Adjuvant chemotherapy for non-metastatic osteosarcoma of the extremities in two New Zealand cancer centres
- PMID: 7487690
- DOI: 10.1111/j.1445-5994.1995.tb01527.x
Adjuvant chemotherapy for non-metastatic osteosarcoma of the extremities in two New Zealand cancer centres
Abstract
Background: Adjuvant chemotherapy significantly improves survival of patients with non-metastatic osteosarcoma but most of the data come from trials conducted in major international cancer centres.
Aim: To review the efficacy and toxicity of an adjuvant chemotherapy regimen used in two regional cancer centres in New Zealand.
Methods: Retrospective review of patients treated for non-metastatic high-grade osteosarcoma of the extremities. The regimen (POMA) consists of high-dose-methotrexate 8 g/m2 and vincristine 1.5 mg/m2 (maximum 2 mg) on days 1 and 8 followed by folinic acid then doxorubicin 50 mg/m2 and cisplatin 100 mg/m2 on day 15. This cycle was repeated every 35 days. Following amputation patients received six cycles while in selected patients two cycles were planned prior to limb salvage surgery followed by a further four cycles. Actuarial survival was calculated using the Kaplan-Meier method.
Results: Twenty patients were treated with POMA between 1986 and 1993. Amputation was performed in 16 patients and limb-salvage surgery in four. Sixteen patients (80%) remain alive with no evidence of disease at a median follow-up of 40 months. Thirteen patients (65%) have been continuously disease-free. Actuarial survival at five years is 70%. Seven patients relapsed, six in lungs, of whom four underwent pulmonary metastasectomy; three of these remain free of disease 31, 35 and 40 months later. There was no local relapse. The toxicity of POMA is significant but tolerable.
Conclusion: The results obtained at two regional cancer centres in New Zealand using POMA compare favourably to those achieved in clinical trials performed at major international cancer centres.
Comment in
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Adjuvant chemotherapy for non-metastatic osteosarcoma of the extremities in two New Zealand cancer centres.Aust N Z J Med. 1996 Apr;26(2):230. doi: 10.1111/j.1445-5994.1996.tb00890.x. Aust N Z J Med. 1996. PMID: 8744624 Clinical Trial. No abstract available.
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