Sarcomas of Soft Tissue and Bone

被引:51
|
作者
Ferrari, Andrea [1 ]
Dirksen, Uta [2 ]
Bielack, Stefan [3 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Pediat Oncol Unit, Via G Venezian 1, IT-20133 Milan, Italy
[2] Univ Hosp Munster, Dept Pediat Hematol & Oncol, Munster, Germany
[3] Olga Hosp, Klinikum Stuttgart, Zentrum Kinder Jugend & Frauenmed, Onkol,Hamatol,Immunol,Padiatrie 5, Stuttgart, Germany
来源
关键词
CHILDRENS-ONCOLOGY-GROUP; RANDOMIZED CONTROLLED-TRIAL; STUDY-GROUP PROTOCOLS; EURO-EWING; 99; CONTROLLED PHASE-3 TRIAL; HIGH-GRADE OSTEOSARCOMA; END RESULTS PROGRAM; SYNOVIAL SARCOMA; ADJUVANT CHEMOTHERAPY; PROGNOSTIC-FACTORS;
D O I
10.1159/000447083
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The definition of soft tissue and bone sarcomas include a large group of several heterogeneous subtypes of mesenchymal origin that may occur at any age. Among the different sarcomas, rhabdomyosarcoma, synovial sarcoma, Ewing sarcoma and osteosarcoma are aggressive high-grade malignancies that often arise in adolescents and young adults. Managing these malignancies in patients in this age bracket poses various clinical problems, also because different therapeutic approaches are sometimes adopted by pediatric and adult oncologists, even though they are dealing with the same condition. Cooperation between pediatric oncologists and adult medical oncologists is a key step in order to assure the best treatment to these patients, preferably through their inclusion into international clinical trials. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:128 / 141
页数:14
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