期刊文献+

卡培他滨联合多西紫杉醇治疗蒽环类耐药的晚期乳腺癌 被引量:3

Capecitabine in combination with docetaxel in the treatment of anthracycline-resistant advanced breast carcinoma
原文传递
导出
摘要 目的观察卡培他滨联合多西紫杉醇治疗蒽环类耐药的晚期乳腺癌的疗效与安全性。方法于2001年9月至2005年5月,41例蒽环类耐药的晚期乳腺癌患者实施了卡培他滨联合多西紫杉醇方案化疗,卡培他滨1000~1250mg/m2口服,每日2次,第1~14天;多西紫杉醇60~75mg/m2,静滴,第1天或30~37.5mg/m2,静滴,第1、8天;21d为1周期。每例至少治疗2周期后评价疗效,中位化疗周期数为4(2~8)周期。结果在38例可评价疗效的患者中,完全缓解(CR)4例(10.5%),部分缓解(PR)18例(47.4%),稳定(SD)11例(28.9%),进展(PD)5例(13.2%),总有效率(CR+PR)为57.9%,疾病控制率(CR+PR+SD)为86.8%,中位肿瘤进展时间(TTP)9.1个月,中位生存期18.4个月。主要毒性反应为骨髓抑制和胃肠道反应。结论卡培他滨和多西紫杉醇联合方案治疗蒽环类耐药的转移性乳腺癌疗效好,使用方便,耐受性良好,适合于体质状态稍差的老年患者,可作为蒽环类耐药的晚期乳腺癌的有效解救治疗方案。 Objective To evaluate the efficacy and safety of oral capecitabine in combination with dneetaxel for patients with anthracycline-resistant advanced breast carcinoma. Methods Forty-one patients with anthracycline - resistant advanced breast cancer received oral capecitabine 1000-1250 mg/m^2 twice daily, days 1 -14, plus i.v. docetaxel 60-75 mg/m^2 on day 1 or 30-37.5 mg/m2 on days 1 and 8 of each 21 day treatment cycle. Every patient was administered at least 2 cycles and with a median of 4 cycles (2 -8 cycles). Results All 41 patients were evaluable for safety and 38 for efficacy. The overall combination chemotherapy objective response rate was 57. 9% including complete responses (CR) in 4 (10.5%) patients, paritical responses (PR) in 18 (47. 4% ) patients, stable disease (SD) in 11 (28. 9% ) patients, and progressive disease (PD) in 5 ( 13. 2% ) patients. Disease control rate (CR + PR + SD) was 86. 8%. The median time to disease progression or TTP was 9. 1 months. The main side effects were hematologic and gastrointestinal toxicities including grade 3-4 leukopenia in 5 patients (12. 2% ) and nausea and vomiting in 1 patient. Conclusions Capecitabine and docetaxel combination regimen has important antitumor activity in the treatment of anthracyclin-resistant advanced breast cancer patients, with an acceptable safety profile in this setting, especially for older patients. It may be regarded as the salvage chemotherapy afte r anthracycline regimen has failed.
出处 《中华乳腺病杂志(电子版)》 CAS 2007年第5期146-149,共4页 Chinese Journal of Breast Disease(Electronic Edition)
关键词 卡培他滨 多西紫杉醇 晚期乳腺癌 蒽环类 Capecitabine Docetaxel Advanced breast carcinoma Anthracycline
  • 相关文献

参考文献11

  • 1郝春芳,江泽飞,宋三泰.紫杉特尔在乳腺癌化疗中的应用[J].国外医学(肿瘤学分册),2003,30(2):129-132. 被引量:37
  • 2刘晓晴,宋三泰,管忠震,吴世凯,段玉峰,于静新,杨丽芳.希罗达治疗复发转移乳腺癌的临床研究[J].中华肿瘤杂志,2002,24(1):71-73. 被引量:61
  • 3Valero V,Jones SE,Von Hoff DD,et al.A phase II study of docetaxel in patients with paclitaxel-resistant metastatic breast cancer[].Journal of Clinical Oncology.1998 被引量:1
  • 4Fumoleau P,Largillier R.Multicentre,phase II study evaluatingcapecitabine monotherapy in patients with anthracycline-and taxane-pretreated metastatic breast cancer[].European Journal of Cancer.2004 被引量:1
  • 5DC Talbot,V Moiseyenko,S Belle.Randomised, phase II trial comparing oral capecitabine (Xeloda) with paclitaxel in patients with metastatic/advanced breast cancer pretreated with anthracyclines[].British Journal of Cancer.2002 被引量:1
  • 6Sawada N,Ishikawa T,Fukase Y,et al.Induction of thymidine phosphorylase activity and enhancement of capecitabine efficacy by taxol/taxotere in human cancer xenografts[].Clinical Cancer Research.1998 被引量:1
  • 7O’Shaughnessy J,Miles D,Vukelja S,et al.Superior survival with capecitabine plus docetaxel combination therapy in anthracycline-pretreated patients with advanced breast cancer: phase Ⅲ trial results[].Journal of Clinical Oncology.2002 被引量:1
  • 8Eda H,Fujimoto K,Watanabe S,et al.Cytokines induce uridine phosphorylase in mouse colon 26 carcinoma cells and make the cells more susceptible to 5’-deoxy-5-fluorouridine[].Japanese Journal of Cancer Research.1993 被引量:1
  • 9Ellis M J,Hayes D F,Lippman ME.Treatment of metastatic breast cancer[].Diseases of the Breast.2000 被引量:1
  • 10Reichardt P,Von Minckwitz G,Thuss Patience P C,et al.Multicenter phaseⅡstudy of oral capecitabine(Xeloda)in patients with metastatic breast cancer relapsing after treatment with a taxane-containing therapy[].Annals of Oncology.2003 被引量:1

二级参考文献35

  • 1Ibrahim NK, Rahman Z, Valero V, et al. Phase Ⅰ study of vinorelbine and docetaxel with granulocyte colony-stimulating factor support in the treatment of metastatic breast cancer [J]. Cancer Invest, 2002,20(1): 29-37. 被引量:1
  • 2Venturini M, Del Mastro L, Garrone O, et al. Phase Ⅰ, dose-finding study of capecitabine in combination with docetaxel and epirubicin as first-line chemotherapy for advanced breast cancer [ J ]. Ann Oncol, 2002,13(4): 546-552. 被引量:1
  • 3Schwetz BA. From the Food and Drug Administration [J]. JAMA,2001,286(17) : 2085. 被引量:1
  • 4O'Shaughnessy J, Miles D, Vukelja S, et al. Superior survival with capecitabine plus docetaxel combination therapy in anthracyclin-pretreated patients with advanced breast cancer: phase Ⅲ trial results [J]. J Clin Oncol, 2002,20(12): 2812-2823. 被引量:1
  • 5Brugnatelli S, Danova M, De Bella MT, et al. Weekly administration of gemcitabine plus docetaxel in patients with advanced breast cancer: a phase 1 study [J]. Oncology, 2002,62(1): 33-38. 被引量:1
  • 6Frasci G, Comella P, D' Aiuto G, et al. Weekly docetaxel plus gemcitabine or vinorelbine in refractory advanced breast cancer patients: a parallel dose-finding study [J]. Ann Oncol, 2000, 11(3):367-371. 被引量:1
  • 7Burris HA 3rd.Docetaxel (Taxotere) plus trasuzumab (Herceptin) in breast cancer [J]. Semin Oncol, 2001,28(1 Suppl 3) : 38-44. 被引量:1
  • 8Esteva FJ, Valero V, Booser D, et al. Phase I1 study of weekly docetaxel and trastuzumab for patients with HER-2-overexpressing metastatic breast cancer [J]. J Clin Oncol, 2002,20(7): 1800-1808. 被引量:1
  • 9Smith IC, Heys SD, Hutcheon AW, et al. Neoadjuvant chemotherapy in breast cancer: significantly enhanced response with docetaxel [J]. J Clin Oncol, 2002, 20(6): 1456-1466. 被引量:1
  • 10Estevez LG, Cuevas JM, Anton A, et al. Weekly docetaxel as neoadjuvant vhemotherapy for stage Ⅱ and Ⅲ Breast Cancer: Efficacy and Correlation with Biological Markers in a Phase Ⅱ , Multicenter Study [J]. Clin Cancer Res, 2003,9(2): 686-692. 被引量:1

共引文献95

同被引文献41

引证文献3

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部