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苯达莫司汀联合利妥昔单抗治疗既往未治疗的老年弥漫性大B细胞淋巴瘤的II期试验。

A phase II trial of bendamustine in combination with rituximab in older patients with previously untreated diffuse large B-cell lymphoma.

作者信息

Park Steven I, Grover Natalie S, Olajide Oludamilola, Asch Adam S, Wall James G, Richards Kristy L, Sobol Anna L, Deal Allison M, Ivanova Anastasia, Foster Matthew C, Muss Hyman B, Shea Thomas C

机构信息

Division of Hematology/Oncology, University of North Carolina, Chapel Hill, NC, USA.

Rex Hematology Oncology Associates, Raleigh, NC, USA.

出版信息

Br J Haematol. 2016 Oct;175(2):281-289. doi: 10.1111/bjh.14232. Epub 2016 Jul 22.

Abstract

Bendamustine in combination with rituximab (BR) has been associated with high response rates and acceptable toxicity in older patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL). Evaluation of BR is warranted in the front-line setting for DLBCL patients not eligible for anthracyclines or for the elderly. In this phase II study, we enrolled DLBCL patients aged ≥65 years who were poor candidates for R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) to determine the efficacy and safety of BR in previously untreated stage II-IV DLBCL. Twenty-three patients were enrolled with a median age of 80 years. 52% of patients presented with poor functional status (Eastern Cooperative Oncology Group performance score of ≥2). The overall response rate was 78% with 12 complete responses (52%). At a median follow up of 29 months, the median overall survival was 10·2 months and the median progression-free survival was 5·4 months. The most common grade 3/4 adverse events were haematological. Combination therapy with BR demonstrates high response rates as front-line therapy in frail older patients with DLBCL, but survival rates were low. BR should be used with caution in future clinical trials involving older DLBCL patients with poor functional status.

摘要

苯达莫司汀联合利妥昔单抗(BR)已被证实,对于复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)的老年患者具有较高的缓解率和可接受的毒性。对于不符合蒽环类药物治疗条件的DLBCL患者或老年患者,在一线治疗中对BR进行评估是必要的。在这项II期研究中,我们纳入了年龄≥65岁、不适合接受R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松)治疗的DLBCL患者,以确定BR在先前未经治疗的II-IV期DLBCL中的疗效和安全性。共纳入23例患者,中位年龄为80岁。52%的患者功能状态较差(东部肿瘤协作组体能状态评分为≥2)。总缓解率为78%,其中12例完全缓解(52%)。中位随访29个月时,中位总生存期为10.2个月,中位无进展生存期为5.4个月。最常见的3/4级不良事件为血液学事件。BR联合治疗作为DLBCL体弱老年患者的一线治疗显示出较高的缓解率,但生存率较低。在未来涉及功能状态较差的老年DLBCL患者的临床试验中,应谨慎使用BR。

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