Evidence map›Paper›PMID 41316332›Full record

ArticleEuropean journal of medical research2025

Brown adipose tissue activation and cardiovascular risk following PD-1 antibody therapy in cancer patients: a retrospective cohort study.

Bingqian Lin, Duanyu Lin, Xiaodan Ou, Jinwen Wang, Shun Yu, Gan Chen, Junping Wen

Registry-linked trialAbstract read
In one paragraph

Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07538479 (NIVALIS Trial), which is not on this 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.

NCT07538479 phase1recruitingnot on this mapstarted 2026, after this paper: background citation

NIVALIS Trial: A Single-Center, Prospective, Single-Arm, Open-Label Phase I Exploratory Study Evaluating the Safety, Feasibility, and Preliminary Antitumor Activity of Controlled Cold Exposure Combined With PD-1/PD-L1 Immunotherapy in Patients With Solid Tumors

TypeinterventionalSponsorWest China HospitalRan2026 to 2029Enrolled24ConditionsSolid Tumors, Solid Malignancies, Cold Exposure, ImmunotherapyArmsControlled Cold Exposure, Investigator-Selected Standard PD-1/PD-L1 Inhibitor-Based Therapy
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.

Bingqian Lin *Department of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Duanyu Lin *Fujian Cancer Hospital, Fujian Medical University Cancer Hospital, Fuzhou, China.
Xiaodan Ou *Department of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Jinwen Wang *Department of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Shun YuDepartment of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Gan ChenDepartment of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Junping WenDepartment of Endocrinology, Key Laboratory of Endocrinology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China. junpingwen@163.com.

Funding

Fujian Provincial Clinical Research Center 2022Y2013Joint Funds for the innovation of science And Technology 2024Y9057National Key Clinical Specialty Discipline Construction Program of China 2023001National Major Science and Technology Projects of China 2024ZD0531600National Natural Science Foundation of China 82370786
6 · The paper itself

Abstract

backgroundThis study aimed to investigate whether PD-1 antibody therapy modulates brown adipose tissue (BAT) activity and whether BAT activation is associated with cardiovascular risk parameters in cancer patients. METHODS

designRetrospective cohort study.

settingTwo tertiary hospitals in Fujian Province, China (Fujian Provincial Hospital and Fujian Cancer Hospital), between January 2019 and January 2024.

participantsSixty-eight cancer patients (54 males, 14 females) who received PD-1 antibody therapy (e.g., pembrolizumab, 200 mg Q3W) and underwent paired EXCLUSION CRITERIA: hypothyroidism (n = 3), severe renal insufficiency (n = 2), and incomplete PET/CT or laboratory data. OUTCOME MEASURES: primary outcome: change in BAT activity (quantified by supraclavicular fossa SUVmax via PET/CT) pre- versus post-PD-1 therapy. SECONDARY OUTCOMES: changes in VAT/SAT SUVmax, lipid profiles (triglycerides [TG], total cholesterol [TC], LDL-C, and HDL-C), arterial stiffness index (ASI), cardiac biomarkers (cTnT and NT-proBNP), and thyroid function (TSH, FT3, FT4).

resultsFollowing immunotherapy, BAT SUV

conclusionsPD-1 antibodies enhance BAT activity in cancer patients, and higher BAT activity is associated with reduced arterial stiffness. PET/CT-derived BAT SUVmax may serve as a novel biomarker for cardiovascular risk stratification during PD-1 antibody therapy.

Indexed as

Adipose Tissue, BrownCardiovascular DiseasesImmune Checkpoint InhibitorsNeoplasmsProgrammed Cell Death 1 ReceptorAdultAgedAntibodies, Monoclonal, HumanizedFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedPositron Emission Tomography Computed TomographyRetrospective StudiesAntibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 ReceptorArterial stiffnessBrown adipose tissueCancerOncology immunotherapyPD-1 antibodies

Identifiers

PMID41316332
PMCPMC12664139

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