Melanoma
Keshav Kooragayala, MD (he/him/his)
Resident
Cooper University Hospital, Pennsylvania, United States
Keshav Kooragayala, MD (he/him/his)
Resident
Cooper University Hospital, Pennsylvania, United States
Keshav Kooragayala, MD (he/him/his)
Resident
Cooper University Hospital, Pennsylvania, United States
Francis Spitz, BS
Graduate Student
Cooper University Hospital, United States
Yupeng Li, PhD
Professor of Economics
Rowan University, United States
Young K. Hong, MD MPH
Assistant Professor
Cooper University Hospital
Camden, New Jersey, United States
Treatment for metastatic melanoma has evolved with immune checkpoint inhibition (CPI) infusions. In contrast, tumor-infiltrating lymphocytes (TIL) have been utilized as a novel therapeutic modality for malignant melanoma with durable, long-lasting effects from a single treatment. Recent data has shown that progression-free survival (PFS) is significantly longer for patients treated with TIL therapy than CPI monotherapy. Still, more is needed to know about the cost-effectiveness of this treatment modality, which is associated with high up-front costs and adverse events during the acute treatment phase. This study proposes a framework to assess cost-effectiveness by comparing checkpoint inhibition versus TIL therapy for metastatic melanoma.
Methods:
We performed a three-state Markov model (progression-free, progression, death) to compare the cost-effectiveness of pembrolizumab versus TIL therapy. Outcome data from the Keynote 006 trial and outcome data for TIL therapy were extracted from a recent multi-center randomized trial to create transition probabilities. The cost for TIL therapy was estimated from adoptive cell therapies, such as CAR-T, while costs for Pembrolizumab was determined from Centers for Medicare and Medicaid data. Utility and direct adverse event costs were estimated from published literature. Quality-adjusted life-years (QALYs), lifetime costs, and incremental cost-effectiveness ratio (ICER) were calculated at a willingness-to-pay threshold of $200,000 per QALY. Pembrolizumab administration every three weeks was less costly than TIL therapy, with incremental QALY and ICER for TIL therapy favoring Pembrolizumab. Over a lifetime, TIL accrued a total cost of $412,975 (95% CI 403,392, 421,220) and a QALY of 19.66(95% CI 15.98, 23.57). Pembrolizumab monotherapy accrued a total cost of $211,600 (95% CI $193,600, $230,300). The incremental QALY for Pembrolizumab was 21.92 (19.43,24.64). At our willingness-to-pay threshold of $200,000, the ICER for TIL therapy was larger than that for immunotherapy. Cost-effectiveness analysis demonstrated pembrolizumab monotherapy for patients with metastatic melanoma was cost-effective to TIL therapy based on current cost assumptions similar to CAR-T. As cell therapy becomes a more prevalent treatment modality for melanoma upon commercialization, strategies to reduce costs will be critical for managing metastatic melanoma.
Results:
Conclusions: