Impact of Oncology Drug Review Times on Public Funding Recommendations

Author:

Hussain Marya1ORCID,Wong Chelsea2ORCID,Taguedong Eddy3,Verma Saurav4ORCID,Mahsin Md5ORCID,Karim Safiya1,Lee-Ying Richard1,Ezeife Doreen A.1

Affiliation:

1. Department of Oncology, University of Calgary, Calgary, AB T2N 4N2, Canada

2. Faculty of Arts, Department of Psychology, University of Calgary, Calgary, AB T2N 1N4, Canada

3. Department of Medicine, McGill University, Montreal, QC H3A 0G4, Canada

4. London Regional Cancer Program, Department of Medical Oncology, London Health Sciences Centre, London, ON N6A 5W9, Canada

5. Precision Oncology Hub, Alberta Health Services, Calgary, AB T2N 4Z6, Canada

Abstract

New oncology drugs undergo detailed review prior to public funding in a single-payer healthcare system. The aim of this study was to assess how cancer drug review times impact funding recommendations. Drugs reviewed by the pan-Canadian Oncology Drug Review (pCODR) between the years 2012 and 2020 were included. Data were collected including Health Canada approval dates, initial and final funding recommendations, treatment intent, drug class, clinical indications, and incremental cost-effectiveness ratios (ICER). Univariable and multivariable analyses were used to determine the association between funding recommendations and review times. Of the 164 applications submitted, 130 received a positive final recommendation. Median time from Health Canada (HC) approval to final recommendation was longer for drugs indicated for the treatment of gastrointestinal (GI) and lung cancer compared to breast, genitourinary (GU), and other tumours (205 vs. 198 vs. 111 vs. 129 vs. 181 days, respectively; Kruskal–Wallis p = 0.0312). Drugs with longer review times were more likely to receive a negative pCODR recommendation, even when adjusting for tumour type, drug class, and intent of therapy (157 vs. 298 days; Wilcoxon p = 0.0003, OR 1.002 95% CI [1.000–1.004].). There was no association between funding recommendation and tumour type or class of drug. The exploration of factors associated with variance in review times will be important in ensuring timely patient access to cancer drugs.

Publisher

MDPI AG

Reference19 articles.

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4. Canada’s Drug and Health Technology Agency (2020). Procedures for the CADTH Pan-Canadian Oncology Drug Review, Canada’s Drug and Health Technology Agency. Available online: https://www.cadth.ca/sites/default/files/pcodr/pCODR%27sDrugReviewProcess/pcodr-procedures.pdf.

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