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临床试验/JPRN-UMIN000005613
JPRN-UMIN000005613已完成2 期

Clinical PhII Study: Investigation for safety and efficacy of bendamustine and rituximab, B-R combination therapy for the patients of recurrent and/or refractory low-grade B cell lymphoma or mantle cell lymphoma previously treated with one or two regimen including rituximab - BRB Study

Keio BRB Study group0 个研究点目标入组 44 人开始时间: 2011年5月20日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
44

研究概览

简要总结

Fifty-three patients were enrolled in this study and analyzed. The diagnosis included follicular lymphoma (FL) (77 %), mucosa-associated lymphoid tissue lymphoma (13 %) and others (10 %). Forty-seven (90 %) patients completed four cycles of treatment as per schedule. Best overall response rate (ORR) and complete response rate (CRR) was 94 and 71 %, respectively (for FL, ORR 95 % and CRR 80 %). The treatment was well tolerated and the primary toxicity was myelosuppression; the incidence of grade 3/4 leukopenia and neutropenia were 42 and 40 %, respectively. There were no grade 5 toxicities. For the evaluation of late toxicity, especially infection, longer follow-up of this cohort is needed.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Pregnancy, brest-feedings, or pts who would be pregnant 2. Active double cancer 3. Psychotics judged could not be difficutlt to attend 4. Severe complication and/or infection 5. Liver cirrhosis 6. Interstitial pneumonitis 7. Tumor cells in PB are 25000/uL or more 8. CNS invasion 9. Past history of bendamustine administration 10.Inappropriate to administer rituximab 11.Sever hypersensitity on any agents 12.Judged to be inappropriate

研究者

发起方
Keio BRB Study group

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