Evidence map›Paper›PMID 34028627›Full record

Trial reportAngiogenesis2022

Plasma levels of angiopoietin-2, VEGF-A, and VCAM-1 as markers of bevacizumab-induced hypertension: CALGB 80303 and 90401 (Alliance).

Julia C F Quintanilha, Yingmiao Liu, Amy S Etheridge, Akram Yazdani, Hedy L Kindler, William Kevin Kelly, Andrew B Nixon, Federico Innocenti

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Angiogenesis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Observational
  6. 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

8 authors at 4 institutions in 1 country.

Julia C F QuintanilhaUNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Genetic Medicine Bldg. 120 Mason Farm Rd, Campus Box 7361, Chapel Hill, NC, 27599-7361, USA.
Yingmiao LiuDuke University School of Medicine, Duke University, Durham, NC, USA.
Amy S EtheridgeUNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Genetic Medicine Bldg. 120 Mason Farm Rd, Campus Box 7361, Chapel Hill, NC, 27599-7361, USA.
Akram YazdaniUNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Genetic Medicine Bldg. 120 Mason Farm Rd, Campus Box 7361, Chapel Hill, NC, 27599-7361, USA.
Hedy L KindlerDepartment of Medicine, University of Chicago, Chicago, IL, USA.
William Kevin KellyDepartment of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.
Andrew B NixonDuke University School of Medicine, Duke University, Durham, NC, USA.
Federico InnocentiUNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Genetic Medicine Bldg. 120 Mason Farm Rd, Campus Box 7361, Chapel Hill, NC, 27599-7361, USA. innocent@email.unc.edu.
University of North Carolina at Chapel Hill · USDuke University · USUniversity of Chicago · USYale University · US

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
Yale Cancer Center NCTN LAPSUG1CA233337 · NCI · YALE UNIVERSITY · PI ANNE C CHIANG · 2019 to 2026
$6.0M
UG1 - NCTN (Network Lead)UG1CA233327 · NCI · UNIVERSITY OF CHICAGO · PI STEVEN J CHMURA, HEDY L KINDLER · 2019 to 2026
$4.4M
The Duke University - Duke Cancer Institute National Clinical Trials Network LAPS (UG1) Support GrantUG1CA233253 · NCI · DUKE UNIVERSITY · PI John H Strickler, Alexandra Thomas · 2019 to 2026
$3.7M
UNC Lead Academic Participating SiteUG1CA233373 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A, DEES, ELIZABETH CLAIRE · 2019 to 2025
$3.5M
Foundation for the National Institutes of Health (US) UG1CA233327National Cancer Institute of the National Institutes of Health U10CA180821National Cancer Institute of the National Institutes of Health U24CA196171National Cancer Institute of the National Institutes of Health UG1CA233253National Cancer Institute of the National Institutes of Health UG1CA233337National Cancer Institute of the National Institutes of Health UG1CA233373NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA233253NCI NIH HHS UG1 CA233327NCI NIH HHS UG1 CA233337NCI NIH HHS UG1 CA233373
6 · The paper itself

Abstract

Hypertension is a common toxicity induced by bevacizumab and other antiangiogenic drugs. There are no biomarkers to predict the risk of bevacizumab-induced hypertension. This study aimed to identify plasma proteins related to the function of the vasculature to predict the risk of severe bevacizumab-induced hypertension. Using pretreated plasma samples from 398 bevacizumab-treated patients in two clinical trials (CALGB 80303 and 90401), the levels of 17 proteins were measured via ELISA. The association between proteins and grade 3 bevacizumab-induced hypertension was performed by calculating the odds ratio (OR) from logistic regression adjusting for age, sex, and clinical trial. Using the optimal cut-point of each protein, sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for hypertension were estimated. Five proteins showed no difference in levels between clinical trials and were used for analyses. Lower levels of angiopoietin-2 (p = 0.0013, OR 3.41, 95% CI 1.67-7.55), VEGF-A (p = 0.0008, OR 4.25, 95% CI 1.93-10.72), and VCAM-1 (p = 0.0067, OR 2.68, 95% CI 1.34-5.63) were associated with an increased risk of grade 3 hypertension. The multivariable model suggests independent effects of angiopoietin-2 (p = 0.0111, OR 2.71, 95% CI 1.29-6.10), VEGF-A (p = 0.0051, OR 3.66, 95% CI 1.54-9.73), and VCAM-1 (p = 0.0308, OR 2.27, 95% CI 1.10-4.92). The presence of low levels of 2-3 proteins had an OR of 10.06 (95% CI 3.92-34.18, p = 1.80 × 10

Indexed as

HypertensionPharmaceutical PreparationsAngiogenesis InhibitorsAngiopoietin-2BevacizumabHumansVascular Cell Adhesion Molecule-1Vascular Endothelial Growth Factor AAngiogenesis InhibitorsAngiopoietin-2BevacizumabPharmaceutical PreparationsVascular Cell Adhesion Molecule-1Vascular Endothelial Growth Factor AAngiopoietin-2BevacizumabHypertensionVCAM-1VEGF-A

Identifiers

PMID34028627
PMCPMC8611102
OpenAlexW3164804569

What Socratic 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 Socratic graph.