Razoxane and vindesine in advanced soft tissue sarcomas: impact on metastasis, survival and radiation response

Walter Rhomberg1, Helmut Eiter, Franz Schmid

  • 1Department of Radiation Oncology, Academic Teaching Hospital, Feldkirch, Austria. walter.rhomberg@gmx.at

Anticancer Research
|November 2, 2007
PubMed
Abstract

Insights

This study explored a novel treatment for advanced soft tissue sarcomas (STS), combining razoxane and vindesine with radiotherapy and surgery. The combination therapy significantly reduced new metastases and improved survival rates in patients with STS.

Area of Science:

  • Oncology
  • Medical Research
  • Pharmacology

Background:

  • Advanced soft tissue sarcomas (STS) present limited treatment options.
  • A pilot study investigated an antimetastatic and radiosensitizing treatment concept for STS.

Purpose of the Study:

  • To evaluate the efficacy of a combined treatment regimen including razoxane and vindesine, supported by radiotherapy and surgery.
  • To assess the antimetastatic and radiosensitizing effects of this novel therapeutic approach in advanced STS patients.

Main Methods:

  • Twenty-one patients with unresectable/oligometastatic STS received razoxane and vindesine with radiotherapy/surgery.
  • Forty-one comparable STS patients receiving contemporary chemotherapy served as non-randomized controls.
  • Prognostic parameters between the study and control groups were comparable.

Main Results:

  • The study group showed a median of 0 new metastases at 6 and 9 months, versus 4.5 and 9 in controls (p<0.001).
  • Progression-free survival at 6 months was 71% (study) vs. 23% (controls); median survival post-metastasis was 16 vs. 9 months.
  • Major response rates were 88% (study) vs. 62% (controls) (p=0.007), with low to moderate toxicity.

Conclusions:

  • The combined treatment effectively inhibited remote metastasis development in most STS patients.
  • This therapeutic strategy demonstrated a survival benefit in advanced soft tissue sarcoma patients.

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