Immunotherapy in Sarcoma: Future Horizons

被引:17
|
作者
Burgess, Melissa [1 ,4 ]
Gorantla, Vikram [2 ]
Weiss, Kurt [3 ,4 ]
Tawbi, Hussein [1 ,4 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Med, Div Hematol Oncol, Pittsburgh, PA 15213 USA
[2] Amer Oncol Inst, Med Oncol, Hyderabad, Andhra Pradesh, India
[3] Univ Pittsburgh, Div Musculoskeletal Oncol, Dept Orthoped Surg, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Sarcoma Program, Inst Canc, Pittsburgh, PA 15232 USA
关键词
Soft tissue sarcoma; Immunosurveillance; Immunotherapy; Programmed death-1 (PD-1); Tumor-infiltrating lymphocyte (TIL); Immune checkpoint blockade; LIPOSOMAL MURAMYL TRIPEPTIDE; COMBINING TARGETED THERAPY; AUTOLOGOUS TUMOR-CELLS; ACTIVATED KILLER-CELLS; SOFT-TISSUE SARCOMA; T-CELLS; KAPOSIS-SARCOMA; ADOPTIVE IMMUNOTHERAPY; ANTIRETROVIRAL THERAPY; MONOCLONAL-ANTIBODY;
D O I
10.1007/s11912-015-0476-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页数:10
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