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完全切除的局限期弥漫性大 B 细胞淋巴瘤(CISL 12-09)患者接受短疗程 R-CHOP 化疗免疫治疗的长期随访结果。

Long-term follow-up of abbreviated R-CHOP chemoimmunotherapy for completely resected limited-stage diffuse large B cell lymphoma (CISL 12-09).

机构信息

Department of Internal Medicine, Asan Medical Center, Seoul, South Korea.

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.

出版信息

Ann Hematol. 2020 Dec;99(12):2831-2836. doi: 10.1007/s00277-020-04284-z. Epub 2020 Sep 28.

Abstract

The standard of treatment for completely resected limited-stage diffuse large B cell lymphoma (DLBCL) in patients without residual lesions has not yet been established. Previously, we designed a phase II trial to evaluate the safety and efficacy of three cycles of abbreviated R-CHOP in patients with completely resected limited-stage DLBCL and reported favorable survival outcomes. We present the long-term follow-up results to taking into account the importance of delayed relapse in patients with limited-stage DLBCL. With a median follow-up duration of 62.7 months (range, 60.2-75.5 months), the 5-year OS and DFS rates were both 95.0% (95% confidence interval, 85.59-104.11%). Only one patient experienced disease progression which was confirmed at 12.3 months, and one patient with primary intestinal DLBCL developed non-small cell lung cancer 6 years after treatment. The long-term results of our data support the use of three cycles of abbreviated R-CHOP for patients with completely resected limited-stage DLBCL. The study was reviewed and approved by the review boards of the participating institutes and registered at ClinicalTrials.gov , number NCT01279902, in August 3, 2010.

摘要

完全切除的局限性弥漫性大 B 细胞淋巴瘤(DLBCL)患者的标准治疗方法尚未确定。此前,我们设计了一项 II 期临床试验,以评估完全切除的局限性 DLBCL 患者接受三周期短疗程 R-CHOP 的安全性和有效性,并报告了良好的生存结果。我们考虑到局限性 DLBCL 患者延迟复发的重要性,现将长期随访结果呈现出来。中位随访时间为 62.7 个月(范围为 60.2-75.5 个月),5 年 OS 和 DFS 率均为 95.0%(95%置信区间,85.59-104.11%)。仅 1 例患者出现疾病进展,于 12.3 个月时确诊,1 例原发性肠道 DLBCL 患者在治疗 6 年后发生非小细胞肺癌。我们数据的长期结果支持对完全切除的局限性 DLBCL 患者使用三周期短疗程 R-CHOP。该研究经过参与机构的审查委员会审查和批准,并于 2010 年 8 月 3 日在 ClinicalTrials.gov 注册,编号为 NCT01279902。

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