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10.1016/j.ctrv.2015.03.008

http://scihub22266oqcxt.onion/10.1016/j.ctrv.2015.03.008
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suck abstract from ncbi


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pmid25869102      Cancer+Treat+Rev 2015 ; 41 (5): 391-400
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  • Targeted therapies for advanced Ewing sarcoma family of tumors #MMPMID25869102
  • Jiang Y; Ludwig J; Janku F
  • Cancer Treat Rev 2015[May]; 41 (5): 391-400 PMID25869102show ga
  • The prognosis of adolescent and young adult patients battling metastatic Ewing sarcoma family of tumors (ESFT) remains less than 30% despite the development of systemic therapies. In the era of personalized medicine, novel molecular targets have been tested in preclinical or clinical settings in ESFT. In this review, we focus on early clinical and translational research that identified multiple molecular targets, including IGF-1R; mTOR; tyrosine kinase inhibitors; EWS-FLI1-related targets, and others. Overall, novel targeted therapies demonstrated modest efficacy; however pronounced and durable antineoplastic responses have been observed in small subsets of treated patients, for example with IGF-1R antibodies. Identifying outcome-predicting biomarkers and overcoming treatment resistance remain major challenges. Due to the rarity of ESFT, multi-institutional collaboration efforts of clinicians, basic and translational scientists are needed in order to understand biology of therapeutic response or resistance, which can lead to development of novel therapeutic methods and improved patient outcomes.
  • |*Molecular Targeted Therapy[MESH]
  • |Antineoplastic Agents/*therapeutic use[MESH]
  • |Bone Neoplasms/*drug therapy[MESH]
  • |Humans[MESH]


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