Evidence map›Paper›PMID 20878444›Full record

ArticleInvestigational new drugs2012

Treatment of bevacizumab-induced hypertension by amlodipine.

Olivier Mir, Romain Coriat, Stanislas Ropert, Laure Cabanes, Benoit Blanchet, Sandra Camps, Bertrand Billemont, Bertrand Knebelmann, François Goldwasser

Abstract read
PubMed Publisher
In one paragraph

Article in Investigational new drugs, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Navigating the Complexities of Cancer Treatment-Induced Hypertension.Journal of cardiovascular development and disease · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Hypertension in neonates treated with intravitreal bevacizumab for retinopathy of prematurity.Journal of perinatology : official journal of the California Perinatal Association · 2021
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Tyrosine Kinase Inhibitor-Induced Hypertension.Current oncology reports · 2018
    Review
  20. 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

9 authors at 4 institutions in 1 country.

Olivier MirCentre for Research on Angiogenesis Inhibitors, Department of Medical Oncology, Cochin Teaching Hospital, AP-HP, Paris Descartes University, 27 rue du faubourg Saint Jacques, 75014 Paris, France. olivier.mir@cch.aphp.fr
Romain Coriat
Stanislas Ropert
Laure Cabanes
Benoit Blanchet
Sandra Camps
Bertrand Billemont
Bertrand Knebelmann
François Goldwasser
Université Paris Cité · FRDélégation Paris 5 · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Cochin · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypertension is a common toxicity of anti-VEGF agents, but its optimal treatment remains to define. This study aimed to describe the efficacy and tolerability of amlodipine, a calcium channel blocker, in patients with metastatic malignancies treated with bevacizumab, a humanized monoclonal antibody to VEGF. PATIENTS AND

methodsOne hundred and eighty-seven patients with advanced or metastatic NSCLC, colorectal or ovarian cancer receiving bevacizumab (5 mg/kg every 2 weeks or 7.5 mg/kg every 3 weeks) and chemotherapy were eligible for this analysis. Blood pressure was measured at home twice daily according to international guidelines. Patients received amlodipine 5 mg daily for grade ≥ 2 bevacizumab-induced hypertension.

resultsTwenty-six patients received amlodipine 5 mg daily for de novo hypertension (group A), and another 10 patients received amlodipine for exacerbation of previously existing hypertension (group B). Hypertension was controlled within 7 days under amlodipine in 23/26 (88.5%, 95%CI: 76.2-100) patients in group A, and 8/10 (80%, 95%CI: 55.2-100) patients in group B, with a favourable toxicity profile.

conclusionsAmlodipine 5 mg daily appears safe and efficient for the treatment of hypertension in patients receiving bevacizumab at a dose-intensity of 2.5 mg/kg/week. Further prospective studies are warranted to confirm these results.

Indexed as

AdultAgedAmlodipineAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedAntihypertensive AgentsBevacizumabBlood PressureCalcium Channel BlockersCarcinoma, Non-Small-Cell LungChi-Square DistributionColorectal NeoplasmsDrug Administration ScheduleFemaleHumansHypertensionAmlodipineAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedAntihypertensive AgentsBevacizumabCalcium Channel BlockersVascular Endothelial Growth Factor AVasodilator AgentsVEGFA protein, human

Identifiers

PMID20878444
OpenAlexW2027671567

What OpenQuestion holds

Textmetadata
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.