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BR方案与R-miniCHOP方案治疗不适合接受常规治疗的B细胞非霍奇金淋巴瘤患者的疗效比较:一项随机、双中心、队列研究

BR vs. R‑miniCHOP in unfit patients with B‑cell non‑Hodgkin lymphoma: A randomized, two‑center, cohort study.

作者信息

Zhang Dongdong, Lin Yong, Dong Youhong, Zhang Liling

机构信息

Department of Oncology, Xiangyang No. 1 People's Hospital, Hubei University of Medicine, Xiangyang, Hubei 441000, P.R. China.

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430071, P.R. China.

出版信息

Oncol Lett. 2023 Aug 23;26(4):440. doi: 10.3892/ol.2023.14027. eCollection 2023 Oct.

Abstract

The aim of the present study was to compare the efficacy and safety between the bendamustine plus rituximab (BR) regimen and rituximab combined with low-dose doxorubicin, cyclophosphamide, vincristine and prednisone (R-miniCHOP) in the treatment of 'unfit' patients with diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma grade 3B (FL3B). Patients, >70 years of age with DLBCL or FL3B, defined as unfit according to Comprehensive Geriatric Assessment, were included in the present study. All patients received 4-6 cycles of a BR or R-miniCHOP regimen at a three-week interval. The objective remission rate (ORR) and adverse reactions were evaluated between the two groups. A total of 35 patients, recruited between January 2020 and December 2021, were included in this prospective study. The median age was 74 years (range, 70-82 years). The ORR in the BR group was similar to that in the R-miniCHOP group (73.3 vs. 75.0%; P=0.606). However, the BR group exhibited a lower incidence of leukopenia than the R-miniCHOP group (20.0 vs. 60.0%; P=0.037). The univariate analysis revealed that the ORR was influenced by the serum β microglobulin level. The BR regimen showed equivalent efficacy but more improved safety compared with R-miniCHOP in unfit patients with DLBCL and FL3B. The BR regimen may be considered as an alternative treatment in these subgroups of patients.

摘要

本研究的目的是比较苯达莫司汀联合利妥昔单抗(BR)方案与利妥昔单抗联合低剂量多柔比星、环磷酰胺、长春新碱和泼尼松(R-miniCHOP)方案治疗“不适合”的弥漫性大B细胞淋巴瘤(DLBCL)和3B级滤泡性淋巴瘤(FL3B)患者的疗效和安全性。本研究纳入了年龄>70岁、患有DLBCL或FL3B且根据综合老年评估被定义为不适合的患者。所有患者均接受每三周一次的BR或R-miniCHOP方案,共4 - 6个周期。评估两组之间的客观缓解率(ORR)和不良反应。本前瞻性研究共纳入了2020年1月至2021年12月期间招募的35例患者。中位年龄为74岁(范围70 - 82岁)。BR组的ORR与R-miniCHOP组相似(73.3%对75.0%;P = 0.606)。然而,BR组白细胞减少的发生率低于R-miniCHOP组(20.0%对60.0%;P = 0.037)。单因素分析显示,ORR受血清β微球蛋白水平影响。在不适合的DLBCL和FL3B患者中,与R-miniCHOP相比,BR方案显示出等效的疗效,但安全性更优。BR方案可被视为这些亚组患者的替代治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738c/10472019/7b0211effe65/ol-26-04-14027-g00.jpg

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