High Cost Sharing and Specialty Drug Initiation Under Medicare Part D: A Case Study in Patients With Newly Diagnosed Chronic Myeloid Leukemia

被引:0
|
作者
Doshi, Jalpa A. [1 ,2 ]
Li, Pengxiang [1 ,2 ]
Huo, Hairong [1 ]
Pettit, Amy R. [3 ]
Kumar, Rishab [4 ]
Weiss, Brendan M. [5 ,6 ]
Huntington, Scott F. [7 ,8 ]
机构
[1] Univ Penn, Perelman Sch Med, Div Gen Internal Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Leonard Davis Inst Hlth Econ, Philadelphia, PA 19104 USA
[3] Univ Penn, Ctr Publ Hlth Initiat, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Arts & Sci, Philadelphia, PA 19104 USA
[5] Univ Penn, Abramson Canc Ctr, Dept Med, Div Hematol Oncol, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[7] Yale Univ, Sch Med, Dept Med, Sect Hematol, New Haven, CT 06510 USA
[8] Yale Univ, Sch Med, Canc Outcomes Publ Policy & Effectiveness Res COP, New Haven, CT USA
关键词
OF-POCKET COSTS; IMPACT; ADHERENCE; SURVIVAL; IMATINIB;
D O I
暂无
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objectives: Specialty drugs often offer medical advances but are frequently subject to high cost sharing. This is particularly true with Medicare Part D, where after meeting a deductible, patients without low-income subsidies (non-LIS) typically face 25% to 33% coinsurance (initial coverage phase with "specialty tier" cost sharing), followed by similar to 50% coinsurance (coverage gap phase), and then 5% coinsurance (catastrophic phase). Yet, no studies have examined the impact of such high cost sharing on specialty drug initiation under Part D. Oral tyrosine kinase inhibitors (TKIs) have revolutionized the treatment of chronic myeloid leukemia (CML), making it an apt case study. Study Design: A retrospective claims-based analysis utilizing 2011 to 2013 100% Medicare claims. Methods: TKI initiation rates and time to initiation were compared between fee-for-service non-LIS Part D patients newly diagnosed with CML and their LIS counterparts who faced nominal cost sharing of <=$5. Results: The first 30-day TKI fill "straddled" benefit phases, for a mean out-of-pocket cost of $2600 or more for non-LIS patients. Non-LIS patients were less likely than LIS patients to have a TKI claim within 6 months of diagnosis (45.3% vs 66.9%; P<.001) and those initiating a TKI took twice as long to fill it (mean = 50.9 vs 23.7 days; P<.001). Cox regressions controlling for sociodemographic, clinical, and plan characteristics confirmed descriptive findings (hazard ratio, 0.59; 95% CI, 0.45-0.76). Extensive sensitivity analyses confirmed the robustness of our findings. Conclusions: High cost sharing was associated with reduced and/or delayed initiation of TKIs. We discuss policy strategies to reduce current financial barriers that adversely impact access to critical therapies under Medicare Part D.
引用
收藏
页码:S78 / +
页数:11
相关论文
共 25 条
  • [1] Tyrosine Kinase Inhibitors Initiation, Cost Sharing, and Health Care Utilization in Patients with Newly Diagnosed Chronic Myeloid Leukemia: A Retrospective Claims-Based Study
    Phuar, Hsiao Ling
    Begley, Charles E.
    Chan, Wenyaw
    Krause, Trudy Millard
    JOURNAL OF MANAGED CARE & SPECIALTY PHARMACY, 2019, 25 (10) : 1140 - 1150
  • [2] Is imatinib a cost-effective treatment for newly diagnosed chronic myeloid leukemia patients?
    Goldman, J
    NATURE CLINICAL PRACTICE ONCOLOGY, 2005, 2 (03): : 126 - 127
  • [3] High-Cost, High-Value Oral Specialty Drugs: More Evidence on the Impact of Cost Sharing in Medicare Part D
    Huntington, Scott F.
    Davidoff, Amy J.
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (36) : 4307 - +
  • [4] Phase 2 study of bosutinib in Japanese patients with newly diagnosed chronic phase chronic myeloid leukemia
    Hino, Masayuki
    Matsumura, Itaru
    Fujisawa, Shin
    Ishizawa, Kenichi
    Ono, Takaaki
    Sakaida, Emiko
    Sekiguchi, Naohiro
    Tanetsugu, Yusuke
    Fukuhara, Kei
    Ohkura, Masayuki
    Koide, Yuichiro
    Takahashi, Naoto
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2020, 112 (01) : 24 - 32
  • [5] Financial Burden for Patients With Chronic Myeloid Leukemia Enrolled in Medicare Part D Taking Targeted Oral Anticancer Medications
    Shen, Chan
    Zhao, Bo
    Liu, Lei
    Shih, Ya-Chen Tina
    JOURNAL OF ONCOLOGY PRACTICE, 2017, 13 (02) : E152 - E162
  • [6] Phase 3 study of nilotinib vs imatinib in Chinese patients with newly diagnosed chronic myeloid leukemia in chronic phase: ENESTchina
    Wang, Jianxiang
    Shen, Zhi-Xiang
    Saglio, Giuseppe
    Jin, Jie
    Huang, He
    Hu, Yu
    Du, Xin
    Li, Jianyong
    Meng, Fanyi
    Zhu, Huanling
    Hu, Jianda
    Wang, Jianmin
    Hou, Ming
    Hertle, Sabine
    Menssen, Hans D.
    Ortmann, Christine-Elke
    Tribouley, Catherine
    Yuan, Ye
    Baccarani, Michele
    Huang, Xiaojun
    BLOOD, 2015, 125 (18) : 2771 - 2778
  • [7] Evaluation of Medication Adherence and Pharmacokinetics of Dasatinib for Earlier Molecular Response in Japanese Patients With Newly Diagnosed Chronic Myeloid Leukemia: A Pilot Study
    Iwamoto, Takuya
    Monma, Fumihiko
    Ohishi, Kohshi
    Umino, Akira
    Suzuki, Kei
    Oka, Koji
    Kawakami, Keiki
    Sekine, Takao
    Okuda, Masahiro
    Katayama, Naoyuki
    THERAPEUTIC DRUG MONITORING, 2019, 41 (05) : 575 - 581
  • [8] The current role of high-dose imatinib in chronic myeloid leukemia patients, newly diagnosed or resistant to standard dose
    Breccia, Massimo
    Alimena, Giuliana
    EXPERT OPINION ON PHARMACOTHERAPY, 2011, 12 (13) : 2075 - 2087
  • [9] A phase II study of continuous infusion homoharringtonine and cytarabine in newly diagnosed patients with chronic myeloid leukemia: CALGB study 19804
    Stone, Richard M.
    Donohue, Kathleen A.
    Stock, Wendy
    Hars, Vera
    Linker, Charles A.
    Shea, Thomas
    DeAngelo, Daniel J.
    Marcucci, Guido
    Bloomfield, Clara D.
    Larson, Richard A.
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2009, 63 (05) : 859 - 864
  • [10] Long-term outcome of patients with newly diagnosed chronic myeloid leukemia: a randomized comparison of stem cell transplantation with drug treatment
    Gratwohl, A.
    Pfirrmann, M.
    Zander, A.
    Kroger, N.
    Beelen, D.
    Novotny, J.
    Nerl, C.
    Scheid, C.
    Spiekermann, K.
    Mayer, J.
    Sayer, H. G.
    Falge, C.
    Bunjes, D.
    Doehner, H.
    Ganser, A.
    Schmidt-Wolf, I.
    Schwerdtfeger, R.
    Baurmann, H.
    Kuse, R.
    Schmitz, N.
    Wehmeier, A.
    Fischer, J. Th
    Ho, A. D.
    Wilhelm, M.
    Goebeler, M-E
    Lindemann, H. W.
    Bormann, M.
    Hertenstein, B.
    Schlimok, G.
    Baerlocher, G. M.
    Aul, C.
    Pfreundschuh, M.
    Fabian, M.
    Staib, P.
    Edinger, M.
    Schatz, M.
    Fauser, A.
    Arnold, R.
    Kindler, T.
    Wulf, G.
    Rosselet, A.
    Hellmann, A.
    Schaefer, E.
    Pruemmer, O.
    Schenk, M.
    Hasford, J.
    Heimpel, H.
    Hossfeld, D. K.
    Kolb, H-J
    Buesche, G.
    LEUKEMIA, 2016, 30 (03) : 562 - 569