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Cost-Effectiveness of Chimeric Antigen Receptor T-Cell Therapy in Pediatric Relapsed/Refractory B-Cell Acute Lymphoblastic Leukemia.
Sarkar, Reith R; Gloude, Nicholas J; Schiff, Deborah; Murphy, James D.
Affiliation
  • Sarkar RR; University of California San Diego School of Medicine, UCSD School of Medicine, La Jolla, CA.
  • Gloude NJ; Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA.
  • Schiff D; University of California San Diego School of Medicine, UCSD School of Medicine, La Jolla, CA.
  • Murphy JD; Department of Pediatrics, Division of Pediatric Hematology/Oncology, Rady Children's Hospital, San Diego, CA.
J Natl Cancer Inst ; 111(7): 719-726, 2019 07 01.
Article in En | MEDLINE | ID: mdl-30551196
BACKGROUND: Chimeric antigen receptor T-cell (CAR-T) therapy is a promising new class of cancer therapy but has a high up-front cost. We evaluated the cost-effectiveness of CAR-T therapy among pediatric patients with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL). METHODS: We built a microsimulation model for pediatric patients with relapsed/refractory B-ALL receiving either CAR-T therapy or standard of care. Outcomes included costs, quality of life (health utility), complications, and survival. We measured cost-effectiveness with the incremental cost-effectiveness ratio (ICER), with ICERs under $100 000 per quality-adjusted life-year (QALY) considered cost effective. One-way and probabilistic sensitivity analyses were used to test model uncertainty. RESULTS: Compared to standard of care, CAR-T therapy increased overall cost by $528 200 and improved effectiveness by 8.18 QALYs, resulting in an ICER of $64 600/QALY. The model was sensitive to assumptions about long-term CAR-T survival, the complete remission rate of CAR-T patients, and the health utility of long-term survivors. The base model assumed a 76.0% one-year survival with CAR-T, although if this decreased to 57.8%, then CAR-T was no longer cost effective. If the complete remission rate of CAR-T recipients decreased from 81% to 56.2%, or if the health utility of disease-free survivors decreased from 0.94 to 0.66, then CAR-T was no longer cost effective. Probabilistic sensitivity analysis found that CAR-T was cost effective in 94.8% of iterations at a willingness to pay of $100 000/QALY. CONCLUSION: CAR-T therapy may represent a cost-effective option for pediatric relapsed/refractory B-ALL, although longer follow-up of CAR-T survivors is required to confirm validity of these findings.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunotherapy, Adoptive / Cost-Benefit Analysis / Precursor Cell Lymphoblastic Leukemia-Lymphoma Type of study: Health_economic_evaluation / Prognostic_studies Aspects: Patient_preference Limits: Child / Female / Humans / Male Language: En Journal: J Natl Cancer Inst Year: 2019 Document type: Article Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunotherapy, Adoptive / Cost-Benefit Analysis / Precursor Cell Lymphoblastic Leukemia-Lymphoma Type of study: Health_economic_evaluation / Prognostic_studies Aspects: Patient_preference Limits: Child / Female / Humans / Male Language: En Journal: J Natl Cancer Inst Year: 2019 Document type: Article Country of publication: Estados Unidos