Evidence map›Paper›PMID 42189435›Full record

ArticleCardiovascular toxicology2026

Clinical Characteristics and Outcomes of Heart Failure with Preserved Ejection Fraction Versus Reduced Ejection Fraction in Patients Receiving Anticancer Drugs.

Yuma Shibutani, Fuka Aoki, Takuro Imaoka, Atsuko Suzuki, Kazuko Tajiri

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Cardiovascular toxicology, 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.

Yuma ShibutaniDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.
Fuka AokiDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.
Takuro ImaokaDepartment of Cardiology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba, 277-8577, Japan.
Atsuko SuzukiDepartment of Clinical Laboratory, National Cancer Center Hospital East, Kashiwa, Japan.
Kazuko TajiriDepartment of Cardiology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba, 277-8577, Japan. ktajiri@east.ncc.go.jp.

Funding

JSPS KAKENHI 23K07518National Cancer Center Research and Development Fund 2023-A-12
6 · The paper itself

Abstract

This study aimed to compare prevalence, clinical features, and outcomes between patients with heart failure (HF) with preserved ejection fraction (HFpEF) and those with reduced ejection fraction (HFrEF) who received anticancer drugs. This single-center, retrospective study included 126 patients who developed new-onset HF or worsening HF after starting anticancer drug treatment between April 2018 and December 2023. HFrEF was defined as HF symptoms and signs with left ventricular ejection fraction (LVEF) < 50%, and HFpEF as LVEF ≥ 50%. Among the cohort, 49 patients (39%) had HF with New York Heart Association functional class ≥ 3, and the proportions of HFrEF and HFpEF were similar (61 [48%] vs. 65 [52%], respectively). Patients with HFrEF had a significantly higher history of anthracycline use, whereas fluoropyrimidine or other cytotoxic chemotherapy use was lower. Overall, 84% discontinued or interrupted anticancer therapy after HF onset. There were no significant differences in overall survival (log-rank p = 0.27) or cancer treatment continuation rates (log-rank p = 0.83) between HFpEF and HFrEF. All-cause mortality was associated with anemia (odds ratio [OR]: 3.46, 95% confidence interval [CI]; 1.36-8.82, p = 0.009) and performance status ≥ 3 (OR: 3.13, 95% CI; 1.18-8.26, p = 0.021), but not with LVEF. In patients who developed HF after anticancer treatment, HFrEF and HFpEF occurred at similar rates. There were no significant differences in overall survival or cancer treatment continuation between groups. Anemia and poor performance status, but not LVEF, independently predicted all-cause mortality.

Indexed as

Antineoplastic AgentsHeart FailureNeoplasmsStroke VolumeVentricular Function, LeftAgedCardiotoxicityFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsAntineoplastic AgentsCardio-oncologyCardiotoxicityHeart failureOnco-cardiology

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