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Cost-effectiveness of Tyrosine Kinase Inhibitor Treatment Strategies for Chronic Myeloid Leukemia in Chronic Phase After Generic Entry of Imatinib in the United States

Padula, William V. (författare)
Johns Hopkins Univ, Dept Hlth Policy & Management, Baltimore, MD 21218 USA.
Larson, Richard A. (författare)
Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA.
Dusetzina, Stacie B. (författare)
Univ N Carolina, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA.;Univ N Carolina, Gillings Sch Global Publ Hlth, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA.;Univ N Carolina, Cecil G Sheps Ctr Hlth Serv Res, Chapel Hill, NC 27599 USA.
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Apperley, Jane F. (författare)
Imperial Coll, Hammersmith Hosp, Dept Haematol, London, England.
Hehlmann, Rudiger (författare)
Heidelberg Univ, Dept Med, Mannheim, Germany.
Baccarani, Michele (författare)
S Orsola Malpighi Univ Hosp, Dept Haematol & Oncol, Bologna, Italy.
Eigendorff, Ekkehard (författare)
Univ Hosp, Dept Haematol & Oncol, Jena, Germany.
Guilhot, Joelle (författare)
CHU Poitiers, INSERM, CIC 1402, Poitiers, France.
Guilhot, Francois (författare)
CHU Poitiers, INSERM, CIC 1402, Poitiers, France.
Mahon, Francois-Xavier (författare)
Univ Victor Segalen, Lab Hematol, Pessac, France.
Martinelli, Giovanni (författare)
Univ Bologna, Dept Hematol, L & A Seragnoli, Bologna, Italy.
Mayer, Jiri (författare)
Univ Hosp Brno, Dept Internal Med Hematol & Oncol, Brno, Czech Republic.
Müller, Martin C. (författare)
Heidelberg Univ, Dept Hematol & Oncol, Mannheim, Germany.
Niederwieser, Dietger (författare)
Univ Hosp Leipzig, Dept Hematol & Oncol, Leipzig, Germany.
Saussele, Susanne (författare)
Heidelberg Univ, Dept Med, Mannheim, Germany.
Schiffer, Charles A. (författare)
Wayne State Univ, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA.
Silver, Richard T. (författare)
Weill Cornell Med Ctr, Dept Med, New York, NY 10065 USA.
Simonsson, Bengt (författare)
Uppsala universitet,Hematologi
Conti, Rena M. (författare)
Univ Chicago, Dept Pediat, Chicago, IL 60637 USA.;Univ Chicago, Dept Publ Hlth Sci, Chicago, IL 60637 USA.
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Johns Hopkins Univ, Dept Hlth Policy & Management, Baltimore, MD 21218 USA Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA. (creator_code:org_t)
2016-03-04
2016
Engelska.
Ingår i: Journal of the National Cancer Institute. - : Oxford University Press (OUP). - 0027-8874 .- 1460-2105. ; 108:7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: We analyzed the cost-effectiveness of treating incident chronic myeloid leukemia in chronic phase (CML-CP) with generic imatinib when it becomes available in United States in 2016. In the year following generic entry, imatinib's price is expected to drop 70% to 90%. We hypothesized that initiating treatment with generic imatinib in these patients and then switching to the other tyrosine-kinase inhibitors (TKIs), dasatinib or nilotinib, because of intolerance or lack of effectiveness ("imatinib-first") would be cost-effective compared with the current standard of care: "physicians' choice" of initiating treatment with any one of the three TKIs. Methods: We constructed Markov models to compare the five-year cost-effectiveness of imatinib-first vs physician's choice from a US commercial payer perspective, assuming 3% annual discounting ($US 2013). The models' clinical endpoint was five-year overall survival taken from a systematic review of clinical trial results. Per-person spending on incident CML-CP treatment overall care components was estimated using Truven's MarketScan claims data. The main outcome of the models was cost per quality-adjusted life-year (QALY). We interpreted outcomes based on a willingness-to-pay threshold of $100 000/QALY. A panel of European LeukemiaNet experts oversaw the study's conduct. Results: Both strategies met the threshold. Imatinib-first ($277 401, 3.87 QALYs) offered patients a 0.10 decrement in QALYs at a savings of $88 343 over five years to payers compared with physician's choice ($365 744, 3.97 QALYs). The imatinibfirst incremental cost-effectiveness ratio was approximately $883 730/QALY. The results were robust to multiple sensitivity analyses. Conclusion: When imatinib loses patent protection and its price declines, its use will be the cost-effective initial treatment strategy for CML-CP.

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