Prognostic Value of Each Codon-specific KRAS Mutation in Colorectal Cancer

NCT ID: NCT05657210

Last Updated: 2022-12-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

2203 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-01-01

Study Completion Date

2021-12-31

Brief Summary

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This retrospective study reviewed 3,144 patients who underwent surgery for colorectal cancer. This study was designed to comprehend the clinicopathological characteristics associated with individual codon-specific KRAS mutations in colorectal cancer.

Detailed Description

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This study was designed to comprehend the clinicopathological characteristics associated with individual codon-specific KRAS mutations in colorectal cancer including codon 12, 13, and 61. Furthermore, the main objective of this study was to determine whether KRAS codon 13 mutation could serve as a prognostic biomarker of colorectal cancer in a relatively large cohort of subjects. Overall survival (OS) and recurrence-free survival (RFS) were calculated from the date of surgery and compared using the Kaplan-Meier method and log-rank test. For analysis of risk factors for tumor recurrence, Cox proportional hazards regression model was used with the covariance input criterion set as \< 0.1. Patients were subdivided based on primary tumor location (colon versus rectum), and MSI status (MSS/MSI-low versus MSI-high).

Conditions

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Colorectal Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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KRAS wildtype

No interventions assigned to this group

KRAS codon 12 mutation

Mutation

Intervention Type GENETIC

KRAS codon 13 mutation

Mutation

Intervention Type GENETIC

KRAS codon 61 mutation

Mutation

Intervention Type GENETIC

Interventions

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Mutation

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* Patients underwent surgery for colorectal cancer from January 2009 to December 2019.

Exclusion Criteria

* incomplete data on KRAS mutation
* incomplete data on microsatellite instability (MSI) status
* dual or triple KRAS mutation
* stage IV
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Seoul National University Bundang Hospital

OTHER

Sponsor Role lead

Responsible Party

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Duck-Woo Kim

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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B-2203-742-101

Identifier Type: -

Identifier Source: org_study_id