <xref rid="R36" ref-type="bibr">Laryea et al., 2014</xref>; <xref rid="R44" ref-type="bibr">Siegel et al., 2018</xref>; <xref rid="R50" ref-type="bibr">Tammana and Laiyemo, 2014</xref>; <xref rid="R53" ref-type="bibr">Wagner et al., 2012</xref>) including esophageal and pancreatic cancers.(<xref rid="R17" ref-type="bibr">Cronin et al., 2018</xref>; <xref rid="R26" ref-type="bibr">Gold and Goldin, 1998</xref>; <xref rid="R37" ref-type="bibr">Lowenfels and Maisonneuve, 2002</xref>). Further, as additional years of post-Affordable Care Act data accumulate to minimize the occurrence of unstable rate estimates/data suppression, the dynamic of race and Medicaid expansion status should be explored further, In the meantime, however, we should remain mindful of work by Zerhouni et al highlighting the relevance of Medicaid expansion in helping to reduce overall cancer disparities (<xref rid="R62" ref-type="bibr">Zerhouni et al., 2019</xref>).</p><p id="P19">As with other work based on MIRs (<xref rid="R5" ref-type="bibr">Adams et al., 2015a</xref>, <xref rid="R6" ref-type="bibr">2015b</xref>; <xref rid="R10" ref-type="bibr">Babatunde et al., 2016</xref>; <xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>; <xref rid="R31" ref-type="bibr">Hebert et al., 2009</xref>; <xref rid="R40" ref-type="bibr">Odahowski et al., 2018</xref>; <xref rid="R48" ref-type="bibr">Sunkara and Hebert, 2016a</xref>, <xref rid="R49" ref-type="bibr">2016b</xref>; <xref rid="R53" ref-type="bibr">Wagner et al., 2012</xref>), these finding can help guide dissemination and implementation research focused on cancer prevention and control (<xref rid="R54" ref-type="bibr">Wheeler and Basch, 2017</xref>). Many of these cancers have known modifiable risk factors and there are evidence-based interventions that can be applied in many populations. Future work also could include targeting the cancer care continuum ranging from age- and other factor-appropriate screening to, especially, post-diagnosis care. It also is true that not all such interventions are tested for use in rural and minority populations (<xref rid="R55" ref-type="bibr">Wheeler and Davis, 2017</xref>); so, that issue needs to be addressed irrespective of our specific findings.</p><p id="P20">It is worth noting that other investigations have compared the MIR to 1-surival functions and found the MIR to have variable accuracy with the survival function, dependent upon cancer type (<xref rid="R22" ref-type="bibr">Ellis et al., 2019</xref>). We do not dispute that modeling survival data is the most accurate method available to ascertain true, absolute survival rates; however, we must point out that the data needed for survival calculations is not publicly available for our entire nation. All US cancer registries report to either SEER or the National Program of Cancer Registries (NPCR). SEER makes survival variables publicly available for all its cancer cases; however, NPCR does not have the capacity to do this. As SEER covers only about a third of the cancer population in the newest, most expansive version (<xref rid="R20" ref-type="bibr">Duggan et al., 2016</xref>), we are not able to run survival models on the vast majority of cancer cases. Hence, the MIR has enhanced utility as it is the only methodology practically available to compare cancer mortality accounting for cancer incidence. By virtue of the limitations listed by others, the MIR should not be taken as an absolute measure of survival; however, it provides a useful statistic to make geographic and demographic comparisons as we have done here.</p><p id="P21">This study is not without limitations. First, for all analyses, there were no data for three Midwestern states, which includes 30 congressional districts (7% of all districts in the U.S.). Additionally, due to limited availability of race-specific data for individual cancer types due to data suppression, we were unable to fully explore racial differences by congressional district across the United States. It also should be noted that racial comparisons do not generalize nationwide, as racial/ethnic subgroups are not uniformly distributed across states or districts. Further, as with any spatial analysis, we must be cognizant of the modifiable areal unit problem and zoning effects, where MIR values may vary dependent upon where the boundaries are drawn (<xref rid="R56" ref-type="bibr">Wong, 2009</xref>). This problem is particularly salient with congressional districts whose boundaries are not derived independently or objectively. Despites these weakness, this study has several strengths. It is the first to examine MIR by congressional district, as previous studies had examined mortality rates alone (<xref rid="R28" ref-type="bibr">Hao et al., 2006</xref>; <xref rid="R43" ref-type="bibr">Siegel et al., 2015</xref>). Second, this paper displays policy-relevant maps, which can be helpful tools to inform the public and policymakers alike (<xref rid="R11" ref-type="bibr">Bell et al., 2006</xref>). Finally, although more work needs to be done to verify its relationship with 1-survival (<xref rid="R16" ref-type="bibr">Cordero-Morales et al., 2016</xref>; <xref rid="R22" ref-type="bibr">Ellis et al., 2019</xref>), the MIR has been shown to be a good proxy where it is cumbersome, difficult, expensive or impossible to compute survival (J.R. <xref rid="R31" ref-type="bibr">Hebert et al., 2009</xref>; <xref rid="R40" ref-type="bibr">Odahowski et al., 2018</xref>; <xref rid="R47" ref-type="bibr">Sunkara and Hebert, 2015</xref>, <xref rid="R48" ref-type="bibr">2016a</xref>, <xref rid="R49" ref-type="bibr">2016b</xref>). Although some work has been done to examine the relationship between MIR values and 1-survival (<xref rid="R40" ref-type="bibr">Odahowski et al., 2018</xref>), research should explore the relationship between MIR and 1-survival for various cancer types.</p><p id="P22">In summary, our results confirmed previous findings regarding rurality, showing that populations with larger rural constituencies had higher MIRs than their counterparts. These results also confirm what we demonstrated earlier regarding higher MIRs in states without Medicaid expansion (<xref rid="R7" ref-type="bibr">Adams et al., 2016</xref>; <xref rid="R15" ref-type="bibr">Choi et al., 2015</xref>). Moreover, lack of health insurance is a major underlying and modifiable risk factor. While studies have shown the advantages of Medicaid expansion for a variety of health outcomes, expansion alone will not ensure full and high-quality coverage for all residents, particularly given the prevalence of high-deductible and &#x0201c;junk insurance&#x0201d; plans (<xref rid="R38" ref-type="bibr">Mazurenko et al., 2019</xref>; <xref rid="R63" ref-type="bibr">Zhao et al., 2019</xref>;<xref rid="R64" ref-type="bibr">Zheng et al., 2019a</xref>, <xref rid="R65" ref-type="bibr">2019b</xref>). That is, states that have rejected Medicaid expansion start out from a worse position in terms of cancer mortality given incidence. It also is important to note that some results were inconsistent with other studies, especially the lack of consistently lower MIRs in Whites. Additional work is needed to examine these race-specific MIRs across regions rather than aggregated nationally. Future work should also move beyond descriptive studies toward meaningful use of the MIR to inform dissemination and implementation research and health policy efforts. As a final note, this work also highlights the need for one central cancer registry system with common data elements which are publicly available or at least available through a standardized requesting process that does not require membership fees in order to be considered.</p></sec><sec id="S5"><label>5.</label><title>Conclusions</title><p id="P23">Using newly available data based on U.S. congressional districts we found significant differences in MIRs according to region, race and Medicaid expansion. In general, Blacks have higher MIRs than Whites, rural areas have higher rates than urban and suburban districts, and congressional districts in states that have refused Medicaid expansion have higher rates than those of states that have adopted Medicaid expansion. Future work should include monitoring MIRs in relation to demographic trends and changes in health care financing and utilization.</p></sec></body><back><ack id="S6"><title>Acknowledgments</title><p id="P24">Funding was provided by the Centers for Disease Control and Prevention under the Prevention Research Centers through Special Interest Project Cancer Prevention and Control Research Networks #3 U48 DP005000&#x02013;01S2 to the University of South Carolina at Columbia (JRH, JME, WEZ, SAA, DBF) and #3 U48 DP005017&#x02013;01S8 to the University of North Carolina Chapel Hill (SBW).</p><p id="P25">Publication of this supplement was supported by the Cancer Prevention and Control Network (CPCRN), University of North Carolina at Chapel Hill and the following co-funders: Case Western Reserve University, Oregon Health &#x00026; Science University, University of South Carolina, University of Iowa, University of Kentucky, University of Pennsylvania and University of Washington.</p></ack><ref-list><title>References</title><ref id="R1"><mixed-citation publication-type="journal"><name><surname>Aboagye</surname><given-names>JK</given-names></name>, <name><surname>Kaiser</surname><given-names>HE</given-names></name>, <name><surname>Hayanga</surname><given-names>AJ</given-names></name>, <year>2014</year>
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<volume>125</volume> (<issue>10</issue>), <fpage>1737</fpage>&#x02013;<lpage>1747</lpage>. <pub-id pub-id-type="doi">10.1002/cncr.31913</pub-id><comment>.</comment><pub-id pub-id-type="pmid">30663039</pub-id></mixed-citation></ref></ref-list></back><floats-group><fig id="F1" orientation="portrait" position="float"><label>Fig. 1.</label><caption><p id="P26">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for All Cancers Combined</p></caption><graphic xlink:href="nihms-1566286-f0001"/></fig><fig id="F2" orientation="portrait" position="float"><label>Fig. 2.</label><caption><p id="P27">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Breast Cancer</p></caption><graphic xlink:href="nihms-1566286-f0002"/></fig><fig id="F3" orientation="portrait" position="float"><label>Fig. 3.</label><caption><p id="P28">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0003"/></fig><fig id="F4" orientation="portrait" position="float"><label>Fig. 4.</label><caption><p id="P29">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0004"/></fig><fig id="F5" orientation="portrait" position="float"><label>Fig. 5.</label><caption><p id="P30">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0005"/></fig><fig id="F6" orientation="portrait" position="float"><label>Fig. 6.</label><caption><p id="P31">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0006"/></fig><fig id="F7" orientation="portrait" position="float"><label>Fig. 7.</label><caption><p id="P32">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0007"/></fig><fig id="F8" orientation="portrait" position="float"><label>Fig. 8.</label><caption><p id="P33">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0008"/></fig><fig id="F9" orientation="portrait" position="float"><label>Fig. 9.</label><caption><p id="P34">Depiction of the Mortality-to-Incidence Ratio by US Congressional District for Cervical Cancer</p></caption><graphic xlink:href="nihms-1566286-f0009"/></fig><table-wrap id="T1" position="float" orientation="landscape"><label>Table 1</label><caption><p id="P35">Mean mortality-to-incidence ratio by U.S. Census Division.</p></caption><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/></colgroup><thead><tr><th rowspan="3" align="left" valign="top" colspan="1"/><th colspan="2" align="left" valign="top" rowspan="1">Northeast</th><th colspan="2" align="left" valign="top" rowspan="1">Midwest</th><th colspan="3" align="left" valign="top" rowspan="1">South</th><th colspan="2" align="left" valign="top" rowspan="1">West</th><th align="left" valign="top" rowspan="1" colspan="1"/></tr><tr><th colspan="2" align="left" valign="top" rowspan="1"><hr/></th><th colspan="2" align="left" valign="top" rowspan="1"><hr/></th><th colspan="3" align="left" valign="top" rowspan="1"><hr/></th><th colspan="2" align="left" valign="top" rowspan="1"><hr/></th><th align="left" valign="top" rowspan="1" colspan="1"><hr/></th></tr><tr><th align="left" valign="top" rowspan="1" colspan="1">New England Mean (SD) (n=21 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">Middle Atlantic Mean (SD) (n=57 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">East nNorth cCentral Mean (SD) (n=65 districts)<sup><xref rid="TFN1" ref-type="table-fn">a</xref></sup></th><th align="left" valign="top" rowspan="1" colspan="1">West nNorth cCentral Mean (SD) (n=29 districts)<sup><xref rid="TFN1" ref-type="table-fn">a</xref></sup></th><th align="left" valign="top" rowspan="1" colspan="1">South Atlantic Mean (SD) (n=85 Districts)</th><th align="left" valign="top" rowspan="1" colspan="1">East sSouth cCentral Mean (SD) (n=26 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">West sSouth cCentral Mean (SD) (n=51 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">Mountain Mean (SD) (n=31 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">Pacific Mean (SD) (n=71 districts)</th><th align="left" valign="top" rowspan="1" colspan="1">P-value</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Overall</td><td align="left" valign="top" rowspan="1" colspan="1">0.34 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.33 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.37 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.37 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.40 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.39 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.36 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.36 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Breast (female)</td><td align="left" valign="top" rowspan="1" colspan="1">0.14 (0.01)</td><td align="left" valign="top" rowspan="1" colspan="1">0.16 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.17 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.16 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.17 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.17 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.16 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Cervix</td><td align="left" valign="top" rowspan="1" colspan="1">0.25 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.06)</td><td align="left" valign="top" rowspan="1" colspan="1">0.31 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.35 (0.06)</td><td align="left" valign="top" rowspan="1" colspan="1">0.32 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Colorectal</td><td align="left" valign="top" rowspan="1" colspan="1">0.34 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.35 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.36 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.37 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.39 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.37 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Esophagus</td><td align="left" valign="top" rowspan="1" colspan="1">0.83 (0.06)</td><td align="left" valign="top" rowspan="1" colspan="1">0.86 (0.09)</td><td align="left" valign="top" rowspan="1" colspan="1">0.94 (0.06)</td><td align="left" valign="top" rowspan="1" colspan="1">0.92 (0.09)</td><td align="left" valign="top" rowspan="1" colspan="1">0.87 (0.07)</td><td align="left" valign="top" rowspan="1" colspan="1">0.88 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">0.86 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">0.92 (0.07)</td><td align="left" valign="top" rowspan="1" colspan="1">0.90 (0.07)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Lung</td><td align="left" valign="top" rowspan="1" colspan="1">0.66 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.67 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.74 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.72 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.72 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.76 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.74 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.73 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.74 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Oral</td><td align="left" valign="top" rowspan="1" colspan="1">0.19 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.19 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.22 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.20 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.21 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.23 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.24 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.21 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.24 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Pancreas</td><td align="left" valign="top" rowspan="1" colspan="1">0.87 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.82 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.90 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.87 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.86 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.89 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.87 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.88 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.88 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Prostate</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.15 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.19 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.19 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.21 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.20 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr></tbody></table><table-wrap-foot><fn id="TFN1"><label>a</label><p id="P36">East north central = 47 districts and west north central = 25 districts for cancer-specific MIRs due to data suppression.</p></fn></table-wrap-foot></table-wrap><table-wrap id="T2" position="float" orientation="portrait"><label>Table 2</label><caption><p id="P37">Mean mortality-to-incidence ratio by race.</p></caption><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/></colgroup><thead><tr><th align="left" valign="top" rowspan="1" colspan="1"/><th align="left" valign="top" rowspan="1" colspan="1">White Mean (SD)</th><th align="left" valign="top" rowspan="1" colspan="1">Black Mean (SD)</th><th align="left" valign="top" rowspan="1" colspan="1">P-value<sup><xref rid="TFN2" ref-type="table-fn">a</xref></sup></th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Breast (female)</td><td align="left" valign="top" rowspan="1" colspan="1">0.16 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.23 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Cervix</td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Colorectal</td><td align="left" valign="top" rowspan="1" colspan="1">0.43 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.44 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">0.40</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Esophagus</td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Lung</td><td align="left" valign="top" rowspan="1" colspan="1">0.85 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">0.73 (0.10)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Oral</td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Pancreas</td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Prostate</td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1"><sup><xref rid="TFN3" ref-type="table-fn">b</xref></sup></td></tr></tbody></table><table-wrap-foot><fn id="TFN2"><label>a</label><p id="P38">Independent t-test.</p></fn><fn id="TFN3"><label>b</label><p id="P39">Not reported due to at least 33% of districts with suppressed data.</p></fn></table-wrap-foot></table-wrap><table-wrap id="T3" position="float" orientation="portrait"><label>Table 3</label><caption><p id="P40">Mean mortality-to-incidence ratio by Medicaid expansion status.</p></caption><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/></colgroup><thead><tr><th align="left" valign="top" rowspan="1" colspan="1"/><th align="left" valign="top" rowspan="1" colspan="1">Districts in expansion states (n = 291 districts) Mean (SD)</th><th align="left" valign="top" rowspan="1" colspan="1">Districts in non-expansion states (n = 144 districts) Mean (SD)</th><th align="left" valign="top" rowspan="1" colspan="1">P-value</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">All</td><td align="left" valign="top" rowspan="1" colspan="1">0.36 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Colorectal<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.37 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.38 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.002</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Esophagus<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.89 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">0.86 (0.08)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Cervical<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.30 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.32 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Breast (female)<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.17 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.02)</td><td align="left" valign="top" rowspan="1" colspan="1">&#x0003c;0.001</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Lung<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.72 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.73 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.003</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Oral<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.22 (0.04)</td><td align="left" valign="top" rowspan="1" colspan="1">0.22 (0.03)</td><td align="left" valign="top" rowspan="1" colspan="1">0.14</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Pancreas<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.87 (0.05)<sup><xref rid="TFN5" ref-type="table-fn">b</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.86 (0.05)</td><td align="left" valign="top" rowspan="1" colspan="1">0.05</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Prostate<sup><xref rid="TFN4" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.18 (0.03)<sup><xref rid="TFN6" ref-type="table-fn">c</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.19 (0.03)<sup><xref rid="TFN7" ref-type="table-fn">d</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.28</td></tr></tbody></table><table-wrap-foot><fn id="TFN4"><label>a</label><p id="P41">Includes 265 expansion state districts and 140 non-expansion districts due to data suppression.</p></fn><fn id="TFN5"><label>b</label><p id="P42">Based on analysis of variance.</p></fn><fn id="TFN6"><label>c</label><p id="P43">Includes 247 and 261 expansion state districts for white and black, respectively and 140 non-expansion districts for both black and white MIRs due to data suppression.</p></fn><fn id="TFN7"><label>d</label><p id="P44">Includes 247 and 231 expansion state districts for white and black, respectively and 140 and 133 non-expansion districts for white and black, respectively, due to data suppression.</p></fn></table-wrap-foot></table-wrap><table-wrap id="T4" position="float" orientation="portrait"><label>Table 4</label><caption><p id="P45">Pearson correlation coefficients between mortality-to-incidence ratio and rural and racial/ethnic composition.</p></caption><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/></colgroup><thead><tr><th align="left" valign="top" rowspan="1" colspan="1"/><th align="left" valign="top" rowspan="1" colspan="1">% Rural</th><th align="left" valign="top" rowspan="1" colspan="1">% Non-Hispanic Black</th><th align="left" valign="top" rowspan="1" colspan="1">% Hispanic</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">All</td><td align="left" valign="top" rowspan="1" colspan="1">0.47<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.15<sup><xref rid="TFN10" ref-type="table-fn">**</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.08</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Breast (female)<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.17<sup><xref rid="TFN10" ref-type="table-fn">**</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.36<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.14<sup><xref rid="TFN10" ref-type="table-fn">**</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Cervical<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.10</td><td align="left" valign="top" rowspan="1" colspan="1">0.30<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.02</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Colorectal<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.23<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.21<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.002</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Esophagus<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.22<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.14<sup><xref rid="TFN9" ref-type="table-fn">*</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.15<sup><xref rid="TFN10" ref-type="table-fn">**</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Lung<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.31<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.009</td><td align="left" valign="top" rowspan="1" colspan="1">0.04</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Oral<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.04</td><td align="left" valign="top" rowspan="1" colspan="1">0.21<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.25<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Pancreas<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.28<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.13<sup><xref rid="TFN9" ref-type="table-fn">*</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.08</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Prostate<sup><xref rid="TFN8" ref-type="table-fn">a</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">0.16<sup><xref rid="TFN10" ref-type="table-fn">**</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">&#x02212;0.06</td><td align="left" valign="top" rowspan="1" colspan="1">0.18<sup><xref rid="TFN11" ref-type="table-fn">***</xref></sup></td></tr></tbody></table><table-wrap-foot><fn id="TFN8"><label>a</label><p id="P46">Includes 405 congressional districts due to data suppression.</p></fn><fn id="TFN9"><label>*</label><p id="P47">p &#x0003c; .05.</p></fn><fn id="TFN10"><label>**</label><p id="P48">p &#x0003c; .01.</p></fn><fn id="TFN11"><label>***</label><p id="P49">p &#x0003c; .001.</p></fn></table-wrap-foot></table-wrap></floats-group></article>