Casali, P GBielack, SAbecassis, NAro, H TBauer, SBiagini, RBonvalot, SBoukovinas, IBovee, J V M GBrennan, BBrodowicz, TBroto, J MBrugieres, LBuonadonna, ADe-Alava, EDei-Tos, A PDel-Muro, X GDileo, PDhooge, CEriksson, MFagioli, FFedenko, AFerraresi, VFerrari, AFerrari, SFrezza, A MGaspar, NGasperoni, SGelderblom, HGil, TGrignani, GGronchi, AHaas, R LHassan, BHecker-Nolting, SHohenberger, PIssels, RJoensuu, HJones, R LJudson, IJutte, PKaal, SKager, LKasper, BKopeckova, KKrakorova, D ALadenstein, RLe-Cesne, ALugowska, IMerimsky, OMontemurro, MMorland, BPantaleo, M APiana, RPicci, PPiperno-Neumann, SPousa, A LReichardt, PRobinson, M HRutkowski, PSafwat, A ASchöffski, PSleijfer, SStacchiotti, SStrauss, S JSundby-Hall, KUnk, MVan-Coevorden, Fvan-der-Graaf, W T AWhelan, JWardelmann, EZaikova, OBlay, J Y2025-01-072025-01-072018Casali PG, Bielack S, Abecassis N, Aro HT, Bauer S, Biagini R, et al. Bone sarcomas: ESMO-PaedCan-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018 Oct 1;29(Suppl 4):iv79-iv95.https://hdl.handle.net/10668/27470Primary 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].enAge FactorsBone NeoplasmsEuropeLong-Term CareNeoadjuvant TherapyOsteosarcomaRadionuclide ImagingSocieties, MedicalAdultAftercareAntineoplastic Combined Chemotherapy ProtocolsBiopsyBone and BonesChildHumansIncidenceMagnetic Resonance ImagingMedical OncologyNeoplasm StagingOrthopedic ProceduresPatient ParticipationPositron Emission Tomography Computed TomographyRadiotherapy, AdjuvantSelf-Help GroupsSurvivorshipTreatment Outcomeresearch article30285218Restricted AccessNeoplasiasIncidenciaHuesosSarcoma de EwingSistema de RegistrosPacientesSobrevidaOsteosarcomaCondrosarcoma10.1093/annonc/mdy3101569-8041http://www.annalsofoncology.org/article/S0923753419317120/pdf