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The prognostic value of KRAS mutation in locally advanced rectal cancer.
Asawa, Palash; Bakalov, Veli; Kancharla, Pragnan; Abel, Stephen; Chahine, Zena; Monga, Dulabh K; Kirichenko, Alexander V; Wegner, Rodney E.
Afiliación
  • Asawa P; Department of Internal Medicine, Allegheny Health Network, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Bakalov V; Division of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Kancharla P; Division of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Abel S; Division of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Chahine Z; Markey Cancer Center, University of Kentucky, 800 Rose St, Lexington, KY, 40536, USA.
  • Monga DK; Division of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Kirichenko AV; Division of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
  • Wegner RE; Division of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA. Rodney.wegner@ahn.org.
Int J Colorectal Dis ; 37(5): 1199-1207, 2022 May.
Article en En | MEDLINE | ID: mdl-35484252
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / Proteínas Proto-Oncogénicas p21(ras) Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: Int J Colorectal Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / Proteínas Proto-Oncogénicas p21(ras) Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: Int J Colorectal Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos