Phase III trial of carboplatin and paclitaxel compared with cisplatin and paclitaxel in patients with optimally resected stage III ovarian cancer: A Gynecologic Oncology Group study

被引:1659
作者
Ozols, RF
Bundy, BN
Greer, BE
Fowler, JM
Clarke-Pearson, D
Burger, RA
Mannel, RS
DeGeest, K
Hartenbach, EM
Baergen, R
机构
[1] Fox Chase Canc Ctr, Gynecol Oncol Grp, Dept Med Sci, Philadelphia, PA 19103 USA
[2] Roswell Pk Canc Inst, Gynecol Oncol Grp, Stat & Data Ctr, Buffalo, NY USA
[3] New York Presbyterian Hosp, Cornell Med Ctr, Dept Pathol, New York, NY USA
[4] Univ Washington, Sch Med, Div Gynecol Oncol, Seattle, WA USA
[5] Ohio State Univ, James Canc Hosp, Div Gynecol Oncol, Columbus, OH 43210 USA
[6] Ohio State Univ, Solove Res Inst, Columbus, OH 43210 USA
[7] Duke Univ, Sch Med, Dept Gynecol Oncol, Durham, NC USA
[8] Duke Univ, Sch Med, Dept Obstet, Durham, NC USA
[9] Duke Univ, Sch Med, Dept Gynecol, Durham, NC USA
[10] Univ Calif Irvine, Div Gynecol Oncol, Orange, CA 92668 USA
[11] Univ Oklahoma, Hlth Sci Ctr, Dept Obstet & Gynecol, Oklahoma City, OK 73190 USA
[12] Rush Presbyterian St Lukes Med Ctr, Dept Obstet & Gynecol, Chicago, IL USA
[13] Univ Wisconsin, Div Gynecol Oncol, Madison, WI USA
[14] Univ Texas, SW Med Ctr, Dallas, TX USA
关键词
D O I
10.1200/JCO.2003.02.153
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
(P) under bar(u) under bar(r) under bar(p) under bar(o) under bar(s) under bar(e) under bar: In randomized trials the combination of cisplatin and paclitaxel was superior to cisplatin and cyclophosphamide in advanced-stage epithelial ovarian cancer. Although in nonrandomized trials, carboplatin and paclitaxel was a less toxic and highly active combination regimen, there remained concern regarding its efficacy in patients with small-volume, resected, stage III disease. Thus, we conducted a noninferiority trial of cisplatin and paclitaxel versus carboplatin and paclitaxel in this population. (P) under bar(a) under bar(t) under bar(i) under bar(e) under bar(n) under bar(t) under bar(s) under bar (a) under bar(n) under bar(d) under bar (M) under bar(e) under bar(t) under bar(h) under bar(o) under bar(d) under bar(s) under bar: Patients with advanced ovarian cancer and no residual mass greater than 1.0 cm after surgery were randomly assigned to receive cisplatin 75 mg/m(2) plus a 24-hour infusion of paclitaxel 135 mg/m(2) (arm I), or carboplatin area under the curve 7.5 intravenously plus paclitaxel 175 mg/m(2) over 3 hours (arm II). (R) under bar(e) under bar(s) under bar(u) under bar(l) under bar(t) under bar(s) under bar: Seven hundred ninety-two eligible patients were enrolled onto the study. Prognostic factors were similar in the two treatment groups. Gastrointestinal, renal, and metabolic toxicity, as well as grade 4 leukopenia, were significantly more frequent in arm I. Grade 2 or greater thrombocytopenia was more common in arm II. Neurologic toxicity was similar in both regimens. Median progression-free survival and overall survival were 19.4 and 48.7 months, respectively, for arm I compared with 20.7 and 57.4 months, respectively, for arm II. The relative risk (RR) of progression for the carboplatin plus paclitaxel group was 0.88 (95% confidence interval [CI], 0.75 to 1.03) and the RR of death was 0.84 (95% CI, 0.70 to 1.02). (C) under bar(o) under bar(n) under bar(c) under bar(l) under bar(u) under bar(s) under bar(i) under bar(o) under bar(n) under bar: In patients with advanced ovarian cancer, a chemotherapy regimen consisting of carboplatin plus paclitaxel results in less toxicity, is easier to administer, and is not inferior, when compared with cisplatin plus paclitaxel. (C) 2003 by American Society of Clinical Oncology.
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页码:3194 / 3200
页数:7
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