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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >White paper on adoptive cell therapy for cancer with tumor-infiltrating lymphocytes: a report of the CTEP subcommittee on adoptive cell therapy.
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White paper on adoptive cell therapy for cancer with tumor-infiltrating lymphocytes: a report of the CTEP subcommittee on adoptive cell therapy.

机译:肿瘤浸润淋巴细胞对癌症的过继细胞疗法白皮书:CTEP分委员会关于过继细胞疗法的报告。

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Adoptive T-cell therapy (ACT) using expanded autologous tumor-infiltrating lymphocytes (TIL) and tumor antigen-specific T cell expanded from peripheral blood are complex but powerful immunotherapies directed against metastatic melanoma. A number of nonrandomized clinical trials using TIL combined with high-dose interleukin-2 (IL-2) have consistently found clinical response rates of 50% or more in metastatic melanoma patients accompanied by long progression-free survival. Recent studies have also established practical methods for the expansion of TIL from melanoma tumors with high success rates. These results have set the stage for randomized phase II/III clinical trials to determine whether ACT provides benefit in stage IV melanoma. Here, we provide an overview of the current state-of-the art in T-cell-based therapies for melanoma focusing on ACT using expanded TIL and address some of the key unanswered biological and clinical questions in the field. Different phase II/III randomized clinical trial scenarios comparing the efficacy of TIL therapy to high-dose IL-2 alone are described. Finally, we provide a roadmap describing the critical steps required to test TIL therapy in a randomized multicenter setting. We suggest an approach using centralized cell expansion facilities that will receive specimens and ship expanded TIL infusion products to participating centers to ensure maximal yield and product consistency. If successful, this approach will definitively answer the question of whether ACT can enter mainstream treatment for cancer.
机译:使用扩增的自体肿瘤浸润淋巴细胞(TIL)和从外周血扩增的肿瘤抗原特异性T细胞的过继性T细胞疗法(ACT)是复杂而有效的针对转移性黑色素瘤的免疫疗法。大量使用TIL联合大剂量白介素2(IL-2)的非随机临床试验一致地发现,转移性黑素瘤患者的临床缓解率为50%或更高,并伴有无进展的长生存期。最近的研究还建立了从黑素瘤肿瘤中扩增TIL的实用方法,成功率很高。这些结果为II / III期临床随机试验奠定了基础,以确定ACT是否可在IV期黑色素瘤中获益。在这里,我们提供了基于黑色素瘤的T细胞疗法的最新技术概述,重点是使用扩展的TIL进行ACT,并解决了该领域中一些关键的尚未解决的生物学和临床问题。描述了不同的II / III期随机临床试验方案,这些方案比较了TIL治疗与单独大剂量IL-2的疗效。最后,我们提供了一个路线图,描述了在随机多中心环境中测试TIL治疗所需的关键步骤。我们建议使用集中式细胞扩增设施的方法,该设施将接收标本并将扩增的TIL输液产品运送到参与中心,以确保最大的产量和产品一致性。如果成功的话,这种方法将最终回答ACT是否可以进入癌症的主流治疗的问题。

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