Cancer Treatment Data in Central Cancer Registries: When Are Supplemental Data Needed?

Author:

Bradley Cathy J12,Liang Rifei1,Jasem Jagar1,Lindrooth Richard C2,Sabik Lindsay M3,Perraillon Marcelo C12

Affiliation:

1. University of Colorado Cancer Center, Aurora, CO, USA

2. Colorado School of Public Health, Aurora, CO, USA

3. University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, USA

Abstract

Background: We evaluated treatment concordance between the Colorado All Payer Claims Database (APCD) and the Colorado Central Cancer Registry (CCCR) to explore whether APCDs can augment registry data. We compare treatment concordance for breast cancer, an extensively studied site with an inpatient reporting source and select leukemias that are often diagnosed outpatient. Methods: We analyzed concordance by cancer type and treatment, patient demographics, reporting source, and health insurance, calculating the sensitivity, specificity, positive predictive values (PPV) and Kappa statistics. We estimated an adjusted logistic regression model to assess whether the APCD statistically significantly reports additional cancer-directed treatments. Results: Among women with breast cancer, 14% had chemotherapy treatments that were absent from the CCCR. Missing treatments were more common among women younger than age 50 (15%) and patients aged 75 and older (19%), rural residents (17%), and when the reporting source was outpatient (22%). Similar and more pronounced patterns for people with leukemia were observed. Concordance for oral treatments was lower for each cancer. Sensitivity and PPVs were high, with moderate Kappa statistics. The APCD was 5.3 percentage points less likely to identify additional treatments for breast cancer patients and 10 percentage points more likely to identify additional treatments when the reporting source was an outpatient facility. Conclusion: A robust data infrastructure is needed to investigate research questions that require population-level analyses, particularly for questions seeking to reduce health inequity and comparisons across payers, including Medicare Advantage and fee-for-service. APCD data are a step toward creating an infrastructure for cancer, particularly for patients who reside in rural areas and/or receive care from outpatient centers.

Funder

National Cancer Institute

Publisher

SAGE Publications

Subject

Cancer Research,Oncology

Reference21 articles.

1. North American Association of Central Cancer Registries. 2022. Accessed January 20, 2022. https://www.naaccr.org/

2. Centers for Disease Control and Prevention. National Program of Cancer Registries (NPCR). Accessed May 20, 2022. https://www.cdc.gov/cancer/npcr/

3. NIH National Cancer Institute Surveillance Epidemiology and End Results Program. SEER Program Coding and Staging Manual 2021. 2021. Accessed May 20, 2022. https://seer.cancer.gov/archive/manuals/2021/SPCSM_2021_MainDoc.pdf

4. Feasibility of Capturing Cancer Treatment Data in the Utah All-Payer Claims Database

5. Agency for Healthcare Research and Quality. All-Payer Claims Databases. Updated February 2018. Accessed January 20, 2022. https://www.ahrq.gov/data/apcd/index.html

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