Evidence map›Paper›PMID 41602789›Full record

ArticleTherapeutic advances in drug safety2026

Integration of pre‑existing cardiovascular comorbidity into CDK4/6 inhibitor selection for breast cancer.

Chanhyun Park, Kiyoung Kim, Nora B Abifaraj, Sydney D Bryant, Ji Haeng Heo

Abstract read
In one paragraph

Article in Therapeutic advances in drug safety, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Chanhyun ParkCollege of Pharmacy, The University of Texas at Austin, 2409 University Avenue, Austin, TX 78712, USA.ORCID https://orcid.org/0000-0002-1081-0950
Kiyoung KimCollege of Pharmacy, The University of Texas at Austin, Austin, TX, USA.
Nora B AbifarajCollege of Pharmacy, The University of Texas at Austin, Austin, TX, USA.
Sydney D BryantCollege of Pharmacy, The University of Texas at Austin, Austin, TX, USA.
Ji Haeng HeoCollege of Pharmacy, The University of Texas at Austin, Austin, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors differ in cardiovascular (CV) safety. Ribociclib has been associated with a higher risk of CV adverse events compared to palbociclib and abemaciclib. Objectives: We examined patterns of CDK4/6 inhibitor selection among patients with breast cancer who had pre-existing cardiovascular disease (CVD) or cardiometabolic conditions (hypertension, hyperlipidemia, or diabetes). Design: We conducted a retrospective cohort study. Methods: Using 2017-2021 Merative MarketScan claims, we identified women ⩾18 years with breast cancer who initiated a first CDK4/6 inhibitor. The outcome was the type of CDK4/6 inhibitor. Primary factors were preexisting CVD and cardiometabolic risk factors measured in the prior 12 months. Multinomial logistic regression estimated unadjusted and adjusted odds of initiating palbociclib or abemaciclib versus ribociclib. Results: Among 5002 initiators (palbociclib Conclusion: Despite its potential higher risk of CV adverse events, ribociclib is more frequently prescribed to patients with breast cancer who have hypertension. Incorporating CV risk prediction into CDK4/6 inhibitor selection could help prevent costly CV complications.

Indexed as

breast cancercardiotoxicityCDK4/6 inhibitorshypertensionreal-world dataribociclib

Identifiers

PMID41602789
PMCPMC12833206

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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.