Department of Internal Medicine, Henan Cancer Hospital, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, China.
J Cancer Res Clin Oncol. 2019 Jan;145(1):235-240. doi: 10.1007/s00432-018-2764-8. Epub 2018 Oct 6.
To evaluate the efficacy of maintenance apatinib after chemotherapy for extensive-stage (ED) small-cell lung cancer (SCLC).
This was a retrospective analysis of 23 cases of extensive-stage SCLC admitted to the Affiliated Cancer Hospital of Zhengzhou University from January 2015 to December 2017. The patients without progression after induction chemotherapy received apatinib 250 mg per day until disease progression or unacceptable toxicity occurred. We analyzed the median progression-free survival (PFS), median overall survival (OS) and safety.
Of 23 enrolled patients, 1 was lost to follow-up. The median PFS from the time of maintenance therapy was 4.1 months (95% CI 3.63-4.57 months). The median PFS from the time of induction chemotherapy was 8.3 months (95% CI 7.20-9.40 months). The median OS from the time of maintenance therapy was 12.5 months (95% CI 5.51-19.49 months). The median OS from the time of induction chemotherapy was 17.0 months (95% CI 9.86-24.14 months). The most frequent treatment-related adverse events were hand-foot syndrome (43.5%, 10/23) and secondary hypertension (30.4%, 7/23), followed by fatigue, proteinuria, nausea, and oral mucositis (17.4%, 13.0%, 13.0%, and 8.7%, respectively). Hematologic toxicity included thrombocytopenia (30.4%), leucopenia (26.1%), and anemia (17.4%). The main grade 3 or 4 toxicities were hand-foot syndrome (8.7%, 2/23) and hypertension (4.3%, 1/23).
Maintenance apatinib was safe and achieved encouraging PFS and OS in extensive-stage SCLC.
评估化疗后维持阿帕替尼治疗广泛期(ED)小细胞肺癌(SCLC)的疗效。
这是一项回顾性分析,纳入了 2015 年 1 月至 2017 年 12 月期间郑州大学附属肿瘤医院收治的 23 例广泛期 SCLC 患者。诱导化疗后无进展的患者接受阿帕替尼 250mg/天治疗,直至疾病进展或出现不可耐受的毒性。我们分析了中位无进展生存期(PFS)、中位总生存期(OS)和安全性。
23 例纳入患者中,1 例失访。维持治疗开始后的中位 PFS 为 4.1 个月(95%CI 3.63-4.57 个月)。诱导化疗开始后的中位 PFS 为 8.3 个月(95%CI 7.20-9.40 个月)。维持治疗开始后的中位 OS 为 12.5 个月(95%CI 5.51-19.49 个月)。诱导化疗开始后的中位 OS 为 17.0 个月(95%CI 9.86-24.14 个月)。最常见的治疗相关不良反应为手足综合征(43.5%,23/53)和继发性高血压(30.4%,7/23),其次为乏力、蛋白尿、恶心和口腔黏膜炎(17.4%、13.0%、13.0%和 8.7%)。血液学毒性包括血小板减少症(30.4%)、白细胞减少症(26.1%)和贫血(17.4%)。主要的 3 级或 4 级毒性为手足综合征(8.7%,23/266)和高血压(4.3%,1/23)。
维持阿帕替尼治疗广泛期 SCLC 安全有效,可获得令人鼓舞的 PFS 和 OS。