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帕博利珠单抗联合乐伐替尼用于肝移植前肝细胞癌患者的新辅助治疗——PLENTY 试点研究

Pembrolizumab in combination with LEnvatinib in participants with hepatocellular carcinoma before liver transplant as Neoadjuvant TherapY-PLENTY pilot study.

作者信息

Lv Zicheng, Xiang Xuelin, Yong June-Kong, Zhou Yi, Wu Yichi, Li Linman, Wang Yuanhao, Zhang Zijie, Xia Qiang, Feng Hao

机构信息

Department of Liver Surgery, Renji Hospital (Punan Branch), School of Medicine, Shanghai Jiao Tong University.

Clinical Research Unit, Renji Hospital, School of Medicine, Shanghai Jiao Tong University.

出版信息

Int J Surg. 2024 Oct 1;110(10):6647-6657. doi: 10.1097/JS9.0000000000001813.

Abstract

BACKGROUND

The high recurrent rate after liver transplantation (LT) remains a clinical challenge, especially for those exceeding the Milan criteria (MC) and with high RETREAT scores. Therefore, the authors aim to investigate whether neoadjuvant systemic therapy allows safely administered and effectively reduces post-LT recurrence for those patients.

METHODS

In this prospective, randomized, open-label, pilot study, patients with HCC exceeding the MC were randomly assigned to PLENTY or control group before LT. The primary endpoint of the study was the recurrence-free survival after LT.

RESULTS

Twenty-two patients were enrolled and randomly assigned: 11 to the PLENTY group and 11 to the control group. The 30-month tumor-specific RFS was 37.5% in the PLENTY group and 12.5% in the control group. The 12-month tumor-specific RFS after LT was significantly improved in the PLENTY group (87.5%) compared to the control group (37.5%) ( P =0·0022). The objective response rate in the PLENTY group was 30 and 60% when determined by RECIST 1.1 and mRECIST, respectively. Six patients (60%) had significant tumor necrosis, including three (30%) who had complete tumor necrosis at histopathology. No acute allograft rejection after LT occurred in the PLENTY and Control group.

CONCLUSION

Neoadjuvant pembrolizumab plus lenvatinib before LT appears to be safe and feasible, associated with significantly better RFS for patients exceeding the MC. Despite the limitations of small sample size, this is the first RCT to evaluate neoadjuvant PD-1 blockade combined with tyrosine kinase inhibitors in LT recipients, the results of this study will inform future research.

摘要

背景

肝移植(LT)后高复发率仍是一项临床挑战,尤其是对于那些超出米兰标准(MC)且RETREAT评分高的患者。因此,作者旨在研究新辅助全身治疗是否能安全给药并有效降低这些患者肝移植后的复发率。

方法

在这项前瞻性、随机、开放标签的试点研究中,超出MC的肝癌患者在肝移植前被随机分配至PLENTY组或对照组。该研究的主要终点是肝移植后的无复发生存期。

结果

22例患者入组并随机分配:11例至PLENTY组,11例至对照组。PLENTY组30个月的肿瘤特异性无复发生存率为37.5%,对照组为12.5%。与对照组(37.5%)相比,PLENTY组肝移植后12个月的肿瘤特异性无复发生存率显著提高(87.5%)(P =0.0022)。根据RECIST 1.1和mRECIST标准测定时,PLENTY组的客观缓解率分别为30%和60%。6例患者(60%)出现显著肿瘤坏死,其中3例(30%)在组织病理学检查时出现完全肿瘤坏死。PLENTY组和对照组肝移植后均未发生急性移植物排斥反应。

结论

肝移植前新辅助使用帕博利珠单抗联合乐伐替尼似乎安全可行,对于超出MC的患者,其无复发生存期显著更好。尽管样本量小存在局限性,但这是第一项评估LT受者中PD - 1阻断联合酪氨酸激酶抑制剂的随机对照试验,本研究结果将为未来研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eefb/11487031/c3433f07c2f3/js9-110-6647-g001.jpg

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