Department of Respiratory Medicine, Tohoku University Hospital, Sendai, Japan.
Department of Respiratory Medicine, Hirosaki University Hospital, Hirosaki, Japan.
Thorac Cancer. 2021 Nov;12(21):2886-2893. doi: 10.1111/1759-7714.14149. Epub 2021 Sep 14.
NJLCG1402 was a phase I/II trial investigating biweekly nanoparticle albumin-bound paclitaxel (nab-PTX) in patients with advanced non-small cell lung cancer (NSCLC).
The study included patients aged ≥20 years with previously treated NSCLC. Nab-PTX (100-150 mg/m ) was administered biweekly in a 28-day cycle. The phase I portion was performed to determine the recommended phase II dose of nab-PTX. In the phase II portion, the primary endpoint was the objective response rate. Secondary endpoints were disease control rate, progression-free survival, overall survival, and safety.
A total of 15 patients received biweekly nab-PTX (100-150 mg/m ) and 12 patients in phase II were treated with 150 mg/m . In the phase I portion, 150 mg/m was determined as the recommended dose. Among those treated with 150 mg/m , the objective response rate was 22%, and the median progression-free and overall survival was 3.6 and 11.2 months, respectively. Adverse events grade ≥3 were observed in 39% of patients.
Biweekly nab-PTX monotherapy was well tolerated and exhibited favorable antitumor activity in patients with previously treated NSCLC.
NJLCG1402 是一项评估每周两次白蛋白结合型紫杉醇纳米粒(nab-PTX)治疗晚期非小细胞肺癌(NSCLC)患者的 I/II 期临床试验。
该研究纳入了年龄≥20 岁、既往治疗过的 NSCLC 患者。nab-PTX(100-150mg/m )每 28 天给药一次,2 周为一个周期。I 期部分旨在确定 nab-PTX 的推荐 II 期剂量。II 期部分的主要终点是客观缓解率。次要终点为疾病控制率、无进展生存期、总生存期和安全性。
共 15 例患者接受了每周两次的 nab-PTX(100-150mg/m )治疗,12 例患者进入 II 期,接受 150mg/m 治疗。I 期部分确定 150mg/m 为推荐剂量。在接受 150mg/m 治疗的患者中,客观缓解率为 22%,中位无进展生存期和总生存期分别为 3.6 个月和 11.2 个月。≥3 级不良事件发生率为 39%。
每周两次 nab-PTX 单药治疗既往治疗的 NSCLC 患者耐受性良好,抗肿瘤活性较好。