Department of Radiation Oncology, Affiliated Hospital of Guilin Medical University, Guilin, China.
Department of Radiation Oncology, Wuzhou Red Cross Hospital, Wuzhou, China.
Cancer. 2021 Sep 1;127(17):3163-3171. doi: 10.1002/cncr.33626. Epub 2021 May 27.
The authors aimed to investigate the efficacy and safety of apatinib in patients with metastatic or locoregionally recurrent nasopharyngeal carcinoma (NPC).
A multicenter, single-arm, prospective phase 2 study was conducted on patients (18-70 years of age) with metastatic or recurrent NPC who had failed chemotherapy. Patients with recurrent disease involving vascular structure invasion were excluded. All enrolled patients received apatinib (500 mg daily) in continuous 4-week cycles until disease progression or development of unacceptable toxicity. The primary end point of this study was objective response rate (ORR), and the secondary end points were progression-free survival (PFS), overall survival (OS), and toxicity. This study was registered with ClinicalTrials.gov (NCT03130270).
Between January 2017 and June 2018, 33 patients were enrolled. At the end of the data collection (May 20, 2020), the 33 patients had completed a total of 261.2 cycles of apatinib. Although 12 patients achieved a partial response, no patient achieved a complete response; thus, the ORR in the 33 patients was 36.4% (95% CI, 19.0%-53.7%). At the end of follow-up (median, 30 months; 95% CI, 24.9-35.1), median OS and median PFS were 16 months (95% CI, 14.6-17.4 months) and 5.0 months (95% CI, 3.6-6.4 months), respectively. The most common adverse events (grade 1/2) were hand-foot syndrome (18 [54.5%]), hypertension (14 [42.4%]), oral ulcer (8 [24.2%]), and proteinuria (4 [12.1%]). Two patients (1 with diabetes and 1 with hypertension) developed cerebral infarction. Grade 3/4 toxicities were uncommon.
Apatinib shows promising activity, with manageable toxicities, in patients with metastatic or locoregionally recurrent NPC. Further evaluation of apatinib in large-scale studies is warranted.
Clinical studies on vascular endothelial growth factor receptor (VEGFR)-targeted therapy for recurrent or metastatic nasopharyngeal carcinoma (NPC) are limited. A recent preclinical study that evaluated apatinib in models of NPC showed a high objective response rate and a favorable safety profile. Our data further confirmed good efficacy in patients with lung metastasis. Further studies of the efficacy and safety of apatinib combined with immune checkpoint inhibitors or chemotherapy in NPC is warranted.
作者旨在研究阿帕替尼在转移性或局部复发性鼻咽癌(NPC)患者中的疗效和安全性。
这是一项多中心、单臂、前瞻性 2 期研究,纳入了化疗失败的转移性或复发性 NPC 患者(18-70 岁)。排除了复发性疾病涉及血管结构侵犯的患者。所有入组患者接受阿帕替尼(500mg 每日)连续 4 周的治疗周期,直至疾病进展或出现不可接受的毒性。本研究的主要终点为客观缓解率(ORR),次要终点为无进展生存期(PFS)、总生存期(OS)和毒性。本研究在 ClinicalTrials.gov 注册(NCT03130270)。
2017 年 1 月至 2018 年 6 月期间,共纳入 33 例患者。截至数据收集结束(2020 年 5 月 20 日),33 例患者共完成了 261.2 个周期的阿帕替尼治疗。尽管 12 例患者达到部分缓解,但无患者达到完全缓解;因此,33 例患者的 ORR 为 36.4%(95%CI,19.0%-53.7%)。随访结束时(中位随访时间 30 个月;95%CI,24.9-35.1 个月),中位 OS 和中位 PFS 分别为 16 个月(95%CI,14.6-17.4 个月)和 5.0 个月(95%CI,3.6-6.4 个月)。最常见的不良事件(1/2 级)为手足综合征(18 例[54.5%])、高血压(14 例[42.4%])、口腔溃疡(8 例[24.2%])和蛋白尿(4 例[12.1%])。2 例患者(1 例合并糖尿病,1 例合并高血压)发生脑梗死。3/4 级毒性并不常见。
阿帕替尼在转移性或局部复发性 NPC 患者中显示出良好的疗效和可管理的毒性。需要进一步在大规模研究中评估阿帕替尼的疗效。
针对复发性或转移性鼻咽癌(NPC)的血管内皮生长因子受体(VEGFR)靶向治疗的临床研究有限。最近一项评估阿帕替尼在 NPC 模型中的研究显示出较高的客观缓解率和良好的安全性。我们的数据进一步证实了该药在肺转移患者中的良好疗效。阿帕替尼联合免疫检查点抑制剂或化疗治疗 NPC 的疗效和安全性值得进一步研究。