Abstract | OBJECTIVES: METHODS: Frequencies of BCR-ABL1 mutations and the impact of mutations on responses to 2G-TKIs were obtained from published literature and used as inputs in a decision analytics model. Complete hematologic response (CHR) and major cytogenetic response (MCyR) were estimated after 12 months of 2G-TKI treatment. Total annual 2G-TKI drug costs per CHR and MCyR were estimated and compared among 3 2G-TKI access scenarios: (1) open access to both 2G-TKIs; (2) access restricted to dasatinib ( DASA-only); and (3) access restricted to nilotinib (NILO-only). RESULTS: Among a hypothetical cohort of 1000 2G-TKI-treated chronic myelogenous leukemia patients, the percentage of patients with CHR and MCyR were greatest for the open access plan (CHR: 93%, MCyR: 56%), followed by DASA-only (88%, 53%) and NILO-only (67%, 47%). Compared with the 2G-TKI costs per CHR in open access ($120,706/CHR), the costs were 5% higher ($126,753/CHR) in DASA-only and 41% higher ($169,990/CHR) in NILO-only. Likewise, compared with the 2G-TKI costs per MCyR in open access ($198,284/MCyR), the costs were 6% higher ($209,259/MCyR) in DASA-only and 22% higher ($241,515/MCyR) in NILO-only. CONCLUSION: Open access to both 2G-TKIs is associated with improved clinical and economic outcomes: greater treatment response rates (CHR and MCyR) and lower drug costs compared with restricted access to 2G-TKIs.
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Authors | Elias Jabbour, Dinara Makenbaeva, Melissa Lingohr-Smith, Jay Lin |
Journal | American journal of clinical oncology
(Am J Clin Oncol)
Vol. 41
Issue 3
Pg. 213-217
(03 2018)
ISSN: 1537-453X [Electronic] United States |
PMID | 26580245
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- BCR-ABL1 fusion protein, human
- Protein Kinase Inhibitors
- Pyrimidines
- Fusion Proteins, bcr-abl
- nilotinib
- Dasatinib
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Topics |
- Antineoplastic Agents
(economics, therapeutic use)
- Dasatinib
(economics, therapeutic use)
- Decision Support Techniques
- Drug Costs
- Fusion Proteins, bcr-abl
(genetics)
- Health Services Accessibility
- Humans
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
(drug therapy, economics, genetics)
- Mutation
- Protein Kinase Inhibitors
(economics, therapeutic use)
- Pyrimidines
(economics, therapeutic use)
- Treatment Outcome
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