4.7 Article

Long-term outcomes in patients with relapsed or refractory hairy cell leukemia treated with vemurafenib monotherapy

Journal

BLOOD
Volume 140, Issue 25, Pages 2663-2671

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood.2022016183

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Funding

  1. NIH/NCI [1P50 254838-01]
  2. Hairy Cell Leukemia Foundation/Leukemia & Lymphoma Society Synergistic Team Award

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In patients with relapsed/refractory hairy cell leukemia (HCL), vemurafenib has shown high response rates. This study reports that the overall response rate was 86% in 36 patients treated with vemurafenib, with 33% complete response and 53% partial response. Relapses occurred in 68% of responders, but retreatment with vemurafenib showed a 86% complete hematologic response rate.
Vemurafenib, an oral BRAF inhibitor, has demonstrated high response rates in relapsed/ refractory (R/R) hairy cell leukemia (HCL). However, little is known about long-term out-comes and response to retreatment. Herein, we report the results of 36 patients with R/R HCL treated with vemurafenib from the United States arm of the phase 2 clinical trial (NCT01711632). The best overall response rate was 86%, including 33% complete response (CR) and 53% partial response (PR). After a median follow-up of 40 months, 21 of 31 responders (68%) experienced relapse with a median relapse-free survival (RFS) of 19 months (range, 12.5-53.9 months). There was no significant difference in the RFS for patients with CR vs PR. Fourteen of 21 (67%) relapsed patients were retreated with vemurafenib, with 86% achieving complete hematologic response. Two patients acquired resistance to vemurafenib with the emergence of new KRAS and CDKN2A mutations, respectively. Six of 12 (50%) responders to vemurafenib retreatment experienced another relapse with a median RFS of 12.7 months. Overall survival (OS) was 82% at 4 years, with a significantly shorter OS in patients who relapsed within 1 year of initial treatment with vemurafenib. Higher cumulative doses or a longer duration of treatment did not lengthen the durability of response. All adverse events in the retreatment cohort were grade 1/2 except for 1 case of a grade 3 rash and 1 grade 3 fever/pneumonia. Our data suggest that vemur-afenib retreatment is a safe and effective option for patients with R/R HCL.

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