Efficacy and safety of first- or second-line irinotecan, cisplatin, and mitomycin in mesothelioma

Cancer. 2007 Jan 1;109(1):93-9. doi: 10.1002/cncr.22366.

Abstract

Background: Malignant pleural mesothelioma (MPM) is a rapidly progressive lethal tumor. Treatment options remain limited and the outcome in recurrent disease is poor.

Methods: A Phase II open-label noncomparative study was conducted to assess the safety and efficacy of the triplet combination irinotecan, cisplatin, and mitomycin-C (IPM) chemotherapy in untreated patients and in those with previous exposure to chemotherapy.

Results: In 62 patients an objective response rate of 25% was observed. In the first-line setting progression-free survival measured 6.4 months (95% confidence interval [CI]: 4.5-7.3) and overall survival was 10.8 months (95% CI: 7.9-13.7). In the second-line setting progression-free survival was 7.3 months (95% CI: 3.4-11.2) and overall survival was also 7.3 months (95% CI: 4.8-9.8). Psychosocial well-being improved during chemotherapy and the main toxicity observed was neutropenia (40%).

Conclusions: IPM appeared to have a reasonable response rate with an acceptable toxicity profile in the first- and second-line treatment of MPM.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / toxicity
  • Camptothecin / administration & dosage
  • Camptothecin / analogs & derivatives
  • Cisplatin / administration & dosage
  • Clinical Trials, Phase II as Topic
  • Female
  • Humans
  • Irinotecan
  • Male
  • Mesothelioma / drug therapy*
  • Mesothelioma / mortality
  • Middle Aged
  • Mitomycin / administration & dosage
  • Pleural Neoplasms / drug therapy*
  • Quality of Life
  • Survival Rate
  • Treatment Outcome

Substances

  • Mitomycin
  • Irinotecan
  • Cisplatin
  • Camptothecin