Evidence map›Paper›PMID 38213548›Full record

ReviewCurrent treatment options in cardiovascular medicine2023

Immunotherapy-Associated Atherosclerosis: A Comprehensive Review of Recent Findings and Implications for Future Research.

Antonia Chan, Stefan Torelli, Evaline Cheng, Ryan Batchelder, Sarah Waliany, Joel Neal, Ronald Witteles, Patricia Nguyen, Paul Cheng, Han Zhu

Open access · hybridAbstract readReview
In one paragraph

Review in Current treatment options in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 13 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

10 authors at 3 institutions in 1 country.

Antonia ChanDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.ORCID 0000-0002-7496-9581
Stefan TorelliDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Evaline ChengDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA USA.
Ryan BatchelderDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA USA.
Sarah WalianyDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Joel NealDepartment of Medicine, Division of Oncology, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA USA.
Ronald WittelesDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Patricia NguyenDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Paul ChengDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Han ZhuDepartment of Medicine, Stanford University School of Medicine, Stanford, CA USA.
Stanford Medicine · USCardiovascular Institute of the South · USStanford University · US

Funding

From Locus to Function: Role of ZEB2 in Human Risk of Coronary Artery DiseaseK08HL153798 · NHLBI · STANFORD UNIVERSITY · PI CHENG, PAUL PO SHENG · 2020 to 2024
$933k
NHLBI NIH HHS K08 HL153798
6 · The paper itself

Abstract

Purpose of the Review: Even as immune checkpoint inhibitors (ICIs) have transformed the lifespan of many patients, they may also trigger acceleration of long-term cardiovascular disease. Our review aims to examine the current landscape of research on ICI-mediated atherosclerosis and address key questions regarding its pathogenesis and impact on patient management. Recent Findings: Preclinical mouse models suggest that T cell dysregulation and proatherogenic cytokine production are key contributors to plaque development after checkpoint inhibition. Clinical data also highlight the significant burden of atherosclerotic cardiovascular disease (ASCVD) in patients on immunotherapy, although the value of proactively preventing and treating ASCVD in this population remains an open area of inquiry. Current treatment options include dietary/lifestyle modification and traditional medications to manage hypertension, hyperlipidemia, and diabetes risk factors; no current targeted therapies exist. Summary: Early identification of high-risk patients is crucial for effective preventive strategies and timely intervention. Future research should focus on refining screening tools, elucidating targetable mechanisms driving ICI atherosclerosis, and evaluating long-term cardiovascular outcomes in cancer survivors who received immunotherapy. Moreover, close collaboration between oncologists and cardiologists is essential to optimize patient outcomes.

Indexed as

AtherosclerosisCardio-oncologyImmunotherapy

Identifiers

PMID38213548
PMCPMC10776491
OpenAlexW4389789043

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.