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KRAS Variant Frequency and Colorectal Cancer-Specific Survival by Race and Ethnicity.

JAMA network open 2026 Vol.9(3) p. e261585

Rodriguez GM, Aljehani M, DePuy D, Patel SR, Fisher GA, Lin AY

📝 환자 설명용 한 줄

[IMPORTANCE] Colorectal cancer is the third most commonly diagnosed cancer and the third leading cause of cancer-associated deaths in the US.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value P < .001
  • 95% CI 1.01-1.22
  • 연구 설계 cross-sectional

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BibTeX ↓ RIS ↓
APA Rodriguez GM, Aljehani M, et al. (2026). KRAS Variant Frequency and Colorectal Cancer-Specific Survival by Race and Ethnicity.. JAMA network open, 9(3), e261585. https://doi.org/10.1001/jamanetworkopen.2026.1585
MLA Rodriguez GM, et al.. "KRAS Variant Frequency and Colorectal Cancer-Specific Survival by Race and Ethnicity.." JAMA network open, vol. 9, no. 3, 2026, pp. e261585.
PMID 41817523

Abstract

[IMPORTANCE] Colorectal cancer is the third most commonly diagnosed cancer and the third leading cause of cancer-associated deaths in the US. Hispanic and non-Hispanic Black patients experience higher colorectal cancer mortality rates compared with non-Hispanic White patients. More data are needed to understand the role of cancer biology in colorectal cancer survival disparities among racial and ethnic minority groups.

[OBJECTIVE] To evaluate racial and ethnic differences in KRAS variant frequency and the association of presence of a KRAS variant with colorectal cancer-specific survival.

[DESIGN, SETTING, AND PARTICIPANTS] This population-based cross-sectional study used data from the Surveillance, Epidemiology, and End Results Program and included patients diagnosed with colorectal cancer from 2010 through 2015, with follow-up through December 31, 2018. Data were analyzed between December 2023 and August 2024.

[EXPOSURE] Racial and ethnic differences in KRAS variant frequency.

[MAIN OUTCOMES AND MEASURES] Outcomes of interest were cumulative incidence of colorectal cancer-specific death, assessed using cumulative incidence functions, and subdistribution hazard ratio (sHR) for colorectal cancer-specific death, assessed using Fine-Gray regression models.

[RESULTS] A total of 21 354 patients (mean [SD] age at diagnosis, 62.54 [13.78] years; 9653 females [45.2%]; median [IQR] follow-up, 2.67 [1.25-4.17] years) were included in the analysis, including 1680 Asian or Pacific Islander patients (7.8%), 2459 Hispanic patients (11.5%), 2761 non-Hispanic Black patients (12.9%), and 14 454 non-Hispanic White patients (67.7%). Hispanic patients and non-Hispanic Black patients had higher KRAS variant frequencies than non-Hispanic Asian or Pacific Islander patients and non-Hispanic White patients (44.2% and 48.3% vs 37.5% and 39.3%, respectively). Among patients with KRAS wild-type tumors, the unadjusted cumulative incidence of colorectal cancer-specific death was highest for Hispanic patients (59.5%; 95% CI, 55.4%-63.3%; P < .001); among patients with KRAS variant tumors, colorectal cancer-specific death was highest for non-Hispanic Black patients (67.3%; 95% CI, 63.3%-70.9%; P < .001). Among patients with KRAS wild-type tumors, Hispanic patients showed a significantly increased risk of colorectal cancer-specific death (sHR, 1.11; 95% CI, 1.01-1.22; P = .03). Among patients with KRAS variant tumors, non-Hispanic Black patients had a significantly increased risk of colorectal cancer-specific death (sHR, 1.18; 95% CI, 1.07-1.29; P < .001).

[CONCLUSIONS AND RELEVANCE] In this cross-sectional study of patients with colorectal cancer, Hispanic patients and non-Hispanic Black patients had higher KRAS variant prevalence than non-Hispanic White patients. Among patients with a KRAS variant, non-Hispanic Black patients had worse cause-specific survival than non-Hispanic White patients. Among patients with wild-type KRAS, Hispanic patients had worse survival compared with non-Hispanic White patients. These findings highlight the need for further research on racial and ethnic differences in KRAS-related outcomes.

MeSH Terms

Humans; Colorectal Neoplasms; Female; Proto-Oncogene Proteins p21(ras); Male; Middle Aged; Cross-Sectional Studies; Aged; United States; Hispanic or Latino; Ethnicity; White People; Black or African American; SEER Program; Racial Groups; White