Evidence map›Paper›PMID 42332608›Full record

SynthesisBMC cancer2026

Long-term cardiovascular risk in survivors of hematologic malignancies: a meta-analysis.

Siqing Liu, Shuran Liu, Yining Hu, Jiawen Deng, Guoli Sun, Xuexian Fang

Abstract readMeta-Analysis
In one paragraph

Synthesis in BMC cancer, 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

6 authors.

Siqing LiuSchool of Public Health and Nursing, Zhejiang Key Laboratory of Medical Epigenetics, Hangzhou Normal University, Building No.7 in Shenyuan, 2318 Yuhangtang Road, Hangzhou, 311121, China.
Shuran LiuSchool of Public Health and Nursing, Zhejiang Key Laboratory of Medical Epigenetics, Hangzhou Normal University, Building No.7 in Shenyuan, 2318 Yuhangtang Road, Hangzhou, 311121, China.
Yining HuSchool of Public Health and Nursing, Zhejiang Key Laboratory of Medical Epigenetics, Hangzhou Normal University, Building No.7 in Shenyuan, 2318 Yuhangtang Road, Hangzhou, 311121, China.
Jiawen DengSchool of Public Health and Nursing, Zhejiang Key Laboratory of Medical Epigenetics, Hangzhou Normal University, Building No.7 in Shenyuan, 2318 Yuhangtang Road, Hangzhou, 311121, China.
Guoli SunDepartment of Cardiology, Guangdong Provincial People's Hospital, Guangzhou, China. sunguoli2019@outlook.com.
Xuexian FangSchool of Public Health and Nursing, Zhejiang Key Laboratory of Medical Epigenetics, Hangzhou Normal University, Building No.7 in Shenyuan, 2318 Yuhangtang Road, Hangzhou, 311121, China. xfang@hznu.edu.cn.

Funding

National Natural Science Foundation of China 82170644Natural Science Foundation of Zhejiang Province LR23H020001
6 · The paper itself

Abstract

backgroundThe survival rate for hematologic malignancies is steadily improving. With the encouraging trend and the aging of these survivors, there is an ever-increasing responsibility for identifying adverse cardiovascular outcomes associated with carcinogenesis and/or anti-cancer therapies across the span of their lives. However, prospective studies have yielded inconsistent results.

methodsWe performed a meta-analysis to summarize the evidence regarding the association between leukemia, Hodgkin lymphoma (HL), and non-Hodgkin lymphoma (NHL) in relation to later risk of cardiovascular disease (CVD). Relevant literatures were identified from PubMed and Web of Science databases through May 2024 and reviewing reference lists of retrieved articles.

resultsFrom the 2412 studies screened, we included 50 studies with 550,385 participants, spanning 1940-2020 for leukemia and 1940-2016 for both Hodgkin and non-Hodgkin lymphoma. The pooled fully adjusted RRs of total CVD, ischemic heart disease (IHD), heart failure (HF), and stroke associated with leukemia were 2.68 (95% confidence interval: 2.22-3.25), 1.46 (1.25-1.70), 4.13 (2.41-7.06), and 3.05 (2.16-4.32), respectively. For HL or NHL survivors, similar positive associations were observed in our study. In addition, compared with survivors with chemotherapy (2.12; 1.89-2.38), radiotherapy-treated survivors had a greater risk of CVD (4.06; 2.84-5.81).

conclusionsIn summary, survivors of hematologic malignancies, especially those who receive radiotherapy, are at highest risk of developing CVD, emphasizing the need for targeted prevention strategies.

Indexed as

Cancer SurvivorsCardiovascular DiseasesHematologic NeoplasmsHodgkin DiseaseHumansLeukemiaLymphoma, Non-HodgkinRisk FactorsCardiovascular diseaseHodgkin lymphomaLeukemiaMeta-analysisNon-Hodgkin lymphoma

Identifiers

PMID42332608
PMCPMC13540886

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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.