Carboplatin alone vs carboplatin plus epidoxorubicin as second-line therapy for cisplatin- or carboplatin-sensitive ovarian cancer

被引:67
作者
Bolis, G [1 ]
Scarfone, G
Giardina, G
Villa, A
Mangili, G
Melpignano, M
Presti, M
Tateo, S
Franchi, M
Parazzini, F
机构
[1] Univ Milan, Clin Ostetr Ginecol, I-20122 Milan, Italy
[2] Ist Nazl Tumori, Div Oncol Chirurg Ginecol, I-20133 Milan, Italy
[3] Osped S Anna, Div Osterticia & Ginecol, Turin, Italy
[4] Univ Milan, Osped S Raffaele, Clin Ostetr Ginecol, I-20122 Milan, Italy
[5] Univ Parma, Clin Ostetr Ginecol, I-43100 Parma, Italy
[6] Osped Civile, Div Ostetricia & Ginecol, Voghera, PV, Italy
[7] Univ Pavia, Clin Ostetr Ginecol, I-27100 Pavia, Italy
[8] Univ Insurbria, Clin Ostetr Ginecol, Varese, Italy
[9] Mario Negri Inst Pharmacol Res, I-20157 Milan, Italy
关键词
ovarian cancer; chemotherapy; recurrence;
D O I
10.1006/gyno.2001.6151
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The aim of the study was to analyze the benefit/ toxicity profile of a second-line treatment with carboplatin alone or carboplatin plus another non-cross-resistant drug (epidoxorubicin) in ovarian cancer patients sensitive to cisplatin-based chemotherapy at first-line treatment. Methods. We conducted a randomized clinical trial. Women with epithelial ovarian cancer FIGO Stage II-IV who had a complete or partial response to first-line treatment with cisplatin or carboplatin-based regiments and subsequently progressed or relapsed more than 6 months after discontinuation of first-line treatment were eligible for the study. A total of 190 subjects entered the study. They were randomly allocated to either 300 mg/m(2) of carboplatin every 28 days for five cycles (95 patients) or 120 mg/m(2) of epidoxorubicin and 300 mg/m(2) of carboplatin every 28 days for five cycles (95 patients). Results. A complete response was reported, respectively, in 32 (36%) women allocated to carboplatin alone and in 28 (31.8%) of those allocated to carboplatin plus epidoxorubicin, The corresponding figures for partial response were 18 (20.2%) and 26 (29.9%). Comparing the frequency of complete response, partial response, no change, and progression, the differences between the two groups were not significant (chi (2)(3) 5.10, P = 0,16). The median duration of response was 16 months in the carboplatin alone and 20 months in the carboplatin plus epidoxorubicin group (P = not significant). The 3-year percentage of survival was 29% in the carboplatin alone and 42% in the carboplatin plus epidoxorubicin group; this difference was not statistically significant, The frequency of leukopenia, anemia, and thrombocytopenia grade 3-4 was higher in the epidoxorubicin plus carboplatin than in the carboplatin alone group. Alopecia G3 was present in 88% of women treated with epidoxorubicin plus carboplatin. Conclusions. The general results of this study do not show any marked differences in response to second-line treatment among women treated with single-agent (carboplatin) or multiagent (carboplatin plus epidoxorubicin) schedules. Toxicity, particularly hematological, was more relevant in women treated with the multiagent schedule. (C) 2001 Academic Press.
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页码:3 / 9
页数:7
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