Annals of Oncology 4:669-672, 1993
© 1993 European Society for Medical Oncology
research-article |
Epirubicin and ifosfamide in advanced soft tissue sarcomas
1Division of Medical Oncology, Centro di Riferimento Oncologico Aviano, Italy
2Department of Radiation Therapy, Centro di Riferimento Oncologico Aviano, Italy
3Div. of Pathology, Centro di Riferimento Oncologico Aviano, Italy
4Radiology Service, Centro di Riferimento Oncologico Aviano, Italy
Correspondence to: Sergio Frustaci, M.D., Division of Medical Oncology, Centro di Riferimento Oncologjco, V. Pedemontana Occidentale, 33081 Aviano (PN), Italy
Background: To evaluate the feasibility, toxicity and efficacy of the combination of (IFO) ifosfamide and epirubicin (EPI) given at conventional doses for monochemotherapy, we started a phase II study in advanced/metastatic soft tissue sarcoma patients.
Patients and methods: Treatment consisted of: epirubicin 75 mg/m2 i.v. day 1; IFO 1.8 g/m2 days 1 to 5; MESNA 20% of the IFO dose at 4-hour intervals three times a day during IFO administration. Cycles were given every 34 weeks for at least three cycles.
Results: The overall response rate for non-visceral sarcomas (51 pts) ws 31% (95% confidence limits ± 13%). Among the 13 visceral sarcomas no response was seen for the leio-myosarcomas of the gastrointestinal tract, whereas one complete and one partial remission were observed for the uterine sarcomas. The duration of response was 10 months (range 534+) for complete responses and 9 (range 442+) for partial responses. The median survival for responders is 18 months (range 260+) and for non-responders 10 months (range 133) (p ± 0.004). Conclusions: This combination proved to be feasible and tolerable. The overall response rate does not appear to be superior to those with other standard treatments, but it should be pointed out that our patient population was totally unselected.
chemotherapy, epirubicin, ifosfamide, metastatic soft tissue sarcomas
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