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Continuous-infusion Ifosfamide and Doxorubicin Combination as Second-Line Chemotherapy for Recurrent or Refractory Osteosarcoma Patients in China: a Retrospective Study

  • Huang, Yu-Jing (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University) ;
  • He, Ai-Na (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University) ;
  • Sun, Yuan-Jue (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University) ;
  • Shen, Zan (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University) ;
  • Min, Da-Liu (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University) ;
  • Yao, Yang (Department of Oncology, Affiliated Sixth People's Hospital, Shanghai Jiaotong University)
  • Published : 2015.04.03

Abstract

Objective: The aim of this retrospective study was to evaluate the feasibility and efficacy of response to continuous-infusion ifosfamide and doxorubicin combination as second-line chemotherapy for patients with recurrent or refractory osteosarcoma. Materials and Methods: Eighteen recurrent or refractory osteosarcoma patients who were treated with continuous-infusion ifosfamide and doxorubicin combination between May 1999 and April 2011 were included in the analysis. Ifosfamide at $12g/m^2$ was administered by intravenous continuous infusion over 3 days, and doxorubicin $60mg/m^2$ was administered as an intravenous bolus injection on day 1. The combination therapy was repeated every 3 weeks. Treatment was continued until evidence of disease progression or unacceptable toxicity. Results: The patients (ages 7-53 years) received a total of 42 cycles of chemotherapy (median: 2 courses; range: 2-5 courses). The overall response rate was 0% and the disease control rate was 22.3%, with four patients having stable disease. The median time to progression and overall survival time were 2 months (range: 2-5 months) and 9 months (range: 3-29 months), respectively. Major severe toxicities were leucopenia 7 (38.9%), nausea and vomiting 3 (16.7%) and alopecia 9 (50%). There were no treatment-related deaths. Conclusions: In our experience, continuous-infusion ifosfamide and doxorubicin combination therapy at this dosage and schedule was found to be well tolerated and moderate effective, which could be considered as salvage therapy for patients with recurrent or refractory osteosarcoma. Further assessment is necessary to confirm the safety and efficacy of this treatment.

Keywords

References

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