Determinants of Treatment Benefit and Post-Treatment Survival for Patients with Hepatocellular Carcinoma Enrolled in Second-Line Trials after the Failure of Sorafenib Treatment.

hepatocellular carcinoma immune checkpoint inhibitors second-line sorafenib systemic therapy targeted agents

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
17 Oct 2022
Historique:
received: 29 09 2022
revised: 09 10 2022
accepted: 11 10 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

Second-line treatments are standard care for advanced hepatocellular carcinoma (HCC) patients with preserved liver function who are intolerant of or progress on first-line therapy. However, determinants of treatment benefit and post-treatment survival (PTS) remain unknown. HCC patients previously treated with sorafenib and enrolled in second-line clinical trials were pooled according to the investigational treatment received and the subsequent regulatory approval: approved targeted agents and immune checkpoint inhibitors (AT) or other agents (OT) not subsequently approved. Univariate and multivariate analyses using Cox proportional hazards models established relationships among treatments received, clinical variables, and overall survival (OS) or PTS. For 174 patients (80 AT; 94 OT) analyzed, baseline factors for longer OS in multivariate analysis were second-line AT, absence of both portal vein thrombosis and extrahepatic spread (EHS). Treatment with AT (versus OT) was associated with significantly longer OS among patients with EHS (pinteraction = 0.005) and patients with low neutrophil-to-lymphocyte ratio (NLR; pinteraction = 0.032). Median PTS was 4.0 months (95% CI 2.8−5.3). At second-line treatment discontinuation, alpha-fetoprotein (AFP) levels <400 ng/dl, albumin-bilirubin (ALBI) grade 1, and enrolment onto subsequent trials independently predicted longer PTS. Treatment with AT, PVT, and EHS were prognostic factors for OS, while AFP, ALBI grade and enrolment onto a third-line trial were prognostic for PTS. Presence of EHS and low NLR were predictors of greater OS benefit from AT.

Identifiants

pubmed: 36294865
pii: jpm12101726
doi: 10.3390/jpm12101726
pmc: PMC9604940
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Nicola Personeni (N)

Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.

Tiziana Pressiani (T)

Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.

Valentina Zanuso (V)

Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.

Andrea Casadei-Gardini (A)

Department of Oncology, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Antonio D'Alessio (A)

Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.

Martina Valgiusti (M)

Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "DinoAmadori", 47014 Meldola, Italy.

Vincenzo Dadduzio (V)

Oncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.

Francesca Bergamo (F)

Oncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.

Caterina Soldà (C)

Oncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.

Mario Domenico Rizzato (MD)

Oncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.
Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua, 35122 Padua, Italy.

Laura Giordano (L)

Biostatistic Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Milan, Italy.

Armando Santoro (A)

Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.

Lorenza Rimassa (L)

Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.

Classifications MeSH