晚期胃腺癌患者生存结果的性别差异。

Minggui Pan, Meng M Tong, Jack Stover, Tina Huang, Arun Dang, Chen Jiang, Ninah S Achacoso, Jeffrey Bien, Aleyda V Solorzano, Pamela Tse, Elaine Chung, Vishnu P Kanakaveti, Dean Felsher, George A Fisher, Sachdev Thomas, Laurel Habel
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引用次数: 0

摘要

目的:探讨男性和女性晚期胃(GAC)、胃食管交界处(GEJAC)和食管(EAC)腺癌患者的潜在总生存率(OS)差异。患者和方法:该研究包括来自北加州凯撒医疗机构的新发转移性或复发性EAC、GEJAC和GAC患者。我们使用Cox回归模型来检验性别与OS的关系,调整人口统计学、运动状态、Charlson合病指数、组织学(Lauren分类)、接受化疗、HER2扩增或过表达、p53、KRAS、CDKN2A、PIK3CA共突变和MYC扩增。结果:875例符合条件的患者中,有426例GAC,其中男性224例,女性202例。在GAC患者中,男性的OS优于女性(HR = 0.73; [95% CI, 0.59-0.92]),这种OS差异在除mutKRAS外的各个分子亚组中都保持不变。有趣的是,在p53突变的GAC患者中,如果肿瘤携带非功能获得性突变,男性比女性的OS更好(非GOF, HR = 0.59; [95% CI, 0.40-0.85]),但如果肿瘤携带功能获得性突变,男性的OS更差(GOF, HR = 1.80; [95% CI, 0.83-3.99])。GEJAC患者的性别与OS无关(HR = 1.14);(CI, 0.77 - -1.67)(95%)或EAC (HR = 1.0; [95% CI, 0.57 - -1.74])。当对接受和未接受化疗的患者进行单独分析时,这些结果仍然相似。结论:晚期GAC患者中,男性的OS优于女性。此外,在突变p53的GAC患者中,GOF与非GOF的存在与性别和OS的相关性呈负相关。我们的数据揭示了晚期GAC患者生存结果的性别差异。如果得到证实,这一发现将对临床实践和进一步了解GAC的生物学具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sex disparity in survival outcomes of advanced gastric adenocarcinoma.

Sex disparity in survival outcomes of advanced gastric adenocarcinoma.

Sex disparity in survival outcomes of advanced gastric adenocarcinoma.

Sex disparity in survival outcomes of advanced gastric adenocarcinoma.

Purpose: To examine potential overall survival (OS) differences between males and females with advanced gastric (GAC), gastroesophageal junction (GEJAC) and esophageal (EAC) adenocarcinoma.

Patients and methods: The study included patients from Kaiser Permanente Northern California with de novo metastatic or relapsed EAC, GEJAC and GAC. We used Cox regression modeling to examine association of sex with OS adjusting for demographics, performance status, Charlson comorbidity index, histology (Lauren's classification), receipt of chemotherapy, and HER2 amplification or overexpression, p53, KRAS, CDKN2A, PIK3CA co-mutations and MYC amplification.

Results: Of 875 total eligible patients, 426 had GAC, of whom 224 were male and 202 were female. Among patients with GAC, males had better OS than females (HR = 0.73; [95% CI, 0.59-0.92]), and this OS difference was preserved across the molecular subgroups except mutKRAS. Intriguingly, among GAC patients with a p53 mutation, males versus females had better OS if tumor carried a non-gain-of-function mutation (non-GOF, HR = 0.59; [95% CI, 0.40-0.85]) but worse OS if tumor carried gain-of-function mutation (GOF, HR = 1.80; [95% CI, 0.83-3.99]). Sex was not associated with OS among patients with GEJAC (HR = 1.14); (95% [CI, 0.77-1.67]) or EAC (HR = 1.0; [95% CI, 0.57-1.74]). These results remained similar when separate analyses were performed among patients who received and among patients who did not receive chemotherapy.

Conclusions: Males had better OS than females among patients with advanced GAC. In addition, among GAC patients with a mutp53, sex and OS association was inversely driven by the presence of GOF versus non-GOF. Our data reveal a previously unappreciated sex disparity in survival outcomes among patients with advanced GAC. If confirmed, this finding could have important implications for clinical practice and for further understanding the biology of GAC.

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