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弥漫性大B细胞淋巴瘤L265P突变在R-CHOP治疗中的高频性及预后价值

High frequency and prognostic value of L265P mutation in diffuse large B-cell lymphoma with R-CHOP treatment.

作者信息

Yu Sisi, Luo Huaichao, Pan Meiling, Palomino Luis Angel, Song Xiaoyu, Wu Ping, Huang Jian-Ming, Zhang Zhihui

机构信息

Department of Medical Oncology, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610051, P.R China.

Department of Clinical Laboratory, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610051, P.R China.

出版信息

Oncol Lett. 2018 Feb;15(2):1707-1715. doi: 10.3892/ol.2017.7472. Epub 2017 Nov 22.

Abstract

The aim of this study was to analyze the prevalence and prognostic value of myeloid differentiation factor 88 () L265P in diffuse large B-cell lymphoma (DLBCL) patients treated with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). We assessed the L265P mutation using an allele-specific semi-nested polymerase chain reaction method in 53 DLBCL patients treated with R-CHOP. The L265P mutation was detected in 16 of 53 DLBCL (30.19%) samples from patients treated with R-CHOP. Age and location were statistically significantly associated with L265P (P=0.025, 0.033, respectively), while treatment response and tumor recurrence were not. Univariate analysis showed that B symptoms (P=0.004) and Ki-67 (P=0.03) were significantly associated with progression-free survival (PFS), while L265P showed no significant association with overall survival and PFS. Multivariate analysis showed that B symptoms were significantly associated with PFS. Our study suggests that the prognostic value of L265P in DLBCL patients with R-CHOP requires further research.

摘要

本研究的目的是分析髓样分化因子88(MyD88)L265P在接受利妥昔单抗联合环磷酰胺、阿霉素、长春新碱和泼尼松(R-CHOP)治疗的弥漫性大B细胞淋巴瘤(DLBCL)患者中的发生率及预后价值。我们采用等位基因特异性半巢式聚合酶链反应方法,对53例接受R-CHOP治疗的DLBCL患者的MyD88 L265P突变进行了评估。在53例接受R-CHOP治疗的DLBCL患者的样本中,有16例(30.19%)检测到MyD88 L265P突变。年龄和病变部位与MyD88 L265P有统计学显著相关性(P分别为0.025和0.033),而治疗反应和肿瘤复发则无相关性。单因素分析显示,B症状(P=0.004)和Ki-67(P=0.03)与无进展生存期(PFS)显著相关,而MyD88 L265P与总生存期和PFS无显著相关性。多因素分析显示,B症状与PFS显著相关。我们的研究表明,MyD88 L

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ff/5780752/0ac19ab21dc8/ol-15-02-1707-g00.jpg

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