A Phase I/II Study of Docetaxel and Gemcitabine Combination for Chemotherapy-resistant Ovarian Cancer

被引:0
作者
Itani, Yoshio [1 ]
Hosokawa, Kenichi [2 ]
Ito, Kimihiko [3 ]
Takeuchi, Satoshi [4 ]
Tabata, Tsutomu [5 ]
Tsubamoto, Hiroshi [6 ]
Fujita, Hiroyuki [7 ]
Akiyama, Minoru [8 ]
Adachi, Susumu [6 ,9 ]
机构
[1] Nara Prefectural Nara Hosp, Nara, Japan
[2] Kyoto Prefectural Univ Med, Kyoto, Japan
[3] Kansai Rosai Hosp, Hyogo, Japan
[4] Kobe Natl Hosp, Kobe, Hyogo, Japan
[5] Mie Univ, Tsu, Mie, Japan
[6] Hyogo Coll Med, Nishinomiya, Hyogo, Japan
[7] Kyoto Second Red Cross Hosp, Kyoto, Japan
[8] Shiga Med Univ, Shiga, Japan
[9] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
关键词
Epithelial ovarian cancer; treatment resistant; phase I/II study; gemcitabine; docetaxel; PEGYLATED LIPOSOMAL DOXORUBICIN; PLATINUM-BASED CHEMOTHERAPY; II TRIAL; FALLOPIAN-TUBE; PACLITAXEL; CARCINOMA; RECURRENT; MALIGNANCIES; CARBOPLATIN; PERITONEUM;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A phase I/II study of docetaxel (DOC) and gemcitabine (GEM) combination for treatment-resistant ovarian cancer (OC) was conducted. Materials and Methods: Eligible patients exhibited recurrent OC within 12 months after initial treatment, or after more than 2 chemotherapy regimens. Planned dose levels (DL) were as follows: DOC 70 mg/m(2), GEM 800 mg/m(2) (DL1); DOC 70 mg/m(2), GEM 1000 mg/m(2) (DL2). DOC was administered on day 1 combined with GEM on days 1 and 8 every 3 weeks. Adverse events were assessed by NCI-CTC2.0J. Response was evaluated by RECIST or Rustin's criteria. Results: The recommended dose was DL1. For all enrolled patients, the median interval from last chemotherapy was 2.5 (1-11) months and 32 patients were assessable for response. One complete response, 6 partial responses and 6 stable disease were noted. Median time to progression was 4.8 months. Toxicities were mainly hematological and Manageable. Conclusion: This combination could be an acceptable treatment option before palliation.
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页码:1521 / 1526
页数:6
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