Thirty-six previously treated adult patients with advanced soft tissue sarcomas received CPDD 120 mg/m2 with mannitol diuresis. There were only two (6%) partial responses and five (15%) minor responses in 34 evaluable patients. Toxicity included nausea and vomiting, myelosuppression, mild ototoxicit
A phase II trial of temozolomide in patients with unresectable or metastatic soft tissue sarcoma
โ 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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โฆ 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
Twentyโfive of 26 patients were eligible and assessable for toxicity and response. Temozolomide was administered twice daily on a 12โhour 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 followโup of 13.2 months, the median progressionโfree survival and the median overall survival were 2.0 months (95% confidence interval [95% CI], 1.7โ2.3) and 13.2 months (95% CI, 4.7โ31.1), 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 followโup of 24.4 months, the median progressionโfree survival and the median overall survival were 3.9 months (95% CI, 1.9โ21.9) and 30.8 months (lowerโbound 95% CI, 7.8), respectively. There were no treatmentโrelated 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.
๐ SIMILAR VOLUMES
## Abstract ## BACKGROUND The authors conducted a twoโarm Phase II study of temozolomide to determine its efficacy and toxicity in patients with soft tissue sarcomas (STSs) who had received, had refused, or were not eligible for standard chemotherapy with doxorubicin and ifosfamide (Arm 1) and in