SELNET clinical practice guidelines for soft tissue sarcoma and GIST

Autor: Shreyaskumar Patel, Jean-Yves Blay, S. Moura David, Y. Pfluger, K. Scotlandi, M. Angel, M. Chacón, A. Carvajal Montoya, J. Haro, J. Bollard, N. Jimenez, Bernd Kasper, Claudia Haydee Sarai Caro-Sánchez, A. G. Nascimento, T. Soule, S. Casavilca-Zambrano, R. Badilla, Héctor Martínez-Said, F. Campos, M. Farias-Loza, Alberto Righi, A. P. Dei Tos, Armelle Dufresne, E. J. Ortiz-Cruz, Hans Gelderblom, G. Lutter, B. B. Lopes David, J. M. Morales Pérez, C. A. Mello, Daniel Bernabeu, T. T. G. Santos, V. Castro-Oliden, Jorge Luis Martínez-Tlahuel, D. Donati, L. Huanca, M. C. Gómez-Mateo, D.Y. Garcia-Ortega, Paola Collini, M. Clara, P. Fernandez, Emanuela Palmerini, F. Waisberg, E. Zamora Estrada, J. Martin-Broto, Antonio Lopez-Pousa, Mikael Eriksson, A. Rodriguez, François Gouin, Claudia Valverde, S. Provenzano, B. Araya, Nadia Hindi, S. Aguiar, Silvia Stacchiotti, H. R. Dominguez Malagon, M. Cuellar, T. Frisoni, Alessandro Gronchi, R. Correa Genoroso, A.M. Frezza, Marie Karanian, R. Salas, B. Carvajal, F. D. Costa

Publikováno v: CANCER TREATMENT REVIEWS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Cancer Treatment Reviews, 102. ELSEVIER SCI LTD

Soft tissue sarcoma (STS) is a heterogeneous group of neoplasms, encompassing >80 different histologic subtypes. Approximately three quarter of sarcoma arise from soft-tissue, about 15% are gastrointestinal stromal tumours (GISTs) and bone sarcoma re

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