%0 Journal Article
%A Casali, P G
%A Bielack, S
%A Abecassis, N
%A Aro, H T
%A Bauer, S
%A Biagini, R
%A Bonvalot, S
%A Boukovinas, I
%A Bovee, J V M G
%A Brennan, B
%A Brodowicz, T
%A Broto, J M
%A Brugieres, L
%A Buonadonna, A
%A De-Alava, E
%A Dei-Tos, A P
%A Del-Muro, X G
%A Dileo, P
%A Dhooge, C
%A Eriksson, M
%A Fagioli, F
%A Fedenko, A
%A Ferraresi, V
%A Ferrari, A
%A Ferrari, S
%A Frezza, A M
%A Gaspar, N
%A Gasperoni, S
%A Gelderblom, H
%A Gil, T
%A Grignani, G
%A Gronchi, A
%A Haas, R L
%A Hassan, B
%A Hecker-Nolting, S
%A Hohenberger, P
%A Issels, R
%A Joensuu, H
%A Jones, R L
%A Judson, I
%A Jutte, P
%A Kaal, S
%A Kager, L
%A Kasper, B
%A Kopeckova, K
%A Krakorova, D A
%A Ladenstein, R
%A Le-Cesne, A
%A Lugowska, I
%A Merimsky, O
%A Montemurro, M
%A Morland, B
%A Pantaleo, M A
%A Piana, R
%A Picci, P
%A Piperno-Neumann, S
%A Pousa, A L
%A Reichardt, P
%A Robinson, M H
%A Rutkowski, P
%A Safwat, A A
%A Schöffski, P
%A Sleijfer, S
%A Stacchiotti, S
%A Strauss, S J
%A Sundby-Hall, K
%A Unk, M
%A Van-Coevorden, F
%A van-der-Graaf, W T A
%A Whelan, J
%A Wardelmann, E
%A Zaikova, O
%A Blay, J Y
%T Bone sarcomas: ESMO-PaedCan-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
%D 2018
%U https://hdl.handle.net/10668/27470
%X Primary bone tumours are rare, accounting for < 0.2% of malignant neoplasms registered in the EUROCARE (European Cancer Registry based study on survival and care of cancer patients) database [1]. Different bone tumour subtypes have distinct patterns of incidence, and each has no more than 0.3 incident cases per 100 000 per year. Osteosarcoma (OS) and Ewing sarcoma (ES) have a relatively high incidence in the second decade of life, whereas chondrosarcoma (CS) is more common in older age [2–4].
%K Age Factors
%K Bone Neoplasms
%K Europe
%K Long-Term Care
%K Neoadjuvant Therapy
%K Osteosarcoma
%K Radionuclide Imaging
%K Societies, Medical
%~