Aims: Chondrosarcoma, osteosarcoma and Ewing sarcoma form the majority of malignant primary tumours of bone. High-grade bone sarcomas require intensive treatment due to their rapid and invasive growth pattern and metastasising capabilities. This nationwide study covers overall incidence, treatment and survival patterns of bone sarcomas in a 15-year period (2000-2014) in the total population of the Netherlands. Patients and methods: Data for this study were derived from the Netherlands Cancer Registry, which receives primary notification from the national pathology database. Classification and categorisation was based on the ICD-O-3 classification and the WHO classification 2013 applied according to our clinicopathological expertise. Overall...
The objectives of this study were to present changes in referral patterns, treatment and survival in...
INTRODUCTION: The EUROpean Bone Over 40 Sarcoma Study (EURO-B.O.S.S.) was the first prospective inte...
Malignant bone tumours in children are rare, accounting for approximately 5% of all childhood cancer...
Aims: Chondrosarcoma, osteosarcoma and Ewing sarcoma form the majority of malignant primary tumours ...
AIM: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
Aim: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
AIM: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
For over two decades now, bone sarcoma care has been centralised in the Netherlands. To obtain a cle...
Primary bone tumours are rare, accounting for < 0.2% of malignant neoplasms registered in the EUROCA...
Background: Knowledge of chondrosarcoma (CS) of bone to date is based on institutional reports and r...
Background: Knowledge of chondrosarcoma (CS) of bone to date is based on institutional reports and r...
Research on soft-tissue sarcoma (STS) and bone sarcoma (BS) is increasingly in the focus of physicia...
The purpose of the study was to calculate population-based survival rates for osteosarcoma (OS) and ...
Background Research on soft-tissue sarcoma (STS) and bone sarcoma (BS) is increasingly in the focus...
Objectives: As diagnosis and treatment guidelines for bone sarcomas continue updating, it is importa...
The objectives of this study were to present changes in referral patterns, treatment and survival in...
INTRODUCTION: The EUROpean Bone Over 40 Sarcoma Study (EURO-B.O.S.S.) was the first prospective inte...
Malignant bone tumours in children are rare, accounting for approximately 5% of all childhood cancer...
Aims: Chondrosarcoma, osteosarcoma and Ewing sarcoma form the majority of malignant primary tumours ...
AIM: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
Aim: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
AIM: Follow-up strategies for high-grade bone sarcomas have been optimized to facilitate early detec...
For over two decades now, bone sarcoma care has been centralised in the Netherlands. To obtain a cle...
Primary bone tumours are rare, accounting for < 0.2% of malignant neoplasms registered in the EUROCA...
Background: Knowledge of chondrosarcoma (CS) of bone to date is based on institutional reports and r...
Background: Knowledge of chondrosarcoma (CS) of bone to date is based on institutional reports and r...
Research on soft-tissue sarcoma (STS) and bone sarcoma (BS) is increasingly in the focus of physicia...
The purpose of the study was to calculate population-based survival rates for osteosarcoma (OS) and ...
Background Research on soft-tissue sarcoma (STS) and bone sarcoma (BS) is increasingly in the focus...
Objectives: As diagnosis and treatment guidelines for bone sarcomas continue updating, it is importa...
The objectives of this study were to present changes in referral patterns, treatment and survival in...
INTRODUCTION: The EUROpean Bone Over 40 Sarcoma Study (EURO-B.O.S.S.) was the first prospective inte...
Malignant bone tumours in children are rare, accounting for approximately 5% of all childhood cancer...