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TP53 Gene Polymorphism at Codon 72 as a Response Predictor for Neoadjuvant Chemotherapy
被引:1
|作者:
Vieira, Jussane Oliveira
[1
]
Pesquero, Joao Bosco
[2
]
Nazario, Afonso Celso Pinto
[1
]
机构:
[1] Fed Univ Sao Paulo UNIFESP, Dept Gynecol, Sao Paulo, Brazil
[2] Fed Univ Sao Paulo UNIFESP, Ed Pesquisa II Ctr Pesquisa & Diagnost Mol Doencas, Dept Biophys, Mol Biol, Sao Paulo, Brazil
来源:
关键词:
Breast cancer;
TP53;
Polymorphism;
Neoadjuvant chemotherapy;
PATHOLOGICAL COMPLETE RESPONSE;
BREAST-CANCER;
COMPLETE ERADICATION;
SURVIVAL;
RISK;
PACLITAXEL;
APOPTOSIS;
OUTCOMES;
SURGERY;
IMPACT;
D O I:
10.1159/000536115
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Introduction: Breast cancer is the most prevalent cancer 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 pCR 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 (RECIST) were used. The study was approved by the University of S & atilde;o Paulo Ethics and Research Committee. Results: Of the 168 patients, 44.6% were Arg72Arg, 17.3% were Pro72Pro, and 38.0% were Arg72Pro; pCR was achieved in 21.4% of the patients; 10.1% had progressive disease, 13.7% had 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 evolving 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 pCR, but it can be a predictor of stable disease.
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页码:96 / 105
页数:10
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