Evidence map›Paper›PMID 41784693›Full record

ArticleJournal of gastrointestinal cancer2026

KRAS Mutation Status as a Prognostic Marker and Predictor of Therapy Response in Colorectal Cancer: an NCDB Analysis.

Mohyeddine El Sayed, Melhem El Harati, Miller W Shealy, Sassine Youssef

Abstract read
In one paragraph

Article in Journal of gastrointestinal cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Mohyeddine El SayedHollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA. elsayedm@musc.edu.ORCID http://orcid.org/0000-0001-7661-7865
Melhem El HaratiDepartment of Pulmonary and Critical Care, Medical University of South Carolina, Charleston, SC, USA.
Miller W ShealyDepartment of Surgery, Medical University of South Carolina, Charleston, SC, USA.
Sassine YoussefHollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKRAS mutation is a prominent biomarker in colorectal cancer (CRC) and is associated with resistance to anti-EGFR therapy in metastatic disease. However, its prognostic value across stages and its association with survival within common treatment pathways remain incompletely defined in large real-world cohorts.

methodsWe performed a retrospective cohort study using the National Cancer Database, identifying 52,534 patients with CRC diagnosed between 2010 and 2021 with documented KRAS mutation status. Demographic, clinicopathological, and treatment variables were analyzed. Overall survival (OS) was evaluated using Kaplan–Meier methods and multivariable Cox proportional hazards models, performed overall and stratified by AJCC stage. Exploratory analyses evaluated the association of KRAS status with OS within stage-specific treatment pathways.

resultsKRAS-mutant tumors comprised 39.9% of the cohort and were more frequently right-sided and metastatic at presentation and were less often poorly differentiated. KRAS mutation was independently associated with worse OS in the overall cohort (HR 1.12). Stage-specific associations were modest but statistically significant in stage II (HR 1.14), stage III (HR 1.16), and stage IV disease (HR 1.07). In exploratory treatment-pathway analyses, KRAS mutation was associated with inferior OS in several common regimens (e.g., surgery + chemotherapy in stage III and stage IV).

conclusionKRAS mutation independently predicts poorer survival in CRC, particularly in earlier stages, and influences outcomes under multiple therapeutic regimens. These findings underscore the importance of KRAS testing to optimize individualized treatment strategies and guide novel interventions targeting KRAS-mutant CRC.

Indexed as

Biomarkers, TumorColorectal NeoplasmsProto-Oncogene Proteins p21(ras)AgedFemaleHumansMaleMiddle AgedMutationNeoplasm StagingPrognosisRetrospective StudiesBiomarkers, TumorKRAS protein, humanProto-Oncogene Proteins p21(ras)Colorectal cancerKRAS mutationNational Cancer Database (NCDB)Overall survivalStage-specific survivalTreatment pathways

Identifiers

PMID41784693
PMCPMC12963201

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.