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DIRECT‐ACTING ANTIVIRALS DURING OR AFTER IMMUNO‐CHEMOTHERAPY IN HEPATITIS C VIRUS‐ASSOCIATED DIFFUSE LARGE B‐CELL LYMPHOMAS

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vs 10.7%, p = 0.18) GVHD were also comparable as well as 2‐year GVHD free/relapse‐free survival (FB2: 44.4% vs 42.8%, p = 0.38). In multivariate analysis, there was a trend… Click to show full abstract

vs 10.7%, p = 0.18) GVHD were also comparable as well as 2‐year GVHD free/relapse‐free survival (FB2: 44.4% vs 42.8%, p = 0.38). In multivariate analysis, there was a trend for worse outcome using FB3/FB4 regimens (OS: HR 1.46, 95%CI: 0.96‐2.23, p = 0.07; LFS: HR 1.43, 95%CI: 0.99‐2.06, p = 0.05; RI: HR 1.54, 95%CI: 0.95‐2.48, p = 0.07). These results were also confirmed using a propensity score‐matching strategy including 184 FB2 and 98 FB3/4 patients. Conclusion: This large retrospective study showed that reduced toxicity myeloablative fludarabine/busulfan regimens did not improve outcomes of adults allografted for NHL. FB2 conditioning regimen still should be considered as the standard of care conditioning regimen in this setting.

Keywords: chemotherapy hepatitis; direct acting; antivirals immuno; hepatitis virus; immuno chemotherapy; acting antivirals

Journal Title: Hematological Oncology
Year Published: 2017

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