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Clinical benefit and cost of breakthrough cancer drugs approved by the US Food and Drug Administration
- Source :
- CANCER, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, instname, r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
- Publication Year :
- 2020
- Publisher :
- WILEY, 2020.
-
Abstract
- Background The clinical benefit and pricing of breakthrough-designated cancer drugs are uncertain. This study compares the magnitude of the clinical benefit and monthly price of new and supplemental breakthrough-designated and non-breakthrough-designated cancer drug approvals. Methods A cross-sectional cohort comprised approvals of cancer drugs for solid tumors from July 2012 to December 2017. For each indication, the clinical benefit from the pivotal trials was scored via validated frameworks: the American Society of Clinical Oncology Value Framework (ASCO-VF), the American Society of Clinical Oncology Cancer Research Committee (ASCO-CRC), the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS), and the National Comprehensive Cancer Network (NCCN) Evidence Blocks. A high clinical benefit was defined as scores ≥ 45 for the ASCO-VF, overall survival gains ≥ 2.5 months or progression-free survival gains ≥ 3 months for all cancer types for the ASCO-CRC criteria, a grade of A or B for trials of curative intent and a grade of 4 or 5 for trials of noncurative intent for the ESMO-MCBS, and scores of 4 and 5 and a combined score ≥ 16 for the NCCN Evidence Blocks. Monthly Medicare drug prices were calculated with Medicare prices and DrugAbacus. Results This study identified 106 trials supporting approval of 52 drugs for 96 indications. Forty percent of these indications received the breakthrough designation. Among the included trials, 33 (43%), 46 (73%), 35 (34%), and 67 (69%) met the thresholds established by the ASCO-VF, ASCO-CRC, ESMO-MCBS, and NCCN, respectively. In the metastatic setting, there were higher odds of clinically meaningful grades in trials supporting breakthrough drugs with the ASCO-VF (odds ratio [OR], 3.69; P = .022) and the NCCN Evidence Blocks (OR, 5.80; P = .003) but not with the ASCO-CRC (OR, 3.54; P = .11) or version 1.1 (v1.1) of the ESMO-MCBS (OR, 1.22; P = .70). The median costs of breakthrough therapy drugs were significantly higher than those of nonbreakthrough therapies (P = .001). Conclusions In advanced solid cancers, drugs that received the breakthrough therapy designation were more likely than nonbreakthrough therapy drugs to be scored as providing a high clinical benefit with the ASCO-VF and the NCCN Evidence Blocks but not with the ESMO-MCBS v1.1 or the ASCO-CRC scale.
- Subjects :
- Cancer Research
medicine.medical_specialty
Breakthrough therapy
Cancer drugs
value frameworks
Antineoplastic Agents
Odds
Food and drug administration
03 medical and health sciences
0302 clinical medicine
Internal medicine
cost
medicine
Humans
030212 general & internal medicine
American Society of Clinical Oncology (ASCO)
European Society for Medical Oncology (ESMO)
Clinical Oncology
United States Food and Drug Administration
business.industry
clinical benefit
Cancer
Odds ratio
medicine.disease
United States
Cross-Sectional Studies
Oncology
030220 oncology & carcinogenesis
Cohort
breakthrough therapy designation
Quality of Life
business
Subjects
Details
- ISSN :
- 0008543X
- Database :
- OpenAIRE
- Journal :
- CANCER, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, instname, r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
- Accession number :
- edsair.doi.dedup.....a13633f21006518d5bce8d4686f9017c