He Zhen, Zhou Hanqiong, Wang Junsheng, Li Ding, Zhang Xudong, Wang Pengyuan, Ma Tianjiang, Zhang Yueqiang, Tian Chuntao, Chen Yunfang, Zou Minglei, Han Yu, Xu Cong, Ma Shuxiang, Wang Lili, Wu Xuan, Chen Gongbin, Wang Qiming
Department of Internal Medicine, Henan Cancer Hospital, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
Department of Medical Oncology, Anyang Cancer Hospital, Anyang, China.
Transl Lung Cancer Res. 2021 Feb;10(2):889-899. doi: 10.21037/tlcr-20-1235.
Patients with extensive-stage small-cell lung cancer (ES-SCLC) have a particularly poor prognosis. And the treatment options for patients with relapsed or refractory ES-SCLC are limited. Thus, we conducted an open-label, multicenter, single-arm phase II clinical trial to assess the efficacy and safety of apatinib plus etoposide capsules as the third- or further-line treatment in ES-SCLC patients.
Patients with ES-SCLC who experienced disease progression following 2 to 3 previous therapies from 11 medical centers in China were enrolled to receive apatinib (250 mg/d, continuously) and etoposide capsules (50 mg/d, on day 1-21, per 28 days). The treatment continued until disease progression, treatment intolerance, or death. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were objective response rate (ORR), overall survival (OS), and safety.
Fifty-six patients with relapsed or refractory ES-SCLC were enrolled from January 2018 to February 2020 and 53 of them were eventually included in the evaluation population. The median follow-up was 9.8 months. At the data cut-off time (March 5, 2020), 39 patients (74%) had died and 44 (83%) had progressed. The median PFS was 3.0 months (95% CI, 2.1-3.9) and the median OS was 5.0 months (95% CI, 3.6-6.4). No complete responses were seen. Eleven patients (21%) showed a best response of partial response and 37 (70%) patients achieved stable disease. The ORR was 20.8% (11/53), and the disease control rate (DCR) was 90.6% (48/53). The 6-month OS rate was 40.1% (95% CI, 26.2-54). After 12 months, the OS rate was 18.4% (95% CI, 4.7-32.1). Possible treatment-related grade III/IV adverse events included leukopenia [8 (15.1%)], neutropenia [7 (13.2%)], anemia [4 (7.4%)], and hand-foot syndrome [2 (3.8%)]. During the study, no mortality occurred as a consequence of treatment.
Apatinib combined with etoposide capsules exhibits efficacy and has an acceptable safety profile. It could be used as a later-line treatment for ES-SCLC patients who have been heavily pretreated with standard therapies. Further exploration of apatinib combined with etoposide capsules in phase III trials is warranted.
广泛期小细胞肺癌(ES-SCLC)患者的预后特别差。而复发性或难治性ES-SCLC患者的治疗选择有限。因此,我们开展了一项开放标签、多中心、单臂II期临床试验,以评估阿帕替尼联合依托泊苷胶囊作为ES-SCLC患者三线或更后线治疗的疗效和安全性。
来自中国11个医学中心的ES-SCLC患者,在接受过2至3线先前治疗后疾病进展,入组接受阿帕替尼(250mg/d,持续用药)和依托泊苷胶囊(50mg/d,第1 - 21天用药,每28天为一周期)治疗。治疗持续至疾病进展、出现治疗不耐受或死亡。主要终点为无进展生存期(PFS),次要终点为客观缓解率(ORR)、总生存期(OS)和安全性。
2018年1月至2020年2月共纳入56例复发性或难治性ES-SCLC患者,其中53例最终纳入评估人群。中位随访时间为9.8个月。在数据截止时间(2020年3月5日),39例患者(74%)死亡,44例患者(83%)疾病进展。中位PFS为3.0个月(95%CI,2.1 - 3.9),中位OS为5.0个月(95%CI,3.6 - 6.4)。未观察到完全缓解。11例患者(21%)最佳疗效为部分缓解,37例患者(70%)疾病稳定。ORR为20.8%(11/53),疾病控制率(DCR)为90.6%(48/53)。6个月OS率为40.1%(95%CI,26.2 - 54)。12个月后,OS率为18.4%(95%CI,4.7 - 32.1)。可能与治疗相关的III/IV级不良事件包括白细胞减少[8例(15.1%)]、中性粒细胞减少[7例(13.2%)]、贫血[4例(7.4%)]和手足综合征[2例(3.8%)]。研究期间,未发生因治疗导致的死亡。
阿帕替尼联合依托泊苷胶囊显示出疗效且安全性可接受。它可作为经标准疗法充分预处理后的ES-SCLC患者的后线治疗。有必要在III期试验中进一步探索阿帕替尼联合依托泊苷胶囊的疗效。