Mature outcomes and prognostic indices in diffuse large B-cell lymphoma in Malawi: a prospective cohort
Supporting Files
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2 2019
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File Language:
English
Details
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Alternative Title:Br J Haematol
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Personal Author:Painschab, Matthew S.
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Kasonkanji, Edwards
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Zuze, Takondwa
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Kaimila, Bongani
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Tomoka, Tamiwe
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Nyasosela, Richard
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Nyirenda, Ruth
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Dhungel, Bal M.
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Mulenga, Maurice
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Chikasema, Maria
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Tewete, Blessings
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Mtangwanika, Asekanadziwa
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Chiyoyola, Sarah
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Mhango, Wilberforce
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Chimzimu, Fred
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Kampani, Coxcilly
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Krysiak, Robert
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Shea, Thomas C.
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Montgomery, Nathan D.
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Fedoriw, Yuri
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Gopal, Satish
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Description:Outcomes for diffuse large B-cell lymphoma (DLBCL) in sub-Saharan Africa (SSA) are poorly described. We report mature data from one of the first prospective SSA cohorts. Patients aged ≥18 years with DLBCL were enrolled in Malawi 2013-2017. Participants were treated with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy and concurrent antiretroviral therapy (ART) if positive for human immunodeficiency virus (HIV+). Eighty-six participants (mean age 47 years, standard deviation 13) were enrolled: 54 (63%) were male and 51 (59%) were HIV+, of whom 34 (67%) were on ART at DLBCL diagnosis. Median CD4 count was 0·113 cells × 10| /l (interquartile range [IQR] 0·062-0·227) and 25 (49%) had HIV viral load <400 copies/μl. Participants received median six cycles CHOP (IQR 4-6). No patients were lost to follow-up and the 2-year overall survival was 38% (95% confidence interval 28-49). In multivariable analyses, Eastern Cooperative Oncology Group performance status (PS) ≥2 and lactate dehydrogenase (LDH) >2× upper limit of normal (ULN) were associated with mortality. HIV status was not associated with mortality. A simplified prognostic model of LDH >2× ULN and PS ≥2 performed at least as well as the age-adjusted International Prognostic Index. DLBCL can be successfully treated in SSA and outcomes did not differ by HIV status. A simplified prognostic model prognosticates well and may be easier to use in resource-limited settings but requires validation.
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Keywords:
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Source:Br J Haematol. 184(3):364-372
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Pubmed ID:30450671
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Pubmed Central ID:PMC6340743
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Document Type:
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Funding:K01 TW009488/TW/FIC NIH HHSUnited States/ ; U54 CA190152/CA/NCI NIH HHSUnited States/ ; P20 CA210285/CA/NCI NIH HHSUnited States/ ; P30 CA016086/CA/NCI NIH HHSUnited States/ ; L30 CA233709/CA/NCI NIH HHSUnited States/ ; UM1 CA121947/CA/NCI NIH HHSUnited States/ ; R21 CA180815/CA/NCI NIH HHSUnited States/ ; U01 CA121947/CA/NCI NIH HHSUnited States/ ; D43 TW009340/TW/FIC NIH HHSUnited States/
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Volume:184
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Issue:3
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Collection(s):
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Main Document Checksum:urn:sha256:96facb6f8564744a40c3a8113e655ec944c78a2a69399e6d93a81e6a5b317deb
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Download URL:
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File Type:
Supporting Files
File Language:
English
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