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Bendamustine plus rituximab in Japanese patients with relapsed or refractory diffuse large B-cell lymphoma
被引:0
|作者:
Kayoko Murayama
Toru Kiguchi
Koji Izutsu
Yoshihiro Kameoka
Michihiro Hidaka
Harumi Kato
Shinya Rai
Junya Kuroda
Kenichi Ishizawa
Satoshi Ichikawa
Kiyoshi Ando
Michinori Ogura
Koji Fukushima
Yasuhito Terui
机构:
[1] Gunma Prefectural Cancer Center,Department of Hematology
[2] Chugoku Central Hospital,Department of Hematology
[3] Dokkyo Medical University Saitama Medical Center,Department of Diabetes, Endocrinology and Hematology
[4] National Cancer Center Hospital,Department of Hematology Tokyo
[5] Akita University Graduate School of Medicine and Faculty of Medicine,Department of Hematology, Nephrology and Rheumatology
[6] National Hospital Organization Kumamoto Medical Center,Department of Hematology
[7] Aichi Cancer Center Hospital,Department of Hematology and Cell Therapy
[8] Kindai University Faculty of Medicine,Department of Hematology and Rheumatology
[9] Kyoto Prefectural University of Medicine,Division of Hematology and Oncology, Department of Medicine
[10] Yamagata University Faculty of Medicine,Department of Internal Medicine III
[11] Tohoku University Graduate School of Medicine,Department of Hematology and Rheumatology
[12] Tokai University School of Medicine,Department of Hematology & Oncology
[13] Kasugai Municipal Hospital,Department of Hematology and Oncology
[14] SymBio Pharmaceutical Ltd.,Medical Affairs Department
[15] Research & Development Division,Department of Hematology Oncology
[16] Cancer Institute Hospital of JFCR,Department of Hematology
[17] Saitama Medical University,undefined
来源:
关键词:
Bendamustine hydrochloride;
Lymphoma;
Large B cell;
Diffuse;
Recurrence;
Rituximab;
Salvage therapy;
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摘要:
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/m2 IV on day 1 and B 120 mg/m2/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.
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页码:979 / 989
页数:10
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