Comparison of conventional dose and double dose carboplatin in patients receiving cyclophosphamide plus carboplatin for advanced ovarian carcinoma: a North Central Cancer Treatment Group Study.

Autor:	Edmonson, John H., Suman, Vera J., Dalton, Robert J., Bro, Walter C., Gallenberg, Mary M., Long, Harry J., Levitt, Ralph, Hatfield, Alan K., Krook, James E., Mailliard, James A., Gerstner, James B., Edmonson, J H, Suman, V J, Dalton, R J, Bro, W C, Gallenberg, M M, Long, H J, Levitt, R, Hatfield, A K, Krook, J E
Předmět:	GRANULOCYTE-macrophage colony-stimulating factor OVARIAN cancer DOSAGE forms of drugs ANTINEOPLASTIC agents BLACK people CLINICAL trials COMBINED modality therapy COMPARATIVE studies DRUG administration DOSE-effect relationship in pharmacology RESEARCH methodology MEDICAL cooperation OVARIAN tumors RESEARCH RECOMBINANT proteins SURVIVAL WHITE people EVALUATION research RANDOMIZED controlled trials CYCLOPHOSPHAMIDE CARBOPLATIN THERAPEUTICS
Zdroj:	Cancer Investigation; Aug2001, Vol. 19 Issue 6, p597-602, 6p, 3 Charts
Abstrakt:	Between March 1992 and November 1994, 91 patients with stage III and IV ovarian carcinoma were enrolled in a randomized comparative study of cyclophosphamide 600 mg/m2 plus carboplatin 300 mg/m2 vs. cyclophosphamide 600 mg/m2 plus carboplatin 600 mg/m2, each regimen given monthly for six cycles. Patients on the intensive regimen also received 10 micrograms/kg of granulocyte macrophage colony stimulating factor (GM-CSF) (molgramostim) daily for 14 days following each chemotherapy treatment. The study was closed prematurely because of very poor case accrual following the preliminary announcement (in May 1993) that paclitaxel appeared superior to cyclophosphamide in the platinum-based treatment of ovarian cancer. More than 4 years after our last case entry, we analyzed the survival results for the 44 eligible patients who received the conventional dose of carboplatin and the 43 eligible patients receiving our intensified dose of carboplatin. More than 90% of the treated patients receiving the conventional dose regimen received at least 75% of the planned doses at each of the six treatment intervals, whereas the percentage of treated patients able to receive at least 75% of the assigned intensive dose regimen had declined from 95% in cycle 2 to 53% by cycle 6. Furthermore, although 32 patients received all six planned cycles of treatment in the conventional regimen group, only 15 received all six cycles of the intensified regimen. Patients receiving the intensive regimen had more fever, dermatitis, lethargy, musculoskeletal pain, and pulmonary complications than did the conventional dose patients. Median survival times for the two treatment groups were very similar (38.5 and 38.1 months, respectively, for the conventional and intensive regimens), and we saw no evidence that the distribution of survival times differed between the treatment regimens (p = 0.95). [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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