Suo Jiaojiao, Sun Yu, Fu Yan, Xiu Weigang, Zhang Xuanwei, Wang Yan, Zhu Jiang
Department of Thoracic Oncology, West China Hospital, Sichuan University, Chengdu, China.
Radiation Physics Center, West China Hospital, Sichuan University, Chengdu, China.
Front Oncol. 2021 Dec 23;11:788837. doi: 10.3389/fonc.2021.788837. eCollection 2021.
The purpose of this study was to initially investigate the effect of previous antiangiogenic therapy (bevacizumab and endostatin) on the efficacy of anlotinib in patients with advanced or metastatic lung cancer (LC).
We retrospectively collected the clinical data of patients with LC treated with anlotinib and divided them into group A (treated with anlotinib after the failure of previous antiangiogenic drugs and group B (no prior use of antiangiogenic drugs). We used propensity score matching (PSM) for confounding factors between the groups. Progression-free survival (PFS) and overall survival (OS) were also recorded.
A total of 160 patients were included in the analysis. The median OS in groups A and group B was 11.8 months and 16.1 months (P=0.120), whereas the median PFS was 3.1 months and 4.7 months (P=0.009), respectively. Moreover, the objective response rate (ORR) of the two groups was 9.6% and 10.4% (P=0.874), and the disease control rate (DCR) was 71.1% and 80.5% (P=0.165).After PSM (n=46), baseline characteristics were comparable between groups A and B. Furthermore, the median OS of the two groups was 14.6 months and 16.2 months (P=0.320), whereas the median PFS was 3.5 months and 4.5 months (P=0.040), respectively. Moreover, the ORR of the two groups were 13.0% and 10.9% (P=0.748), and the DCR were 78.3% and 82.6% (P=0.599), respectively.
Previous antiangiogenic treatments may affect the PFS of patients who receive anlotinib later, but it might not affect the patient's ORR and OS.
本研究旨在初步探究既往抗血管生成治疗(贝伐单抗和内皮抑素)对晚期或转移性肺癌(LC)患者使用安罗替尼疗效的影响。
我们回顾性收集了接受安罗替尼治疗的LC患者的临床数据,并将他们分为A组(既往抗血管生成药物治疗失败后使用安罗替尼)和B组(未使用过抗血管生成药物)。我们对两组之间的混杂因素采用倾向评分匹配(PSM)。还记录了无进展生存期(PFS)和总生存期(OS)。
共有160例患者纳入分析。A组和B组的中位OS分别为11.8个月和16.1个月(P = 0.120),而中位PFS分别为3.1个月和4.7个月(P = 0.009)。此外,两组的客观缓解率(ORR)分别为9.6%和10.4%(P = 0.874),疾病控制率(DCR)分别为71.1%和80.5%(P = 0.165)。PSM后(n = 46),A组和B组的基线特征具有可比性。此外,两组的中位OS分别为14.6个月和16.2个月(P = 0.320),而中位PFS分别为3.5个月和4.5个月(P = 0.040)。此外,两组的ORR分别为13.0%和10.9%(P = 0.748),DCR分别为78.3%和82.6%(P = 0.599)。
既往抗血管生成治疗可能会影响后来接受安罗替尼治疗患者的PFS,但可能不会影响患者的ORR和OS。