Literature DB >> 30212291

Cost Effectiveness of Chimeric Antigen Receptor T-Cell Therapy in Relapsed or Refractory Pediatric B-Cell Acute Lymphoblastic Leukemia.

John K Lin1, Benjamin J Lerman1, James I Barnes1, Brian C Boursiquot1, Yuan Jin Tan1, Alex Q L Robinson1, Kara L Davis1, Douglas K Owens1, Jeremy D Goldhaber-Fiebert1.   

Abstract

PURPOSE: The anti-CD19 chimeric antigen receptor T-cell therapy tisagenlecleucel was recently approved to treat relapsed or refractory pediatric acute lymphoblastic leukemia. With a one-time infusion cost of $475,000, tisagenlecleucel is currently the most expensive oncologic therapy. We aimed to determine whether tisagenlecleucel is cost effective compared with currently available treatments.
METHODS: Markov modeling was used to evaluate tisagenlecleucel in pediatric relapsed or refractory acute lymphoblastic leukemia from a US health payer perspective over a lifetime horizon. The model was informed by recent multicenter, single-arm clinical trials. Tisagenlecleucel (under a range of plausible long-term effectiveness) was compared with blinatumomab, clofarabine combination therapy (clofarabine, etoposide, and cyclophosphamide), and clofarabine monotherapy. Scenario and probabilistic sensitivity analyses were used to explore uncertainty. Main outcomes were life-years, discounted lifetime costs, discounted quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (3% discount rate).
RESULTS: With an assumption of a 40% 5-year relapse-free survival rate, tisagenlecleucel increased life expectancies by 12.1 years and cost $61,000/QALY gained. However, at a 20% 5-year relapse-free survival rate, life-expectancies were more modest (3.8 years) and expensive ($151,000/QALY gained). At a 0% 5-year relapse-free survival rate and with use as a bridge to transplant, tisagenlecleucel increased life expectancies by 5.7 years and cost $184,000/QALY gained. Reduction of the price of tisagenlecleucel to $200,000 or $350,000 would allow it to meet a $100,000/QALY or $150,000/QALY willingness-to-pay threshold in all scenarios.
CONCLUSION: The long-term effectiveness of tisagenlecleucel is a critical but uncertain determinant of its cost effectiveness. At its current price, tisagenlecleucel represents reasonable value if it can keep a substantial fraction of patients in remission without transplantation; however, if all patients ultimately require a transplantation to remain in remission, it will not be cost effective at generally accepted thresholds. Price reductions would favorably influence cost effectiveness even if long-term clinical outcomes are modest.

Entities:  

Year:  2018        PMID: 30212291     DOI: 10.1200/JCO.2018.79.0642

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  33 in total

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Authors:  Ajaikumar B Kunnumakkara; Devivasha Bordoloi; Bethsebie Lalduhsaki Sailo; Nand Kishor Roy; Krishan Kumar Thakur; Kishore Banik; Mehdi Shakibaei; Subash C Gupta; Bharat B Aggarwal
Journal:  Exp Biol Med (Maywood)       Date:  2019-04-08

2.  Cost-Effectiveness of Tisagenlecleucel in Paediatric Acute Lymphoblastic Leukaemia (pALL) and Adult Diffuse Large B-Cell Lymphoma (DLBCL) in Switzerland.

Authors:  Maziar Moradi-Lakeh; Mohsen Yaghoubi; Patrick Seitz; Mehdi Javanbakht; Elisabeth Brock
Journal:  Adv Ther       Date:  2021-05-22       Impact factor: 3.845

Review 3.  Chimeric Antigen Receptor T-Cell Therapy: What the Neuroradiologist Needs to Know.

Authors:  H A Valand; F Huda; R K Tu
Journal:  AJNR Am J Neuroradiol       Date:  2019-05-02       Impact factor: 3.825

Review 4.  Chimeric antigen receptor T cell therapy comes to clinical practice.

Authors:  D A Wall; J Krueger
Journal:  Curr Oncol       Date:  2020-04-01       Impact factor: 3.677

Review 5.  Fueling chimeric antigen receptor T cells with cytokines.

Authors:  Jin Jin; Jiali Cheng; Meijuan Huang; Hui Luo; Jianfeng Zhou
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Review 6.  The long road to the first FDA-approved gene therapy: chimeric antigen receptor T cells targeting CD19.

Authors:  Peter Braendstrup; Bruce L Levine; Marco Ruella
Journal:  Cytotherapy       Date:  2020-02-01       Impact factor: 5.414

Review 7.  Value and affordability of CAR T-cell therapy in the United States.

Authors:  Salvatore Fiorenza; David S Ritchie; Scott D Ramsey; Cameron J Turtle; Joshua A Roth
Journal:  Bone Marrow Transplant       Date:  2020-05-30       Impact factor: 5.483

8.  Anti-CD19 CAR-T cell therapy bridge to HSCT decreases the relapse rate and improves the long-term survival of R/R B-ALL patients: a systematic review and meta-analysis.

Authors:  Linhui Hu; Alice Charwudzi; Qian Li; Weiwei Zhu; Qianshan Tao; Shudao Xiong; Zhimin Zhai
Journal:  Ann Hematol       Date:  2021-02-15       Impact factor: 3.673

9.  A Systematic Review of Pediatric Phase I Trials in Oncology: Toxicity and Outcomes in the Era of Targeted Therapies.

Authors:  Julia W Cohen; Srivandana Akshintala; Eli Kane; Helen Gnanapragasam; Brigitte C Widemann; Seth M Steinberg; Nirali N Shah
Journal:  Oncologist       Date:  2020-01-14

Review 10.  Immunotherapy for the Treatment of Acute Lymphoblastic Leukemia.

Authors:  Valentin Barsan; Sneha Ramakrishna; Kara L Davis
Journal:  Curr Oncol Rep       Date:  2020-01-29       Impact factor: 5.075

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