TY - JOUR
T1 - Patient- And Provider-Level Predictors of Survival Among Patients With Metastatic Renal Cell Carcinoma Initiating Oral Anticancer Agents
AU - Spees, Lisa P.
AU - Dinan, Michaela A.
AU - Jackson, Bradford E.
AU - Baggett, Christopher D.
AU - Wilson, Lauren E.
AU - Greiner, Melissa A.
AU - Kaye, Deborah R.
AU - Zhang, Tian
AU - George, Daniel J.
AU - Scales, Charles D.
AU - Pritchard, Jessica E.
AU - Leapman, Michael
AU - Gross, Cary P.
AU - Wheeler, Stephanie B.
N1 - Funding Information:
LPS and BEJ receive unrelated funding paid to their institution from AstraZeneca. SBW has received unrelated grant funding paid to her institution from Pfizer Foundation/NCCN and AstraZeneca. TZ has research funding relationships with Personal Genome Diagnostics, Pfizer, Janssen, Acerta, Abbvie/StemCentrx, Novartis, Merrimack, OmniSeq, PGDx, Merck, Mirati Therapeutics, Regeneron, and Astellas, and consulting relationships with Genentech Roche, Exelixis, Genomic Health, Sanofi Aventis, AstraZeneca, Bayer, Pfizer, Foundation Medicine, Janssen, Amgen, Bristol Myers Squibb, MJH Associates, Calithera, Dendreon, QED Therapeutics, Aravive, Seattle Genetics, Eisai, Pacific Genuity, IQVIA, Capio Biosciences, and Archimmune Therapeutics, & Nanorobotics. DG has a current relationship with Bayer, Novartis, Merck&Co., Exelixis, and Pfizer. CG has received research funding from the NCCN Foundation, Genentech, Johnson & Johnson and funding from Flatiron Inc. for travel to and speaking at a scientific conference. CS has research funding with Pfizer, Exelixis, Merck, and BMS.
Funding Information:
Funding : Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health (NIH) ( R01CA226842 ). Federal money is financing 100% of the cost. Database infrastructure was supported through the UNC Clinical and Translational Science Award ( UL1TR001111 ) and the UNC LCCC, University Cancer Research Fund via the State of North Carolina . The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022
Y1 - 2022
N2 - Purpose: In an era of rapid expansion of FDA approvals for oral anticancer agents (OAAs), it is important to understand the factors associated with survival among real-world populations, which include groups not well-represented in pivotal clinical trials of OAAs, such as the elderly, racial minorities, and medically complex patients. Our objective was to evaluate patient- and provider-level characteristics’ associations with mortality among a multi-payer cohort of metastatic renal cell carcinoma (mRCC) patients who initiated OAAs. Methods: This retrospective cohort study was conducted using data from the North Carolina state cancer registry linked to multi-payer claims data for the years 2004 to 2015. Provider data were obtained from North Carolina Health Professions Data System and the National Plan & Provider Enumeration System. Included patients were individuals with mRCC who initiated an OAA and survived ≥90 days after beginning treatment. We estimated hazard ratios (HR) and corresponding 95% confidence limits (CL) using Cox hazard models for associations between patient demographics, patient clinical characteristics, provider-level factors, and 2-year all-cause mortality. Results: The cohort included 207 patients with mRCC who received OAAs. In multivariable models, clinical variables such as frailty (HR: 1.36, 95% CL: 1.11-1.67) and de novo metastatic diagnosis (HR: 2.63, 95%CL: 1.67-4.16) were associated with higher all-cause mortality. Additionally, patients solely on Medicare had higher adjusted all-cause mortality compared with patients with any private insurance (HR: 2.35, 95% CL: 1.32-4.18). No provider-level covariates investigated were associated with all-cause mortality. Conclusions: Within a real-world population of mRCC patients taking OAAs, survival differed based on patient characteristics. In an era of rapid expansion of FDA approvals for OAAs, these real-world data underscore the continued importance of access to high-quality care, particularly for medically complex patients with limited resources.
AB - Purpose: In an era of rapid expansion of FDA approvals for oral anticancer agents (OAAs), it is important to understand the factors associated with survival among real-world populations, which include groups not well-represented in pivotal clinical trials of OAAs, such as the elderly, racial minorities, and medically complex patients. Our objective was to evaluate patient- and provider-level characteristics’ associations with mortality among a multi-payer cohort of metastatic renal cell carcinoma (mRCC) patients who initiated OAAs. Methods: This retrospective cohort study was conducted using data from the North Carolina state cancer registry linked to multi-payer claims data for the years 2004 to 2015. Provider data were obtained from North Carolina Health Professions Data System and the National Plan & Provider Enumeration System. Included patients were individuals with mRCC who initiated an OAA and survived ≥90 days after beginning treatment. We estimated hazard ratios (HR) and corresponding 95% confidence limits (CL) using Cox hazard models for associations between patient demographics, patient clinical characteristics, provider-level factors, and 2-year all-cause mortality. Results: The cohort included 207 patients with mRCC who received OAAs. In multivariable models, clinical variables such as frailty (HR: 1.36, 95% CL: 1.11-1.67) and de novo metastatic diagnosis (HR: 2.63, 95%CL: 1.67-4.16) were associated with higher all-cause mortality. Additionally, patients solely on Medicare had higher adjusted all-cause mortality compared with patients with any private insurance (HR: 2.35, 95% CL: 1.32-4.18). No provider-level covariates investigated were associated with all-cause mortality. Conclusions: Within a real-world population of mRCC patients taking OAAs, survival differed based on patient characteristics. In an era of rapid expansion of FDA approvals for OAAs, these real-world data underscore the continued importance of access to high-quality care, particularly for medically complex patients with limited resources.
KW - Insurance
KW - Metastatic
KW - Oral anti-cancer agents
KW - Renal cell carcinoma
KW - Survival
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U2 - 10.1016/j.clgc.2022.04.010
DO - 10.1016/j.clgc.2022.04.010
M3 - Article
C2 - 35595633
AN - SCOPUS:85130323498
SN - 1558-7673
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
ER -