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Part of the book series: Pediatric Oncology ((PEDIATRICO))

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Abstract

Multimodal approach to treatment has led to the dramatically improved outcome of patients with osteosarcoma and Ewing sarcoma. However, despite intensive therapies and incorporation of novel agents in trials, the therapeutic plateau in recurrent osteosarcoma and Ewing sarcoma has not yet been overcome. Cure for these patients remain a daunting challenge with dismal survival rate after relapse despite best efforts. Certain clinical factors help prognosticate quality of relapse of these tumors. Because patient characteristics are different upon disease recurrence, therapeutic approach to these patients vary widely.

Further improvements in outcome for patients with recurrent disease will depend on refinement of therapy using agents with clinical activity based on understanding of tumor biology, and within a trial design that optimally detects drug activity. There is a growing list of targets for osteosarcoma and Ewings sarcoma. A significant biology effort has been established by cooperative groups, as well as preclinical drug evaluation systems created towards more rapid identification and validation of compounds active in osteosarcoma and Ewing sarcoma. High throughput screens of novel agents should accelerate clinical trial development. Finally, there are now various national and international cooperative groups to efficiently test new agents in these rare tumors.

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Correspondence to Joanne Lagmay MD .

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Lagmay, J., Yeager, N.D. (2015). Recurrent Bone Tumors. In: Cripe, T., Yeager, N. (eds) Malignant Pediatric Bone Tumors - Treatment & Management. Pediatric Oncology. Springer, Cham. https://doi.org/10.1007/978-3-319-18099-1_14

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