Impact of real-world clinical factors on an analysis of the cost-effectiveness of 'immediate CAR-T' versus 'late CAR-T' as second-line treatment for DLBCL patients: Immediate or late CAR-T as second-line DLBCL treatment.
{"title":"Impact of real-world clinical factors on an analysis of the cost-effectiveness of 'immediate CAR-T' versus 'late CAR-T' as second-line treatment for DLBCL patients: Immediate or late CAR-T as second-line DLBCL treatment.","authors":"Chihiro Yamamoto, Seina Honda, Ryutaro Tominaga, Daizo Yokoyama, Shuka Furuki, Atsuto Noguchi, Shunsuke Koyama, Rui Murahashi, Hirotomo Nakashima, Shin-Ichiro Kawaguchi, Kazuki Hyodo, Yumiko Toda, Kento Umino, Daisuke Minakata, Masahiro Ashizawa, Masuzu Ueda, Kaoru Hatano, Kazuya Sato, Ken Ohmine, Shin-Ichiro Fujiwara, Yoshinobu Kanda","doi":"10.1016/j.jtct.2025.02.013","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>While chimeric antigen receptor (CAR-T) targeting CD19 as second-line therapy for diffuse large B cell lymphoma (DLBCL) is a promising strategy, the high costs and limited access to CAR-T pose significant challenges. When assessing the cost-effectiveness of CAR-T, we need to consider not only individual outcomes but also how to effectively integrate CAR-T into the overall treatment approach for relapsed DLBCL.</p><p><strong>Objectives/study design: </strong>We conducted a cost-effective analysis for patients with DLBCL in early relapse or primary refractory, to compare 'immediate CAR-T,' which proceeds directly to CAR-T, and 'late CAR-T,' which initially aims at ASCT and quickly switches to third-line CAR-T if non-responsive. The primary analysis used a patient age of 60 years, and it also examined variations from 40 to 70 years. The analysis was performed for both Japanese and US settings using a Markov model incorporating life expectancy in both countries, with extensive sensitivity analysis including factors such as age, the choice of CAR-T (lisocabtagene maraleucel or axicabtagene ciloleucel), and the opportunity to receive third-line CAR-T, to reflect real-world situations. The length of a Markov cycle was defined to be one month, and patients in the model were assumed to age one year every 12 Markov cycles. The analysis was made over a lifetime horizon, and the outcome was measured based on incremental cost-effectiveness ratio (ICER), with willingness-to-pay (WTP) thresholds of \\7,500,000 and $150,000 per quality-adjusted life years (QALY) in Japan and the US, respectively, with an annual discount rate of 3%.</p><p><strong>Results: </strong>Compared with 'late CAR-T,' the 'immediate CAR-T' strategy gained QALYs of 0.97 and 0.89 with an incremental cost of \\5,998,354 and $88,440 in Japan and the US, respectively. The ICERs were \\6,170,058/QALY in Japan and $99,596/QALY in the US. In the probabilistic sensitivity analysis for patients aged 60, 'immediate CAR-T' was cost-effective in 54.8% and 61.7% of the 10,000 Monte Carlo iterations in Japan and the US, respectively. Sensitivity analyses showed that 'immediate CAR-T' was not cost-effective when patients were over 68.4 in Japan, when the standardized mortality ratio of CAR-T and ASCT survivors was close, and when utility during treatment-free remission was low.</p><p><strong>Conclusions: </strong>Incorporating various clinical factors, the analysis showed that 'immediate CAR-T' is more cost-effective than 'late CAR-T.' However, this conclusion should be interpreted with caution, as the ICERs were very close to the WTP thresholds, and the results were highly sensitive to parameter changes.</p>","PeriodicalId":23283,"journal":{"name":"Transplantation and Cellular Therapy","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation and Cellular Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jtct.2025.02.013","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: While chimeric antigen receptor (CAR-T) targeting CD19 as second-line therapy for diffuse large B cell lymphoma (DLBCL) is a promising strategy, the high costs and limited access to CAR-T pose significant challenges. When assessing the cost-effectiveness of CAR-T, we need to consider not only individual outcomes but also how to effectively integrate CAR-T into the overall treatment approach for relapsed DLBCL.
Objectives/study design: We conducted a cost-effective analysis for patients with DLBCL in early relapse or primary refractory, to compare 'immediate CAR-T,' which proceeds directly to CAR-T, and 'late CAR-T,' which initially aims at ASCT and quickly switches to third-line CAR-T if non-responsive. The primary analysis used a patient age of 60 years, and it also examined variations from 40 to 70 years. The analysis was performed for both Japanese and US settings using a Markov model incorporating life expectancy in both countries, with extensive sensitivity analysis including factors such as age, the choice of CAR-T (lisocabtagene maraleucel or axicabtagene ciloleucel), and the opportunity to receive third-line CAR-T, to reflect real-world situations. The length of a Markov cycle was defined to be one month, and patients in the model were assumed to age one year every 12 Markov cycles. The analysis was made over a lifetime horizon, and the outcome was measured based on incremental cost-effectiveness ratio (ICER), with willingness-to-pay (WTP) thresholds of \7,500,000 and $150,000 per quality-adjusted life years (QALY) in Japan and the US, respectively, with an annual discount rate of 3%.
Results: Compared with 'late CAR-T,' the 'immediate CAR-T' strategy gained QALYs of 0.97 and 0.89 with an incremental cost of \5,998,354 and $88,440 in Japan and the US, respectively. The ICERs were \6,170,058/QALY in Japan and $99,596/QALY in the US. In the probabilistic sensitivity analysis for patients aged 60, 'immediate CAR-T' was cost-effective in 54.8% and 61.7% of the 10,000 Monte Carlo iterations in Japan and the US, respectively. Sensitivity analyses showed that 'immediate CAR-T' was not cost-effective when patients were over 68.4 in Japan, when the standardized mortality ratio of CAR-T and ASCT survivors was close, and when utility during treatment-free remission was low.
Conclusions: Incorporating various clinical factors, the analysis showed that 'immediate CAR-T' is more cost-effective than 'late CAR-T.' However, this conclusion should be interpreted with caution, as the ICERs were very close to the WTP thresholds, and the results were highly sensitive to parameter changes.