Evidence map›Paper›PMID 34068398›Full record

ReviewCancers2021

Novel Pharmacological Options in the Treatment of Cholangiocarcinoma: Mechanisms of Resistance.

Jose J G Marin, Paula Sanchon-Sanchez, Candela Cives-Losada, Sofía Del Carmen, Jesús M González-Santiago, Maria J Monte, Rocio I R Macias

Abstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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

7 authors.

Jose J G MarinExperimental Hepatology and Drug Targeting (HEVEPHARM) Group, Biomedical Research Institute (IBSAL), University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-1186-6849
Paula Sanchon-SanchezExperimental Hepatology and Drug Targeting (HEVEPHARM) Group, Biomedical Research Institute (IBSAL), University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-2649-8778
Candela Cives-LosadaExperimental Hepatology and Drug Targeting (HEVEPHARM) Group, Biomedical Research Institute (IBSAL), University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-0430-838X
Sofía Del CarmenDepartment of Pathology, Biomedical Research Institute (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0001-9565-2009
Jesús M González-SantiagoDepartment of Gastroenterology and Hepatology, Biomedical Research Institute (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.
Maria J MonteExperimental Hepatology and Drug Targeting (HEVEPHARM) Group, Biomedical Research Institute (IBSAL), University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-1844-7428
Rocio I R MaciasExperimental Hepatology and Drug Targeting (HEVEPHARM) Group, Biomedical Research Institute (IBSAL), University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0002-4748-0326

Funding

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas EHD15PI05/2016Centro Internacional sobre el Envejecimiento 0348_CIE_6_EConsejería de Educación, Junta de Castilla y León SA074P20Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III PI19/00819 and PI20/00189Fundació Marato TV3 201916-31Fundación Científica Asociación Española Contra el Cáncer 2017/2020
6 · The paper itself

Abstract

Despite the crucial advances in understanding the biology of cholangiocarcinoma (CCA) achieved during the last decade, very little of this knowledge has been translated into clinical practice. Thus, CCA prognosis is among the most dismal of solid tumors. The reason is the frequent late diagnosis of this form of cancer, which makes surgical removal of the tumor impossible, together with the poor response to standard chemotherapy and targeted therapy with inhibitors of tyrosine kinase receptors. The discovery of genetic alterations with an impact on the malignant characteristics of CCA, such as proliferation, invasiveness, and the ability to generate metastases, has led to envisage to treat these patients with selective inhibitors of mutated proteins. Moreover, the hope of developing new tools to improve the dismal outcome of patients with advanced CCA also includes the use of small molecules and antibodies able to interact with proteins involved in the crosstalk between cancer and immune cells with the aim of enhancing the immune system's attack against the tumor. The lack of effect of these new therapies in some patients with CCA is associated with the ability of tumor cells to continuously adapt to the pharmacological pressure by developing different mechanisms of resistance. However, the available information about these mechanisms for the new drugs and how they evolve is still limited.

Indexed as

biliary cancerimmunotherapypharmacoresistancetargeted therapy

Identifiers

PMID34068398
PMCPMC8153564

What Socratic holds

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LicenceCC BY
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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 Socratic graph.