Abstract | OBJECTIVE: METHODS: 83 Patients with at least one measurable lesion were randomized to receive the treatment arms: docetaxel 37.5 mg/m(2) on days 1 and 8, oral capecitabine 950 mg/m(2) twice daily on days 1-14 (Group A); docetaxel 75 mg/m(2) on days 1, oral capecitabine 950 mg/m(2) twice daily on days 1-14 (Group B). Each cycle was repeated every 3 weeks. RESULTS: Eighty-three patients were enrolled, 78 eligible for tumor assessment. The overall clinical response rate of all groups was 61.4% (51/83). There was no progressive disease (PD) after two cycles. Efficacy outcomes were similar in the two groups. The response rate of group A and B were 61.8% (21/34) and 61.2% (30/49) respectively. There were no drug-related deaths observed. Neutropenia was the most common toxicity. In all, the frequency of Grade 3/4 neutropenia were 45.8% (38/83), but Grade 3/4 neutropenia of Group B 55.1% (27/49) was higher than Group A 32.4% (11/34), P = 0.04. CONCLUSION:
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Authors | Shao-hua Zhang, Ze-fei Jiang, Xiao-dong Xie, Yan Wei, Jun Ren, Ji-wei Liu, Wen-chao Liu, Xia Li, Yu-xian Bai, Shun-chang Jiao, Qiang Sun, Duan-qi Liu, Ju-xiang Xiao, Hua-qing Wang, Li-li Tang, Ying Cheng, Yu Wang, Yong-sheng Wang |
Journal | Zhonghua yi xue za zhi
(Zhonghua Yi Xue Za Zhi)
Vol. 90
Issue 26
Pg. 1813-5
(Jul 13 2010)
ISSN: 0376-2491 [Print] China |
PMID | 20979824
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Anthracyclines
- Taxoids
- Deoxycytidine
- Docetaxel
- Capecitabine
- Fluorouracil
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Topics |
- Adult
- Aged
- Anthracyclines
(therapeutic use)
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Breast Neoplasms
(drug therapy, secondary)
- Capecitabine
- Deoxycytidine
(administration & dosage, analogs & derivatives)
- Docetaxel
- Female
- Fluorouracil
(administration & dosage, analogs & derivatives)
- Humans
- Middle Aged
- Neoplasm Recurrence, Local
(drug therapy)
- Pilot Projects
- Taxoids
(administration & dosage)
- Treatment Failure
- Treatment Outcome
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