Ng Kimmie, Meyerhardt Jeffrey A, Chan Andrew T, Sato Kaori, Chan Jennifer A, Niedzwiecki Donna, Saltz Leonard B, Mayer Robert J, Benson Al B, Schaefer Paul L, Whittom Renaud, Hantel Alexander, Goldberg Richard M, Venook Alan P, Ogino Shuji, Giovannucci Edward L, Fuchs Charles S
: Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA (KN, JAM, KS, JAC, RJM, SO, CSF); Division of Gastroenterology, Massachusetts General Hospital, Boston, MA (ATC); Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA (ATC, ELG, CSF); Alliance Statistics and Data Center, Duke University Medical Center, Durham, NC (DN); Memorial Sloan-Kettering Cancer Center, New York, NY (LBS); Division of Hematology/Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL (ABB); Toledo Community Hospital Oncology Program, Toledo, OH (PLS); Hopital du Sacre-Coeur de Montreal, Universite de Montreal, Quebec, Canada (RW); Edward Cancer Center, Naperville, IL (AH); Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH (RMG); Division of Medical Oncology, University of California at San Francisco, San Francisco, CA (APV); Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (SO); Department of Epidemiology (SO, ELG) and Department of Nutrition (ELG), Harvard School of Public Health, Boston, MA.
J Natl Cancer Inst. 2014 Nov 27;107(1):345. doi: 10.1093/jnci/dju345. Print 2015 Jan.
We conducted a prospective, observational study of aspirin and COX-2 inhibitor use and survival in stage III colon cancer patients enrolled in an adjuvant chemotherapy trial. Among 799 eligible patients, aspirin use was associated with improved recurrence-free survival (RFS) (multivariable hazard ratio [HR] = 0.51, 95% confidence interval [CI] = 0.28 to 0.95), disease-free survival (DFS) (HR = 0.68, 95% CI = 0.42 to 1.11), and overall survival (OS) (HR = 0.63, 95% CI = 0.35 to 1.12). Adjusted HRs for DFS and OS censored at five years (in an attempt to minimize misclassification from noncancer death) were 0.61 (95% CI = 0.36 to 1.04) and 0.48 (95% CI = 0.23 to 0.99). Among 843 eligible patients, those who used COX-2 inhibitors had multivariable HRs for RFS, DFS, and OS of 0.53 (95% CI = 0.27 to 1.04), 0.60 (95% CI = 0.33 to 1.08), and 0.50 (95% CI = 0.23 to 1.07), and HRs of 0.47 (95% CI = 0.24 to 0.91) and 0.26 (95% CI = 0.08 to 0.81) for DFS and OS censored at five years. Aspirin and COX-2 inhibitor use may be associated with improved outcomes in stage III colon cancer patients.
我们对参加辅助化疗试验的III期结肠癌患者使用阿司匹林和COX-2抑制剂与生存情况进行了一项前瞻性观察研究。在799名符合条件的患者中,使用阿司匹林与无复发生存期(RFS)改善相关(多变量风险比[HR]=0.51,95%置信区间[CI]=0.28至0.95)、无病生存期(DFS)(HR=0.68,95%CI=0.42至1.11)和总生存期(OS)(HR=0.63,95%CI=0.35至1.12)。五年时进行截尾的DFS和OS的校正HR分别为0.61(95%CI=0.36至1.04)和0.48(95%CI=0.23至0.99)(旨在尽量减少非癌症死亡导致的错误分类)。在843名符合条件的患者中,使用COX-2抑制剂的患者RFS、DFS和OS的多变量HR分别为0.53(95%CI=0.27至1.04)、0.60(95%CI=0.33至1.08)和0.50(95%CI=0.23至1.07),五年时进行截尾的DFS和OS的HR分别为0.47(95%CI=0.24至0.91)和0.26(95%CI=0.08至0.81)。使用阿司匹林和COX-2抑制剂可能与III期结肠癌患者的预后改善相关。