TY - JOUR
T1 - Association of KRAS mutation with tumor deposit status and overall survival of colorectal cancer
AU - Zhang, Meifang
AU - Hu, Wenwei
AU - Hu, Kun
AU - Lin, Yong
AU - Feng, Zhaohui
AU - Yun, Jing Ping
AU - Gao, Nan
AU - Zhang, Lanjing
N1 - Funding Information:
The study was in part supported by an Initiative for Multidisciplinary Research Teams (IMRT) award from Rutgers University, Newark, NJ (to N.G. and L.Z.), the U.S. National Institute of Health (R01 AT010243 to N.G.), the National Natural Science Foundation of China (No. 81872387 to M.Z.) and China Scholarship Council (to M.Z.). The funders have no roles in the study design or manuscript preparation.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Purpose: To examine associations of KRAS mutation with tumor deposit status and overall survival in colorectal cancer (CRC) patients. Methods: This retrospective cohort study included patients with incidental CRC diagnosed during 2010–2014 and recorded statuses of KRAS and tumor deposit in the National Cancer Database of the USA. Multivariable logistic regression and time-varying Cox regression analyses were used. Results: We included 45,761 CRC patients with KRAS status (24,027 [52.5%] men, 24,240 [53.0%] < 65 years old, 17,338 [37.9%] with KRAS mutation). Adjusted for microsatellite instability, age, pathologic stage and tumor grade, KRAS mutation (versus wild type) was associated with tumor deposit presence (odds ratio = 1.11, 95% CI 1.02–1.20). KRAS mutation was also linked to worse overall survival of CRC patients regardless of tumor deposit status (adjusted Hazard ratio [HR] = 1.20, 95% CI 1.07–1.33 for CRC with tumor deposits, and adjusted HR = 1.24, 95% CI 1.14–1.35 or CRC without) or tumor stage (adjusted HR = 1.32, 95% CI 1.14–1.54 for early-stage and adjusted HR = 1.18, 95% CI 1.10–1.27 for late-stage). Microsatellite instability was associated with better overall survival in CRC without tumor deposit (adjusted HR = 0.89, 95% CI 0.79–0.99), but not in CRC with tumor deposit (adjusted HR = 1.12, 95% CI 0.97–1.30). Conclusion: KRAS mutation is independently associated with tumor deposit presence and a worse overall survival in CRC patients.
AB - Purpose: To examine associations of KRAS mutation with tumor deposit status and overall survival in colorectal cancer (CRC) patients. Methods: This retrospective cohort study included patients with incidental CRC diagnosed during 2010–2014 and recorded statuses of KRAS and tumor deposit in the National Cancer Database of the USA. Multivariable logistic regression and time-varying Cox regression analyses were used. Results: We included 45,761 CRC patients with KRAS status (24,027 [52.5%] men, 24,240 [53.0%] < 65 years old, 17,338 [37.9%] with KRAS mutation). Adjusted for microsatellite instability, age, pathologic stage and tumor grade, KRAS mutation (versus wild type) was associated with tumor deposit presence (odds ratio = 1.11, 95% CI 1.02–1.20). KRAS mutation was also linked to worse overall survival of CRC patients regardless of tumor deposit status (adjusted Hazard ratio [HR] = 1.20, 95% CI 1.07–1.33 for CRC with tumor deposits, and adjusted HR = 1.24, 95% CI 1.14–1.35 or CRC without) or tumor stage (adjusted HR = 1.32, 95% CI 1.14–1.54 for early-stage and adjusted HR = 1.18, 95% CI 1.10–1.27 for late-stage). Microsatellite instability was associated with better overall survival in CRC without tumor deposit (adjusted HR = 0.89, 95% CI 0.79–0.99), but not in CRC with tumor deposit (adjusted HR = 1.12, 95% CI 0.97–1.30). Conclusion: KRAS mutation is independently associated with tumor deposit presence and a worse overall survival in CRC patients.
KW - Biomarker
KW - Colorectal cancer
KW - KRAS
KW - Microsatellite instability
KW - Survival rate
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U2 - 10.1007/s10552-020-01313-0
DO - 10.1007/s10552-020-01313-0
M3 - Article
C2 - 32394229
AN - SCOPUS:85084472495
VL - 31
SP - 683
EP - 689
JO - Cancer Causes and Control
JF - Cancer Causes and Control
SN - 0957-5243
IS - 7
ER -