Evidence map›Paper›PMID 31973908›Full record

Observational studyAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2020

Acute Kidney Injury and Electrolyte Abnormalities After Chimeric Antigen Receptor T-Cell (CAR-T) Therapy for Diffuse Large B-Cell Lymphoma.

Shruti Gupta, Harish Seethapathy, Ian A Strohbehn, Matthew J Frigault, Elizabeth K O'Donnell, Caron A Jacobson, Shveta S Motwani, Samir M Parikh, Gary C Curhan, Kerry L Reynolds and 2 more

Open access · greenAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 121 citations in OpenAlex.

  1. Pooled it
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  8. CAR-T Cell Therapy for Autoimmune Kidney Diseases: Where Do We Stand Now?International journal of molecular sciences · 2025
    Review
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  14. Contemporary Perspectives on Chronic Renal Disorders.Chronic diseases and translational medicine · 2025
    Review
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10 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

12 authors at 4 institutions in 1 country.

Shruti GuptaDivision of Renal Medicine, Department of Internal Medicine, Brigham and Women's Hospital, Boston, MA.
Harish SeethapathyRenal Division, Department of Internal Medicine, Massachusetts General Hospital, Boston, MA.
Ian A StrohbehnRenal Division, Department of Internal Medicine, Massachusetts General Hospital, Boston, MA.
Matthew J FrigaultOncology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA.
Elizabeth K O'DonnellOncology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA.
Caron A JacobsonDana Farber Cancer Institute, Boston, MA.
Shveta S MotwaniDivision of Renal Medicine, Department of Internal Medicine, Brigham and Women's Hospital, Boston, MA; Dana Farber Cancer Institute, Boston, MA.
Samir M ParikhDivision of Nephrology, Beth Israel Deaconess Medical Center, Boston, MA.
Gary C CurhanDivision of Renal Medicine, Department of Internal Medicine, Brigham and Women's Hospital, Boston, MA.
Kerry L ReynoldsOncology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA.
David E LeafDivision of Renal Medicine, Department of Internal Medicine, Brigham and Women's Hospital, Boston, MA.
Meghan E SiseRenal Division, Department of Internal Medicine, Massachusetts General Hospital, Boston, MA. Electronic address: msise@partners.org.
Massachusetts General Hospital · USBrigham and Women's Hospital · USBeth Israel Deaconess Medical Center · USDana-Farber Cancer Institute · US

Funding

Sex-related differences in incidence rates of nephrolithiasisK24DK091417 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI CURHAN, GARY C. · 2011 to 2020
$1.5M
Effect of Hepatitis C Virus Eradication on Chronic Kidney Disease ProgressionK23DK117014 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SISE, MEGHAN E. · 2018 to 2022
$865k
Chronic kidney disease as a risk factor for incident hearing lossF32DC017342 · NIDCD · BRIGHAM AND WOMEN'S HOSPITAL · PI GUPTA, SHRUTI · 2018 to 2019
$167k
NIDCD NIH HHS F32 DC017342NIDDK NIH HHS K23 DK117014NIDDK NIH HHS K24 DK091417
6 · The paper itself

Abstract

RATIONALE &

objectiveCytokine release syndrome is a well-known complication of chimeric antigen receptor T-cell (CAR-T) therapy and can lead to multiorgan dysfunction. However, the nephrotoxicity of CAR-T therapy is unknown. We aimed to characterize the occurrence, cause, and outcomes of acute kidney injury (AKI), along with the occurrence of electrolyte abnormalities, among adults with diffuse large B-cell lymphoma receiving CAR-T therapy. STUDY

designCase series. SETTING &

participantsWe reviewed the course of 78 adults receiving CAR-T therapy with axicabtagene ciloleucel or tisagenlecleucel at 2 major cancer centers between October 2017 and February 2019. Baseline demographics, comorbid conditions, medications, and laboratory values were obtained from electronic health records. AKI was defined using KDIGO (Kidney Disease: Improving Global Outcomes) criteria. The cause, clinical course, and outcome of AKI events and electrolyte abnormalities in the first 30 days after CAR-T infusion were characterized using data contained in electronic health records.

resultsAmong 78 patients receiving CAR-T therapy, cytokine release syndrome occurred in 85%, of whom 62% were treated with tocilizumab. AKI occurred in 15 patients (19%): 8 had decreased kidney perfusion, 6 developed acute tubular necrosis, and 1 patient had urinary obstruction related to disease progression. Those with acute tubular necrosis and obstruction had the longest lengths of stay and highest 60-day mortality. Electrolyte abnormalities were common; hypophosphatemia, hypokalemia, and hyponatremia occurred in 75%, 56%, and 51% of patients, respectively. LIMITATIONS: Small sample size; AKI adjudicated by retrospective chart review; lack of biopsy data.

conclusionsIn this case series of patients with diffuse large B-cell lymphoma receiving CAR-T therapy, AKI and electrolyte abnormalities occurred commonly in the context of cytokine release syndrome.

Indexed as

Acute Kidney InjuryAgedFemaleHumansImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseMaleMiddle AgedWater-Electrolyte BalanceWater-Electrolyte Imbalanceacute kidney injury (AKI)adverse eventcase seriesChimeric antigen receptor T-cell (CAR-T)cytokine release syndromediffuse large B-cell lymphoma (DLBCL)electrolyte abnormalitieshypokalemiahyponatremiahypophosphatemiaimmunotherapynephrotoxicitypre-renal azotemiarenal failure

Identifiers

PMID31973908
PMCPMC7311244
OpenAlexW3002479067

What OpenQuestion holds

Textmetadata
LicenceTDM
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.