Evidence map›Paper›PMID 42332688›Full record

SynthesisBMC cancer2026

Exploring the relationship between potential hepatotoxicity and novel hormonal therapies in prostate cancer: a systematic review and meta-analysis.

Liang Ma, Liwei Fan, Xiaoli Luo, Zhuangcheng Huang, Jiacheng Dai, Yuejun Wu, Wenhua Zhang

Abstract readSystematic ReviewMeta-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

7 authors.

Liang Ma *Department of Gastroenterology, Shaoxing Second Hospital, Shaoxing, Zhejiang, 312000, China. markma0926@163.com.
Liwei Fan *Department of Biochemistry, V.N. Karazin Kharkiv National University, Kharkiv, 61022, Ukraine.
Xiaoli Luo *Department of Laboratory Medicine, Western Theater Command Air Force Hospital, No. 18 Shunjiang Road, Chengdu, 610000, China.
Zhuangcheng HuangThe First Affiliated Hospital of Shantou University Medical College, Medical College of Shantou University, Shantou, 515041, China.
Jiacheng DaiSchool of Stomatology, Changsha Medical University, Changsha, 410219, China.
Yuejun WuDepartment of Internal Medicine, Didang Subdistrict Community Health Service Center, Yuecheng District, Shaoxing City, China.
Wenhua ZhangDepartment of Gastroenterology, Shaoxing Second Hospital, Shaoxing, Zhejiang, 312000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNovel hormonal therapies (NHTs) have substantially improved outcomes in prostate cancer across multiple disease states. However, their hepatic safety remains clinically relevant because treatment is often prolonged and may be combined with androgen-deprivation therapy, corticosteroids, or chemotherapy. We performed a systematic review and meta-analysis to quantify the risk of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) elevations associated with NHT-based therapy.

methodsThis study was conducted in accordance with PRISMA guidelines. Randomized controlled trials comparing NHT-containing regimens with control regimens in patients with prostate cancer were eligible if they reported extractable ALT and/or AST adverse-event data. Pooled risk ratios (RRs) with 95% confidence intervals (CIs) were calculated for four prespecified outcomes: all-grade ALT elevation, grade ≥ 3 ALT elevation, all-grade AST elevation, and grade ≥ 3 AST elevation.

resultsTen randomized studies reported in 11 publications were included, involving 10,173 participants treated with abiraterone, enzalutamide, darolutamide, or abiraterone plus enzalutamide combination regimens. Compared with controls, NHT-based therapy significantly increased the risk of all-grade ALT elevation (RR 1.49, 95% CI 1.12-2.00; I

conclusionsNHT-based therapy for prostate cancer was associated with an increased risk of hepatic enzyme abnormalities, particularly severe ALT elevation. The hepatic safety signal appeared more evident for abiraterone-containing and combination regimens, whereas drug-specific estimates for enzalutamide and darolutamide remained limited. Because this analysis focused on laboratory-defined ALT and AST elevations, careful liver function monitoring remains warranted during NHT-based therapy, especially in patients receiving abiraterone-containing or prolonged combination regimens.

Indexed as

Antineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsChemical and Drug Induced Liver InjuryProstatic NeoplasmsAlanine TransaminaseAspartate AminotransferasesHumansMaleRandomized Controlled Trials as TopicAlanine TransaminaseAntineoplastic Agents, HormonalAspartate AminotransferasesAndrogen receptor pathway inhibitorHepatotoxicityLiver toxicityNovel hormonal therapyProstate cancer

Identifiers

PMID42332688
PMCPMC13488195

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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.