Patterns and Predictors of Oral Anticancer Agent Use in Diverse Patients With Metastatic Renal Cell Carcinoma.


Journal

JCO oncology practice
ISSN: 2688-1535
Titre abrégé: JCO Oncol Pract
Pays: United States
ID NLM: 101758685

Informations de publication

Date de publication:
12 2021
Historique:
pubmed: 18 6 2021
medline: 1 2 2022
entrez: 17 6 2021
Statut: ppublish

Résumé

Availability of targeted oral anticancer agents (OAAs) has transformed care for patients with metastatic renal cell carcinoma (mRCC). Our objective was to identify patterns and predictors of OAA use within 12 months after mRCC was detected to understand real-world adoption of OAAs. We used a novel, North Carolina cancer registry-linked multipayer claims data resource to examine patterns of use of five oral therapies among patients with mRCC diagnosed in 2006-2015, with claims through 2016. Patients were required to have 12 months of continuous enrollment before metastatic index date. Log-Poisson models estimated unadjusted and adjusted risk ratios (RRs) for associations between patient characteristics and OAA use. In sensitivity analyses, we used a competing risk framework to estimate adjusted risk differences in OAA use. Our population-based study of 713 patients demonstrated low (37%) OAA use during the first year after metastatic index date among both publicly and privately insured patients, with shifting patterns of use consistent with regulatory approvals over time. Compared with patients age 18-49 years, patients age 70-74 years were half likely to use OAAs (95% confidence limit [CL], 0.34 to 0.78) and patients age 80+ years were 71% less likely to use OAAs (95% CL, 0.17 to 0.50). Patients with two comorbidities (RR, 0.73; 95% CL, 0.55 to 0.98) and those with 3+ comorbidities (RR, 0.68; 95% CL, 0.50 to 0.91) were less likely to receive OAA than those without comorbidities. Patients with higher frailty also had lower OAA utilization (RR, 0.67; 95% CL, 0.52 to 0.85). These findings suggest a need to better understand the system-level and provider-level drivers of OAA underuse, as well as OAA adherence and associated survival.

Identifiants

pubmed: 34138665
doi: 10.1200/OP.20.01082
pmc: PMC8678030
doi:

Substances chimiques

Antineoplastic Agents 0
Antipsychotic Agents 0
Paliperidone Palmitate R8P8USM8FR

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1895-e1904

Subventions

Organisme : NCI NIH HHS
ID : R01 CA226842
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001111
Pays : United States

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Auteurs

Stephanie B Wheeler (SB)

Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill (UNC-CH), Chapel Hill, NC.
Lineberger Comprehensive Cancer Center, UNC-CH, Chapel Hill, NC.

Lisa P Spees (LP)

Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill (UNC-CH), Chapel Hill, NC.
Lineberger Comprehensive Cancer Center, UNC-CH, Chapel Hill, NC.

Bradford E Jackson (BE)

Lineberger Comprehensive Cancer Center, UNC-CH, Chapel Hill, NC.

Christopher D Baggett (CD)

Lineberger Comprehensive Cancer Center, UNC-CH, Chapel Hill, NC.
Department of Epidemiology, Gillings School of Global Public Health, UNC-CH, Chapel Hill, NC.

Lauren E Wilson (LE)

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC.

Melissa A Greiner (MA)

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC.

Deborah R Kaye (DR)

Department of Medicine, Duke University School of Medicine, Durham, NC.
Department of Surgery (Urology), Duke University School of Medicine, Durham, NC.

Tian Zhang (T)

Department of Surgery (Urology), Duke University School of Medicine, Durham, NC.
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Daniel George (D)

Department of Surgery (Urology), Duke University School of Medicine, Durham, NC.
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Charles D Scales (CD)

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC.
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Jessica E Pritchard (JE)

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC.

Michaela A Dinan (MA)

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC.
Duke Cancer Institute, Durham, NC.

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Classifications MeSH