Evidence map›Paper›PMID 29670046›Full record

ReviewInternational journal of molecular sciences2018

Resistance to Anti-Angiogenic Therapy in Cancer-Alterations to Anti-VEGF Pathway.

Yoshiro Itatani, Kenji Kawada, Takamasa Yamamoto, Yoshiharu Sakai

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04863768 (Molecular Profiling of Colorectal Cancer), which is not on this map. Cited by 216 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
216citing papers in PubMed, 4 pooled it
9.0field-weighted citation impact, top 1% 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.

NCT04863768 unknown statusnot on this map

Molecular Profiling of Colorectal Cancer: A Translational Research Study With a Next Generation Sequencing Panel.

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan2006 to 2022Enrolled300ConditionsColorectal Cancer, Colon Cancer, Colon AdenocarcinomaArmsGene panel
3 · Its place in the literature

Who cites it

216 citing papers in PubMed, 4 syntheses or guidelines pooled it, 334 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Article
  8. H2AC19 promotes lung adenocarcinoma progressionActa pharmaceutica Sinica. B · 2026
    Article
  9. Article
  10. Review
  11. Exploring the potential role of miR-124 in angiogenesis in colorectal cancer.Journal of cancer research and clinical oncology · 2026
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Histology and histopathology · 2026
    Article
  20. Review

156 more citing papers are in PubMed but not listed here.

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 2 countries.

Yoshiro ItataniDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan. itatani@kuhp.kyoto-u.ac.jp.
Kenji KawadaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan. kkawada@kuhp.kyoto-u.ac.jp.ORCID 0000-0003-4336-6937
Takamasa YamamotoDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan. masayama@kuhp.kyoto-u.ac.jp.
Yoshiharu SakaiDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan. ysakai@kuhp.kyoto-u.ac.jp.
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-angiogenic therapy is one of the promising strategies for many types of solid cancers. Bevacizumab (Avastin), a recombinant humanized monoclonal antibody of vascular endothelial growth factor (VEGF) A, was approved for the first time as an anti-angiogenic drug for the treatment of metastatic colorectal cancer (CRC) by the Food and Drug Administration (FDA) in 2004. In addition, the other VEGF pathway inhibitors including small molecule tyrosine kinase inhibitors (sunitinib, sorafenib, and pazopanib), a soluble VEGF decoy receptor (aflibercept), and a humanized monoclonal antibody of VEGF receptor 2 (VEGFR2) (ramucirumab) have been approved for cancer therapy. Although many types of VEGF pathway inhibitors can improve survival in most cancer patients, some patients have little or no beneficial effect from them. The primary or acquired resistance towards many oncological drugs, including anti-VEGF inhibitors, is a common problem in cancer treatment. This review summarizes the proposed alternative mechanisms of angiogenesis other than the VEGF pathway. These mechanisms are involved in the development of resistance to anti-VEGF therapies in cancer patients.

Indexed as

Drug Resistance, NeoplasmSignal TransductionAngiogenesis InhibitorsHumansNeoplasmsPhenotypeVascular Endothelial Growth Factor AAngiogenesis InhibitorsVascular Endothelial Growth Factor Aanti-angiogenic therapyresistance to anti-VEGFtumor microenvironment

Identifiers

PMID29670046
PMCPMC5979390
OpenAlexW2800353792

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.