Evidence map›Paper›PMID 26341657›Full record

ReviewJournal of nephrology2015

Renal toxicity of anticancer agents targeting HER2 and EGFR.

Laura Cosmai, Maurizio Gallieni, Camillo Porta

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of nephrology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  6. Article
  7. Review
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  12. Review
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  14. TRPM7, Magnesium, and Signaling.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Review
  17. Cardiotoxicity of Novel Targeted Chemotherapeutic Agents.Current treatment options in cardiovascular medicine · 2018
    Review
  18. Article
  19. Role of adaptor protein p66Shc in renal pathologies.American journal of physiology. Renal physiology · 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

3 authors at 3 institutions in 1 country.

Laura CosmaiDivision of Nephrology and Dialysis, Istituti Ospitalieri di Cremona, Largo Priori, 1, 26100, Cremona, Italy. lacos@iol.it.
Maurizio GallieniNephrology and Dialysis, San Carlo Borromeo Hospital, Milan, Italy.
Camillo PortaMedical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Pavia, Italy. c.porta@smatteo.pv.it.
Italian Society of Physiotherapy · ITOspedale San Carlo · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EGFR and HER2 are found overexpressed and/or activated in many different human malignancies (e.g. breast and colon cancer), and a number of drugs specifically targeting these two tyrosine kinases have been developed over the years as anticancer agents. In the present review, the renal safety profile of presently available agents targeting either HER2 or EGFR will be discussed, together with the peculiarities related to their clinical use in patients with impaired renal function, or even in dialysis. Indeed, even though renal toxicity is not so common with these agents, it may nevertheless happen, especially when these agents are combined with traditional chemotherapeutic agents. As a whole, kidney impairment or dialysis should not be regarded per se as reasons not to administer or to stop an active anti-HER or anti-EGFR anticancer treatment, especially given the possibility of significantly improving the life expectancy of many cancer patients with the use of these agents.

Indexed as

Acute Kidney InjuryAdo-Trastuzumab EmtansineAfatinibAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCetuximabErb-b2 Receptor Tyrosine KinasesErbB ReceptorsErlotinib HydrochlorideGefitinibHumansLapatinibMaytansineNeoplasmsProtein Kinase InhibitorsQuinazolinesAdo-Trastuzumab EmtansineAfatinibAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCetuximabERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsErlotinib HydrochlorideGefitinibLapatinibMaytansinepertuzumabProtein Kinase InhibitorsQuinazolinesTrastuzumabDialysisEGFR inhibitorsHER2-targeting agentsKidney impairmentKidney toxicity

Identifiers

PMID26341657
OpenAlexW1272134337

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.