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西达本胺联合利妥昔单抗在中国复发或难治性B细胞淋巴瘤老年患者中的安全性:一项多中心、单臂、II期研究。

Safety of chidamide plus rituximab in elderly patients with relapsed or refractory B-cell lymphoma in China: a multicenter, single-arm, phase II study.

作者信息

Chen Xinrui, Wang Huaqing, Sun Xiuhua, Su Liping, Liu Fengting, Zhao Ke, Xu Liye, Wu Shaohua, Song Teng

机构信息

Department of Oncology, Tianjin Union Medical Center, Nankai University, Tianjin, China.

The Institute of Translational Medicine, Tianjin Union Medical Center, Nankai University, Tianjin, China.

出版信息

Ann Transl Med. 2021 Dec;9(24):1769. doi: 10.21037/atm-21-6019.

Abstract

BACKGROUND

Patients over 65 years old with diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma (FL) relapse or being refractory to rituximab-associated chemotherapy have limited treatment options. Chidamide has the ability to enhance the sensitivity of rituximab-resistant tumors has been confirmed. We aimed to assess the activity and safety profile of chidamide plus rituximab in elderly Chinese patients with recurrent or refractory B-cell lymphoma.

METHODS

In this prospective, single-arm phase II trial, we enrolled patients from three hospitals in China with histopathological diagnoses of DLBCL and FL who had relapsed or were refractory to previous lines of rituximab-associated chemotherapy. Patients were given chidamide (10 mg on days 1-6 and 8-14) and rituximab (375 mg/m on day 7). The treatments were repeated every 21 days. The primary endpoint was the objective response rate (ORR). The secondary endpoints included the disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety.

RESULTS

Thirteen patients were enrolled and commenced treatment between November 12, 2018, and December 24, 2020. As of March 20, 2021, two patients (15.4%) were still receiving treatment. The median follow-up was 13.4 months. The ORR was 40% for the DLBCL cohort (n=10), and 100% for the FL cohort (n=3). DLBCL patients had a median PFS (mPFS) of 2.6 months (0.9-31.2 months) and a median OS (mOS) of 16.7 months (2.3-13.6 months). Neither mPFS nor mOS was reached in the FL cohort. The most frequent treatment-related adverse events (TRAEs) were leukopenia (38.5%), neutropenia (30.8%), lymphopenia (30.8%), thrombocytopenia (30.8%), fatigue (38.5%), and hyperuricemia (30.8%).

CONCLUSIONS

Chidamide plus rituximab is clinically effective with an acceptable toxicity profile in elderly patients over 65 years old with relapsed or refractory DLBCL and FL. Further investigation is ongoing.

摘要

背景

65岁以上弥漫性大B细胞淋巴瘤(DLBCL)或滤泡性淋巴瘤(FL)复发或对利妥昔单抗相关化疗难治的患者治疗选择有限。西达本胺增强利妥昔单抗耐药肿瘤敏感性的能力已得到证实。我们旨在评估西达本胺联合利妥昔单抗在中国老年复发或难治性B细胞淋巴瘤患者中的活性和安全性。

方法

在这项前瞻性单臂II期试验中,我们纳入了来自中国三家医院的组织病理学诊断为DLBCL和FL且对先前利妥昔单抗相关化疗复发或难治的患者。患者接受西达本胺(第1 - 6天和第8 - 14天10毫克)和利妥昔单抗(第7天375毫克/平方米)治疗。每21天重复治疗。主要终点是客观缓解率(ORR)。次要终点包括疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和安全性。

结果

2018年11月12日至2020年12月24日期间共纳入13例患者并开始治疗。截至2021年3月20日,2例患者(15.4%)仍在接受治疗。中位随访时间为13.4个月。DLBCL队列(n = 10)的ORR为40%,FL队列(n = 3)为100%。DLBCL患者的中位PFS(mPFS)为2.6个月(0.9 - 31.2个月),中位OS(mOS)为16.7个月(2.3 - 13.6个月)。FL队列未达到mPFS和mOS。最常见的治疗相关不良事件(TRAEs)为白细胞减少(38.5%)、中性粒细胞减少(30.8%)、淋巴细胞减少(30.8%)、血小板减少(

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c3/8756245/84ce44b35d5b/atm-09-24-1769-f1.jpg

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