TY - JOUR
T1 - Socioeconomic determinants of the use of molecular testing in stage iv colorectal cancer
AU - Punekar, Salman R.
AU - Griffin, Megan M.
AU - Masri, Lena
AU - Roman, Stefanie D.
AU - Makarov, Danil V.
AU - Sherman, Scott E.
AU - Becker, Daniel J.
N1 - Funding Information:
Supported by the VA HSRD CDA # HX-18-012.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Objectives: Treatment with epidermal growth factor receptor monoclonal antibodies extends life for patients with advanced colorectal cancers (CRCs) whose tumors exhibit wild-Type KRAS, but KRAS testing may be underused. We studied the role of socioeconomic factors in the application of KRAS testing. Materials and Methods: We identified subjects with stage IV colorectal adenocarcinoma diagnosed 2010-2015 in the Surveillance, Epidemiology, and End Results (SEER) database. We used multivariable logistic regression models to evaluate associations between clinical/demographic factors and the rate of KRAS testing. We used multivariable-Adjusted Cox proportional hazards models to assess survival. Results: We identified 37,676 patients with stage IV CRC, 31.1% of whom were tested for KRAS mutations, of those who had documented KRAS testing, 44% were KRAS mutant. Patients were more likely to be tested if they were younger (odds ratio [OR]= 5.10 for age 20 to 29 vs. 80+, 95% confidence interval [CI]: 3.99-6.54, P<0.01), diagnosed more recently (OR=1.92 for 2015 vs. 2010, 95% CI: 1.77-2.08, P< 0.01), or lived in an area of high median household income (OR=1.24 for median household income of >69,311 vs. <49,265, 95% CI: 1.14-1.35, P<0.01). Patients were less likely to be tested if they had Medicaid (OR=0.83, 95% CI: 0.77-0.88, P< 0.01) or were unmarried (OR= 0.78, 95% CI: 0.75-0.82, P<0.0001). The risk of death was decreased in patients who received KRAS testing (hazard ratio= 0.77, 95% CI: 0.75-0.80, P <0.01). Conclusions: We found a low rate of KRAS testing in CRC patients with those living in low-income areas less likely to be tested, even after controlling for Medicaid insurance. Our study suggests that socioeconomic disparities persist despite Medicaid insurance.
AB - Objectives: Treatment with epidermal growth factor receptor monoclonal antibodies extends life for patients with advanced colorectal cancers (CRCs) whose tumors exhibit wild-Type KRAS, but KRAS testing may be underused. We studied the role of socioeconomic factors in the application of KRAS testing. Materials and Methods: We identified subjects with stage IV colorectal adenocarcinoma diagnosed 2010-2015 in the Surveillance, Epidemiology, and End Results (SEER) database. We used multivariable logistic regression models to evaluate associations between clinical/demographic factors and the rate of KRAS testing. We used multivariable-Adjusted Cox proportional hazards models to assess survival. Results: We identified 37,676 patients with stage IV CRC, 31.1% of whom were tested for KRAS mutations, of those who had documented KRAS testing, 44% were KRAS mutant. Patients were more likely to be tested if they were younger (odds ratio [OR]= 5.10 for age 20 to 29 vs. 80+, 95% confidence interval [CI]: 3.99-6.54, P<0.01), diagnosed more recently (OR=1.92 for 2015 vs. 2010, 95% CI: 1.77-2.08, P< 0.01), or lived in an area of high median household income (OR=1.24 for median household income of >69,311 vs. <49,265, 95% CI: 1.14-1.35, P<0.01). Patients were less likely to be tested if they had Medicaid (OR=0.83, 95% CI: 0.77-0.88, P< 0.01) or were unmarried (OR= 0.78, 95% CI: 0.75-0.82, P<0.0001). The risk of death was decreased in patients who received KRAS testing (hazard ratio= 0.77, 95% CI: 0.75-0.80, P <0.01). Conclusions: We found a low rate of KRAS testing in CRC patients with those living in low-income areas less likely to be tested, even after controlling for Medicaid insurance. Our study suggests that socioeconomic disparities persist despite Medicaid insurance.
KW - Colorectal cancer
KW - KRAS testing
KW - Socioeconomic status
KW - Wild-Type EGFR
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U2 - 10.1097/COC.0000000000000875
DO - 10.1097/COC.0000000000000875
M3 - Article
C2 - 34753883
AN - SCOPUS:85120330838
VL - 44
SP - 597
EP - 602
JO - American Journal of Clinical Oncology
JF - American Journal of Clinical Oncology
SN - 0277-3732
IS - 12
ER -