Neoadjuvant Chemotherapy With Doxorubicin and Cisplatin in Malignant Fibrous Histiocytoma of Bone: A European Osteosarcoma Intergroup Study

Author:

Bramwell Vivien H.C.1,Steward William P.1,Nooij Marianne1,Whelan Jeremy1,Craft Alan W.1,Grimer Robert J.1,Taminau Antonie H.M.1,Cannon Steven R.1,Malcolm Archie J.1,Hogendoorn Pancras C.W.1,Uscinska Barbara1,Kirkpatrick Anne L.1,Machin David1,Van Glabbeke Martine M.1

Affiliation:

1. From the London Regional Cancer Centre, London, Ontario, Canada; Leicester Royal Infirmary, Leicester, University College London Hospitals National Health Service Trust, London, Royal Victoria Infirmary, Newcastle upon Tyne, Royal Orthopaedic Hospital National Health Service Trust, Birmingham, Royal National Orthopedic Hospital, London, and Medical Research Council Cancer Trials Office, Cambridge, United Kingdom; Leiden University Medical Centre, Leiden, the Netherlands; and European Organization for...

Abstract

PURPOSE: Studies involving small case series have suggested that malignant fibrous histiocytoma of bone (MFH-B) is a chemosensitive tumor and that chemotherapy may improve survival. In this study, we evaluated clinical and pathologic response rates and survival in a series of patients treated with a consistent chemotherapy regimen of doxorubicin and cisplatin (DOX/DDP). PATIENTS AND METHODS: Study patients were required to have biopsy-proven MFH-B, no previous chemotherapy, and primary or metastatic measurable disease and to be ≤ 65 years of age. Treatment consisted of doxorubicin 25 mg/m2/d days 1 through 3 and cisplatin 100 mg/m2 by 4-hour intravenous infusion every 3 weeks for six cycles. In patients with operable primary tumors, chemotherapy was planned to start within 42 days of biopsy, with definitive surgery performed after three cycles. RESULTS: Forty-one patients had operable nonmetastatic limb sarcomas, and 23 (56%) completed six chemotherapy cycles. Limb salvage was possible in 33 patients (80%), and 16 (42%) of 38 assessable specimens showed a good pathologic response (≥ 90% necrosis). Median time to progression was 56 months, and the 5-year progression-free survival rate was 56% (95% confidence interval [CI], 40% to 72%). Median survival time was 63 months, and the 5-year survival rate was 59% (95% CI, 41% to 77%). Patients with a good pathologic response had longer survival times and times to progression than did those with a poor response. Also treated were two patients with locally recurrent and nine with metastatic disease, and these patients had a median survival time of 17.5 months. CONCLUSION: Our study suggests that adjuvant or neoadjuvant chemotherapy with DOX/DDP is beneficial in MFH-B. Good pathologic response rates and survivals are quite comparable with those for osteosarcoma, a related bone tumor for which adjuvant or neoadjuvant chemotherapy is an accepted practice.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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