학술논문

Sarcoma treatment in the era of molecular medicine
Document Type
article
Source
EMBO Molecular Medicine, Vol 12, Iss 11, Pp n/a-n/a (2020)
Subject
bone sarcoma
molecular diagnostics
molecular medicine
soft tissue sarcoma
targeted therapy
Medicine (General)
R5-920
Genetics
QH426-470
Language
English
ISSN
1757-4684
1757-4676
Abstract
Abstract Sarcomas are heterogeneous and clinically challenging soft tissue and bone cancers. Although constituting only 1% of all human malignancies, sarcomas represent the second most common type of solid tumors in children and adolescents and comprise an important group of secondary malignancies. More than 100 histological subtypes have been characterized to date, and many more are being discovered due to molecular profiling. Owing to their mostly aggressive biological behavior, relative rarity, and occurrence at virtually every anatomical site, many sarcoma subtypes are in particular difficult‐to‐treat categories. Current multimodal treatment concepts combine surgery, polychemotherapy (with/without local hyperthermia), irradiation, immunotherapy, and/or targeted therapeutics. Recent scientific advancements have enabled a more precise molecular characterization of sarcoma subtypes and revealed novel therapeutic targets and prognostic/predictive biomarkers. This review aims at providing a comprehensive overview of the latest advances in the molecular biology of sarcomas and their effects on clinical oncology; it is meant for a broad readership ranging from novices to experts in the field of sarcoma.