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肉瘤的免疫疗法:未来展望

Immunotherapy in Sarcoma: Future Horizons.

作者信息

Burgess Melissa, Gorantla Vikram, Weiss Kurt, Tawbi Hussein

机构信息

Division of Hematology/Oncology, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Sarcoma Program, University of Pittsburgh Cancer Institute, 5150 Centre Avenue, Fifth Floor, Pittsburgh, PA, 15232, USA.

出版信息

Curr Oncol Rep. 2015 Nov;17(11):52. doi: 10.1007/s11912-015-0476-7.

Abstract

Immunologic approaches to cancer are over a century old. Over the years, the strategy has been fine-tuned from inciting infections in subjects to inhibiting negative regulatory signals from the innate immune system. Sarcomas are among the first tumors to be considered for immune interventions. From Coley's toxin to cytokine-based therapies to adoptive cell therapy, there have been numerous immunotherapeutic investigations in this patient population. A promising strategy includes adoptive T cell therapy which has been studied in small cohorts of synovial sarcoma, a subtype that is known to widely express the cancer testis antigen, NY-ESO-1. Additionally, recent data in metastatic melanoma and renal cell carcinoma demonstrate the utility and tremendous efficacy of immune checkpoint blockade with increased rates of durable responses compared to standard therapies. Responses in traditionally "non-immunogenic" tumors, such as lung and bladder cancers, provide ample rationale for the study of immune checkpoint inhibitors in sarcoma. While immunotherapy has induced some responses in sarcomas, further research will help clarify optimal patient selection for future clinical trials and new combinatorial immunotherapeutic strategies.

摘要

癌症的免疫治疗方法已有一个多世纪的历史。多年来,该策略已从激发受试者感染调整为抑制来自先天免疫系统的负调节信号。肉瘤是最早被考虑进行免疫干预的肿瘤之一。从科利毒素到基于细胞因子的疗法再到过继性细胞疗法,在这一患者群体中已经进行了大量的免疫治疗研究。一种有前景的策略包括过继性T细胞疗法,该疗法已在滑膜肉瘤的小队列中进行了研究,滑膜肉瘤是一种已知广泛表达癌胚抗原NY-ESO-1的亚型。此外,转移性黑色素瘤和肾细胞癌的最新数据表明,与标准疗法相比,免疫检查点阻断具有实用性和巨大疗效,持久反应率更高。在传统的“非免疫原性”肿瘤(如肺癌和膀胱癌)中的反应为肉瘤中免疫检查点抑制剂的研究提供了充分的理论依据。虽然免疫疗法已在肉瘤中诱导了一些反应,但进一步的研究将有助于明确未来临床试验的最佳患者选择和新的联合免疫治疗策略。

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