Evidence map›Paper›PMID 27468204›Full record

ReviewWorld journal of gastroenterology2016

Hepatocellular carcinoma: Will novel targeted drugs really impact the next future?

Liliana Montella, Giovannella Palmieri, Raffaele Addeo, Salvatore Del Prete

Open access · bronzeAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Plumbagin Restrains Hepatocellular Carcinoma Angiogenesis by Stromal Cell-Derived Factor (SDF-1)/CXCR4-CXCR7 Axis.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  12. Review
  13. Article
  14. High RNF40 expression indicates poor prognosis of hepatocellular carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  15. Review
  16. Review
  17. Genetic alterations in hepatocellular carcinoma: An update.World journal of gastroenterology · 2016
    Review
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.

Liliana MontellaLiliana Montella, Raffaele Addeo, Salvatore Del Prete, Medical Oncology Unit, "San Giovanni di Dio" Hospital, Frattamaggiore, 80027 Naples, Italy.
Giovannella PalmieriLiliana Montella, Raffaele Addeo, Salvatore Del Prete, Medical Oncology Unit, "San Giovanni di Dio" Hospital, Frattamaggiore, 80027 Naples, Italy.
Raffaele AddeoLiliana Montella, Raffaele Addeo, Salvatore Del Prete, Medical Oncology Unit, "San Giovanni di Dio" Hospital, Frattamaggiore, 80027 Naples, Italy.
Salvatore Del PreteLiliana Montella, Raffaele Addeo, Salvatore Del Prete, Medical Oncology Unit, "San Giovanni di Dio" Hospital, Frattamaggiore, 80027 Naples, Italy.
University of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer treatment has been revolutionized by the advent of new molecular targeted and immunotherapeutic agents. Identification of the role of tumor angiogenesis changed the understanding of many tumors. After the unsuccessful results with chemotherapy, sorafenib, by interfering with angiogenic pathways, has become pivotal in the treatment of hepatocellular carcinoma. Sorafenib is the only systemic treatment to show a modest but statistically significant survival benefit. All novel drugs and strategies for treatment of advanced hepatocellular carcinoma must be compared with the results obtained with sorafenib, but no new drug or drug combination has yet achieved better results. In our opinion, the efforts to impact the natural history of the disease will be directed not only to drug development but also to understanding the underlying liver disease (usually hepatitis B virus- or hepatitis C virus-related) and to interrupting the progression of cirrhosis. It will be important to define the role and amount of mutations in the complex pathogenesis of hepatocellular carcinoma and to better integrate locoregional and systemic therapies. It will be important also to optimize the therapeutic strategies with existing chemotherapeutic drugs and new targeted agents.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsCarcinoma, HepatocellularDrug DiscoveryErbB ReceptorsHumansLiver NeoplasmsMitogen-Activated Protein Kinase KinasesMolecular Targeted TherapyNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsProto-Oncogene Proteins c-metReceptors, Vascular Endothelial Growth FactorSorafenibVascular Endothelial Growth FactorsAngiogenesis InhibitorsAntineoplastic AgentsErbB ReceptorsMET protein, humanMitogen-Activated Protein Kinase KinasesNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsProto-Oncogene Proteins c-metReceptors, Vascular Endothelial Growth FactorSorafenibVascular Endothelial Growth FactorsAngiogenesisHepatocellular carcinomaPathwaySorafenibTargeted therapy

Identifiers

PMID27468204
PMCPMC4945973
OpenAlexW2502104717

What OpenQuestion holds

Textmetadata
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.