Literature DB >> 2155645

High dose intensity combination chemotherapy for advanced epithelial ovarian carcinoma: results of a pilot study.

J W Sweetenham1, J J McKendrick, D H Jones, J M Whitehouse, C J Williams.   

Abstract

Retrospective studies have recently demonstrated a significant correlation between dose intensity of chemotherapy and response rates and survival in various diseases including epithelial ovarian carcinoma. As part of a proposed randomised trial to assess the effect of dose intensity on outcome in ovarian carcinoma, a pilot study has been undertaken to determine the toxicity and efficacy of the high intensity therapy. Nineteen patients with advanced ovarian carcinoma received initial treatment with cisplatin 120 mg m-2 i.v. day 1, and cyclophosphamide 1,000 mg-2 i.v. day 1, given at 21-day intervals for six cycles. The average relative dose intensity of this therapy is 1.14 when compared with the CHAP regimen. Severe toxicity was experienced by most patients. The median received average relative dose intensity was 0.90, with only one patient receiving treatment to the proposed intensity. Randomised studies of the effect of dose intensity in ovarian carcinoma are essential, but an initial step must be to assess whether the proposed high dose treatment can be delivered.

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Year:  1990        PMID: 2155645      PMCID: PMC1971386          DOI: 10.1038/bjc.1990.61

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  13 in total

1.  Prediction of creatinine clearance from serum creatinine.

Authors:  D W Cockcroft; M H Gault
Journal:  Nephron       Date:  1976       Impact factor: 2.847

2.  High-dose cisplatin in hypertonic saline in refractory ovarian cancer.

Authors:  R F Ozols; Y Ostchega; C E Myers; R C Young
Journal:  J Clin Oncol       Date:  1985-09       Impact factor: 44.544

3.  High-dose-intensity regimen of weekly doxorubicin and cisplatin in the treatment of patients with stage III and IV epithelial ovarian carcinoma.

Authors:  G O'Connell; W Shelley; J Carmichael; R Fraser; M E Kirk; G Krepart; L Levin; K Swenerton
Journal:  Cancer Treat Rep       Date:  1987-05

4.  Average relative dose intensity and the impact on design of clinical trials.

Authors:  W M Hryniuk
Journal:  Semin Oncol       Date:  1987-03       Impact factor: 4.929

5.  Randomised trial comparing low-dose cisplatin and chlorambucil with low-dose cisplatin, chlorambucil, and doxorubicin in advanced ovarian carcinoma.

Authors:  G H Barker; E Wiltshaw
Journal:  Lancet       Date:  1981-04-04       Impact factor: 79.321

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.  Cyclophosphamide plus cis-platinum in combination: treatment program for stage III or IV ovarian carcinoma.

Authors:  D G Decker; T R Fleming; G D Malkasian; M J Webb; J A Jeffries; J H Edmonson
Journal:  Obstet Gynecol       Date:  1982-10       Impact factor: 7.661

8.  Therapy of ovarian carcinoma: the relationship of dose level and treatment intensity to survival.

Authors:  A J Jacobs; G M Sommers; S M Homan; H M Camel; J H Axelrod; M S Kao; A E Galakatos; J Parham; L Lippmann
Journal:  Gynecol Oncol       Date:  1988-09       Impact factor: 5.482

9.  Improved chemotherapy for ovarian cancer with cis-diamminedichloroplatinum and adriamycin.

Authors:  H W Bruckner; C J Cohen; J D Goldberg; B Kabakow; R C Wallach; G Deppe; E M Greenspan; S B Gusberg; J F Holland
Journal:  Cancer       Date:  1981-05-01       Impact factor: 6.860

10.  Dose intensity analysis of chemotherapy regimens in ovarian carcinoma.

Authors:  L Levin; W M Hryniuk
Journal:  J Clin Oncol       Date:  1987-05       Impact factor: 44.544

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  1 in total

1.  Hetergeneous tumour response to photodynamic therapy assessed by in vivo localised 31P NMR spectroscopy.

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  1 in total

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