Risk of diffuse large B-cell lymphoma after solid organ transplantation in the United States

Details

• Alternative Title:
  Am J Hematol
• Personal Author:
  Gibson, Todd M. ; Engels, Eric A. ; Clarke, Christina A. ; Lynch, Charles F. ; Weisenburger, Dennis D. ; Morton, Lindsay M.
• Description:
  Non-Hodgkin lymphoma arising in the context of immunosuppression is an important adverse outcome after solid organ transplantation. Diffuse large B-cell lymphoma (DLBCL) is the most commonly diagnosed subtype of post-transplantation non-Hodgkin lymphoma, but few studies of transplant recipients have examined subtype-specific risks. Therefore, we examined DLBCL risk in the Transplant Cancer Match Study, including registry-based cancer ascertainment among 96,615 solid organ transplants performed from 2000 to 2008. We determined standardized incidence ratios (SIRs) and 95% confidence intervals comparing DLBCL risk in transplant recipients with that in the general population, and used multivariable Poisson regression models to assess the impact of potential risk factors. We identified 321 incident cases of DLBCL, over 12 times more than expected based on general population rates (SIR = 12.6, 95% confidence interval = 11.2-14.0). SIRs were highest in young recipients and those receiving a lung or pancreas/kidney-pancreas transplant, and were greatly elevated for extranodal DLBCLs at the site of the transplantation compared with other sites. DLBCL risk was highest in the first year following transplantation, and SIRs for early-onset DLBCL risk were elevated in association with Epstein-Barr virus-negative serostatus and use of polyclonal antibody induction therapy. In conclusion, associations between recipient and transplant factors and post-transplantation DLBCL risk suggest a complicated interrelationship among multiple risk factors and timing of disease.
• Subjects:
  Adolescent Aged Child Child, Preschool Cohort Studies Female Humans Infant Infant, Newborn Lymphoma, Large B-Cell, Diffuse Male Middle Aged Organ Transplantation Risk Factors Young Adult

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• Source:
  Am J Hematol. 89(7):714-720.
• Pubmed ID:
  24753070
• Pubmed Central ID:
  PMC4069221
• Document Type:
  Journal Article
• Funding:
  1U58 DP000807-01/DP/NCCDPHP CDC HHS/United States ; 1US58/DP0039311-01/DP/NCCDPHP CDC HHS/United States ; 5U58DP000812-03/DP/NCCDPHP CDC HHS/United States ; 5U58DP000824-04/DP/NCCDPHP CDC HHS/United States ; 5U58DP003875-01/DP/NCCDPHP CDC HHS/United States ; DP000805-04/DP/NCCDPHP CDC HHS/United States ; HHSN261201000024C/CA/NCI NIH HHS/United States ; HHSN261201000026C/CA/NCI NIH HHS/United States ; HHSN261201000027C/CA/NCI NIH HHS/United States ; HHSN261201000032C/CA/NCI NIH HHS/United States ; HHSN261201000034C/CA/NCI NIH HHS/United States ; HHSN261201000035C/CA/NCI NIH HHS/United States ; HHSN261201000036C/CA/NCI NIH HHS/United States ; HHSN261201000037C/CA/NCI NIH HHS/United States ; N01-PC-20100-027./PC/NCI NIH HHS/United States ; N01-PC-35137/PC/NCI NIH HHS/United States ; N01-PC-35139/PC/NCI NIH HHS/United States ; N01-PC-35142/PC/NCI NIH HHS/United States ; N01-PC-35143/PC/NCI NIH HHS/United States ; P30 CA086862/CA/NCI NIH HHS/United States ; U58 DP000848-04/DP/NCCDPHP CDC HHS/United States ; U58DP000832/DP/NCCDPHP CDC HHS/United States ; U58DP0038789/DP/NCCDPHP CDC HHS/United States ; Intramural NIH HHS/United States
• Place as Subject:
  United States
• Volume:
  89
• Issue:
  7
• Collection(s):
  CDC Public Access
• Main Document Checksum:
  urn:sha256:5748c01b48fa1409f2bcec1f65eec127ba50330105822c1efa3036e65abfaaec
• Download URL:
  https://stacks.cdc.gov/view/cdc/30012/cdc_30012_DS1.pdf
• File Type:
  [PDF - 331.46 KB ]