Julio C Chavez, Marc S Hoffmann, Leslie L Popplewell
{"title":"评估CAR-T细胞治疗在复发或难治性滤泡性淋巴瘤患者当前治疗方案中的作用","authors":"Julio C Chavez, Marc S Hoffmann, Leslie L Popplewell","doi":"10.1016/j.jtct.2025.06.013","DOIUrl":null,"url":null,"abstract":"<p><p>Follicular lymphoma (FL), the most common subtype of indolent non-Hodgkin lymphoma, exhibits significant clinical heterogeneity, with some patients enjoying durable periods of active surveillance and others having a more aggressive course characterized by frequent relapses and sometimes transformation to high-grade lymphoma. Consequently, treatment is highly individualized. Currently, there is no standard regimen established for patients with relapsed or refractory (r/r) FL. The only established curative-intent treatment for r/r FL is hematopoietic stem cell transplantation, but its application is limited by toxicity. Currently there is a need for effective therapies that could provide longer disease control without significant increase in toxicities. Agents in development include chimeric antigen receptor (CAR)-T cell therapy, monoclonal anti-cluster of differentiation (CD)20 antibodies, kinase inhibitors, enhancer of zeste homolog 2 inhibitors, cereblon E3 ligase modulatory drugs, and bispecific antibodies. Some of these therapies have already been approved for use in patients with r/r FL with ≥2 previous lines of therapy, but sequencing and standardization of treatment are still lacking. CAR-T cell therapy has been shown to have durable efficacy with manageable adverse events, such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. Bispecific antibodies have been shown to demonstrate a good overall response rate but their long-term efficacy has not been established. Several trials on targeted therapies have also shown promising results. Clinical trials using a combination of these therapeutic agents are still limited, as are real-world studies in patients with r/r FL given cellular therapy. Despite this expansion of the treatment landscape among patients with third-line r/r FL, there still exists an unmet need for a standardized, stepwise approach in the treatment of this population. Herein we review the efficacy and safety of CAR-T cell therapy and non-CAR-T cell therapy in the management of r/r FL.</p>","PeriodicalId":23283,"journal":{"name":"Transplantation and Cellular Therapy","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluating the Role of CAR-T Cell Therapy in the Context of Current Therapy Options for Patients With Relapsed or Refractory Follicular Lymphoma.\",\"authors\":\"Julio C Chavez, Marc S Hoffmann, Leslie L Popplewell\",\"doi\":\"10.1016/j.jtct.2025.06.013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Follicular lymphoma (FL), the most common subtype of indolent non-Hodgkin lymphoma, exhibits significant clinical heterogeneity, with some patients enjoying durable periods of active surveillance and others having a more aggressive course characterized by frequent relapses and sometimes transformation to high-grade lymphoma. Consequently, treatment is highly individualized. Currently, there is no standard regimen established for patients with relapsed or refractory (r/r) FL. The only established curative-intent treatment for r/r FL is hematopoietic stem cell transplantation, but its application is limited by toxicity. Currently there is a need for effective therapies that could provide longer disease control without significant increase in toxicities. Agents in development include chimeric antigen receptor (CAR)-T cell therapy, monoclonal anti-cluster of differentiation (CD)20 antibodies, kinase inhibitors, enhancer of zeste homolog 2 inhibitors, cereblon E3 ligase modulatory drugs, and bispecific antibodies. Some of these therapies have already been approved for use in patients with r/r FL with ≥2 previous lines of therapy, but sequencing and standardization of treatment are still lacking. CAR-T cell therapy has been shown to have durable efficacy with manageable adverse events, such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. Bispecific antibodies have been shown to demonstrate a good overall response rate but their long-term efficacy has not been established. Several trials on targeted therapies have also shown promising results. Clinical trials using a combination of these therapeutic agents are still limited, as are real-world studies in patients with r/r FL given cellular therapy. Despite this expansion of the treatment landscape among patients with third-line r/r FL, there still exists an unmet need for a standardized, stepwise approach in the treatment of this population. Herein we review the efficacy and safety of CAR-T cell therapy and non-CAR-T cell therapy in the management of r/r FL.</p>\",\"PeriodicalId\":23283,\"journal\":{\"name\":\"Transplantation and Cellular Therapy\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-06-12\",\"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.2025.06.013\",\"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.2025.06.013","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Evaluating the Role of CAR-T Cell Therapy in the Context of Current Therapy Options for Patients With Relapsed or Refractory Follicular Lymphoma.
Follicular lymphoma (FL), the most common subtype of indolent non-Hodgkin lymphoma, exhibits significant clinical heterogeneity, with some patients enjoying durable periods of active surveillance and others having a more aggressive course characterized by frequent relapses and sometimes transformation to high-grade lymphoma. Consequently, treatment is highly individualized. Currently, there is no standard regimen established for patients with relapsed or refractory (r/r) FL. The only established curative-intent treatment for r/r FL is hematopoietic stem cell transplantation, but its application is limited by toxicity. Currently there is a need for effective therapies that could provide longer disease control without significant increase in toxicities. Agents in development include chimeric antigen receptor (CAR)-T cell therapy, monoclonal anti-cluster of differentiation (CD)20 antibodies, kinase inhibitors, enhancer of zeste homolog 2 inhibitors, cereblon E3 ligase modulatory drugs, and bispecific antibodies. Some of these therapies have already been approved for use in patients with r/r FL with ≥2 previous lines of therapy, but sequencing and standardization of treatment are still lacking. CAR-T cell therapy has been shown to have durable efficacy with manageable adverse events, such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. Bispecific antibodies have been shown to demonstrate a good overall response rate but their long-term efficacy has not been established. Several trials on targeted therapies have also shown promising results. Clinical trials using a combination of these therapeutic agents are still limited, as are real-world studies in patients with r/r FL given cellular therapy. Despite this expansion of the treatment landscape among patients with third-line r/r FL, there still exists an unmet need for a standardized, stepwise approach in the treatment of this population. Herein we review the efficacy and safety of CAR-T cell therapy and non-CAR-T cell therapy in the management of r/r FL.