[Clinical characteristics and prognostic analysis of diffuse large B-cell lymphoma with TP53 mutation].

Y Qin, J Xie, Y Q Wang, X Y Liu, L N Chen, X H He, J L Yang, S Y Zhou, P Liu, S Yang, L Gui, C G Zhang, Y K Shi
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Abstract

Exploring the clinical and pathological characteristics and prognostic factors of diffuse large B-cell lymphoma (DLBCL) patients with TP53 mutation. Data of 86 DLBCL patients with TP53 mutation treated with R-CHOP and 19 DLBCL patients with TP53 mutation treated with R-CHOP like regimen as first-line treatment at the Cancer Hospital of Chinese Academy of Medical Sciences (CAMS) and the Cancer Hospital of the CAMS in Shenzhen, China, from January 2006 to June 2023 were retrospectively analyzed. Multivariate Cox analysis was applied to assess the effects of the factors on survival. Among the 105 DLBCL patients with TP53 mutation, 56 were male (53.3%); the median age was 59 years. There were 54 cases with stage Ⅰ-Ⅱ and 51 cases with stage Ⅲ-Ⅳ diseases. The proportion of B-cell lymphoma 2 (BCL2) gene amplification was 9.5% (10/105). The complete response rate in the whole group of patients treated with the R-CHOP regimen was 28.6% (30/105). The median progression-free survival (PFS) was 10.1 (95%CI: 7.3-13.0) months, and the median overall survival (OS) was not reached. Stage Ⅲ-Ⅳ was a risk factor for OS (HR=2.80, 95%CI: 1.04-7.54), and elevated lactic dehydrogenase (LDH) was a risk factor for PFS (HR=2.86, 95%CI: 1.56-5.26) and OS (HR=2.90, 95%CI: 1.08-7.69). The median PFS was lower in patients with BCL2 amplification than in patients without amplification [4.0 (95%CI: 2.7-5.3) vs 11.3 (95%CI: 8.5-14.1) months, P=0.011]. Thirty-one of the 54 (57.4%) patients with stage Ⅰ-Ⅱ disease received combination therapy based on the R-CHOP protocol. In conclusion, stage Ⅲ-Ⅳ and elevated LDH were associated with poor prognosis in TP53 mutation DLBCL patients, and patients with BCL2 amplification had a poor prognosis. For TP53 mutation DLBCL patients with stage Ⅰ-Ⅱ disease, combination of therapeutic modalities based on the R-CHOP may improve the prognosis.

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[伴 TP53 突变的弥漫大 B 细胞淋巴瘤的临床特征和预后分析]。
探讨TP53突变的弥漫大b细胞淋巴瘤(DLBCL)患者的临床病理特点及预后因素。回顾性分析2006年1月至2023年6月在中国医学科学院肿瘤医院(CAMS)和深圳CAMS肿瘤医院一线治疗的86例TP53突变DLBCL患者和19例TP53突变DLBCL患者的资料。采用多因素Cox分析评估各因素对生存率的影响。105例TP53突变的DLBCL患者中,男性56例(53.3%);中位年龄为59岁。其中Ⅰ-Ⅱ期54例,Ⅲ-Ⅳ期51例。b细胞淋巴瘤2 (BCL2)基因扩增比例为9.5%(10/105)。R-CHOP方案治疗的全组患者完全缓解率为28.6%(30/105)。中位无进展生存期(PFS)为10.1个月(95%CI: 7.3-13.0),中位总生存期(OS)未达到。Ⅲ-Ⅳ期是OS的危险因素(HR=2.80, 95%CI: 1.04-7.54),乳酸脱氢酶(LDH)升高是PFS (HR=2.86, 95%CI: 1.56-5.26)和OS (HR=2.90, 95%CI: 1.08-7.69)的危险因素。BCL2扩增患者的中位PFS低于无扩增患者[4.0 (95%CI: 2.7-5.3) vs 11.3 (95%CI: 8.5-14.1)个月,P=0.011]。54例Ⅰ-Ⅱ期患者中有31例(57.4%)接受了基于R-CHOP方案的联合治疗。综上所述,TP53突变的DLBCL患者Ⅲ-Ⅳ期和LDH升高与预后不良相关,且BCL2扩增患者预后不良。对于TP53突变的Ⅰ-Ⅱ期DLBCL患者,基于R-CHOP的联合治疗方式可能改善预后。
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来源期刊
Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
400
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