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Randomized Phase II Trial of weekly paclitaxel alone versus trastuzumab plus weekly paclitaxel as first-line therapy of patients with Her-2 positive advanced breast cancer.

机译:每周单独紫杉醇与曲妥珠单抗加每周紫杉醇作为Her-2阳性晚期乳腺癌患者的一线治疗的随机II期试验。

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摘要

BACKGROUND: ududA randomized Phase II study evaluated the activity of weekly paclitaxel versus its combination with trastuzumab for treatment of patients with advanced breast cancer overexpressing HER-2.ududPATIENTS AND METHODS: ududAmong 124 patients randomized, 123 are assessable for toxicity and 118 for response. Patients received weekly paclitaxel single agent (80 mg/m2) or combined with trastuzumab (4 mg/kg loading dose, then weekly 2 mg/kg). HER-2 overexpression was determined by immunohistochemistry (IHC). Patients with 2+/3+ IHC scores were eligible. IHC was compared with HER-2 serum extracellular domain (ECD).ududRESULTS: ududPatient characteristics were similar in the two arms. Both treatments were feasible and well tolerated with no grade 4 hematologic toxicity. No patient developed cardiac toxicity. The combined treatment was statistically significant superior for overall response rate (ORR) (75% vs. 56.9%; P = 0.037), particularly in the subset of IHC 3+ patients (84.5% vs. 47.5%; P = 0.00050). A statistically significant better median time to progression was seen in the subgroup with IHC 3+ (369 vs. 272 days; P = 0.030) and visceral disease (301 vs. 183 days; P = 0.0080) treated with combination. Multivariable analysis of predictive factors showed that only IHC score retained statistically significant value for ORR (P = 0.0035).ududCONCLUSION: ududWeekly paclitaxel plus trastuzumab is highly active and safe and it is superior to paclitaxel alone in patients with IHC score of 3+.
机译:背景: ud ud一项随机的II期研究评估了每周紫杉醇与曲妥珠单抗联合使用对治疗过度表达HER-2的晚期乳腺癌患者的活性。 ud ud患者和方法: ud ud在124名患者中随机分组,其中123名可评估毒性,可评估118。患者每周接受紫杉醇单药(80 mg / m2)或联合曲妥珠单抗(4 mg / kg负荷剂量,然后每周2 mg / kg)。通过免疫组织化学(IHC)确定HER-2过表达。 IHC评分为2 + / 3 +的患者符合条件。将IHC与HER-2血清细胞外域(ECD)进行了比较。 ud ud结果: ud ud患者的两个手臂的特征相似。两种治疗均可行且耐受性良好,无4级血液学毒性。没有患者出现心脏毒性。联合治疗在总体缓解率(ORR)方面具有统计学显着性(75%比56.9%; P = 0.037),尤其是在IHC 3+患者中(84.5%比47.5%; P = 0.00050)。 IHC 3+(369 vs. 272天; P = 0.030)和内脏疾病(301 vs. 183天; P = 0.0080)联合治疗的亚组的平均进展时间有统计学显着性改善。多因素分析预测因素表明,仅IHC评分对ORR具有统计学意义(P = 0.0035)。 ud ud结论: ud ud每周紫杉醇加曲妥珠单抗治疗均非常有效且安全,在IHC患者中优于单独使用紫杉醇得分3+。

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