Literature DB >> 3621453

High-dose cyclophosphamide followed by cisplatinum in the treatment of ovarian cancer.

R Osborne, B Evans, C Gallagher, C Wood, M Slevin, J Shepherd, E Wiltshaw.   

Abstract

Twenty patients with previously untreated ovarian cancer received intensive chemotherapy after initial surgery. Treatment comprised two courses of cyclophosphamide at 7 g/m2 with mesna, re-evaluation with second-look laparotomy where appropriate, followed by five courses of cisplatin at 100 mg/m2. Three patients achieved pathologically documented complete remission (PDCR) with high-dose cyclophosphamide, and eight patients achieved partial remission. Fifteen patients went on to receive cisplatin. Nine of these patients had no assessable disease; of six patients who were assessed for response two achieved PDCR and three achieved partial remission. The overall response rate to the sequential regimen was 14/20 (70%). High-dose cyclophosphamide was associated with marked haematological toxicity, which was cumulative and fatal in two patients. The median duration of first remission was 14 months, and the median duration of survival was 20 months. It is concluded that sequential treatment with high-dose cyclophosphamide and cisplatin appears to be no more effective than conventional treatment in advanced ovarian cancer, judging by the PDCR rate and median survival achieved.

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Year:  1987        PMID: 3621453     DOI: 10.1007/bf00252959

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  14 in total

1.  EXPERIMENTAL EVALUATION OF POTENTIAL ANTICANCER AGENTS. XIV. FURTHER STUDY OF CERTAIN BASIC CONCEPTS UNDERLYING CHEMOTHERAPY OF LEUKEMIA.

Authors:  H E SKIPPER; F M SCHABEL; W S WILCOX
Journal:  Cancer Chemother Rep       Date:  1965-04

2.  Intermittent high-dose cyclophosphamide (NSC-26271) treatment of stage III ovarian carcinoma.

Authors:  C D Buckner; R Briggs; R A Clift; A Fefer; D D Funk; H Glucksberg; P E Neiman; R Storb; E D Thomas
Journal:  Cancer Chemother Rep       Date:  1974 Sep-Oct

3.  Acceleration of bone-marrow recovery by pre-treatment with cyclophosphamide in patients receiving high-dose melphalan.

Authors:  D W Hedley; T J McElwain; J L Millar; M Y Gordon
Journal:  Lancet       Date:  1978-11-04       Impact factor: 79.321

Review 4.  Cyclophosphamide-induced cardiomyopathy: a report of two cases and review of the English literature.

Authors:  B A Mills; R W Roberts
Journal:  Cancer       Date:  1979-06       Impact factor: 6.860

5.  Serous ovarian neoplastic amylase (SONA): a potentially useful marker for serous ovarian tumors.

Authors:  H Van Kley; S Cramer; D E Bruns
Journal:  Cancer       Date:  1981-09-15       Impact factor: 6.860

6.  Cisplatin combination chemotherapy versus chlorambucil in advanced ovarian carcinoma: mature results of a randomized trial.

Authors:  C J Williams; G M Mead; F R Macbeth; J Thompson; J M Whitehouse; H MacDonald; V J Harvey; M L Slevin; T A Lister; J H Shepherd
Journal:  J Clin Oncol       Date:  1985-11       Impact factor: 44.544

7.  Chemotherapy of advanced ovarian carcinoma: a prospective randomized comparison of phenylalanine mustard and high dose cyclophosphamide.

Authors:  R C Young; G P Canellos; B A Chabner; P S Schein; S P Hubbard; V T DeVita
Journal:  Gynecol Oncol       Date:  1974-12       Impact factor: 5.482

8.  Long-term survival after chemotherapy for advanced epithelial ovarian carcinoma.

Authors:  J T Wharton; C L Edwards; F N Rutledge
Journal:  Am J Obstet Gynecol       Date:  1984-04-01       Impact factor: 8.661

9.  A mathematic model for relating the drug sensitivity of tumors to their spontaneous mutation rate.

Authors:  J H Goldie; A J Coldman
Journal:  Cancer Treat Rep       Date:  1979 Nov-Dec

10.  Prevention of acute deaths in mice after very high dose cyclophosphamide by divided dose schedule.

Authors:  B D Evans; I E Smith; R D Clutterbuck; J L Millar
Journal:  Br J Cancer       Date:  1984-01       Impact factor: 7.640

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