The prognostic value of KRAS mutation in locally advanced rectal cancer
- PMID: 35484252
- DOI: 10.1007/s00384-022-04167-x
The prognostic value of KRAS mutation in locally advanced rectal cancer
Abstract
Background: The prognostic value of the KRAS proto-oncogene mutation in colorectal cancer has been debated. Herein, we analyzed the National Cancer Database (NCDB) to assess the role of KRAS mutation as a prognostic marker in patients with locally advanced rectal cancer (LARC).
Methods: We identified LARC patients treated with neoadjuvant chemoradiation from 2004-2015 excluding those with stage I/IV disease and unknown KRAS status. Multivariable logistic regression identified variables associated with KRAS positivity. Propensity adjusted univariable and multivariable analyses identified predictors of survival.
Results: Of the 784 eligible patients, 506 were KRAS-negative (KRAS -) and 278 were KRAS-positive (KRAS +). Median survival was 63.6 months and 76.3 months for KRAS + and KRAS - patients respectively, with propensity adjusted 3 and 5-year survival of 79.9% vs. 83.6% and 56.7% vs. 61.9% respectively (HR 1.56, p 1.074-2.272). Male sex, no insurance, and KRAS + disease were associated with poorer survival on unadjusted and propensity adjusted multivariable analyses.
Conclusions: Our analysis of KRAS + LARC suggest that KRAS + disease is associated with poorer overall survival. Given the inherent limitations of retrospective data, prospective validation is warranted.
Keywords: Colorectal cancers; Gene mutations; KRAS mutation; Locally advanced rectal cancer; Prognostic value.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
References
-
- Li Y, Wang J, Ma X et al (2016) A review of neoadjuvant chemoradiotherapy for locally advanced rectal cancer. Int J Biol Sci 12(8):1022–31. (In eng). https://doi.org/10.7150/ijbs.15438
-
- Von Moos R, Koeberle D, Schacher S et al (2018) Neoadjuvant radiotherapy combined with capecitabine and sorafenib in patients with advanced KRAS-mutated rectal cancer: A phase I/II trial (SAKK 41/08). Eur J Cancer 89:82–89. (In eng). https://doi.org/10.1016/j.ejca.2017.11.005
-
- Abdul-Jalil KI, Sheehan KM, Toomey S et al (2014) The frequencies and clinical implications of mutations in 33 kinase-related genes in locally advanced rectal cancer: a pilot study. Ann Surg Oncol 21(8):2642–9. (In eng). https://doi.org/10.1245/s10434-014-3658-x
-
- Malumbres M, Barbacid M (2003) RAS oncogenes: the first 30 years. Nat Rev Cancer 3(6):459–65. (In eng). https://doi.org/10.1038/nrc1097
-
- Schubbert S, Shannon K, Bollag G (2007) Hyperactive Ras in developmental disorders and cancer. Nat Rev Cancer 7(4):295–308. (In eng). https://doi.org/10.1038/nrc2109
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