Evidence map›Paper›PMID 42658141›Full record

ArticleJACC. Asia2026

Oncologic Benefits and Cardiovascular Risks of Pembrolizumab: Insights From a Nationwide Lung Adenocarcinoma Cohort.

Chan Soon Park, Yebin Park, Ju Hi Park, Soongu Kwak, Tae-Min Rhee, Heesun Lee, Hyung-Kwan Kim, Yong-Jin Kim, Kyungdo Han, Jun-Bean Park

Abstract read
In one paragraph

Article in JACC. Asia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Chan Soon ParkDivision of Cardiology, Department of Internal Medicine, Asan Medical Center, Seoul, Republic of Korea.
Yebin ParkDepartment of Statistics and Actuarial Science, Soongsil University, Seoul, Republic of Korea.
Ju Hi ParkDivision of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
Soongu KwakDivision of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
Tae-Min RheeDepartment of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital Healthcare System Gangnam Center, Seoul, Republic of Korea.
Heesun LeeDepartment of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital Healthcare System Gangnam Center, Seoul, Republic of Korea.
Hyung-Kwan KimDivision of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
Yong-Jin KimDivision of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
Kyungdo HanDepartment of Statistics and Actuarial Science, Soongsil University, Seoul, Republic of Korea. Electronic address: hkd917@naver.com.
Jun-Bean ParkDivision of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea. Electronic address: nanumy1@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPembrolizumab improves survival in advanced lung adenocarcinoma, but potential cardiovascular toxicity remains.

objectivesThis study evaluated the oncologic benefits and cardiovascular risks of pembrolizumab in a nationwide lung adenocarcinoma cohort.

methodsWe analyzed 39,192 patients newly diagnosed with lung adenocarcinoma between 2012 and 2019 using the nationwide cancer registry. We compared 573 patients treated with pembrolizumab within 1 year of diagnosis with 38,619 patients who were not treated within 3 years. The outcomes included all-cause mortality and myocardial infarction (MI), ischemic stroke (IS), heart failure (HF), pericarditis/myocarditis, and atrial fibrillation (AF) over a 3-year follow-up.

resultsDuring a median follow-up of 3.0 years (IQR: 1.0-3.0 years), 18,241 deaths, 574 MI, 1,157 IS, 2,777 HF, 852 pericarditis/myocarditis, and 1,601 AF events occurred. Model-based adjusted outcome curves showed lower all-cause mortality among users (adjusted P < 0.001) but higher incidences of IS, HF, and AF (adjusted P = 0.028, <0.001, and 0.048, respectively). Nonsignificant trends toward increased risks of MI and pericarditis/myocarditis were observed. Multivariable survival analyses, including Fine-Gray competing risk models for nonfatal cardiovascular outcomes, showed that pembrolizumab use was associated with lower all-cause mortality (HR: 0.77; 95% CI: 0.69-0.86) but with increased risks of IS (HR: 1.56, 95% CI: 1.10-2.23), HF (HR: 2.72, 95% CI: 2.24-3.30), and AF (HR: 1.47, 95% CI: 1.08-2.01); increases in MI and pericarditis/myocarditis were nonsignificant.

conclusionsPembrolizumab was associated with lower all-cause mortality but higher risks of major cardiovascular events. These findings support vigilant cardio-oncologic monitoring in patients treated with pembrolizumab.

Indexed as

all-cause mortalitycardio-oncologyheart failureischemic strokemyocardial infarctionpembrolizumab

Identifiers

PMID42658141
PMCPMC13654415

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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.