Abstract
BackgroundOsteosarcoma is the most common primary malignant bone tumour in children and young adults. Despite advances in the diagnosis and management of osteosarcoma, there have been few recent studies describing the experiences of tertiary referral centres. This paper aims to describe and discuss the clinical features, pre-operative work-up, management and outcomes of these patients at St Vincent's Hospital (Melbourne, Australia).MethodsRetrospective study of fifty-nine consecutive patients managed for osteosarcoma at St Vincent's Hospital between 1995 and 2005.ResultsMedian age at diagnosis was 21 (range, 11–84) years. Gender distribution was similar, with thirty-one male and twenty-eight female patients.Twenty-five patients had osteosarcoma in the femur, eleven each were located in the humerus and tibia, six were identified in the pelvis, and one each in the clavicle, maxilla, fibula, sacrum, ulna and radius.Pre-operative tissue diagnosis of osteosarcoma was obtained through computed tomography-guided percutaneous biopsy in over ninety percent of patients.Following initial therapy, over fifty percent of patients remained relapse-free during the follow-up period, with twelve percent and twenty-seven percent of patients documented as having local and distant disease recurrence, respectively. Of patients with recurrent disease, sixty-two percent remained disease-free following subsequent surgical intervention (most commonly, pulmonary metastatectomy).ConclusionPatient outcomes can be optimised through a multidisciplinary approach in a tertiary referral centre. At St Vincent's Hospital, survival and relapse rates of patients managed for osteosarcoma compare favourably with the published literature.
Highlights
Osteosarcoma is the most common primary malignant bone tumour in children and young adults
Patient outcomes can be optimised through a multidisciplinary approach in a tertiary referral centre
At St Vincent's Hospital, survival and relapse rates of patients managed for osteosarcoma compare favourably with the published literature
Summary
Osteosarcoma is the most common primary malignant bone tumour in children and young adults. Osteosarcomas are highly aggressive spindle cell neoplasms that produce osteoid Overall, this malignancy is rare, with an annual incidence of approximately one per 100,000 persons [1,2,3,4,5]. Developments in imaging techniques have contributed to more effective management of osteosarcoma. These included computed tomography (CT) and magnetic resonance (MR) evaluation of bone and soft tissue involvement to facilitate surgical planning, use of functional nuclear imaging and CT chest for detection of metastatic disease, and imagingguided percutaneous biopsy to enable histopathological diagnosis with minimal morbidity and complication risks. Advances in limb-salvage surgery and reconstructive techniques in selected patients have enabled preservation of limb function without compromising oncological outcomes [2,5]
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