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吉西他滨联合阿帕替尼和特瑞普利单抗治疗复发性或转移性鼻咽癌。

Gemcitabine combined with apatinib and toripalimab in recurrent or metastatic nasopharyngeal carcinoma.

机构信息

Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou 510060, P.R. China; Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, P.R. China; Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangzhou 510060, P.R. China.

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, P.R. China; Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangzhou 510060, P.R. China; Department of Medical Imaging, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou 510060, P.R. China.

出版信息

Med. 2022 Oct 14;3(10):664-681.e6. doi: 10.1016/j.medj.2022.07.009. Epub 2022 Aug 29.

Abstract

BACKGROUND

The role of a triple combination of gemcitabine (chemotherapy) plus apatinib (anti-vascular endothelial growth factor [VEGFR]) and toripalimab (anti-PD-1) (GAT) in recurrent/metastatic nasopharyngeal carcinoma (RM-NPC) is unclear.

METHODS

Between August 2019 and April 2020, 41 patients with RM-NPC were enrolled and received GAT for up to 6 cycles followed by apatinib and toripalimab. The primary endpoint was the safety. The secondary endpoints included the objective response rate (ORR) and progression-free survival (PFS). Integrated genomic and transcriptional analyses were conducted to identify the patients who benefited in response to this novel combination therapy.

FINDINGS

As of April 1, 2022, treatment-related grade 3 or 4 adverse events (AEs) occurred in 23 of 41 patients (56.1%, 95% confidence interval [CI] 41%-70.1%). G3-4 nasopharyngeal necrosis was observed in 9 (9/41, 21.9%) patients. High-risk factors for necrosis included repeated radiotherapy and an interval of less than 12 months from the last radiotherapy. The ORR was 90.2% (95% CI: 76.9%-97.2%). The median PFS was 25.8 months (95% CI: not reached (NR)-NR), and the 24-month PFS rate was 50.7% (95% CI: 34.0%-67.4%). MAS-related GPR family member F (MRGPRF) high expression in tumors correlated with poor PFS from the GAT therapy, characterized by high epithelial mesenchymal transition signatures. Serial circulating tumor DNA (ctDNA) sequencing could predict PFS outcomes to combination therapy.

CONCLUSIONS

GAT therapy exhibits a promising antitumor activity and manageable toxicities in patients with RM-NPC. Patients with repeated radiotherapy and an interval of less than 12 months from the last radiotherapy should be carefully selected for antiangiogenic therapies. MRGPRF expression and serial ctDNA monitoring could identify patients that derive benefits from the combination therapy.

TRIAL REGISTRATION

ClinicalTrials.gov: NCT04073784.

FUNDING

This research was funded by the National Natural Science Foundation of China (nos. 81772895 and 82002857), the Key-Area Research and Development of Guangdong Province (2020B1111190001), the Special Support Program for High-level Talents in Sun Yat-sen University Cancer Center, the Guangzhou Science and Technology Plan Project (202103010001), and the National "Ten Thousand Talents Program" Science and Technology Innovation Leading Talents (84000-41180005).

摘要

背景

吉西他滨(化疗)加阿帕替尼(抗血管内皮生长因子[VEGFR])和替雷利珠单抗(抗 PD-1)(GAT)三联治疗复发性/转移性鼻咽癌(RM-NPC)的作用尚不清楚。

方法

2019 年 8 月至 2020 年 4 月,纳入 41 例 RM-NPC 患者,接受 GAT 治疗,最多 6 个周期,随后接受阿帕替尼和替雷利珠单抗治疗。主要终点是安全性。次要终点包括客观缓解率(ORR)和无进展生存期(PFS)。进行整合基因组和转录组分析,以确定对这种新的联合治疗有反应的患者。

结果

截至 2022 年 4 月 1 日,41 例患者中有 23 例(56.1%,95%置信区间[CI]41%-70.1%)发生与治疗相关的 3 级或 4 级不良事件(AE)。9 例(9/41,21.9%)患者发生 3-4 级鼻咽坏死。坏死的高危因素包括重复放疗和末次放疗后间隔<12 个月。ORR 为 90.2%(95%CI:76.9%-97.2%)。中位 PFS 为 25.8 个月(95%CI:未达到(NR)-NR),24 个月 PFS 率为 50.7%(95%CI:34.0%-67.4%)。肿瘤中与 GAT 治疗相关的高风险 G 蛋白偶联受体家族成员 F(MRGPRF)高表达与较差的 PFS 相关,其特征为高上皮间质转化特征。连续循环肿瘤 DNA(ctDNA)测序可预测联合治疗的 PFS 结果。

结论

GAT 治疗在 RM-NPC 患者中具有良好的抗肿瘤活性和可管理的毒性。应仔细选择接受抗血管生成治疗的重复放疗和末次放疗后间隔<12 个月的患者。MRGPRF 表达和连续 ctDNA 监测可识别从联合治疗中获益的患者。

临床试验注册号

ClinicalTrials.gov:NCT04073784。

资金来源

本研究由国家自然科学基金(编号:81772895 和 82002857)、广东省重点领域研发计划(2020B1111190001)、中山大学肿瘤防治中心高层次人才特殊支持计划、广州市科技计划项目(202103010001)和国家“万人计划”科技创新领军人才(84000-41180005)资助。

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