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Published on: December 28, 2015
Bendamustine plus rituximab for relapsed or refractory diffuse large B cell lymphoma: a multicenter retrospective
Jung Yong Hong1,2, Dok Hyun Yoon1, Cheolwon Suh1
1Department of Oncology, Asan Medical Center, Ulsan University College of Medicine, Seoul, South Korea.
Bendamustine plus rituximab (BR) demonstrated a 55.1% overall response rate in Korean patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL). While effective, higher rates of hematological toxicities like neutropenia and thrombocytopenia were observed.
Area of Science:
- Hematology
- Oncology
- Clinical Trials
Background:
- Bendamustine plus rituximab (BR) is established for indolent lymphomas and mantle cell lymphoma.
- Real-world data on BR in diffuse large B cell lymphoma (DLBCL), particularly in Korean populations, is limited.
Purpose of the Study:
- To evaluate the efficacy and safety of bendamustine plus rituximab (BR) in Korean patients with relapsed or refractory DLBCL.
- To assess treatment outcomes and toxicity profiles in patients ineligible for intensive chemotherapy or autologous stem cell transplantation.
Main Methods:
- An observational, multicenter, retrospective analysis of 58 Korean patients with relapsed/refractory DLBCL treated with BR between December 2011 and December 2015.
- Patients received intravenous rituximab (375 mg/m²) followed by bendamustine (120 or 90 mg/m²) on subsequent days.
- Data collected included response rates, duration of response, progression-free survival (PFS), overall survival (OS), and adverse events.
Main Results:
- The overall response rate (ORR) was 55.1% (31.0% complete response, 24.1% partial response).
- Median progression-free survival was 3.9 months, and median overall survival was 6.7 months.
- The most frequent grade 3/4 adverse events were neutropenia (68.9%) and thrombocytopenia (58.6%). Febrile neutropenia occurred in 18.9% of patients.
Conclusions:
- Bendamustine plus rituximab (BR) shows significant efficacy in Korean patients with relapsed or refractory DLBCL.
- The treatment is associated with acceptable toxicity, although a higher incidence of grade 3/4 hematological toxicities warrants close monitoring in this population.
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