TY - JOUR
T1 - The Impact of KRAS Mutation on the Presentation and Prognosis of Non-Metastatic Colon Cancer
T2 - an Analysis from the National Cancer Database
AU - Scott, Aaron
AU - Goffredo, Paolo
AU - Ginader, Timothy
AU - Hrabe, Jennifer
AU - Gribovskaja-Rupp, Irena
AU - Kapadia, Muneera R.
AU - Weigel, Ronald J.
AU - Hassan, Imran
N1 - Publisher Copyright:
© 2020, The Society for Surgery of the Alimentary Tract.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Introduction: Approximately 40% of colorectal cancers have a KRAS mutation. The prognostic significance of KRAS mutations in patients with non-metastatic colon cancer has not been well elucidated. The National Cancer Database (NCDB) was used to analyze factors associated with KRAS mutation as well as its impact on the presentation and survival of patients with stages I–III colon cancer. Methods: The NCDB was queried to identify patients diagnosed with stages I–III adenocarcinoma of the colon from 2004 to 2015. Results: A total of 19,877 patients with known KRAS status were identified: mutation rates were 33% in stage I, 35% in stage II, and 38% in stage III patients (p < 0.01). On multivariable analysis, black race and right-sided location were independently associated with KRAS-mutated cancers (all p < 0.01). On univariate analysis for overall survival (OS), KRAS mutation was not significantly associated with a worse 5-year OS for stages I and II patients (p = 0.60 and 0.88, respectively). However, stage III KRAS-mutated colon cancers had a lower OS as compared with KRAS wild type cancers both on univariate and multivariable analysis. Right-sided colon cancers were independently associated with a worse prognosis compared with left-sided lesions (p < 0.01). Conclusions: KRAS-mutated colon cancers were more frequently observed in black patients, right-sided locations, and higher-stage tumors. These mutations had a negative prognostic impact for stage III patients, suggesting that the incorporation of genotypic data into colon cancer staging may help to guide systemic therapy and prognostication of colon cancer patients.
AB - Introduction: Approximately 40% of colorectal cancers have a KRAS mutation. The prognostic significance of KRAS mutations in patients with non-metastatic colon cancer has not been well elucidated. The National Cancer Database (NCDB) was used to analyze factors associated with KRAS mutation as well as its impact on the presentation and survival of patients with stages I–III colon cancer. Methods: The NCDB was queried to identify patients diagnosed with stages I–III adenocarcinoma of the colon from 2004 to 2015. Results: A total of 19,877 patients with known KRAS status were identified: mutation rates were 33% in stage I, 35% in stage II, and 38% in stage III patients (p < 0.01). On multivariable analysis, black race and right-sided location were independently associated with KRAS-mutated cancers (all p < 0.01). On univariate analysis for overall survival (OS), KRAS mutation was not significantly associated with a worse 5-year OS for stages I and II patients (p = 0.60 and 0.88, respectively). However, stage III KRAS-mutated colon cancers had a lower OS as compared with KRAS wild type cancers both on univariate and multivariable analysis. Right-sided colon cancers were independently associated with a worse prognosis compared with left-sided lesions (p < 0.01). Conclusions: KRAS-mutated colon cancers were more frequently observed in black patients, right-sided locations, and higher-stage tumors. These mutations had a negative prognostic impact for stage III patients, suggesting that the incorporation of genotypic data into colon cancer staging may help to guide systemic therapy and prognostication of colon cancer patients.
KW - KRAS
KW - Stages I–III colon cancer
KW - Survival
UR - https://www.scopus.com/pages/publications/85081612300
UR - https://www.scopus.com/inward/citedby.url?scp=85081612300&partnerID=8YFLogxK
U2 - 10.1007/s11605-020-04543-4
DO - 10.1007/s11605-020-04543-4
M3 - Article
C2 - 32128676
AN - SCOPUS:85081612300
SN - 1091-255X
VL - 24
SP - 1402
EP - 1410
JO - Journal of Gastrointestinal Surgery
JF - Journal of Gastrointestinal Surgery
IS - 6
ER -