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多西他赛解救治疗紫杉醇耐药的转移性乳腺癌的临床研究 被引量:16

A clinical study of docetaxel in patients with paclitaxel-resistant metastatic breast cancer
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摘要 目的评价多西他赛解救治疗紫杉醇耐药复发转移性乳腺癌的临床疗效。方法回顾性分析60例多西他赛治疗紫杉醇耐药的复发转移性乳腺癌患者的临床资料,对临床疗效及其影响因素等进行统计分析。结果全组患者中位年龄51岁。雌/孕激素受体阳性率65%,Her-2状态阳性率28.3%。多西他赛解救治疗紫杉醇耐药的复发转移性乳腺癌患者,客观缓解率为18.3%,临床获益率25.0%,中位PFS 4.0个月(3.38~4.62个月);耐药亚组分析结果显示原发耐药组与继发耐药组的客观缓解率及临床获益率无明显统计学差异(P=1.000;P=0.762),但多西他赛治疗紫杉醇耐药复发转移性乳腺癌继发耐药组的无进展生存期(PFS)要优于原发耐药组(2个月vs 6个月,P=0.008)。COX多因素分析显示多西他赛PFS与单位体表面积剂量、年龄、病理类型、Her-2状态、雌/孕激素受体表达状态、同侧腋窝淋巴结转移数目、复发转移部位数目等因素均无关,但与耐药情况、无病生存期、解救治疗线数、临床分期(P=0.001;P=0.029;P=0.037;P=0.034)等因素相关。结论紫杉醇耐药患者接受多西他赛解救治疗仍可获得一定的客观缓解率及临床获益率,二者部分交叉耐药。 Objective To evaluate the efficacy of docetaxel in patients with paclitaxel-resistant metastatic breast cancer. Methods 60 clinical records of metastatic breast cancer patients with paelitaxel-resistance were summarized ret- rospectively and the clinical effects and influencing factors of docetaxel were statistically analyzed. Results The median age was fifty-one years in the whole group. The positive rate of estrogen receptor or progesterone receptor was 65%, and the positive status of Her-2 was 28.3%. The objective response rates and the clinical benefit rates of doeetaxel in patients with paclitaxel-resistant metastatic breast cancer were 18.3% and 25.0%, and the median progression-free survival (PFS) was 4. 0 (3.38 -4. 62) months. There was no difference between the effects of primary paclitaxel-resistant group and seconda- ry paclitaxel-resistant group not only in objective response rates, but also in clinical benefit rates ( P = 1. 000 ; P = 0. 762). However, the PFS of the latter was superior to the former (2 months vs 6 months, P = 0. 008). Cox regression showed that the PFS of docetaxel had no association with the dose of body surface area per units, age, pathological type, status of estrogen/progesterone receptor, status of Her-2, lymph node metastatic status in patients with paclitaxel-rcsistant metastatic breast cancer, but was correlated with the resistance to paelitaxel, disease-free survival, treatmenl lines, clinical stages (P = 0. 001 ; P = 0. 029; P = 0. 037 ; P = 0. 034). Conclusion Paclitaxet-resistant patients underwent do- eetaxel treatment still obtained certain objective response rates and clinieal benefit rates, and the paelitaxel and docetaxel were partially cross-resistant in patients.
机构地区 解放军
出处 《癌症进展》 2012年第3期251-256,共6页 Oncology Progress
关键词 乳腺癌 紫杉醇耐药 多西他赛 客观缓解率 无进展生存期 breasl caneer paelitaxel-resistance docetaxel objective response rates progression-free survival
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  • 1Valero V, Jones SE, Von Hoff DD, et al. A phase II study of docetaxel in patients with paclitaxel-resistant metastatic breast cancer [J]. J Clin Oncol, 1998, 16 (10) : 3362 - 3368.
  • 2Taguchi T, Aihara T, Takatsuka Y, et al. Phase 11 Study of Weekly Paelitaxel for Docetaxel-Resistant Metastatic Breast Cancer in Japan [J]. Breast J, 2004, 10 (6): 509 -513.
  • 3徐冰河,孙燕.乳腺癌内科治疗的策略及研究[J].乳腺病杂志,2003,1(1):1-3.
  • 4Nabholtz JM, Tonkin K, Smylie M, et al. Chemotherapy of breast cancer: Are the taxanesgoing to change the natural history of breast cancer [ J ]. Expert Opin Pharmacother, 20001 (2): 187 -206.
  • 5Lavelle F, Bissery MC, Combeau C, et al. Preclinical eval- uation of docetaxel (Taxotere) [ J ]. Semin Oneol, 1995, 22 (2 Suppl4):3-16.
  • 6Hanauske AR, Degen D, Hilsenbeck SG, et al. Effects of Taxotere and Taxol on invitro colony formation of freshly ex- planted human tumor cells [J]. Anti-cancer Drugs, 1992, 3 (2):121-124.
  • 7Riou JF, Naudin A, Lavelle F. Effects of Taxotere on mu- rine and human tumor cell lines [ J ]. Bioehem Biophys Res Commun, 1992, 187 (1) : 164 - 170.
  • 8Diaz JF, Andreu JM. Assembly of purified GDP-tubulin intomicrotubules induced by Taxol and Taxotere: Reversibility, ligand stoichiometry, and competition [ J ]. Biochemistry, 1993, 32 ( 11 ) : 2747 - 2755.
  • 9Ringel I, Horwitz SB. Studies with RP 56976 (Taxotere) : A semisynthetic analogue of Taxol [ J]. J Natl Cancer Inst, 1991, 83 (4):288-291.
  • 10Andreu JM, Diaz JF, Gil R, et al. Solution structure of Taxotere-induced microtubules to 3nm resolution [ J ]. J Biol Chem, 1994, 269:31785 -31792.

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