Literature DB >> 8540118

Combined carboplatin and cytosine arabinoside in metastatic melanoma refractory to dacarbazine.

E Bajetta1, R Buzzoni, G Vicario.   

Abstract

This is a preliminary report on the efficacy and toxicity of the combination chemotherapy regimen with carboplatin and cytosine arabinoside in dacarbazine-resistant metastatic melanoma. Patients were considered eligible in the presence of measurable disease sites, an ECOG performance status of 2 or less, a life expectancy of at least 2 months, and prior dacarbazine treatment. The planned schedule consisted of cytosine arabinoside (150 mg/m2 intravenously plus 50 mg subcutaneously), followed by a rapid infusion of carboplatin (350 mg/m2 on day 1). Courses were administered every 3 weeks according to hematologic recovery. Twenty-one consecutive patients were evaluable for activity and toxicity, the response rate was 19% (95% confidence interval, 5-42%). There was no complete remission. Toxicity was tolerable being myelosuppression the main side effect. In conclusion, the combination of carboplatin and cytosine arabinoside has limited activity as a salvage treatment in melanoma patients failing on dacarbazine chemotherapy. Moreover, the regimen is well tolerated and easy to administer in an outpatient setting.

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Year:  1995        PMID: 8540118     DOI: 10.1177/030089169508100404

Source DB:  PubMed          Journal:  Tumori        ISSN: 0300-8916


  2 in total

1.  Vinblastin-carboplatin for metastatic cutaneous melanoma as first-line chemotherapy and in dacarbazine failures: a single-center study.

Authors:  S Jelić; N Babović; L Stamatović; M Kreacić; S Matković; I Popov
Journal:  Med Oncol       Date:  2001       Impact factor: 3.064

2.  Phase II study of second-line therapy with DTIC, BCNU, cisplatin and tamoxifen (Dartmouth regimen) chemotherapy in patients with malignant melanoma previously treated with dacarbazine.

Authors:  D J Propper; J P Braybrooke; N C Levitt; K O'Byrne; K Christodoulos; C Han; D C Talbot; T S Ganesan; A L Harris
Journal:  Br J Cancer       Date:  2000-06       Impact factor: 7.640

  2 in total

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