Chemotherapy in soft tissue sarcoma. The Scandinavian Sarcoma Group experience

Acta Orthop Scand Suppl. 2004 Apr;75(311):77-86. doi: 10.1080/00016470410001708360.

Abstract

The Scandinavian Sarcoma Group (SSG) started its first chemotherapy study in soft tissue sarcoma (STS) in 1981 (SSG I). This study evaluated single agent doxorubicin given adjuvant in a prospective randomized trial in patients with high-grade STS. Neither overall survival nor disease-free survival was improved. Combination chemotherapy was hereafter studied in a phase II study (1991-1994) combining ifosfamide and continuous infusion etoposide with growth factor support (SSG X). The response rate in previously untreated patients was high (42%), but complete remissions were few. Analysis made on patients operated after chemotherapy indicated improved survival in this subgroup. Meta-analyses of adjuvant chemotherapy for localised resectable STS in adults, including the SSG I trial, has indicated improved disease-free survival and a trend towards improved overall survival. Presently, SSG is testing whether such a benefit can be found for adjuvant ifosfamide and doxorubicin treatment given after primary surgery in selected patients with high-grade STS and other well defined unfavourable prognostic factors (SSG XIII).

Publication types

  • Review

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Benzamides
  • Chemotherapy, Adjuvant
  • Disease-Free Survival
  • Gastrointestinal Neoplasms / metabolism
  • Humans
  • Imatinib Mesylate
  • Meta-Analysis as Topic
  • Piperazines / therapeutic use
  • Prospective Studies
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Pyrimidines / therapeutic use
  • Randomized Controlled Trials as Topic
  • Registries
  • Remission Induction
  • Sarcoma / drug therapy*
  • Sarcoma / mortality
  • Scandinavian and Nordic Countries
  • Soft Tissue Neoplasms / drug therapy*
  • Soft Tissue Neoplasms / mortality
  • Soft Tissue Neoplasms / surgery

Substances

  • Benzamides
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • Protein-Tyrosine Kinases