Evidence map›Paper›PMID 30746132›Full record

ArticleClinical kidney journal2019

Renal toxicities associated with pembrolizumab.

Hassan Izzedine, Alexis Mathian, Stephane Champiat, Cécile Picard, Christine Mateus, Emilie Routier, Andrea Varga, David Malka, Alexandra Leary, Judith Michels and 9 more

Open access · goldAbstract read
In one paragraph

Article in Clinical kidney journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
6.4field-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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 129 citations in OpenAlex.

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  10. Predominant CD8Pathology international · 2024
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  15. Pembrolizumab-induced nephrotoxicity in a patient with breast cancer.Therapeutic advances in medical oncology · 2024
    Article
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  19. Article
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2 more citing papers are in PubMed but not listed here.

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

19 authors at 5 institutions in 1 country.

Hassan IzzedineDepartment of Nephrology, Peupliers Private Hospital, Ramsay Générale de Santé, Paris, France.
Alexis MathianDepartment of Internal Medicine, Pitie-Salpetriere Hospital, Paris, France.
Stephane ChampiatDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
Cécile PicardDepartment of Pathology, Pitie-Salpetriere Hospital, Paris, France.ORCID 0000-0001-9284-4531
Christine MateusDepartment of Supportive Care, Gustave Roussy, Villejuif, France.
Emilie RoutierDepartment of Medical Oncology, Dermatology Unit, Gustave Roussy, Villejuif, France.
Andrea VargaDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
David MalkaDepartment of Medical Oncology, Gastrointestinal Cancer Group, Gustave Roussy, Villejuif, France.
Alexandra LearyDepartment of Medical Oncology, Gynecology Unit, Gustave Roussy, Villejuif, France.
Judith MichelsDepartment of Medical Oncology, Gynecology Unit, Gustave Roussy, Villejuif, France.
Jean-Marie MichotDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
Aurélien MarabelleDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
Olivier LambotteDepartment of Internal Medicine and Clinical Immunology, Bicetre University Hospital, Le Kremlin Bicêtre, France.
Zahir AmouraDepartment of Internal Medicine, Pitie-Salpetriere Hospital, Paris, France.
Jean-Charles SoriaDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
Sihem KaakiDepartement of Pathology, Electron Microscopy Unit, CHU Poitiers, Poitiers, France.
Nathalie QuellardDepartement of Pathology, Electron Microscopy Unit, CHU Poitiers, Poitiers, France.
Jean-Michel GoujonDepartement of Pathology, Electron Microscopy Unit, CHU Poitiers, Poitiers, France.
Isabelle BrocheriouDepartment of Pathology, Pitie-Salpetriere Hospital, Paris, France.
Institut Gustave Roussy · FRSorbonne Université · FRCentre Hospitalier Universitaire de Poitiers · FRBicêtre Hospital · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveExpanded clinical experience with patients treated by pembrolizumab has accumulated. However, renal toxicities associated with this anti-programmed cell death 1 agent are poorly described because kidney histology is rarely sought. As a nephrology referral centre, we aimed to describe the clinic-biological and histopathological characteristics of pembrolizumab-related nephropathy and its response to treatment.

methodsWe conducted a monocentric large case series study, including all pembrolizumab-treated cancer patients presenting a renal toxicity addressed to our centre from 2015 to 2017.

resultsA total of 12 patients (7 men) out of 676 pembrolizumab-treated patients (incidence 1.77%) were included (median age 69.75 years). Patients were referred for acute kidney injury (

conclusionIn our series, ATI, AIN and MCD are the most frequent forms of kidney involvement under pembrolizumab therapy. Kidney dysfunction is usually isolated but can be severe. Use of corticosteroids in case of AIN improves the glomerular filtration rate.

Indexed as

acute interstitial nephritisacute kidney injuryacute tubular injuryminimal change nephropathypembrolizumab

Identifiers

PMID30746132
PMCPMC6366307
OpenAlexW2914696936

What OpenQuestion holds

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LicenceCC BY-NC
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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.