Evidence map›Paper›PMID 42234870›Full record

SynthesisJNCI cancer spectrum2026

Incidence and treatment-modifying impact of immune checkpoint inhibitor-associated peripheral edema: a systematic review and meta-analysis.

Anneliese Markus, Kazuya Tsuchiya, Toshiaki Takahashi, Evelyn Elias MBBCh, Mako Koseki, Yoshito Nishimura, Nicholas C Rohs, Yu Fujiwara

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in JNCI cancer spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Anneliese MarkusDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.ORCID 0000-0002-0677-8556
Kazuya TsuchiyaDepartment of Internal Medicine, Morehouse School of Medicine, Atlanta, GA, United States.
Toshiaki TakahashiDepartment of Internal Medicine, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, United States.ORCID 0009-0003-0364-539X
Evelyn Elias MBBChDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Morningside/West, New York, NY, United States.
Mako KosekiDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Morningside/West, New York, NY, United States.
Yoshito NishimuraDivision of Hematology and Oncology, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0003-0224-7501
Nicholas C RohsCenter for Thoracic Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Yu FujiwaraDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.ORCID 0000-0003-1406-2352

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune-related adverse events disrupt immune checkpoint inhibitor therapy and impact quality of life. Peripheral edema is common among patients with cancer, however the causality of peripheral edema can be unclear in the context of multidrug regimens.

methodsPubMed/MEDLINE, Embase, and Web of Science were searched to identify phase 3 randomized controlled trials (RCTs) evaluating immune checkpoint inhibitors reporting peripheral edema incidence. The incidence of edema was calculated according to adverse event, immune checkpoint inhibitor, and treatment patterns. A random-effects meta-analysis pooled odds ratios (ORs) of edema incidence between immune checkpoint inhibitor and non-immune checkpoint inhibitor groups. A systematic review characterizing the interventions for immune-related peripheral edema was also conducted.

resultsFrom 58 RCTs (22 590 patients), treatment-related peripheral edema (grade 1-5) occurred in 2.80% (n = 195 of 6969) of patients receiving immune checkpoint inhibitor monotherapy, 4.96% (n = 112 of 2257) of patients receiving immune checkpoint inhibitor with chemotherapy, and 8.73% (n = 205 of 2349) of patients receiving immune checkpoint inhibitor with targeted therapy. Meta-analysis showed immune checkpoint inhibitor monotherapy had lower treatment-related peripheral edema incidence compared with chemotherapy (OR = 0.45, 95% CI = 0.27 to 0.73; P = .001, I2 = 69%) with the lowest relative incidence among programmed cell death protein 1 vs chemotherapy (OR = 0.41, 95% CI = 0.23 to 0.73; P = .003) and immune checkpoint inhibitor vs taxane chemotherapy (OR = 0.32, 95% CI = 0.18 to 0.58; P < .001). A systematic review of treatment outcomes for immune-related peripheral edema among 40 patients (19 studies) revealed 82.5% (n = 33 of 40) of cases received glucocorticoid treatment, and immune checkpoint inhibitors were permanently discontinued in 35% (n = 14 of 40).

conclusionsPeripheral edema is a rare but potentially serious adverse event associated with immune checkpoint inhibitors. Immune checkpoint inhibitors likely confer less peripheral edema risk than taxane therapy. To avoid unnecessary treatment interruptions, treatment discontinuation requires careful consideration, particularly when edema develops following immune checkpoint inhibitor combination therapy.

Indexed as

EdemaImmune Checkpoint InhibitorsNeoplasmsAntineoplastic Combined Chemotherapy ProtocolsClinical Trials, Phase III as TopicHumansIncidenceRandomized Controlled Trials as TopicImmune Checkpoint Inhibitors

Identifiers

PMID42234870
PMCPMC13428319

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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.