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Long-term Outcomes in Patients with Relapsed Or refractory Hairy Cell Leukemia Treated with Vemurafenib Monotherapy

Abstract

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 outcomes 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 vemurafenib retreatment is a safe and effective option for patients with R/R HCL.

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References
1.
Antonello Z, Hsu N, Bhasin M, Roti G, Joshi M, Van Hummelen P . Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAF. Oncotarget. 2017; 8(49):84743-84760. PMC: 5689570. DOI: 10.18632/oncotarget.21262. View

2.
Liebers N, Roider T, Bohn J, Haberbosch I, Pircher A, Ferstl B . BRAF inhibitor treatment in classic hairy cell leukemia: a long-term follow-up study of patients treated outside clinical trials. Leukemia. 2019; 34(5):1454-1457. DOI: 10.1038/s41375-019-0646-y. View

3.
Smalley K, Lioni M, Palma M, Xiao M, Desai B, Egyhazi S . Increased cyclin D1 expression can mediate BRAF inhibitor resistance in BRAF V600E-mutated melanomas. Mol Cancer Ther. 2008; 7(9):2876-83. PMC: 2651569. DOI: 10.1158/1535-7163.MCT-08-0431. View

4.
Robert C, Arnault J, Mateus C . RAF inhibition and induction of cutaneous squamous cell carcinoma. Curr Opin Oncol. 2010; 23(2):177-82. DOI: 10.1097/CCO.0b013e3283436e8c. View

5.
Tiacci E, Trifonov V, Schiavoni G, Holmes A, Kern W, Martelli M . BRAF mutations in hairy-cell leukemia. N Engl J Med. 2011; 364(24):2305-15. PMC: 3689585. DOI: 10.1056/NEJMoa1014209. View