Safety and efficacy of PD-1 inhibitor (sintilimab) combined with transarterial chemoembolization as the initial treatment in patients with intermediate-stage hepatocellular carcinoma beyond up-to-seven criteria.

IF 10.3 1区 医学 Q1 IMMUNOLOGY Journal for Immunotherapy of Cancer Pub Date : 2025-01-16 DOI:10.1136/jitc-2024-010035
Lixing Li, Xin Xu, Wentao Wang, Peiran Huang, Lei Yu, Zhenggang Ren, Jia Fan, Jian Zhou, Lan Zhang, Zheng Wang
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Abstract

Background: Numerous studies have demonstrated limited survival benefits of transarterial chemoembolization (TACE) alone in the treatment of intermediate-stage hepatocellular carcinoma (HCC) beyond up-to-seven criteria. The advent of immunotherapy, particularly immune checkpoint inhibitors (ICIs), has opened new avenues for HCC treatment. However, TACE combined with ICIs has not been investigated for patients with intermediate-stage HCC beyond the up-to-seven criteria. The study aims to evaluate the efficacy and safety of this treatment strategy for such patients.

Methods: In this single-arm, prospective, phase II study, we enrolled eligible patients with HCC who were treated with TACE plus programmed cell death protein 1 (PD-1) inhibitors (sintilimab) from April 2021 to February 2023. The study's primary objectives were to assess progression-free survival (PFS) and safety. Secondary objectives included measuring the objective response rate (ORR) and disease control rate (DCR) as per both Response Evaluation Criteria in Solid Tumors (RECIST) V.1.1 and modified RECIST (mRECIST) criteria, as well as overall survival (OS). Additionally, we conducted correlation analyses to identify predictors influencing the efficacy of tumor treatment.

Result: 20 patients participated in this study, with a median follow-up duration of 22.0 months. Median PFS was 8.4 months (95% CI: 4.7 to 19.7) according to both RECIST V.1.1 and mRECIST. The ORR was 30.0% (95% CI: 14.6% to 51.9%) per RECIST 1.1% and 60% (95% CI: 38.7% to 78.1%) per mRECIST. DCR was 95.0% (95% CI: 76.4% to 99.1%) according to both RECIST V.1.1 and mRECIST. Median OS was not yet reached. Notably, 20% (4/20) of patients underwent successful conversion to curative surgical resection. Treatment-related adverse events (TRAEs) mainly included elevated aspartate aminotransferase levels (19/20, 95.0%), elevated alanine aminotransferase levels (18/20, 90.0%), hypothyroidism (18/20, 90.0%), and reduced appetite (10/20, 50.0%). Among all participants, only one experienced grade 3 TRAE (myocarditis). We employed the Elastic Net regression model to analyze radiomic features from tumor and peritumoral areas to predict the efficacy of this treatment strategy.

Conclusion: TACE plus PD-1 inhibitors demonstrated promising efficacy and an acceptable safety profile, suggesting it as a potential treatment option for patients with intermediate-stage HCC beyond up-to-seven criteria. Furthermore, our study indicates that specific image-based features may serve as predictors for patients likely to benefit from this treatment approach.

Trial registration number: NCT04842565.

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PD-1抑制剂(辛替单抗)联合经动脉化疗栓塞作为七级以上中期肝癌患者初始治疗的安全性和有效性
背景:大量研究表明,单独经动脉化疗栓塞(TACE)治疗超过7个标准的中期肝细胞癌(HCC)的生存益处有限。免疫疗法的出现,特别是免疫检查点抑制剂(ICIs),为HCC治疗开辟了新的途径。然而,TACE联合ICIs对于超过7级标准的中期HCC患者尚未进行研究。本研究旨在评估这种治疗策略对此类患者的有效性和安全性。方法:在这项单组前瞻性II期研究中,我们招募了符合条件的HCC患者,这些患者在2021年4月至2023年2月期间接受TACE加程序性细胞死亡蛋白1 (PD-1)抑制剂(sintilimab)治疗。该研究的主要目的是评估无进展生存期(PFS)和安全性。次要目标包括根据实体瘤反应评价标准(RECIST) V.1.1和修订后的RECIST (mRECIST)标准测量客观缓解率(ORR)和疾病控制率(DCR),以及总生存期(OS)。此外,我们进行了相关分析,以确定影响肿瘤治疗疗效的预测因素。结果:20例患者参与本研究,中位随访时间为22.0个月。根据RECIST V.1.1和mRECIST,中位PFS为8.4个月(95% CI: 4.7至19.7)。RECIST的ORR为30.0% (95% CI: 14.6%至51.9%),mRECIST的ORR为60% (95% CI: 38.7%至78.1%)。根据RECIST V.1.1和mRECIST, DCR为95.0% (95% CI: 76.4%至99.1%)。中位OS尚未达到。值得注意的是,20%(4/20)的患者成功转化为根治性手术切除。治疗相关不良事件(TRAEs)主要包括天冬氨酸转氨酶升高(19/ 20,95.0%)、丙氨酸转氨酶升高(18/ 20,90.0%)、甲状腺功能减退(18/ 20,90.0%)和食欲减退(10/ 20,50.0%)。在所有参与者中,只有1人经历了3级TRAE(心肌炎)。我们采用Elastic Net回归模型分析肿瘤和肿瘤周围区域的放射学特征,以预测该治疗策略的疗效。结论:TACE联合PD-1抑制剂显示出良好的疗效和可接受的安全性,表明它是超过7级标准的中期HCC患者的潜在治疗选择。此外,我们的研究表明,特定的基于图像的特征可以作为患者可能受益于这种治疗方法的预测因素。试验注册号:NCT04842565。
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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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