Evidence map›Paper›PMID 25734768›Full record

ReviewNature reviews. Nephrology2015

Renal effects of targeted anticancer therapies.

Camillo Porta, Laura Cosmai, Maurizio Gallieni, Paolo Pedrazzoli, Fabio Malberti

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Nephrology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
9.1field-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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Elucidating Therapeutic Targets in Hereditary Multicentric Carpotarsal Osteolysis FSGS.Journal of the American Society of Nephrology : JASN · 2026
    Article
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  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Development and Validation of a Prediction Model for Kidney Failure in Long-Term Survivors of Childhood Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Lenvatinib-related renal microangiopathy: a case series.Virchows Archiv : an international journal of pathology · 2022
    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 2 institutions in 1 country.

Camillo PortaMedical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Piazzale C. Golgi 19, 27100 Pavia, Italy.
Laura CosmaiNephrology and Dialysis, Istituti Ospitalieri Cremona, Largo Priori 1, 26100 Cremona, Italy.
Maurizio GallieniNephrology and Dialysis, San Carlo Borromeo Hospital, University of Milano, Via Pio II, 3, 20153 Milan, Italy.
Paolo PedrazzoliMedical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Piazzale C. Golgi 19, 27100 Pavia, Italy.
Fabio MalbertiNephrology and Dialysis, Istituti Ospitalieri Cremona, Largo Priori 1, 26100 Cremona, Italy.
University of Pavia · ITIstituti Ospitalieri di Cremona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of novel targeted anticancer agents has led to overall improvement in the prognosis of many patients affected by various malignancies, but has also been associated with an increased risk of poorly characterized toxic effects to different organs, including the kidneys. The high prevalence of kidney impairment in the general population complicates the issue further. Nephrologists most frequently work with patients with cancer when they are asked to investigate kidney function to assess the need for dose adjustments in anticancer therapy. A thorough knowledge of the renal safety profile of novel life-prolonging anticancer therapies, specific features of their metabolism, and pharmacokinetic and pharmacodynamic properties (under normal circumstances as well as in the setting of renal replacement therapy) is, therefore, necessary to preserve kidney function as far as possible and to ensure optimum treatment. In this Review we summarize the present knowledge of renal toxic effects from novel targeted anticancer agents and discuss whether the management of patients' treatment needs to be modified. We also advocate the development of a new onconephrology subspeciality.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsBevacizumabCTLA-4 AntigenEverolimusGenes, erbB-1HumansKidneyKidney Failure, ChronicKidney Tubules, ProximalMolecular Targeted TherapyNeoplasmsReceptors, Vascular Endothelial Growth FactorTOR Serine-Threonine KinasesVascular Endothelial Growth Factor AAngiogenesis InhibitorsAntineoplastic AgentsBevacizumabCTLA-4 AntigenCTLA4 protein, humanEverolimusMTOR protein, humanReceptors, Vascular Endothelial Growth FactorTOR Serine-Threonine KinasesVascular Endothelial Growth Factor A

Identifiers

PMID25734768
OpenAlexW2047255310

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.