A retrospective study of anlotinib in patients with persistent, recurrent or metastatic cervical and endometrial cancer.

IF 1.5 4区 医学 Q4 ONCOLOGY Translational cancer research Pub Date : 2024-07-31 Epub Date: 2024-06-26 DOI:10.21037/tcr-24-272
Lingli Xin, Mei Ye, Yuan Gao, Qi Xiong, Qingxiang Hou
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Abstract

Background: The prognosis of persistent, recurrent or metastatic cervical and endometrial cancer is poor. Anlotinib is a novel multitarget tyrosine kinase inhibitor (TKI). The efficacy and safety of anlotinib in patients with cervical and endometrial cancer need to be evaluated.

Methods: We retrospectively analyzed the efficacy and safety of anlotinib in patients with persistent, recurrent or metastatic cervical and endometrial cancers between March 2020 and June 2023. The objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and adverse events (AEs) were analyzed.

Results: The overall ORR and DCR were 24.14% and 55.17% respectively. The ORR and DCR in patients with cervical cancer were 25.00% and 56.25%; the ORR and DCR in patients with endometrial cancer were 23.08% and 53.85%. The patients received anlotinib plus immunotherapy had significantly higher rate of clinical benefit than those receiving anlotinnb alone (P=0.04). The DCR was significantly higher in patients receiving anlotinib combined with immunotherapy (DCR: 75.00% vs. 30.76%) than those without immunotherapy. The overall median PFS and OS were 12.2 months [95% confidence interval (CI): 6.6-17.8] and 22.3 months (95% CI: 20.9-23.7), respectively. The patients receiving anlotinib plus immunotherapy had significantly longer OS than those without immunotherapy [not reached vs. 12.5 months; hazard ratio (HR): 0.32 (95% CI: 0.1-0.99); P=0.04]. The most common AEs was fatigue (41.4%).

Conclusions: Anlotinib might be a promising agent for persistent, recurrent or metastatic cervical and endometrial cancers with good tolerability. Moreover, anlotinib combined with immunotherapy showed synergistic antitumor effect.

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安罗替尼治疗宫颈癌和子宫内膜癌久治不愈、复发或转移患者的回顾性研究。
背景:久治不愈、复发或转移性宫颈癌和子宫内膜癌的预后很差。安罗替尼是一种新型多靶点酪氨酸激酶抑制剂(TKI)。安罗替尼对宫颈癌和子宫内膜癌患者的疗效和安全性有待评估:我们回顾性分析了2020年3月至2023年6月期间安罗替尼在宫颈癌和子宫内膜癌持续、复发或转移患者中的疗效和安全性。分析了客观反应率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和不良事件(AEs):总的ORR和DCR分别为24.14%和55.17%。宫颈癌患者的ORR和DCR分别为25.00%和56.25%;子宫内膜癌患者的ORR和DCR分别为23.08%和53.85%。接受安罗替尼联合免疫治疗的患者的临床获益率明显高于单独接受安罗替尼治疗的患者(P=0.04)。接受安罗替尼联合免疫疗法的患者的DCR(DCR:75.00% vs. 30.76%)明显高于未接受免疫疗法的患者。总体中位PFS和OS分别为12.2个月[95% 置信区间(CI):6.6-17.8]和22.3个月(95% CI:20.9-23.7)。接受安罗替尼联合免疫疗法的患者的OS明显长于未接受免疫疗法的患者[未达到12.5个月 vs. 12.5个月;危险比(HR):0.32(95% CI:0.1-0.99);P=0.04]。最常见的不良反应是疲劳(41.4%):安罗替尼可能是一种治疗顽固性、复发性或转移性宫颈癌和子宫内膜癌的有前途的药物,且具有良好的耐受性。此外,安罗替尼与免疫疗法联用可产生协同抗肿瘤效应。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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