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Pembrolizumab in combination with lenvatinib in participants with hepatocellular carcinoma (HCC) before liver transplant as neoadjuvant therapY-PLENTY pilot study.
Lv, Zicheng; Xiang, Xuelin; Yong, June-Kong; Zhou, Yi; Wu, Yichi; Li, Linman; Wang, Yuanhao; Zhang, Zijie; Xia, Qiang; Feng, Hao.
Afiliación
  • Lv Z; Department of Liver Surgery, Renji Hospital (Punan Branch), School of Medicine, Shanghai Jiao Tong University.
  • Xiang X; Clinical Research Unit, Renji Hospital, School of Medicine, Shanghai Jiao Tong University.
  • Yong JK; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Zhou Y; Department of Liver Surgery, Renji Hospital (Punan Branch), School of Medicine, Shanghai Jiao Tong University.
  • Wu Y; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Li L; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Wang Y; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Zhang Z; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Xia Q; Shanghai Engineering Research Centre of Transplantation and Immunology.
  • Feng H; Department of Liver Surgery, Renji Hospital (Punan Branch), School of Medicine, Shanghai Jiao Tong University.
Int J Surg ; 2024 Jul 12.
Article en En | MEDLINE | ID: mdl-38995162
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 PLENYT 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.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J Surg Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J Surg Año: 2024 Tipo del documento: Article