Phase 1 study of tazemetostat in Japanese patients with relapsed or refractory B-cell lymphoma
- PMID: 33492746
- PMCID: PMC7935786
- DOI: 10.1111/cas.14822
Phase 1 study of tazemetostat in Japanese patients with relapsed or refractory B-cell lymphoma
Abstract
Background: Tazemetostat is a selective and orally available inhibitor of enhancer of zeste homolog 2 (EZH2), a histone methyltransferase and epigenetic regulator of cellular differentiation programs. We carried out a phase I study of tazemetostat in Japanese patients with relapsed or refractory B-cell non-Hodgkin-type lymphoma (B-NHL) to evaluate its tolerability, safety, pharmacokinetics, and preliminary antitumor activity.
Methods: Tazemetostat was given orally at a single dose of 800 mg on the first day and 800 mg twice daily (BID: total 1600 mg/d) on following days in a 28-day/cycle manner. Tazemetostat dose-limiting toxicity (DLT) was evaluated up to the end of the first treatment cycle. Archival tumor tissues were analyzed for hotspot EZH2 mutations.
Results: As of 15 January 2018, seven patients (four follicular lymphoma [FL] and three diffuse large B-cell lymphoma [DLBCL]) were enrolled. The median age was 73 (range, 59-85) years, and the median number of prior chemotherapy regimens was three (range, one to five). No DLT was observed (one patient was not evaluable due to early disease progression). The common treatment-related adverse events (AEs) were thrombocytopenia and dysgeusia (three patients each; 42.9%). No treatment-related serious AEs were observed. The objective response rate was 57% (4/7 patients), including responses in three of four patients with FL and one of three patients with DLBCL. An EZH2 mutation was detected in one patient with FL responding to treatment.
Conclusions: Tazemetostat at 800 mg BID showed an acceptable safety profile and promising antitumor activity in Japanese patients with relapsed or refractory B-NHL.
Keywords: diffuse large B-cell lymphoma; enhancer of zeste homolog 2; follicular lymphoma; phase I study; tazemetostat.
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
Conflict of interest statement
The authors declare the following potential conflicts. KT: HUYA Bioscience, consultancy, honoraria; Bristol‐Myers Squibb, honoraria; Verastem, honoraria; Takeda Pharmaceutical, consultancy, honoraria, research funding; Eisai, honoraria, research funding; Kyowa Kirin, honoraria, research funding; Celgene, consultancy, honoraria, research funding; Zenyaku Kogyo, consultancy, honoraria; AbbVie, research funding; Yakult, honoraria; Janssen Pharmaceutical, honoraria, research funding; Mundi Pharma, consultancy, honoraria, research funding; Solasia, honoraria; Meiji Seika, honoraria; Daiichi Sankyo, consultancy, honoraria; Ono Pharmaceutical, consultancy, honoraria, research funding; Chugai Pharmaceutical, honoraria, research funding. SM: personal fees (BMS/Celgene, Chugai, Daiichi‐Sankyo, Eisai, Novartis, Symbio, Takeda). DM: personal fees and grant (Ono Pharmaceuticals, Celgene, Takeda Pharmaceutical, Janssen Pharmaceutical, Chugai Pharmaceutical, Bristol‐Myers Squibb), personal fees (Eisai, Kyowa Kirin, Zenyaku Kogyo Company, Synmosa Biopharma, Nippon Sinyaku), grant (Merck, Amgen Astellas BioPharma, Astellas Pharma, Sanofi, Novartis Pharma, Otsuka Pharmaceutical). KI: four honoraria and research funding (Eisai). TN, SS, SH: employees of Eisai Co., Ltd. KA: research funding (Eisai). The other authors have no conflict of interest.
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