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Denileukin diftitox for the treatment of CD25 low-expression mycosis fungoides and Sezary syndrome.


ABSTRACT: In a placebo-controlled study, denileukin diftitox (DD) was effective against cutaneous T-cell lymphoma (CTCL) expressing CD25. An open-label companion study examined the efficacy and safety of DD in 36 patients with skin biopsies containing < 20% CD25 cells by immunohistochemistry staining (CD25 low expression). Patients received DD 18 ?g/kg/day for 5 consecutive days every 3 weeks for up to eight courses. The primary endpoint, overall response rate, was 30.6% (95% confidence interval: 16.3, 48.1), 33.3% for stage IIA or lower disease, and 26.7% for stage IIB or greater disease. Median progression-free survival (PFS) was > 487 days, and median time to treatment failure was 68.5 days. No difference in PFS by disease stage was observed. The safety profile of DD in CD25 low-expression disease was similar to that in CD25+ disease. These findings suggest that CD25 low expression does not preclude a meaningful clinical response to DD in patients with CTCL.

SUBMITTER: Prince HM 

PROVIDER: S-EPMC3523809 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Denileukin diftitox for the treatment of CD25 low-expression mycosis fungoides and Sézary syndrome.

Prince H Miles HM   Martin Ann G AG   Olsen Elise A EA   Fivenson David P DP   Duvic Madeleine M  

Leukemia & lymphoma 20120914 1


In a placebo-controlled study, denileukin diftitox (DD) was effective against cutaneous T-cell lymphoma (CTCL) expressing CD25. An open-label companion study examined the efficacy and safety of DD in 36 patients with skin biopsies containing < 20% CD25 cells by immunohistochemistry staining (CD25 low expression). Patients received DD 18 μg/kg/day for 5 consecutive days every 3 weeks for up to eight courses. The primary endpoint, overall response rate, was 30.6% (95% confidence interval: 16.3, 48  ...[more]

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