| Literature DB >> 30520026 |
Jayadev M Umakanthan1, Javeed Iqbal2, Connie L Batlevi3, Alyssa Bouska2, Lynette M Smith4, Valerie Shostrom4, Heather Nutsch1, Basem M William5, R Gregory Bociek1, Matthew Lunning1, Philip Bierman1, Anas Younes3, James O Armitage1, Julie M Vose1.
Abstract
Relapsed or refractory non-Hodgkin lymphomas (NHLs) often carry poor prognosis and pose management challenges. We evaluated the safety and efficacy of dasatinib, a broad-spectrum multi-kinase inhibitor in relapsed/refractory NHL with correlative genomic analysis in a Phase I/II trial. The study included 33 patients with various sub-types of NHL who had received at least one prior therapy. The most common sub-types were diffuse large B-cell lymphoma (24%), follicular lymphoma, grade 1/2 (21%) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS; 21%). Most patients were heavily pre-treated, including 42% with more than four prior therapies, 67% with rituximab exposure and 24% with prior autologous transplant. In this cohort, dasatinib showed modest activity in evaluable patients with an objective response rate of 29% (7/24) and clinical benefit rate of 71% (17/24). In 32 patients with outcome data, median progression-free survival was 3 months and median overall survival was 22·4 months. There were two patients with sustained complete responses, both with PTCL-NOS histology. The side effect profile was consistent with prior studies, with pleural effusion being the most common non-haematological toxicity. Exploratory genomic analysis showed two cases of PTCL-NOS with sustained response had a common mutation in LRRK2 and high prevalence of FOXO1 mutation in relapsed/refractory follicular lymphoma.Entities:
Keywords: zzm321990NHLzzm321990; dasatinib; mutation analysis; phase 2 study; relapsed/refractory lymphoma
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Year: 2018 PMID: 30520026 PMCID: PMC8281362 DOI: 10.1111/bjh.15702
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998