The Efficacy and Safety of Anlotinib Alone and in Combination with Other Drugs in Previously Treated Advanced Thymic Epithelia Tumors: A Retrospective Analysis.

IF 2.5 4区 医学 Q3 ONCOLOGY Recent patents on anti-cancer drug discovery Pub Date : 2023-01-01 DOI:10.2174/1574892818666221122114753
Shuo Li, Haiyan Zhou, Xiqin Zhang, Bing Bu, Rongjie Tao, Hui Zhang, Jinming Yu
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引用次数: 2

Abstract

Background: Thymic epithelial tumors (TETs) are rare thoracic malignancies with no standard second-line treatment. Tumor angiogenesis is closely associated with the pathogenesis and invasiveness of TETs. Anlotinib is a small-molecule multitarget tyrosine kinase inhibitor (TKI) which inhibits tumor angiogenesis and tumor cell proliferation. Published studies have demonstrated the promising clinical effect of multitarget TKIs sunitinib and lenvatinib in previously treated TETs. However, TKIs have a high incidence of adverse events (AEs).

Objective: In this study, we investigated the clinical efficacy and safety of anlotinib in previously treated TET patients.

Methods: We collected clinical data of 22 patients from Shandong Cancer Hospital and Institute between October 2018 and March 2022. These patients were diagnosed with advanced TETs and received at least the first-line (1st-line) treatment. We analyzed the clinical effects between anlotinib monotherapy and anlotinib combination therapy in the second-line (2nd-line) or anlotinib treatment in different lines.

Results: These 22 patients included 18 cases of thymic carcinoma (TC) and 4 cases of thymoma (T). 68.2% of patients were males, and the median age was 53 years. Fourteen patients (63.6%) received anlotinib monotherapy and 8 patients (36.4%) received anlotinib combination therapy. The objective response rate (ORR) was 9.1% in the overall patients. The median progression-free survival (PFS) in the overall population was 12 months (14 months for T and 9 months for TC), and the median overall survival (OS) was 24 months (survival was not reached for T and was 24 months for TC). The incidence of AEs was 50%, most of them were grades I and II, and the incidence of grades III and IV AEs was 9%.

Conclusion: This is the first study reporting the clinical effect of anlotinib in previously treated TETs patients. The survival data indicate that the efficacy of anlotinib is superior to sunitinib and lenvatinib. Our results suggest that anlotinib is a promising treatment option for previously treated TET patients and its toxicity is tolerable. More research and patents are needed in the future to explore better options for the diagnosis and treatment of TETs.

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Anlotinib单用和联合其他药物治疗晚期胸腺上皮肿瘤的疗效和安全性:回顾性分析。
背景:胸腺上皮肿瘤是一种罕见的胸部恶性肿瘤,没有标准的二线治疗方法。肿瘤血管生成与TETs的发病机制和侵袭性密切相关。Anlotinib是一种小分子多靶点酪氨酸激酶抑制剂(TKI),具有抑制肿瘤血管生成和肿瘤细胞增殖的作用。已发表的研究表明,多靶点TKIs舒尼替尼和lenvatinib在先前治疗的TETs中具有良好的临床效果。然而,tki有很高的不良事件发生率(ae)。目的:本研究探讨安洛替尼治疗TET患者的临床疗效和安全性。方法:收集2018年10月至2022年3月山东省肿瘤医院肿瘤研究所22例患者的临床资料。这些患者被诊断为晚期TETs,并至少接受了一线治疗。我们分析了安洛替尼单药和安洛替尼联合治疗二线(二线)或不同线安洛替尼治疗的临床效果。结果:22例患者中胸腺癌(TC) 18例,胸腺瘤(T) 4例,男性占68.2%,中位年龄53岁。安洛替尼单药治疗14例(63.6%),安洛替尼联合治疗8例(36.4%)。总体患者的客观缓解率(ORR)为9.1%。总体人群的中位无进展生存期(PFS)为12个月(T为14个月,TC为9个月),中位总生存期(OS)为24个月(T未达到生存期,TC为24个月)。ae发生率为50%,以I级和II级为主,III级和IV级发生率为9%。结论:这是首个报道anlotinib在先前治疗过的TETs患者中的临床效果的研究。生存数据表明,anlotinib的疗效优于舒尼替尼和lenvatinib。我们的研究结果表明,对于先前治疗过的TET患者,anlotinib是一个很有希望的治疗选择,其毒性是可以忍受的。未来需要更多的研究和专利来探索诊断和治疗tet的更好选择。
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来源期刊
CiteScore
4.50
自引率
7.10%
发文量
55
审稿时长
3 months
期刊介绍: Aims & Scope Recent Patents on Anti-Cancer Drug Discovery publishes review and research articles that reflect or deal with studies in relation to a patent, application of reported patents in a study, discussion of comparison of results regarding application of a given patent, etc., and also guest edited thematic issues on recent patents in the field of anti-cancer drug discovery e.g. on novel bioactive compounds, analogs, targets & predictive biomarkers & drug efficacy biomarkers. The journal also publishes book reviews of eBooks and books on anti-cancer drug discovery. A selection of important and recent patents on anti-cancer drug discovery is also included in the journal. The journal is essential reading for all researchers involved in anti-cancer drug design and discovery. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to anti-cancer drug discovery.
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