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靶向与细胞毒药物序贯治疗(TACTICS):厄洛替尼、贝伐珠单抗联合标准化疗治疗非小细胞肺癌的Ⅱ期临床试验

Targeted and cytotoxic therapy in coordinated sequence (TACTICS): erlotinib, bevacizumab, and standard chemotherapy for non-small-cell lung cancer, a phase II trial.

机构信息

Section of Hematology and Oncology, Department of Medicine, and Comprehensive Cancer Center, University of Chicago, Chicago, IL, USA.

出版信息

Clin Lung Cancer. 2012 Mar;13(2):123-8. doi: 10.1016/j.cllc.2011.10.001. Epub 2011 Nov 18.

Abstract

BACKGROUND

This trial focused on optimally combining existing targeted therapies and cytotoxic chemotherapy in the treatment of unselected patients with advanced non-small-cell lung cancer (NSCLC).

METHODS

Patients with previously untreated advanced-stage nonsquamous NSCLC were eligible for this trial. In module A, patients received up to 4 cycles of erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks. Patients then received carboplatin (AUC = 6), paclitaxel 200 mg/m2, and bevacizumab 15 mg/kg for 4 cycles in module B. Patients who did not have progressive disease in module A received maintenance erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks in module C.

RESULTS

Forty-eight patients were enrolled in this multicenter phase II trial. Most patients were male (62.5%) and white (77.1%) with stage IV disease (93.8%) and adenocarcinoma histologic type (66.7%). The overall response rate in module A was 10.4%, in module B it was 15.1%, and in module C it was 5.5%. The study achieved its primary endpoint, with a nonprogression rate of 45.8% in module A. The median overall survival (OS) was 12.6 months.

CONCLUSION

The novel systemic therapy regimen is feasible in patients with advanced NSCLC. However there is no further role for developing this regimen in unselected patients with NSCLC.

摘要

背景

本试验专注于优化联合现有靶向治疗和细胞毒化疗药物治疗未经选择的晚期非小细胞肺癌(NSCLC)患者。

方法

这项试验纳入了未经治疗的晚期非鳞状 NSCLC 患者。在模块 A 中,患者接受每日 150mg 厄洛替尼和每 3 周 15mg/kg 贝伐珠单抗最多 4 个周期。然后,患者在模块 B 中接受卡铂(AUC=6)、紫杉醇 200mg/m2 和贝伐珠单抗 15mg/kg,共 4 个周期。在模块 A 中未出现疾病进展的患者在模块 C 中接受每日 150mg 厄洛替尼和每 3 周 15mg/kg 贝伐珠单抗维持治疗。

结果

这项多中心 II 期试验共纳入了 48 例患者。大多数患者为男性(62.5%)和白人(77.1%),疾病分期为 IV 期(93.8%),组织学类型为腺癌(66.7%)。模块 A 的总缓解率为 10.4%,模块 B 为 15.1%,模块 C 为 5.5%。该研究达到了主要终点,模块 A 的无进展率为 45.8%。中位总生存期(OS)为 12.6 个月。

结论

新的系统治疗方案在晚期 NSCLC 患者中是可行的。然而,对于未经选择的 NSCLC 患者,该方案没有进一步的发展作用。

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