A novel cabozantinib-sulfasalazine combination targeting ferroptosis to overcome resistant immunotherapy in advanced hepatocellular carcinoma.

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Bei Wang, Gangcheng Kong, Chaoyang Meng, Chunhui Nie, Dalong Wan
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引用次数: 0

Abstract

Advanced hepatocellular carcinoma (HCC) frequently develops resistance to immunotherapy, resulting in limited treatment options and poor prognosis. Ferroptosis, an iron-dependent regulated form of cell death, may help overcome drug resistance, and cabozantinib has shown clinical efficacy in advanced HCC. In this single-arm retrospective study at the First Affiliated Hospital, Zhejiang University School of Medicine, 60 patients with immunotherapy-refractory HCC received cabozantinib combined with sulfasalazine (1,500 mg/day in three divided oral doses) between August 2021 and August 2024. Tumor response was assessed using RECIST v1.1, while progression-free survival (PFS) and overall survival (OS) were analyzed using Kaplan-Meier methods and exploratory Cox regression. The combination achieved an objective response rate of 40% (95% CI: 28-53%) and a disease control rate of 70% (95% CI: 58-81%), with median PFS of 8.5 months (95% CI: 6.9-10.1) and median OS of 15.3 months (95% CI: 12.9-17.7). Adverse events were mostly grade 1-2 and manageable, consistent with cabozantinib's known safety profile. These findings suggest encouraging antitumor activity, tolerability, and a potential synergistic effect, though the retrospective single-center design may introduce bias. Prospective randomized studies are warranted to confirm these results and further explore this combination's potential in overcoming immunotherapy resistance.

一种新的卡博替尼-磺胺嘧啶联合靶向铁下垂以克服晚期肝细胞癌的耐药免疫治疗。
晚期肝细胞癌(HCC)经常对免疫治疗产生耐药性,导致治疗选择有限和预后不良。铁凋亡是一种铁依赖性细胞死亡的调节形式,可能有助于克服耐药性,卡博赞替尼在晚期HCC中显示出临床疗效。在浙江大学医学院第一附属医院进行的这项单组回顾性研究中,60名免疫治疗难治性HCC患者在2021年8月至2024年8月期间接受了卡博赞替尼联合柳氮磺胺嘧啶(1500 mg/天,分三次口服)的治疗。使用RECIST v1.1评估肿瘤反应,使用Kaplan-Meier方法和探索性Cox回归分析无进展生存期(PFS)和总生存期(OS)。该联合治疗的客观缓解率为40% (95% CI: 28-53%),疾病控制率为70% (95% CI: 58-81%),中位PFS为8.5个月(95% CI: 6.9-10.1),中位OS为15.3个月(95% CI: 12.9-17.7)。不良事件大多为1-2级,可控,与卡博赞替尼已知的安全性一致。尽管回顾性单中心设计可能会引入偏倚,但这些发现提示了抗肿瘤活性、耐受性和潜在的协同效应。有必要进行前瞻性随机研究来证实这些结果,并进一步探索这种组合在克服免疫治疗耐药方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
211
审稿时长
4.5 months
期刊介绍: Pakistan Journal of Pharmaceutical Sciences (PJPS) is a peer reviewed multi-disciplinary pharmaceutical sciences journal. The PJPS had its origin in 1988 from the Faculty of Pharmacy, University of Karachi as a biannual journal, frequency converted as quarterly in 2005, and now PJPS is being published as bi-monthly from January 2013. PJPS covers Biological, Pharmaceutical and Medicinal Research (Drug Delivery, Pharmacy Management, Molecular Biology, Biochemical, Pharmacology, Pharmacokinetics, Phytochemical, Bio-analytical, Therapeutics, Biotechnology and research on nano particles.
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