Literature DB >> 332319

Results with methyl-CCNU and DTIC in metastatic melanoma.

M E Costanza, L Nathanson, D Schoenfeld, J Wolter, J Colsky, W Regelson, T Cunningham, N Sedransk.   

Abstract

This report is the result of an Eastern Cooperative Oncology Group (ECOG) study. Four hundred and 15 patients with inoperable metastatic malignant melanoma, excluding those with cutaneous metastases only, were randomized to one of three drug treatments: DTIC alone, methyl-CCNU alone, or the combination DTIC plus methyl-CCNU. Responses were seen in 14% of DTIC patients (19/127), 15% of methyl-CCNU patients (18/119) and 14% of DTIC plus methyl-CCNU patients (18/122). Duration of response was the same (14 weeks) for all three treatment groups. There was no difference among the treatments in achieving complete responses. Survival was improved significantly for responders (50 weeks) compared with nonresponders (15 weeks) regardless of treatment regimen. Toxicities were generally tolerable. DTIC caused significantly more gastrointestinal toxicity than methyl-CCNU. Methyl-CCNU caused significantly more bone marrow toxicity than DTIC. There were three drug-related deaths. All occurred in patients on combination DTIC plus methyl-CCNU. Important pretreatment characteristics that favor response are ambulatory status, female, less than 50 years old, no prior chemotherapy and no liver or brain metastases. Patients with favorable characteristics combinations had a 30% response rate, while those with unfavorable characteristic combinations had only a 9% response rate.

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Year:  1977        PMID: 332319     DOI: 10.1002/1097-0142(197709)40:3<1010::aid-cncr2820400308>3.0.co;2-c

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  19 in total

1.  Combination chemotherapy of dacarbazine and fotemustine in disseminated malignant melanoma. Experience of the French Study Group.

Authors:  M F Avril; J Bonneterre; M Delaunay; E Grosshans; P Fumoleua; L Israel; R Bugat; M Namer; D Cupissol; P Kerbrat
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

2.  Phase II trial of docetaxel (Taxotere) in patients with metastatic melanoma previously untreated with cytotoxic chemotherapy.

Authors:  A I Einzig; L M Schuchter; A Recio; S Coatsworth; R Rodriquez; P H Wiernik
Journal:  Med Oncol       Date:  1996-06       Impact factor: 3.064

Review 3.  Systematic review and network meta-analysis of overall survival comparing 3 mg/kg ipilimumab with alternative therapies in the management of pretreated patients with unresectable stage III or IV melanoma.

Authors:  Pascale Dequen; Paul Lorigan; Jeroen P Jansen; Marc van Baardewijk; Mario J N M Ouwens; Srividya Kotapati
Journal:  Oncologist       Date:  2012-09-28

Review 4.  Chemotherapy of malignant melanoma.

Authors:  R S Benjamin
Journal:  World J Surg       Date:  1979-07-30       Impact factor: 3.352

Review 5.  Combined modality therapy of malignant melanoma.

Authors:  E M Hersh; J U Gutterman; C M McBride
Journal:  World J Surg       Date:  1979-07-30       Impact factor: 3.352

6.  Vindesine as a single agent in the treatment of advanced malignant melanoma.

Authors:  S Retsas; K A Newton; G Westbury
Journal:  Cancer Chemother Pharmacol       Date:  1979       Impact factor: 3.333

7.  Carboplatinum and cytosine arabinoside in patients with disseminated malignant melanoma. A phase II study.

Authors:  B Jeremic; L Djuric; L Mijatovic
Journal:  Invest New Drugs       Date:  1991-08       Impact factor: 3.850

8.  Phase II study of AMSA alone and in combination with DTIC in patients with metastatic melanoma.

Authors:  A Polyzos; S S Legha; A M Burgess; R S Benjamin; G P Bodey
Journal:  Invest New Drugs       Date:  1988-04       Impact factor: 3.850

Review 9.  Current treatment options for malignant melanoma.

Authors:  G L Cohen; C I Falkson
Journal:  Drugs       Date:  1998-06       Impact factor: 9.546

10.  Weekly Cisplatin during cranial irradiation for malignant melanoma metastatic to brain.

Authors:  D J Stewart; L G Feun; M Maor; M Leavens; M A Burgess; R S Benjamin; G P Bodey
Journal:  J Neurooncol       Date:  1983       Impact factor: 4.130

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