Evidence map›Paper›PMID 27941701›Full record

SynthesisInternational journal of molecular sciences2016

Influence of Tyrosine Kinase Inhibitors on Hypertension and Nephrotoxicity in Metastatic Renal Cell Cancer Patients.

Aleksandra Semeniuk-Wojtaś, Arkadiusz Lubas, Rafał Stec, Cezary Szczylik, Stanisław Niemczyk

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Nephrotoxicity of Anti-Angiogenic Therapies.Diagnostics (Basel, Switzerland) · 2021
    Review
  13. Review
  14. Article
  15. VEGF-A in Cardiomyocytes and Heart Diseases.International journal of molecular sciences · 2020
    Review
  16. Review
  17. Observational
  18. Article
  19. Article
  20. Identification of a Genomic Region betweenClinical cancer research : an official journal of the American Association for Cancer Research · 2018
    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 1 institution in 1 country.

Aleksandra Semeniuk-WojtaśMilitary Institute of Medicine Szaserów, 128 Street, 04-141 Warsaw, Poland. asemeniuk@wim.mil.pl.
Arkadiusz LubasMilitary Institute of Medicine Szaserów, 128 Street, 04-141 Warsaw, Poland. alubas@wim.mil.pl.
Rafał StecMilitary Institute of Medicine Szaserów, 128 Street, 04-141 Warsaw, Poland. rstec@wim.mil.pl.
Cezary SzczylikMilitary Institute of Medicine Szaserów, 128 Street, 04-141 Warsaw, Poland. cszczylik@wim.mil.pl.
Stanisław NiemczykMilitary Institute of Medicine Szaserów, 128 Street, 04-141 Warsaw, Poland. sniemczyk@wim.mil.pl.
Wojskowy Instytut Medycyny Lotniczej · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) is one of the most common kidney malignancies. An upgraded comprehension of the molecular biology implicated in the development of cancer has stimulated an increase in research and development of innovative antitumor therapies. The aim of the study was to analyze the medical literature for hypertension and renal toxicities as the adverse events of the vascular endothelial growth factor (VEGF) signaling pathway inhibitor (anti-VEGF) therapy. Relevant studies were identified in PubMed and ClinicalTrials.gov databases. Eligible studies were phase III and IV prospective clinical trials, meta-analyses and retrospective studies that had described events of hypertension or nephrotoxicity for patients who received anti-VEGF therapy. A total of 48 studies were included in the systematic review. The incidence of any grade hypertension ranged from 17% to 49.6%. Proteinuria and increased creatinine levels were ascertained in 8% to 73% and 5% to 65.6% of patients, respectively. These adverse events are most often mild in severity but may sometimes lead to treatment discontinuation. Nephrotoxicity and hypertension are related to multiple mechanisms; however, one of the main disturbances in those patients is VEGF inhibition. There is a significant risk of developing hypertension and renal dysfunction among patients receiving anti-VEGF treatment; however, there is also some evidence that these side effects may be used as biomarkers of response to antiangiogenic agents.

Indexed as

Angiogenesis InhibitorsAnimalsCarcinoma, Renal CellHumansHypertensionKidney NeoplasmsProtein Kinase InhibitorsProtein-Tyrosine KinasesAngiogenesis InhibitorsProtein Kinase InhibitorsProtein-Tyrosine Kinaseshypertensionnephrotoxicityrenal cell carcinomatyrosine kinase inhibitor

Identifiers

PMID27941701
PMCPMC5187873
OpenAlexW2560124907

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.