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长春瑞滨联合每3周一次曲妥珠单抗治疗转移性乳腺癌:一项单中心2期试验

Vinorelbine plus 3-weekly trastuzumab in metastatic breast cancer: a single-centre phase 2 trial.

作者信息

De Maio Ermelinda, Pacilio Carmen, Gravina Adriano, Morabito Alessandro, Di Rella Francesca, Labonia Vincenzo, Landi Gabriella, Nuzzo Francesco, Rossi Emanuela, Silvestro Pasqualina, Botti Gerardo, Di Bonito Maurizio, Curcio Maria Pia, Formichelli Franca, La Vecchia Franca, Staiano Maria, Maurea Nicola, D'Aiuto Giuseppe, D'Aiuto Massimiliano, Thomas Renato, Signoriello Giuseppe, Perrone Francesco, de Matteis Andrea

机构信息

Clinical Trials Unit, National Cancer Institute, Via M, Semmola, I-80131 Naples, Italy.

出版信息

BMC Cancer. 2007 Mar 20;7:50. doi: 10.1186/1471-2407-7-50.

Abstract

BACKGROUND

After two studies reporting response rates higher than 70% in HER2-positive metastatic breast cancer with weekly trastuzumab and vinorelbine, we planned a phase 2 study to test activity of the same combination, with trastuzumab given every 3 weeks.

METHODS

Patients with HER2-positive metastatic breast cancer (3+ at immunohistochemistry or positive at fluorescence in situ hybridization), PS < or =2, normal left-ventricular ejection fraction (LVEF) and no more than one chemotherapy line for metastatic disease were eligible. Vinorelbine (30 mg/m2) was given on days 1 & 8 every 21 and trastuzumab (8 mg/kg day 1, then 6 mg/kg) every 21 days). A single-stage phase 2 design, with p0 = 0.45, p1 = 0.65, type I and II error = 0.10, was applied; 22 objective responses were required in 39 patients.

RESULTS

From Nov 2002 to May 2005, 50 patients were enrolled, with a median age of 54 years (range 31-81). Among 40 patients eligible for response assessment, there were 7 complete and 13 partial responses (overall response rate 50%; 95% exact CI 33.8-66.2); 11 patients had disease stabilization, lasting more than 6 months in 10 cases. Response rate did not vary according to patients and tumor characteristics, type and amount of previous chemotherapy. Within the whole series, median progression-free survival was 9.6 months (95% CI 7.3-12.3), median overall survival 22.7 months (95% CI 19.5-NA). Fifteen patients (30%) developed brain metastases at a median time of 12 months (range 1-25). There was one toxic death due to renal failure in a patient receiving concomitant pamidronate. Twenty-three patients (46%) had grade 3-4 neutropenia, 2 (4%) grade 3 anemia, 4 (8%) febrile neutropenia. Two patients stopped treatment because of grade 2 decline of LVEF and one patient because of grade 2 liver toxicity concomitant with a grade 1 decline of LVEF. One patient stopped trastuzumab after 50 cycles because of grade 1 decline of LVEF.

CONCLUSION

Although lower than in initial studies, activity of 3-weekly trastuzumab plus vinorelbine fell within the range of results reported with weekly schedules. Toxicity was prevalently manageable. This combination is safe and active for metastatic breast cancer patients who received adjuvant taxanes with anthracyclines.

摘要

背景

两项研究报告了在HER2阳性转移性乳腺癌患者中,使用曲妥珠单抗联合长春瑞滨每周治疗的缓解率高于70%,之后我们计划开展一项2期研究,以测试每3周给予曲妥珠单抗的相同联合方案的活性。

方法

符合条件的患者为HER2阳性转移性乳腺癌患者(免疫组化3+或荧光原位杂交阳性),体力状态(PS)≤2,左心室射血分数(LVEF)正常,且转移性疾病的化疗方案不超过一种。长春瑞滨(30mg/m²)在每21天的第1天和第8天给药,曲妥珠单抗(第1天8mg/kg,之后6mg/kg)每21天给药一次。采用单阶段2期设计,p0 = 0.45,p1 = 0.65,I型和II型错误率 = 0.10;39例患者中需要22例客观缓解。

结果

从2002年11月至2005年5月,共纳入50例患者,中位年龄54岁(范围31 - 81岁)。在40例符合缓解评估条件的患者中,有7例完全缓解和13例部分缓解(总缓解率50%;95%确切可信区间33.8 - 66.2);11例患者疾病稳定,其中10例持续超过6个月。缓解率不因患者和肿瘤特征、既往化疗的类型和剂量而有所不同。在整个队列中,中位无进展生存期为9.6个月(95%可信区间7.3 - 12.3),中位总生存期为22.7个月(95%可信区间19.5 - 未达到)。15例患者(30%)发生脑转移,中位时间为12个月(范围1 - 25个月)。1例接受帕米膦酸二钠治疗的患者因肾衰竭发生毒性死亡。23例患者(46%)出现3 - 4级中性粒细胞减少,2例(4%)出现3级贫血,4例(8%)出现发热性中性粒细胞减少。2例患者因LVEF 2级下降而停止治疗,1例患者因2级肝毒性合并LVEF 1级下降而停止治疗。1例患者在50个周期后因LVEF 1级下降而停止使用曲妥珠单抗。

结论

尽管低于初始研究,但每3周给予曲妥珠单抗联合长春瑞滨的活性仍在每周给药方案报告的结果范围内。毒性大多可控。对于接受过蒽环类辅助紫杉类治疗的转移性乳腺癌患者,该联合方案安全且有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd32/1832208/22188d3597f9/1471-2407-7-50-1.jpg

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