CHEMOTHERAPY OF MALIGNANT FIBROUS HISTIOCYTOMA OF BONE

被引:16
作者
EARL, HM
PRINGLE, J
KEMP, H
MORITTU, L
MILES, D
SOUHAMI, R
机构
[1] UCL, MIDDLESEX HOSP, SCH MED, DEPT ONCOL, MORTIMER ST, LONDON W1N 8AA, ENGLAND
[2] ROYAL NATL ORTHOPAED HOSP, STANMORE, MIDDX, ENGLAND
关键词
BONE SARCOMA; CHEMOTHERAPY;
D O I
10.1093/oxfordjournals.annonc.a058521
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Malignant fibrous histiocytoma of bone (MFHB) is a rare tumour with a 3 year survival of 30%-40% when treated with surgery alone. A small number of patients have previously been treated with pre-operative chemotherapy and responses observed. The aim of the present study was to further determine the response of MFHB to pre-operative chemotherapy. Patients and methods: A non-randomised study of 18 patients with MFHB. Twelve had localised disease and 6 had pulmonary metastases. In 14 patients pre-operative treatment consisted of methotrexate 8 g/m2 on day 1, ifosfamide 3 g/m2 and doxorubicin 60 mg/m2 on day 10. This regimen was given twice and twice post-operatively. A further 4 patients received cisplatin 100 mg/m2 on day 1 and doxorubicin 25 mg/m2 on days 1, 2, 3. Three cycles were given pre- and post-operatively. Results: 15 patients had surgery after chemotherapy. Tumour necrosis was present in all resection specimens and ranged from 50%-100%. 7/15 had > 90% necrosis. Disease free survival is 82% for those patients with a greater than 2 year follow-up. Conclusion: This study confirms previous reports that MFHB is a chemosensitive tumour. In view of its rarity collaborative trials are needed to establish the optimum drug treatment including drug selection dose and duration.
引用
收藏
页码:409 / 415
页数:7
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