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A phase II trial of temozolomide in patients with unresectable or metastatic soft tissue sarcoma

โœ Scribed by Susan M. Talbot; Mary Louise Keohan; Mary Hesdorffer; Russell Orrico; Emilia Bagiella; Andrea B. Troxel; Robert N. Taub


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
69 KB
Volume
98
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Abstract

BACKGROUND

The objective of this study was to assess the efficacy and toxicity of the imidazotetrazine derivative temozolomide for patients with unresectable or metastatic soft tissue sarcoma.

METHODS

Twentyโ€five of 26 patients were eligible and assessable for toxicity and response. Temozolomide was administered twice daily on a 12โ€hour schedule for 5 days as an oral bolus dose of 200 mg/m^2^ followed by 9 doses of 90 mg/m^2^ every 4 weeks.

RESULTS

There were 2 partial responses, 2 mixed responses, and 3 patients with stable disease that lasted > 6 months, for an overall objective response rate of 8%. At a median followโ€up of 13.2 months, the median progressionโ€free survival and the median overall survival were 2.0 months (95% confidence interval [95% CI], 1.7โ€“2.3) and 13.2 months (95% CI, 4.7โ€“31.1), respectively. All responding patients had leiomyosarcoma of uterine or nonuterine origin; and, in a subset analysis of these patients, the objective response rate was 18% (2 of 11 patients), with disease stabilization occurring in 3 of 11 patients (27%). For this subgroup, at a median followโ€up of 24.4 months, the median progressionโ€free survival and the median overall survival were 3.9 months (95% CI, 1.9โ€“21.9) and 30.8 months (lowerโ€bound 95% CI, 7.8), respectively. There were no treatmentโ€related deaths or National Cancer Institute Grade 4 toxicities. Grade 3 toxicities included nausea, anemia, fatigue, elevated alkaline phosphatase levels and nonneutropenic fever (1 patient each).

CONCLUSIONS

Temozolomide at the dose schedule employed in the current study was tolerated well and had modest activity against previously treated unresectable or metastatic leiomyosarcoma of both uterine and nonuterine origin. Cancer 2003. ยฉ 2003 American Cancer Society.


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