Germline mutations of homologous recombination genes and clinical outcomes in pancreatic cancer: a multicenter study in Taiwan

PALB2 支票2 生殖系 穆提 种系突变 医学 胰腺癌 内科学 肿瘤科 BAP1型 卡铂 范卡 外科肿瘤学 癌症 化疗 癌症研究 突变 遗传学 生物 基因 DNA修复 顺铂 范科尼贫血
作者
Siao Muk Cheng,Yung‐Yeh Su,Nai‐Jung Chiang,Chih‐Jung Wang,Ying‐Jui Chao,Chien‐Jui Huang,Hui‐Jen Tsai,Shang‐Hung Chen,Chi‐Yen Chang,Chia‐Rung Tsai,Yijie Li,Chia‐Jui Yen,Shih‐Chang Chuang,Jeffrey Shu-Ming Chang,Yan‐Shen Shan,Daw‐Yang Hwang,Li‐Tzong Chen
出处
期刊:Journal of Biomedical Science [BioMed Central]
卷期号:31 (1): 21-21 被引量:5
标识
DOI:10.1186/s12929-024-01008-7
摘要

Abstract Background Cancer susceptibility germline mutations are associated with pancreatic ductal adenocarcinoma (PDAC). However, the hereditary status of PDAC and its impact on survival is largely unknown in the Asian population. Methods Exome sequencing was performed on 527 blood samples from PDAC individuals and analyzed for mutations in 80 oncogenic genes. Pathogenic and likely pathogenic (P/LP) germline variants were diagnosed according to the ACMG variant classification categories. The association between germline homologous recombination gene mutations ( gHR mut , including BAP1 , BRCA1 , BRCA2 , PALB2 , ATM , BLM , BRIP1 , CHEK2 , NBN , MUTYH , FANCA and FANCC ) and the treatment outcomes was explored in patients with stage III/IV diseases treated with first-line (1L) platinum-based versus platinum-free chemotherapy. Results Overall, 104 of 527 (19.7%) patients carried germline P/LP variants. The most common mutated genes were BRCA2 (3.60%), followed by ATR (2.66%) and ATM (1.9%). After a median follow-up duration of 38.3-months (95% confidence interval, 95% CI 35.0–43.7), the median overall survival (OS) was not significantly different among patients with gHR mut , non- HR germline mutations, or no mutation ( P = 0.43). Among the 320 patients with stage III/IV disease who received 1L combination chemotherapy, 32 (10%) had gHR mut . Of them, patients receiving 1L platinum-based chemotherapy exhibited a significantly longer median OS compared to those with platinum-free chemotherapy, 26.1 months (95% CI 12.7–33.7) versus 9.6 months (95% CI 5.9–17.6), P = 0.001. However, the median OS of patients without gHR mut was 14.5 months (95% CI 13.2–16.9) and 12.6 months (95% CI 10.8–14.7) for patients receiving 1L platinum-based and platinum-free chemotherapy, respectively ( P = 0.22). These results were consistent after adjusting for potential confounding factors including age, tumor stage, performance status, and baseline CA 19.9 in the multivariate Cox regression analysis. Conclusions Our study showed that nearly 20% of Taiwanese PDAC patients carried germline P/LP variants. The longer survival observed in gHR mut patients treated with 1L platinum-based chemotherapy highlights the importance of germline testing for all patients with advanced PDAC at diagnosis.
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