Evidence map›Paper›PMID 35179707›Full record

ReviewCurrent oncology reports2022

VEGF Receptor Inhibitor-Induced Hypertension: Emerging Mechanisms and Clinical Implications.

Nicholas Camarda, Richard Travers, Vicky K Yang, Cheryl London, Iris Z Jaffe

Open access · greenAbstract readReview
In one paragraph

Review in Current oncology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 2% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Review
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  15. Article
  16. VEGFR1 as a Target for Cardiovascular Gene Therapy.Journal of cardiovascular translational research · 2025
    Review
  17. Article
  18. Advancing Cancer-Targeted Nanotherapies with Tumor Homing Peptides.ACS pharmacology & translational science · 2025
    Review
  19. Article
  20. Is lenvatinib-induced blood pressure elevation a favorable prognostic factor in patients with hepatocellular carcinoma?Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    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

5 authors at 3 institutions in 1 country.

Nicholas Camarda *Molecular Cardiology Research Institute, Tufts Medical Center, 800 Washington Street, Box 80, Boston, MA, 02111, USA.
Richard Travers *Molecular Cardiology Research Institute, Tufts Medical Center, 800 Washington Street, Box 80, Boston, MA, 02111, USA.
Vicky K YangCummings School of Veterinary Medicine, Tufts University, MA, Boston, USA.
Cheryl LondonCummings School of Veterinary Medicine, Tufts University, MA, Boston, USA.
Iris Z JaffeMolecular Cardiology Research Institute, Tufts Medical Center, 800 Washington Street, Box 80, Boston, MA, 02111, USA. ijaffe@tuftsmedicalcenter.org.
Tufts Medical Center · USBoston University · USTufts University · US

Funding

Credentialing a Cross-Species Platform to Investigate Cancer Therapy-Associated Cardiovascular ToxicityR01CA243542 · NCI · TUFTS MEDICAL CENTER · PI JAFFE, IRIS Z, LONDON, CHERYL A · 2019 to 2023
$3.1M
Novel strategies to understand, predict, and prevent vascular toxicity of targeted CML therapiesR01HL155078 · NHLBI · TUFTS MEDICAL CENTER · PI JAFFE, IRIS Z · 2021 to 2024
$2.6M
Naturally occurring canine myxomatous mitral valve disease as a large animal model for human non-syndromic mitral valve prolapseK01OD028205 · OD · TUFTS UNIVERSITY BOSTON · PI YANG, VICKY K. · 2019 to 2023
$691k
Endothelium as a mediator of BCR-ABL tyrosine kinase inhibitor vascular toxicityF32HL165838 · NHLBI · TUFTS MEDICAL CENTER · PI TRAVERS, RICHARD · 2022 to 2023
$138k
NCI NIH HHS R01 CA243542NHLBI NIH HHS F32 HL165838NHLBI NIH HHS R01 HL155078NIH HHS K01 OD028205
6 · The paper itself

Abstract

purpose of reviewWhile vascular endothelial growth factor receptor inhibitors (VEGFRis) have dramatically improved cancer survival, these drugs cause hypertension in a majority of patients. This side effect is often dose limiting and increases cardiovascular mortality in cancer survivors. This review summarizes recent advances in our understanding of the molecular mechanisms and clinical findings that impact management of VEGFRi-induced hypertension. RECENT

findingsRecent studies define new connections between endothelial dysfunction and VEGFRi-induced hypertension, including the balance between nitric oxide, oxidative stress, endothelin signaling, and prostaglandins and the potential role of microparticles, vascular smooth muscle cells, vascular stiffness, and microvessel rarefaction. Data implicating genetic polymorphisms that might identify patients at risk for VEGFRi-induced hypertension and the growing body of literature associating VEGFRi-induced hypertension with antitumor efficacy are reviewed. These recent advances have implications for the future of cardio-oncology clinics and the management of VEGFRi-induced hypertension.

Indexed as

HypertensionVascular Endothelial Growth Factor AAngiogenesis InhibitorsHumansReceptors, Vascular Endothelial Growth FactorSignal TransductionAngiogenesis InhibitorsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor ACardio-oncologyEndothelial cellEndothelinHypertensionNitric oxideVascular endothelial growth factor receptor inhibitor

Identifiers

PMID35179707
PMCPMC9218917
OpenAlexW4212783034

What OpenQuestion holds

Textmetadata
LicenceTDM
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.