Evidence map›Paper›PMID 35416635›Full record

ReviewCurrent gastroenterology reports2022

Systemic Therapy in Metastatic Hepatocellular Carcinoma.

Destry Elms, Ami Badami, Asha Dhanarajan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current gastroenterology reports, 2022. 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
0.8field-weighted citation impact, top 30% 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

3 authors at 1 institution in 1 country.

Destry ElmsDivision of Hematology and Oncology, Loyola University Medical Center, Maywood, IL, USA.
Ami BadamiDivision of Hematology and Oncology, Loyola University Medical Center, Maywood, IL, USA.
Asha DhanarajanDivision of Hematology and Oncology, Loyola University Medical Center, Maywood, IL, USA. adhanarajan@lumc.edu.ORCID http://orcid.org/0000-0003-2119-488X
Loyola University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewMultiple new tyrosine kinase inhibitors, immunotherapies and anti-angiogenic therapies are now available for the treatment of advanced hepatocellular carcinoma (HCC). In this article, we reviewed the evidence supporting these new therapies. RECENT

findingsThe combination of atezolizumab and bevacizumab has become a new standard of care for initial systemic therapy in eligible patients, replacing sorafenib in the first line for many patients. Lenvatinib, a multikinase inhibitor, is also a new first line treatment option for patients who are not eligible for immunotherapy. Several additional options for second line treatment were also reviewed in detail in this paper. New systemic therapies for advanced HCC have prolonged overall survival. However, these new therapies are primarily approved for patients with Child-Pugh A classification with few options for patients with Child-Pugh B disease. Further work is needed to expand options for patients with more advanced liver disease and to optimize the sequencing of these new therapies.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsHumansImmunotherapySorafenibSorafenibAdvanced hepatocellular carcinomaHepatocellular carcinomaImmunotherapy in hepatocellular carcinomaMetastatic hepatocellular carcinomaTargeted therapies in hepatocellular carcinoma

Identifiers

PMID35416635
OpenAlexW4223626820

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.