安罗替尼作为一线化疗联合免疫疗法后达到 SD 的晚期非小细胞肺癌患者的维持疗法的有效性和安全性。

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Chemotherapy Pub Date : 2024-09-01 DOI:10.1080/1120009X.2024.2397924
Xiaobing Li, Yi Peng, De Wu, Jing Tang, Yuebing Wu
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引用次数: 0

摘要

晚期非小细胞肺癌(NSCLC)仍然是一项重大的临床挑战,尤其是在一线化疗联合免疫疗法后病情稳定(SD)的患者中。本研究旨在评估新型多靶点酪氨酸激酶抑制剂安罗替尼作为维持疗法在这类患者中的疗效和安全性。这项回顾性单中心研究招募了晚期NSCLC患者,这些患者在接受一线化疗-免疫疗法联合治疗4个周期后出现SD,然后在随后的标准维持治疗中加入安洛替尼,继续治疗直至疾病进展或出现不可耐受的毒副作用。主要终点是无进展生存期(P FS)、总生存期(OS)、客观反应率(ORR)、疾病控制率(DCR)和安全性。共有 52 名患者入组,无进展生存期和总生存期的中位数分别为 5.0m 和 10.0m。亚组分析表明,其疗效与某些不良反应(如高血压、蛋白尿和手足综合征)相关。进一步的机理分析表明,该疗法可能通过消耗Tregs减少免疫抑制,从而进一步激活免疫系统,发挥协同抗肿瘤作用。除了良好的疗效,毒性也是可以耐受的。安罗替尼作为一种维持疗法,对一线化疗联合免疫疗法后达到SD的晚期NSCLC患者具有良好的疗效。可控的安全性以及观察到的P FS和OS延长表明,安罗替尼可能是这一具有挑战性的患者群体的重要治疗选择。有必要进一步开展大规模随机对照试验来证实这些发现,并优化患者选择和管理策略。
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Efficacy and safety of anlotinib as maintenance therapy in patients with advanced non-small cell lung cancer achieving SD post first-line chemotherapy combined with immunotherapy.

Advanced non-small cell lung cancer (NSCLC) remains a significant clinical challenge, particularly in patients who exhibit stable disease (SD) following first-line chemotherapy combined with immunotherapy. This study aims to evaluate the efficacy and safety of Anlotinib, a novel multitarget tyrosine kinase inhibitor, as maintenance therapy in this patient cohort. This retrospective, single-center study enrolled patients with advanced NSCLC who showed SD after receiving a combination of first-line chemo-immunotherapy for 4 cycles, then add anlotinib to subsequent standard maintenance therapy, continuing treatment until disease progression or the occurrence of intolerable toxic side effects. The primary endpoint was progression-free survival (P FS), overall survival (OS), objective response rate (ORR), disease control rate (DCR) and safety profile. A total of 52 patients were enrolled, the median P FS and OS was 5.0m and 10.0m, respectively. The ORR and DCR was 28.85% and 67.31%. subgroup analysis indicated that its efficacy correlate with certain Adverse Effects (AEs, such as hypertension, proteinuria, and hand-foot syndrome). Further mechanistic analysis suggests that this regimen may likely reduce immune suppression by depleting Tregs, thereby further activating the immune system to exert synergistic anti-tumor effects. Besides promising efficacy, the toxicity can be tolerated. Anlotinib demonstrates promising efficacy as a maintenance therapy in patients with advanced NSCLC who have achieved SD following first-line chemotherapy combined with immunotherapy. The manageable safety profile and the observed extension in P FS and OS suggest that Anlotinib could be a valuable therapeutic option for this challenging patient population. Further large-scale randomized controlled trials are warranted to confirm these findings and to optimize patient selection and management strategies.

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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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