Temozolomide in adult patients with advanced soft tissue sarcoma: A phase II study of the EORTC soft tissue and bone sarcoma group

P. J. Woll, I. Judson, S. M. Lee, S. Rodenhuis, O. S. Nielsen, J. M. Buesa, P. C. Lorigan, S. Leyvraz, C. Hermans, M. Van Glabbeke, J. Verweij

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Temozolomide, an oral imidazotetrazine derivative, was given to 31 patients with advanced soft tissue sarcoma. The dose of 750 mg/m2 was divided over 5 consecutive days, and escalated to 1000 mg/m2 over 5 days at cycle 2 if myelosuppression no worse than common toxicity criteria grade 2 was noted in the first 28-day cycle. A total of 99 treatment cycles were given to 31 patients. The drug was well tolerated, with nausea and vomiting as the most common side-effects. Only one partial tumour response was documented, giving a response rate of 3.33%, 95% confidence interval, (CI) 0.1-17.2%. The median time to progression was 8 weeks and the median survival was 27 weeks. These results indicate that temozolomide in this schedule is not active as second-line treatment in advanced soft tissue sarcoma.
    Original languageEnglish
    Pages (from-to)410-412
    Number of pages2
    JournalEuropean Journal of Cancer
    Volume35
    Issue number3
    DOIs
    Publication statusPublished - Mar 1999

    Keywords

    • Chemotherapy
    • Imidazotetrazine
    • Phase II
    • Sarcoma
    • Temozolomide

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