Evidence map›Paper›PMID 32699957›Full record

ArticleMedical oncology (Northwood, London, England)2020

The perplexity of targeting genetic alterations in hepatocellular carcinoma.

Michele Barone, Alfredo Di Leo, Carlo Sabbà, Antonio Mazzocca

Open access · hybridAbstract read
In one paragraph

Article in Medical oncology (Northwood, London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

4 authors at 1 institution in 1 country.

Michele BaroneGastroenterology Unit, Department of Emergency and Organ Transplantation (D.E.T.O.), University of Bari School of Medicine, Piazza G. Cesare, 11, 70124, Bari, Italy.
Alfredo Di LeoGastroenterology Unit, Department of Emergency and Organ Transplantation (D.E.T.O.), University of Bari School of Medicine, Piazza G. Cesare, 11, 70124, Bari, Italy.
Carlo SabbàInterdisciplinary Department of Medicine, University of Bari School of Medicine, Piazza G. Cesare, 11, 70124, Bari, Italy.
Antonio MazzoccaInterdisciplinary Department of Medicine, University of Bari School of Medicine, Piazza G. Cesare, 11, 70124, Bari, Italy. antonio.mazzocca@uniba.it.ORCID http://orcid.org/0000-0003-0940-7352
University of Bari Aldo Moro · IT

Funding

Associazione Italiana per la Ricerca sul Cancro Investigator Grant (IG) 2015 Id.17758Ministero dell'Istruzione, dell'Università e della Ricerca PON-BIOMIS 2018
6 · The paper itself

Abstract

Genetic heterogeneity is a well-recognized feature of hepatocellular carcinoma (HCC). The coexistence of multiple genetic alterations in the same HCC nodule contributes to explain why gene-targeted therapy has largely failed. Targeting of early genetic alterations could theoretically be a more effective therapeutic strategy preventing HCC. However, the failure of most targeted therapies has raised much perplexity regarding the role of genetic alterations in driving cancer as the main paradigm. Here, we discuss the methodological and conceptual limitations of targeting genetic alterations and their products that may explain the limited success of the novel mechanism-based drugs in the treatment of HCC. In light of these limitations and despite the era of the so-called "precision medicine," prevention and early diagnosis of conditions predisposing to HCC remain the gold standard approach to prevent the development of this type of cancer. Finally, a paradigm shift to a more systemic approach to cancer is required to find optimal therapeutic solutions to treat this disease.

Indexed as

MutationBiomarkers, TumorCarcinoma, HepatocellularEarly Detection of CancerHumansLiver NeoplasmsMolecular Targeted TherapyPrecision MedicineBiomarkers, TumorGene-targeted therapyGenetic alterationsHepatocellular carcinomaIntegrative approachPrecision medicineTumor heterogeneity

Identifiers

PMID32699957
PMCPMC7376083
OpenAlexW3044937199

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.