TP53 gene polymorphism at codon 72 as a response predictor for neoadjuvant chemotherapy

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Jussane Oliveira Vieira, J. Pesquero, A. Nazário
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引用次数: 0

Abstract

Introduction: Breast cancer is one of the most prevalent cancers in women worldwide and neoadjuvant chemotherapy is a favored method for achieving pathologic complete response (pCR). The TP53 gene is involved in inducing the response to chemotherapy drugs. Objectives: The present study sought to correlate polymorphism variants at codon 72 with pathologic complete response to neoadjuvant chemotherapy. Casuistry and Methods: The study was conducted in the state of Sergipe, in Northeastern Brazil. A total of 206 patients with a histopathological diagnosis of breast cancer who underwent neoadjuvant chemotherapy from 2019 to 2022 were included. DNA samples were collected for the evaluation of TP53 polymorphism at codon 72. A prospective evaluation of the cases was conducted to verify the surgical pathologic response after chemotherapy; the response evaluation criteria in solid tumors were used (RECIST). The study was approved by the University of São Paulo Ethics and Research Committee. Results: Of the 168 patients, 44.6% were Arg72Arg, 17.3% Pro72Pro, and 38.0% Arg72Pro; pCR was achieved in 21.4% of the patients; 10.1% had progressive disease, 13.7% stable disease, and 54.2% had a partial pathologic response. The only predictor of pCR in multivariate regression was immunohistochemistry (p < 0.001). In the multivariate analysis, Arg72Pro and Pro72Pro increased the odds of the patient evolve with stable disease.This study was innovative in demonstrating a predictor of stable disease in response to neoadjuvant chemotherapy Conclusion: TP53 polymorphism at codon 72 is not a predictor of pathologic complete response, but it can be a predictor of stable disease.
作为新辅助化疗反应预测因子的 TP53 基因 72 号密码子多态性
简介乳腺癌是全球妇女中发病率最高的癌症之一,新辅助化疗是获得病理完全反应(pCR)的首选方法。TP53 基因参与诱导对化疗药物的反应:本研究试图将密码子 72 的多态性变异与新辅助化疗的病理完全反应相关联:研究在巴西东北部的塞尔希培州进行。共纳入了 206 名经组织病理学诊断为乳腺癌的患者,这些患者在 2019 年至 2022 年期间接受了新辅助化疗。采集的DNA样本用于评估TP53第72密码子的多态性。对病例进行前瞻性评估,以核实化疗后的手术病理反应;采用实体瘤反应评估标准(RECIST)。该研究获得了圣保罗大学伦理与研究委员会的批准:168名患者中,44.6%为Arg72Arg型,17.3%为Pro72Pro型,38.0%为Arg72Pro型;21.4%的患者获得了pCR;10.1%的患者病情进展,13.7%的患者病情稳定,54.2%的患者获得了部分病理反应。在多变量回归中,免疫组化是预测 pCR 的唯一指标(p < 0.001)。在多变量分析中,Arg72Pro和Pro72Pro增加了患者病情稳定的几率:结论:TP53 第 72 个密码子的多态性不能预测病理完全反应,但可以预测病情稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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