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DOI 10.3109/10428194.2010.546015

Медицинская библиотека · Leukemia & lymphoma · 2011

A phase II study of bortezomib and gemcitabine in relapsed mantle cell lymphoma from the National Cancer Institute of Canada Clinical Trials Group (IND 172).

Kouroukis C Tom, Fernandez Louis A V, Crump Michael, Gascoyne Randy D, Chua Neil Sun, Buckstein Rena, Turner Robert, Assouline Sarit, Klasa Richard J, Walsh Wendy, Powers Jean, Eisenhauer Elizabeth

Клиническое исследование II фазыСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Bortezomib and gemcitabine have each shown activity as single agents in mantle cell lymphoma (MCL), which is incurable. The purpose of this phase II study was to determine the efficacy and safety of the previously unstudied combination of bortezomib and gemcitabine in patients with relapsed or refractory MCL. Patients were eligible if they had relapsed MCL with 1-3 prior therapies. Patients were treated with gemcitabine 1000 mg/m(2) on days 1 and 8 and bortezomib 1.0 mg/m(2) IV on days 1, 4, 8, and 11, on a 21-day schedule. Twenty-six patients were evaluable for toxicity and 25 for response. The overall response rate was 60% and the median progression free survival was 11.4 months. The main adverse effects were hematological, with 40% and 48% of patients experiencing grade 3/4 thrombocytopenia and granulocytopenia, respectively. Bortezomib and gemcitabine is an active combination in relapsed and refractory MCL with clinically meaningful results. It offers a chemotherapy backbone to which other agents, less myelosuppressive, may be added.

Для цитирования: Kouroukis C Tom, Fernandez Louis A V, Crump Michael, Gascoyne Randy D, Chua Neil Sun, Buckstein Rena, Turner Robert, Assouline Sarit, Klasa Richard J, Walsh Wendy, Powers Jean, Eisenhauer Elizabeth. A phase II study of bortezomib and gemcitabine in relapsed mantle cell lymphoma from the National Cancer Institute of Canada Clinical Trials Group (IND 172).. Leukemia & lymphoma. 2011. DOI: 10.3109/10428194.2010.546015.

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