Mohammed Zuber, Shaimaa Elshafie, Shifa Taj, Lorenzo Villa Zapata
{"title":"美国商业保险b细胞非霍奇金淋巴瘤患者CAR - t细胞治疗后的实际治疗模式和自付费用","authors":"Mohammed Zuber, Shaimaa Elshafie, Shifa Taj, Lorenzo Villa Zapata","doi":"10.1016/j.jtct.2025.06.018","DOIUrl":null,"url":null,"abstract":"<p><p>CAR T-cell therapy has transformed the treatment of B-cell non-Hodgkin Lymphoma (NHL), yet treatment failure remains a major concern. Clinical trial data indicate relapse rates up to 50% within 6 months, but real-world evidence on salvage therapy patterns and financial burdens is limited. This study aims to assess the risk of CAR T failure risk, characterize subsequent therapeutic strategies, and quantify patient out-of-pocket (OOP) health care costs. We conducted a retrospective cohort study using the Merative MarketScan database (2017-2022), identifying adult patients with diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), mantle cell lymphoma (MCL), or primary mediastinal large B-cell lymphoma (PMBCL) who received CAR-T therapy. Additional therapy post-index indicated relapse, with cumulative risk estimated via Kaplan-Meier analysis. OOP costs, including copayments, coinsurance, and deductibles, were calculated. Among 224 eligible patients (median age: 57 years, 70% male, 83% DLBCL), 85 (38%) initiated subsequent therapy, with a cumulative failure risk of 36% at 6 months and 48% at 12 months. Lenalidomide was the most common salvage therapy in DLBCL. Six-month total OOP costs distributed across 121 patients were $273,676, with outpatient claims comprising 67%. Patients requiring additional therapy had higher mean OOP costs ($3,221 versus $1,806), with some reaching $38,889. This study underscores the persistent need for effective salvage therapy options and the financial burden of treatment failure. As CAR T-cell therapy is increasingly utilized in earlier treatment lines, future research should focus on optimizing post-CAR T-cell management and mitigating financial toxicity.</p>","PeriodicalId":23283,"journal":{"name":"Transplantation and Cellular Therapy","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Real-World Treatment Patterns and Out-of-Pocket Costs After CAR T-Cell Therapy in Commercially Insured Patients With B-Cell Non-Hodgkin Lymphoma in the United States.\",\"authors\":\"Mohammed Zuber, Shaimaa Elshafie, Shifa Taj, Lorenzo Villa Zapata\",\"doi\":\"10.1016/j.jtct.2025.06.018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>CAR T-cell therapy has transformed the treatment of B-cell non-Hodgkin Lymphoma (NHL), yet treatment failure remains a major concern. Clinical trial data indicate relapse rates up to 50% within 6 months, but real-world evidence on salvage therapy patterns and financial burdens is limited. This study aims to assess the risk of CAR T failure risk, characterize subsequent therapeutic strategies, and quantify patient out-of-pocket (OOP) health care costs. We conducted a retrospective cohort study using the Merative MarketScan database (2017-2022), identifying adult patients with diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), mantle cell lymphoma (MCL), or primary mediastinal large B-cell lymphoma (PMBCL) who received CAR-T therapy. Additional therapy post-index indicated relapse, with cumulative risk estimated via Kaplan-Meier analysis. OOP costs, including copayments, coinsurance, and deductibles, were calculated. Among 224 eligible patients (median age: 57 years, 70% male, 83% DLBCL), 85 (38%) initiated subsequent therapy, with a cumulative failure risk of 36% at 6 months and 48% at 12 months. Lenalidomide was the most common salvage therapy in DLBCL. Six-month total OOP costs distributed across 121 patients were $273,676, with outpatient claims comprising 67%. Patients requiring additional therapy had higher mean OOP costs ($3,221 versus $1,806), with some reaching $38,889. This study underscores the persistent need for effective salvage therapy options and the financial burden of treatment failure. As CAR T-cell therapy is increasingly utilized in earlier treatment lines, future research should focus on optimizing post-CAR T-cell management and mitigating financial toxicity.</p>\",\"PeriodicalId\":23283,\"journal\":{\"name\":\"Transplantation and Cellular Therapy\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-06-23\",\"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.2025.06.018\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation and Cellular Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jtct.2025.06.018","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Real-World Treatment Patterns and Out-of-Pocket Costs After CAR T-Cell Therapy in Commercially Insured Patients With B-Cell Non-Hodgkin Lymphoma in the United States.
CAR T-cell therapy has transformed the treatment of B-cell non-Hodgkin Lymphoma (NHL), yet treatment failure remains a major concern. Clinical trial data indicate relapse rates up to 50% within 6 months, but real-world evidence on salvage therapy patterns and financial burdens is limited. This study aims to assess the risk of CAR T failure risk, characterize subsequent therapeutic strategies, and quantify patient out-of-pocket (OOP) health care costs. We conducted a retrospective cohort study using the Merative MarketScan database (2017-2022), identifying adult patients with diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), mantle cell lymphoma (MCL), or primary mediastinal large B-cell lymphoma (PMBCL) who received CAR-T therapy. Additional therapy post-index indicated relapse, with cumulative risk estimated via Kaplan-Meier analysis. OOP costs, including copayments, coinsurance, and deductibles, were calculated. Among 224 eligible patients (median age: 57 years, 70% male, 83% DLBCL), 85 (38%) initiated subsequent therapy, with a cumulative failure risk of 36% at 6 months and 48% at 12 months. Lenalidomide was the most common salvage therapy in DLBCL. Six-month total OOP costs distributed across 121 patients were $273,676, with outpatient claims comprising 67%. Patients requiring additional therapy had higher mean OOP costs ($3,221 versus $1,806), with some reaching $38,889. This study underscores the persistent need for effective salvage therapy options and the financial burden of treatment failure. As CAR T-cell therapy is increasingly utilized in earlier treatment lines, future research should focus on optimizing post-CAR T-cell management and mitigating financial toxicity.