Evidence map›Paper›PMID 40843752›Full record

ReviewMedical sciences (Basel, Switzerland)2025

Cardiotoxicity in Breast Cancer Therapy: Risks, Mechanisms, and Prevention Strategies.

Annisa Eka Fitrianti, Nadea Olyvia Wardani, Astri Astuti, Kusnandar Anggadiredja, Lia Amalia, Risani Andalasia Putri, Zulfan Zazuli

Abstract readReview
In one paragraph

Review in Medical sciences (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. 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

7 authors.

Annisa Eka FitriantiMaster's Program in Pharmacy, School of Pharmacy, Institut Teknologi Bandung, Bandung 40132, Indonesia.
Nadea Olyvia WardaniMaster's Program in Pharmacy, School of Pharmacy, Institut Teknologi Bandung, Bandung 40132, Indonesia.
Astri AstutiDepartment of Cardiology, Dr. Hasan Sadikin General Hospital, Bandung 40161, Indonesia.
Kusnandar AnggadiredjaDepartment of Pharmacology-Clinical Pharmacy, Institut Teknologi Bandung, Bandung 40132, Indonesia.ORCID 0000-0001-9879-6112
Lia AmaliaDepartment of Pharmacology-Clinical Pharmacy, Institut Teknologi Bandung, Bandung 40132, Indonesia.
Risani Andalasia PutriDepartment of Pharmacy, Dharmais Cancer Hospital, Jakarta 11420, Indonesia.
Zulfan ZazuliDepartment of Pharmacology-Clinical Pharmacy, Institut Teknologi Bandung, Bandung 40132, Indonesia.ORCID 0000-0002-1264-9558

Funding

2024 Research, Community Service, and Innovation (PPMI 2024) Program, School of Pharmacy, Institut Teknologi Bandung 31/IT1.C10/SK-KU/2024
6 · The paper itself

Abstract

Breast cancer is the most prevalent cancer in women. Anthracyclines are commonly used as the first line of treatment, often combined with other agents, including trastuzumab. Despite their efficacy, both drugs pose a risk of cardiotoxicity, which may impair patients' quality of life (QoL) and hinder treatment persistence. Anthracycline-induced cardiotoxicity is dose-dependent and generally irreversible, whereas trastuzumab is associated with potentially reversible cardiac dysfunction. This review discusses the risk factors and biological mechanisms underlying chemotherapy-induced cardiotoxicity in breast cancer and explores effective strategies for prevention and treatment. It has been demonstrated that several cardioprotective strategies, such as treatments with angiotensin-converting enzyme inhibitors (ACEis), angiotensin receptor blockers (ARBs), beta-blockers, and dexrazoxane, can help lessen cardiotoxic effects. A better understanding of cardioprotective strategies may help optimize cancer treatment without compromising cardiovascular function.

Indexed as

Antineoplastic AgentsBreast NeoplasmsCardiotoxicityAngiotensin-Converting Enzyme InhibitorsAnthracyclinesFemaleHumansRisk FactorsTrastuzumabAngiotensin-Converting Enzyme InhibitorsAnthracyclinesAntineoplastic AgentsTrastuzumabanthracyclinesbreast cancercardioprotectivecardiotoxicitytrastuzumab

Identifiers

PMID40843752
PMCPMC12371923

What OpenQuestion 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 OpenQuestion graph.