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Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas
Initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage–colony-stimulating factor
Version of Record online: 31 JAN 2002
Copyright © 2002 American Cancer Society
Volume 94, Issue 3, pages 786–792, 1 February 2002
How to Cite
Edmonson, J. H., Petersen, I. A., Shives, T. C., Mahoney, M. R., Rock, M. G., Haddock, M. G., Sim, F. H., Maples, W. J., O'Connor, M. I., Gunderson, L. L., Foo, M. L., Pritchard, D. J., Buckner, J. C. and Stafford, S. L. (2002), Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas. Cancer, 94: 786–792. doi: 10.1002/cncr.10259
- Issue online: 31 JAN 2002
- Version of Record online: 31 JAN 2002
- Manuscript Accepted: 26 SEP 2001
- Manuscript Received: 21 SEP 2001
- Manuscript Revised: 21 SEP 2001
- limb-sparing surgery;
- soft tissue sarcoma;
Most institutional teams utilize multimodality therapy in their efforts to cure patients with primary high-grade extremity soft tissue sarcomas, although the value of adjuvant systemic chemotherapy is still disputed by some oncologists. This single-institution Phase II study describes an effort to control metastasis by the use of two cycles of chemotherapy as the initial preoperative treatment.
Between March 1994 and October 1997, 20 women and 19 men with primary extremity or limb girdle high-grade soft tissue sarcomas were registered to a study of preoperative ifosfamide, mitomycin, doxorubicin, cisplatin (IMAP) plus granulocyte macrophage–colony-stimulating factor (GM-CSF) followed by preoperative irradiation and subsequent limb-sparing surgery. The two sequential monthly cycles of IMAP involved intravenous ifosfamide, 2500 mg/m2, and mesna, 2500 mg/m2, on Day 0, followed by identical doses of these agents plus intravenous mitomycin, 4 mg/m2, doxorubicin, 40 mg/m2, and cisplatin, 60 mg/m2, on Day 1. Sargramostim (GM-CSF) 250 μg/m2 was given subcutaneously every 12 hours for 4 days beginning 6 days before the chemotherapy, and then for 14 more days beginning the day after chemotherapy was completed. At the beginning of the third month, external beam irradiation was administered daily, 5 days each week for 5 consecutive weeks to total preoperative doses of 4500 centigrays (cGy). This was accompanied by reduced doses of MAP chemotherapy (mitomycin, 6 mg/m2, doxorubicin, 30 mg/m2, and cisplatin, 45 mg/m2) intravenously on Days 0, 21, and 42 of the radiation therapy segment. Approximately 1 month after preoperative irradiation ended, each patient had complete surgical excision with curative intent, using limb-sparing techniques when possible. Radiation to total doses of 5500–6500 cGy was accomplished by delivery of an additional 1000–2000 cGy to the tumor bed via intraoperative electron beam, brachytherapy, or external beam irradiation at the completion of surgery.
All except 5 patients had tumors at least 5 cm in diameter. Chemotherapy toxicity grade three or higher consisted primarily of vomiting (23%), leukopenia (54%), and thrombocytopenia (77%). Six patients have died of metastatic sarcoma, and one other died in a motorcycle accident. Kaplan–Meier curves indicate estimated 5-year survival of approximately 80% and freedom from metastasis at 2 years of approximately 85%.
IMAP plus GM-CSF is satisfactory as initial treatment for primary extremity soft tissue sarcomas in two monthly cycles preceding irradiation. The prescribed irradiation was generally tolerable and effective in permitting limb-sparing surgery. Although the outcome of patients treated on this regimen has been favorable, the metastasis problem has not been eliminated. Cancer 2002;94:786–92. © 2002 American Cancer Society.