Evidence map›Paper›PMID 40272825›Full record

ArticleJAMA oncology2025

Intravenous Magnesium and Cisplatin-Associated Acute Kidney Injury.

Shruti Gupta, Ilya G Glezerman, Jamie S Hirsch, Api Chewcharat, Sophia L Wells, Jessica L Ortega, Marta Pirovano, Raphael Kim, Kevin L Chen, Kenar D Jhaveri and 7 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Review
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  11. Pharmaceutics · 2026
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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

17 authors.

Shruti GuptaDivision of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Ilya G GlezermanRenal Service, Memorial Sloan Kettering Cancer Center and Department of Medicine, Weill Cornell Medical College, New York, New York.
Jamie S HirschNorthwell Health, New Hyde Park, New York.
Api ChewcharatDivision of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sophia L WellsDivision of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Jessica L OrtegaDivision of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Marta PirovanoAdult Survivorship Program, Dana-Farber Cancer Institute, Boston, Massachusetts.
Raphael KimDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Kevin L ChenDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Kenar D JhaveriNorthwell Health, New Hyde Park, New York.
Valda D PageDivision of Internal Medicine, Section of Nephrology, University of Texas MD Anderson Cancer Center, Houston.
Matthew H AbramsonRenal Service, Memorial Sloan Kettering Cancer Center and Department of Medicine, Weill Cornell Medical College, New York, New York.
Anip BansalDivision of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Campus Aurora, Aurora.
Avisek GhimireDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora.
Melanie S JoyDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora.
Ala AbudayyehDivision of Internal Medicine, Section of Nephrology, University of Texas MD Anderson Cancer Center, Houston.
David E LeafDivision of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Novel Pathways and Therapeutic Targets for Cisplatin-Associated Acute Kidney InjuryK23DK125672 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Shruti Gupta · 2022 to 2026
$998k
NCI NIH HHS P30 CA008748NIDDK NIH HHS K23 DK125672
6 · The paper itself

Abstract

Importance: Cisplatin-associated acute kidney injury (CP-AKI) is a frequent complication of cisplatin chemotherapy and is associated with considerable morbidity and mortality. Prophylactic administration of intravenous (IV) magnesium attenuates CP-AKI in animal models; however, its association with CP-AKI in humans has not been rigorously evaluated. Objective: To evaluate the association of prophylactic IV magnesium administration with CP-AKI in patients with cancer undergoing cisplatin chemotherapy. Design, Settings, and Participants: This multicenter study was conducted at 5 major cancer centers across the US and included adult patients with cancer who were treated with a first dose of IV cisplatin between 2006 to 2022. Data analyses were performed from February to December 2024. Exposure: IV magnesium vs no IV magnesium receipt on the first day of cisplatin treatment. Main Outcomes and Measures: Composite outcome of CP-AKI or death, with CP-AKI defined as a 2-fold or greater increase in serum creatinine levels from baseline or receipt of kidney replacement therapy within 14 days after first dose of IV cisplatin. Secondary outcomes were CP-AKI or death, defined using alternative definitions, as well as major adverse kidney events at 90 days. Inverse probability treatment weighting was used to estimate the association between IV magnesium receipt and CP-AKI. Models were adjusted for demographics, comorbidities, laboratory values, receipt of concurrent nephrotoxic anticancer therapies, site, year of cisplatin administration, and cisplatin dose. Results: A total of 13 719 patients were included (median [IQR] age, 59 [49-67] years; 7817 male [57%]), of whom 3893 (28.4%) received IV magnesium on the first day of cisplatin chemotherapy. The median (IQR) dose of IV magnesium was 2 (1-2) g. CP-AKI or death occurred in 104 of 3893 patients (2.7%) who received IV magnesium, and in 520 of 9826 (5.3%) who did not (adjusted odds ratio, 0.80; 95% CI, 0.66-0.97). Results were similar across a number of sensitivity analyses and secondary outcomes, including major adverse kidney events at 90 days. Conclusions and Relevance: This multicenter cohort study found that patients with cancer who received prophylactic IV magnesium before initiating treatment with IV cisplatin had a lower risk of CP-AKI compared to those who did not receive magnesium. Randomized clinical trials are needed to confirm these findings.

Indexed as

Acute Kidney InjuryAntineoplastic AgentsCisplatinMagnesiumNeoplasmsAdministration, IntravenousAdultAgedFemaleHumansMaleMiddle AgedAntineoplastic AgentsCisplatinMagnesium

Identifiers

PMID40272825
PMCPMC12022858

What OpenQuestion holds

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Registered trials

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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.