Evidence map›Paper›PMID 35068882›Full record

ArticleActa Cardiologica Sinica2022

Clinical Features and Outcomes of Immune Checkpoint Inhibitor-Associated Cardiovascular Toxicities.

Nan-Chun Wu, Yin-Hsun Feng, Yu Hsuan Kuo, Wei-Yu Chen, Hong-Chang Wu, Chien-Tai Huang, Wen-Ching Wang, Nai-Wen Kang, Jhih-Yuan Shih, Zhih-Cherng Chen and 1 more

Open access · greenAbstract read
In one paragraph

Article in Acta Cardiologica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Nan-Chun WuDivision of Cardiovascular Surgery, Department of Surgery, Chi Mei Medical Center.
Yin-Hsun FengDivision of Oncology, Department of Internal Medicine.
Yu Hsuan KuoDivision of Oncology, Department of Internal Medicine.
Wei-Yu ChenDivision of Oncology, Department of Internal Medicine.
Hong-Chang WuDivision of Oncology, Department of Internal Medicine.
Chien-Tai HuangDivision of Oncology, Department of Internal Medicine.
Wen-Ching WangDivision of General Surgery, Department of Surgery.
Nai-Wen KangDivision of Oncology, Department of Internal Medicine.
Jhih-Yuan ShihDivision of Cardiology, Department of Internal Medicine, Chi-Mei Medical Center.
Zhih-Cherng ChenDivision of Cardiology, Department of Internal Medicine, Chi-Mei Medical Center.
Wei-Ting ChangDivision of Cardiology, Department of Internal Medicine, Chi-Mei Medical Center.
Chia Nan University of Pharmacy and Science · TWChi Mei Medical Center · TWSouthern Taiwan University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the increasing prevalence of therapies utilizing immune checkpoint inhibitors (ICIs), the associated cardiovascular complications have been poorly reported. Given the fatality of ICI-related complications, especially myocarditis, optimal risk stratification to predict major adverse cardio- and cerebrovascular events (MACCEs) in patients receiving ICIs is mandatory.

methodsWe collected clinical data from patients receiving ICIs, and the primary outcomes were MACCEs, including myocarditis, heart failure, and ischemic stroke. Other systemic immune responses relating to ICIs were also recorded. The median follow-up duration was 3 years.

resultsAmong 580 patients, the incidence of MACCEs was 3.9%. Older patients, male patients, and patients with lung cancer, liver cirrhosis, or diabetes had higher risks of MACCEs. There was no significant difference between the use of PD-1/PD-L1 inhibitors or CTLA inhibitors in terms of developing cardiovascular toxicities. The development of ICI-related MACCEs was associated with worse survival. Notably, after re-review by specialists, three patients eventually diagnosed with ICI-related myocarditis had not previously been identified. Only one was treated with pulse steroids, and none survived. The most common concomitant extracardiac immune-related adverse events were myositis/dermatitis, endocrine toxicity and hepatitis.

conclusionsCollectively, ICIs may lead to severe cardiovascular toxicities and require more attention. Early identification, proper diagnosis, and prompt treatment are pivotal for improving survival.

Indexed as

Cardiovascular toxicityImmune checkpoint inhibitorMyocarditisPD-1/PD-L1 inhibitor

Identifiers

PMID35068882
PMCPMC8743480
OpenAlexW4206965601

What OpenQuestion holds

Textmetadata
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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.