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The PARP Inhibitor Veliparib Can Be Safely Added to Bendamustine and Rituximab and Has Preliminary Evidence of Activity in B-Cell Lymphoma.


ABSTRACT: Purpose: The PARP inhibitor veliparib enhances the cytotoxicity of alkylating agents. This phase I study evaluated veliparib with the bifunctional alkylator bendamustine (VB) in patients with relapsed/refractory lymphoma, multiple myeloma, and solid malignancies, with a cohort expansion of VB with rituximab (VBR) in patients with B-cell lymphomas.Experimental Design: This dose-escalation study evaluated safety, pharmacokinetics, and preliminary efficacy of veliparib (20-400 mg twice a day, days 1-7 of 28-day cycle) and bendamustine (70 and 90 mg/m2 intravenously, days 1 and 2). A cohort expansion was conducted, which combined veliparib and bendamustine at the maximum tolerated dose (MTD) with rituximab (375 mg/m2, day 1) in patients with B-cell lymphomas. Thirty-four patients were treated in seven dose-escalation cohorts and seven patients in the dose-expansion cohort.Results: The MTD was veliparib 300 mg twice daily plus bendamustine 90 mg/m2 Dose-limiting toxicities (DLT) were anemia, nausea, hypertension, and hyperhidrosis. Grade ≥3 toxicities included lymphopenia (87.8%), anemia (19.5%), neutropenia (12.2%), thrombocytopenia (9.8%), leukopenia (9.8%), nausea (7.3%), and hypophosphatemia (7.3%). Apparent veliparib clearance was slightly lower than previously reported. Of 14 patients with lymphoma evaluable for response, five of seven (71%) on VB and six of seven (86%) on VBR achieved objective response. One patient with multiple myeloma achieved partial response.Conclusions: VB and VBR were generally well-tolerated. VBR had preliminary clinical activity in patients with B-cell lymphoma, which warrants further investigation in a phase II trial. This trial was registered at www.clinicaltrials.gov as NCT01326702 Clin Cancer Res; 23(15); 4119-26. ©2017 AACR.

SUBMITTER: Soumerai JD 

PROVIDER: S-EPMC5541854 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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The PARP Inhibitor Veliparib Can Be Safely Added to Bendamustine and Rituximab and Has Preliminary Evidence of Activity in B-Cell Lymphoma.

Soumerai Jacob D JD   Zelenetz Andrew D AD   Moskowitz Craig H CH   Palomba M Lia ML   Hamlin Paul A PA   Noy Ariela A   Straus David J DJ   Moskowitz Alison J AJ   Younes Anas A   Matasar Matthew J MJ   Horwitz Steven M SM   Portlock Carol S CS   Konner Jason A JA   Gounder Mrinal M MM   Hyman David M DM   Voss Martin H MH   Fury Matthew G MG   Gajria Devika D   Carvajal Richard D RD   Ho Alan L AL   Beumer Jan H JH   Kiesel Brian B   Zhang Zhigang Z   Chen Alice A   Little Richard F RF   Jarjies Christine C   Dang Thu O TO   France Fallon F   Mishra Nishant N   Gerecitano John F JF  

Clinical cancer research : an official journal of the American Association for Cancer Research 20170317 15


<b>Purpose:</b> The PARP inhibitor veliparib enhances the cytotoxicity of alkylating agents. This phase I study evaluated veliparib with the bifunctional alkylator bendamustine (VB) in patients with relapsed/refractory lymphoma, multiple myeloma, and solid malignancies, with a cohort expansion of VB with rituximab (VBR) in patients with B-cell lymphomas.<b>Experimental Design:</b> This dose-escalation study evaluated safety, pharmacokinetics, and preliminary efficacy of veliparib (20-400 mg twic  ...[more]

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