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Bendamustine plus rituximab in Japanese patients with relapsed or refractory diffuse large B-cell lymphoma

This single-arm phase 3 study was conducted to confirm the results of our phase 2 study of bendamustine (B)-rituximab (R) in patients with relapsed/refractory diffuse large B cell lymphoma (rrDLBCL). The primary endpoint was overall response rate (ORR). Autologous stem cell transplantation-ineligibl...

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Detalles Bibliográficos
Autores principales: Murayama, Kayoko, Kiguchi, Toru, Izutsu, Koji, Kameoka, Yoshihiro, Hidaka, Michihiro, Kato, Harumi, Rai, Shinya, Kuroda, Junya, Ishizawa, Kenichi, Ichikawa, Satoshi, Ando, Kiyoshi, Ogura, Michinori, Fukushima, Koji, Terui, Yasuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993776/
https://www.ncbi.nlm.nih.gov/pubmed/35244756
http://dx.doi.org/10.1007/s00277-022-04801-2
Descripción
Sumario:This single-arm phase 3 study was conducted to confirm the results of our phase 2 study of bendamustine (B)-rituximab (R) in patients with relapsed/refractory diffuse large B cell lymphoma (rrDLBCL). The primary endpoint was overall response rate (ORR). Autologous stem cell transplantation-ineligible rrDLBCL patients with ≤ 2 prior chemotherapy regimens received R 375 mg/m(2) IV on day 1 and B 120 mg/m(2)/day IV on days 2 and 3 every 21 days up to 6 cycles. Thirty-eight patients with a median age of 74 years (range, 43–86) received BR. The ORR and complete response rates were 76.3% and 47.4%, respectively. With a median follow-up of 19.5 months including long-term follow-up, median progression-free survival was 11.9 months. Median OS was 29.2 months. Discontinuation of treatment due to Gr3-5 TEAE was observed among 13 of 38 patients (34.2%). One patient with cytomegalovirus enterocolitis died during follow-up. This BR regimen was confirmed to be effective and tolerable in studied patients. ClinicalTrials.gov Identifier: NCT03372837 registered on 14 December 2017, NCT04354402 registered on 21 April, 2020. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-022-04801-2.