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Racial Differences in Stage IV Colorectal Cancer Molecular Profiling and Mutation Rates.
Hinshaw, Tyler P; Fu, Yuanyuan; Irish, William D; Parikh, Alexander A; Snyder, Rebecca A.
Afiliação
  • Hinshaw TP; Division of Surgical Oncology, Department of Surgery, Brody School of Medicine at East Carolina University, Greenville, North Carolina.
  • Fu Y; Division of Surgical Oncology, Department of Surgery, Brody School of Medicine at East Carolina University, Greenville, North Carolina.
  • Irish WD; Division of Surgical Oncology, Department of Surgery, Brody School of Medicine at East Carolina University, Greenville, North Carolina; Department of Public Health, Brody School of Medicine at East Carolina University, Greenville, North Carolina.
  • Parikh AA; Division of Surgical Oncology, Department of Surgery, Brody School of Medicine at East Carolina University, Greenville, North Carolina; Division of Surgical Oncology, The University of Texas Health San Antonio Mays Cancer Center, San Antonio, Texas.
  • Snyder RA; Division of Surgical Oncology, Department of Surgery, Brody School of Medicine at East Carolina University, Greenville, North Carolina; Department of Public Health, Brody School of Medicine at East Carolina University, Greenville, North Carolina; Department of Surgical Oncology, The University of Te
J Surg Res ; 295: 763-769, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38150868
ABSTRACT

INTRODUCTION:

Despite advances in colorectal cancer (CRC) treatment, racial disparities persist. The primary aims of the study were to evaluate differences in molecular testing rates over time by race; and measure the incidence of tumor mutations by race in patients with metastatic CRC.

METHODS:

A retrospective cohort study was performed of all adult patients with stage IV CRC (2008-2018) identified within the cancer registry of a large regional health system. Demographic/clinical characteristics were collected through primary data abstraction of the electronic health record. Molecular profiling results were obtained directly from Caris Molecular Intelligence and electronic health record.

RESULTS:

Three hundred eighty-three patients were included 40.5% (n = 155) were Black and 59.5% (n = 228) were White. Significant increases were observed in microsatellite instability (MSI), KRAS, and BRAF testing rates during the study period (P < 0.0001). The odds of testing over time increased more significantly in Black compared to White patients for MSI testing (White odds ratio [OR] 1.26 [95% confidence interval [CI] 1.12-1.41], Black OR 1.69 [95% CI 1.41-2.02], P = 0.005) and BRAF testing (White OR 1.42 [95% CI 1.26-1.62], Black OR 1.89 [95% CI 1.51-2.36], P = 0.027). An increase in KRAS testing over time was observed for both cohorts and was independent of race (P = 0.58). Mutation rates did not differ by race KRAS (Black 55.8% versus White 45.6%, P = 0.13) and BRAF (Black 4.8% versus White 10.0%, P = 0.33).

CONCLUSIONS:

Within a large regional health system, molecular testing rates in patients with metastatic CRC increased significantly following National Comprehensive Cancer Network guideline changes for both Black and White patients. Black and White patients who underwent molecular testing had similar rates of MSI, KRAS, and BRAF mutations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias do Colo Limite: Adult / Humans Idioma: En Revista: J Surg Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias do Colo Limite: Adult / Humans Idioma: En Revista: J Surg Res Ano de publicação: 2024 Tipo de documento: Article