Bone sarcomas: ESMO–PaedCan–EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up
Population
Patients with primary bone tumours (osteosarcoma, Ewing sarcoma, chondrosarcoma)
Design
Guideline
Authors
Discussion
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Member takes
Implication
Supports referral to expert centers for rare bone sarcomas; extends ESMO guidelines with subtype-specific incidence data for tailored care.
Structured PICO
P
Population
Patients with primary bone tumours (osteosarcoma, Ewing sarcoma, chondrosarcoma)
I
Intervention
Clinical practice guidelines for diagnosis, treatment and follow-up
Provides ESMO-PaedCan-EURACAN clinical practice guidelines for the diagnosis, treatment, and follow-up of bone sarcomas.
Cite This Study
Casali et al. (2018) conducted a review in Bone sarcomas. Primary bone tumours are rare malignancies accounting for <0.2% of malignant neoplasms, with distinct incidence patterns across subtypes like osteosarcoma, Ewing sarcoma, and chondrosarcoma.