|Table of Contents|

Association between genetic polymorphisms of glutathione S-transferase P1 and clinical outcomes of oxaliplatin plus capecitabine chemotherapy in patients with metastatic gastric cancer

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2023 24
Page:
4572-4575
Research Field:
Publishing date:

Info

Title:
Association between genetic polymorphisms of glutathione S-transferase P1 and clinical outcomes of oxaliplatin plus capecitabine chemotherapy in patients with metastatic gastric cancer
Author(s):
DONG Ningning1HAN Lei2
1.Department of Gastroenterology,Beijing Friendship Hospital,Capital Medical University/National Clinical Research Center of Gastrointestinal Disease/Beijing Digestive Disease Center/Beijing Key Laboratory for Precancerous Lesion of Digestive Diseases,Bei
Keywords:
metastatic gastric cancerglutathione S-transferase P1single nucleotide polymorphismdrug therapy
PACS:
R735.2
DOI:
10.3969/j.issn.1672-4992.2023.24.016
Abstract:
Objective:To analyze the association between genetic polymorphisms of glutathione S-transferase P1 (GSTP1) rs1695 and clinical outcomes of oxaliplatin plus capecitabine chemotherapy in patients with metastatic gastric cancer.Methods:102 patients with metastatic gastric cancer were enrolled.They received oxaliplatin in combination with capecitabine chemotherapy (XELOX regimen).GSTP1 rs1695 genotype was detected by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF).The relationship between clinicopathological characteristics (including age,gender,tumor differentiation,location,Eastern Cooperative Oncology Group performance status,and TNM stage) and GSTP1 rs1695 genotypes and clinical outcomes [including objective response rate (ORR) and progression-free survival (PFS)] was analyzed.Results:Among these enrolled patients,73 patients (71.6%) carried GSTP1 rs1695 AA genotype,27 patients (26.5%) AG genotype,and 2 patients (2.0%) GG genotype.Patients harboring GG/AG genotype had both a statistically higher objective response rate than those with AA genotype (69.0% vs 43.8%,P=0.022),and longer progression-free survival[6.1 months (95%CI:5.2~7.0) vs 5.1 months (95%CI:4.6~5.6),P=0.028].None of the clinicopathological characteristics was related to tumor response,whereas,tumor differentiation and TNM stage were associated with progression-free survival (P<0.05).Cox regression analysis suggested that tumor differentiation,TNM stage and GSTP1 rs1695 were independent prognostic factors of progression-free survival.Conclusion:GSTP1 rs1695 genotype is closely related to the clinical outcomes of oxaliplatin plus capecitabine chemotherapy in patients with metastatic gastric cancer,which represents a further step towards individualized therapy.

References:

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Memo

Memo:
National Natural Science Foundation of China(No.82070575);国家自然科学基金(编号:82070575);北京市优秀人才培养资助计划(编号:2015000021469G232)
Last Update: 1900-01-01