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Progression-free survival and overall survival of patients with clear cell carcinoma of the ovary treated with paclitaxel-carboplatin or irinotecan-cisplatin: retrospective analysis.

Authors :
Takano, Masashi
Sugiyama, Toru
Yaegashi, Nobuo
Suzuki, Mitsuaki
Tsuda, Hiroshi
Sagae, Satoru
Udagawa, Yasuhiro
Kuzuya, Kazuo
Kigawa, Junzo
Takeuchi, Satoshi
Tsuda, Hitoshi
Moriya, Takuya
Kikuchi, Yoshihiro
Source :
International Journal of Clinical Oncology. Aug2007, Vol. 12 Issue 4, p256-260. 5p. 2 Charts, 2 Graphs.
Publication Year :
2007

Abstract

Irinotecan hydrochloride, a topoisomerase I inhibitor, has been preliminarily recognized as an effective agent against clear cell carcinoma of the ovary (CCC), but there are few clinical data. Our aim was to compare progression-free survival (PFS) between patients treated with irinotecan hydrochloride and cisplatin (CPT-P) and those with treated with paclitaxel and carboplatin (TC). One hundred and seventeen patients at International Federation of Gynecology and Obstetrics (FIGO) stages Ic (ascites/malignant washing) – IV were identified by scanning the medical records of ten Japanese hospitals. After complete surgical staging procedures including lymphadenectomy, 35 patients received CPT-P and 82 patients received TC. The PFS and overall survival of the two groups were compared using the Kaplan-Meier method. There was no significant difference in median age, performance status, FIGO stage, rate of optimal cytoreduction, or follow-up period between the CPT-P and TC groups. Two-year and 5-year PFS was 48% and 40%, respectively, in the TC group and 55% and 55%, respectively, in the CPT-P group ( P = 0.31). Multiple regression analysis revealed that only residual tumor was an independent prognostic factor for PFS ( P < 0.01). CPT-P showed a potential therapeutic effect, at least no less than that of TC therapy. Although there was no significant survival benefit in the present retrospective analysis, we recommend that the CPT-P regimen be evaluated in a larger, prospective, clinical trial. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13419625
Volume :
12
Issue :
4
Database :
Academic Search Index
Journal :
International Journal of Clinical Oncology
Publication Type :
Academic Journal
Accession number :
26199053
Full Text :
https://doi.org/10.1007/s10147-007-0670-1