| Literature DB >> 30692121 |
Peter Martin1,2, Nancy L Bartlett3, Kristie A Blum4, Steven Park5, Kami Maddocks4, Jia Ruan1,2, LeAnn Ridling3, Christopher Dittus5, Zhengming Chen6, Xiangao Huang1,7, Giorgio Inghirami1,7, Maurizio DiLiberto1,7, Selina Chen-Kiang1,7, John P Leonard1,2.
Abstract
Single-agent ibrutinib is active in patients with previously treated mantle cell lymphoma (MCL); however, nearly half of all patients experience treatment failure during the first year. We previously demonstrated that prolonged early G1 cell cycle arrest induced by the oral, specific CDK4/6 inhibitor palbociclib can overcome ibrutinib resistance in primary human MCL cells and MCL cell lines expressing wild-type Bruton's tyrosine kinase (BTK). Therefore, we conducted a phase 1 trial to evaluate the dosing, safety, and preliminary activity of palbociclib plus ibrutinib in patients with previously treated mantle cell lymphoma. From August 2014 to June 2016, a total of 27 patients (21 men, 6 women) were enrolled. The maximum tolerated doses were ibrutinib 560 mg daily plus palbociclib 100 mg on days 1 to 21 of each 28-day cycle. The dose-limiting toxicity was grade 3 rash. The most common grade 3 to 4 toxicities included neutropenia (41%), thrombocytopenia (30%), hypertension (15%), febrile neutropenia (15%), and lung infection (11%). The overall and complete response rates were 67% and 37%, and with a median follow-up of 25.6 months, the 2-year progression-free survival was 59.4% and the 2-year response duration was 69.8%. A phase 2 multicenter clinical trial to further characterize efficacy is now ongoing. The current trial was registered at www.clinicaltrials.gov as #NCT02159755.Entities:
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Year: 2019 PMID: 30692121 PMCID: PMC6418474 DOI: 10.1182/blood-2018-11-886457
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113