Suppr超能文献

R-分割-EPOCH方案联合大剂量甲氨蝶呤用于未治疗的伴有 重排或双表达的弥漫性大B细胞淋巴瘤。 (你提供的原文中“ rearrangement or double expression of and.”部分内容不完整,请检查补充完整以便能更准确翻译。)

R-split-EPOCH plus high dose methotrexate in untreated diffuse large B cell lymphoma with rearrangement or double expression of and .

作者信息

Sun Peng, Wang Yu, Chen Cui, Yang Hang, Nie Man, Sun Xiao-Qing, He Xiao-Hua, Jiang Wen-Qi, Li Zhi-Ming

机构信息

Department of Medical Oncology, Sun Yat-Sen University Cancer Center, 651 Dong Feng RD East, Guangzhou, Guangdong Province 510060, P. R. China.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dong Feng RD East, Guangzhou, Guangdong Province 510060, P. R. China.

出版信息

J Cancer. 2021 Feb 2;12(7):2059-2064. doi: 10.7150/jca.52958. eCollection 2021.

Abstract

Diffuse large B cell lymphoma (DLBCL) with rearrangement or double expression of and BCL-2 (DE DLBCL) has a relatively poor prognosis and does not respond well to standard R-CHOP. In the current study, we aimed to investigate the efficacy and safety of R-split-EPOCH plus high dose methotrexate (HD-MTX) in the particular patient population. A total of 28 patients diagnosed with DE DLBCL or DLBCL with rearrangement between January 2015 and December 2018 were included and retrospectively analyzed. All the participants underwent R-split-EPOCH plus HD-MTX as introduction therapy, with split infusion of etoposide, doxorubicin, and vincristine for 48 hours on D1-2 and D10-11, respectively. The overall objective response (ORR) rate was 100%, with 24 (85.7%) complete response (CR) and 4 (14.3%) partial response (PR). The CR rate was 76.9% and 93.3% for DLBCL patients with rearrangement and DE DLBCL patients, respectively. The 1- and 3-year PFS rate was 100% and 74.9%, respectively. The 1- and 3-year OS rate was 100% and 92.9%, respectively. Grade 3/4 non-hematological toxicity and grade 3/4 hematological toxicity occurred in 50% and 85.7% of patients, respectively. No treatment-related death was reported. R-split-EPOCH plus HD-MTX regimen is an effective and feasible treatment option for DE DLBCL and DLBCL with rearrangement.

摘要

伴有MYC重排或MYC与BCL-2双重表达的弥漫性大B细胞淋巴瘤(DLBCL)(双表达DLBCL)预后相对较差,对标准R-CHOP方案反应不佳。在本研究中,我们旨在探讨R-split-EPOCH联合大剂量甲氨蝶呤(HD-MTX)在特定患者群体中的疗效和安全性。纳入了2015年1月至2018年12月期间诊断为双表达DLBCL或伴有MYC重排的DLBCL的28例患者,并进行回顾性分析。所有参与者均接受R-split-EPOCH联合HD-MTX作为诱导治疗,依托泊苷、阿霉素和长春新碱分别在第1 - 2天和第10 - 11天分48小时静脉滴注。总体客观缓解(ORR)率为100%,其中完全缓解(CR)24例(85.7%),部分缓解(PR)4例(14.3%)。伴有MYC重排的DLBCL患者和双表达DLBCL患者的CR率分别为76.9%和93.3%。1年和3年无进展生存率(PFS)分别为100%和74.9%。1年和3年总生存率(OS)分别为100%和92.9%。3/4级非血液学毒性和3/4级血液学毒性分别发生在50%和85.7%的患者中。未报告与治疗相关的死亡。R-split-EPOCH联合HD-MTX方案是治疗双表达DLBCL和伴有MYC重排的DLBCL的一种有效且可行的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验