Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma

Ewing sarcoma (ES) family of tumors includes bone and soft tissue tumors that are often characterized by a specific translocation between chromosome 11 and 22, resulting in the EWS-FLI1 fusion gene. With the advent of multi-modality treatment including cytotoxic chemotherapy, surgery, and radiation...

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Main Authors: Dana L. Casey, Tsung-Yi Lin, Nai-Kong V. Cheung
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2019.00537/full
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author Dana L. Casey
Tsung-Yi Lin
Nai-Kong V. Cheung
author_facet Dana L. Casey
Tsung-Yi Lin
Nai-Kong V. Cheung
author_sort Dana L. Casey
collection DOAJ
description Ewing sarcoma (ES) family of tumors includes bone and soft tissue tumors that are often characterized by a specific translocation between chromosome 11 and 22, resulting in the EWS-FLI1 fusion gene. With the advent of multi-modality treatment including cytotoxic chemotherapy, surgery, and radiation therapy, the prognosis for patients with ES has substantially improved. However, a therapeutic plateau is now reached for both localized and metastatic disease over the last two decades. Burdened by the toxicity limits associated with the current frontline systemic therapy, there is an urgent need for novel targeted therapeutic strategies. In this review, we discuss the current treatment paradigm of ES, and explore preclinical evidence and emerging treatments directed at tumor signaling pathways and immune targets.
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spelling doaj.art-76c1017463b54d41a7fdad914380c28c2022-12-22T00:56:23ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-06-01910.3389/fonc.2019.00537454940Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing SarcomaDana L. Casey0Tsung-Yi Lin1Nai-Kong V. Cheung2Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, United StatesDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, United StatesDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, United StatesEwing sarcoma (ES) family of tumors includes bone and soft tissue tumors that are often characterized by a specific translocation between chromosome 11 and 22, resulting in the EWS-FLI1 fusion gene. With the advent of multi-modality treatment including cytotoxic chemotherapy, surgery, and radiation therapy, the prognosis for patients with ES has substantially improved. However, a therapeutic plateau is now reached for both localized and metastatic disease over the last two decades. Burdened by the toxicity limits associated with the current frontline systemic therapy, there is an urgent need for novel targeted therapeutic strategies. In this review, we discuss the current treatment paradigm of ES, and explore preclinical evidence and emerging treatments directed at tumor signaling pathways and immune targets.https://www.frontiersin.org/article/10.3389/fonc.2019.00537/fullEwing sarcomaantibodiesimmunotherapytargeted therapypediatric sarcomas
spellingShingle Dana L. Casey
Tsung-Yi Lin
Nai-Kong V. Cheung
Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
Frontiers in Oncology
Ewing sarcoma
antibodies
immunotherapy
targeted therapy
pediatric sarcomas
title Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
title_full Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
title_fullStr Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
title_full_unstemmed Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
title_short Exploiting Signaling Pathways and Immune Targets Beyond the Standard of Care for Ewing Sarcoma
title_sort exploiting signaling pathways and immune targets beyond the standard of care for ewing sarcoma
topic Ewing sarcoma
antibodies
immunotherapy
targeted therapy
pediatric sarcomas
url https://www.frontiersin.org/article/10.3389/fonc.2019.00537/full
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