Evidence map›Paper›PMID 36294865›Full record

ArticleJournal of personalized medicine2022

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

Nicola Personeni, Tiziana Pressiani, Valentina Zanuso, Andrea Casadei-Gardini, Antonio D'Alessio, Martina Valgiusti, Vincenzo Dadduzio, Francesca Bergamo, Caterina Soldà, Mario Domenico Rizzato and 3 more

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Nicola PersoneniDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0000-0002-7995-272X
Tiziana PressianiMedical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Milan, Italy.
Valentina ZanusoDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0000-0003-4308-6601
Andrea Casadei-GardiniDepartment of Oncology, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.
Antonio D'AlessioDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0000-0002-9164-3671
Martina ValgiustiDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "DinoAmadori", 47014 Meldola, Italy.
Vincenzo DadduzioOncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.
Francesca BergamoOncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.
Caterina SoldàOncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.
Mario Domenico RizzatoOncology 1 Unit, Veneto Institute of Oncology, IOV, IRCCS, 35128 Padua, Italy.
Laura GiordanoBiostatistic Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Milan, Italy.ORCID 0000-0002-9587-7870
Armando SantoroDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.
Lorenza RimassaDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0000-0001-9957-3615

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

hepatocellular carcinomaimmune checkpoint inhibitorssecond-linesorafenibsystemic therapytargeted agents

Identifiers

PMID36294865
PMCPMC9604940

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.