Evidence map›Paper›PMID 31597249›Full record

ReviewInternational journal of molecular sciences2019

Targeting Angiogenesis in Pancreatic Neuroendocrine Tumors: Resistance Mechanisms.

Javier Pozas, María San Román, Teresa Alonso-Gordoa, Miguel Pozas, Laura Caracuel, Alfredo Carrato, Javier Molina-Cerrillo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. CD93 blockade overcomes sunitinib resistance in pancreatic neuroendocrine tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
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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.

Javier PozasMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. pozas.jav@gmail.com.
María San RománMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. marasanroman@gmail.com.
Teresa Alonso-GordoaMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. talonso@oncologiahrc.com.
Miguel PozasMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. pozas.javier@gmail.com.ORCID 0000-0002-9776-9021
Laura CaracuelMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. laura.caracuel@salud.madrid.org.
Alfredo CarratoMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. acarrato@telefonica.net.
Javier Molina-CerrilloMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain. javier.molinace@gmail.com.ORCID 0000-0003-4616-0598

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite being infrequent tumors, the incidence and prevalence of pancreatic neuroendocrine tumors (P-NETs) has been rising over the past few decades. In recent years, rigorous phase III clinical trials have been conducted, allowing the approval of several drugs that have become the standard of care in these patients. Although various treatments are used in clinical practice, including somatostatin analogues (SSAs), biological therapies like sunitinib or everolimus, peptide receptor radionuclide therapy (PRRT) or even chemotherapy, a consensus regarding the optimal sequence of treatment has not yet been reached. Notwithstanding, sunitinib is largely used in these patients after the promising results shown in SUN111 phase III clinical trial. However, both prompt progression as well as tumor recurrence after initial response have been reported, suggesting the existence of primary and acquired resistances to this antiangiogenic drug. In this review, we aim to summarize the most relevant mechanisms of angiogenesis resistance that are key contributors of tumor progression and dissemination. Furthermore, several targeted molecules acting selectively against these pathways have shown promising results in preclinical models, and preliminary results from ongoing clinical trials are awaited.

Indexed as

Molecular Targeted TherapyAngiogenesis InhibitorsAnimalsAntineoplastic AgentsBiomarkersClinical Trials as TopicDisease ManagementDrug Resistance, NeoplasmHumansNeoplasm GradingNeovascularization, PathologicNeuroendocrine TumorsPancreatic NeoplasmsSunitinibTreatment OutcomeAngiogenesis InhibitorsAntineoplastic AgentsBiomarkersSunitinibantiangiogenicneuroendocrine tumorsresistancesunitinib

Identifiers

PMID31597249
PMCPMC6801829

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.