Evidence map›Paper›PMID 36966354›Full record

ArticleClinical and experimental immunology2023

Antinuclear antibody (ANA) status predicts immune-related adverse events in liver cancer patients undergoing anti-PD-1 therapy.

Shu-Jung Hsu, Yen-Cheng Chao, Xia-Hui Lin, Hua-Hua Liu, Yang Zhang, Wei-Feng Hong, Mao-Pei Chen, Xin Xu, Lan Zhang, Zheng-Gang Ren and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

9 citing papers in PubMed, 7 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Shu-Jung HsuLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-4043-7779
Yen-Cheng ChaoDepartment of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Xia-Hui LinDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, China.
Hua-Hua LiuLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Yang ZhangDepartment of Radiation Oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Wei-Feng HongDepartment of Radiation Oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Mao-Pei ChenLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Xin XuLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Lan ZhangLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Zheng-Gang RenLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Shi-Suo DuDepartment of Radiation Oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Rong-Xin ChenLiver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Fudan University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune-related adverse events (irAEs) clinically resemble autoimmune diseases, indicating autoantibodies could be potential biomarkers for the prediction of irAEs. This study aimed to assess the predictive value of peripheral blood antinuclear antibody (ANA) status for irAEs, considering the time and severity of irAEs, as well as treatment outcome in liver cancer patients administered anti-PD-1 therapy. Ninety-three patients with advanced primary liver cancer administered anti-PD-1 treatment were analyzed retrospectively. They were divided into the ANA positive (ANA+, titer ≥ 1:100) and negative (ANA-, titer < 1:100) groups. Development of irAEs, progression-free survival (PFS), and overall survival (OS) were assessed. Compared with ANA- patients, ANA+ cases were more prone to develop irAEs (43.3% vs. 19.2%, P = 0.031). With the increase of ANA titers, the frequency of irAEs increased. The time interval between anti-PD-1 therapy and the onset of irAEs was significantly shorter in ANA+ patients compared with the ANA- group (median, 1.7 months vs. 5.0 months, P = 0.022). Moreover, the time between anti-PD-1 therapy and irAE occurrence decreased with increasing ANA titer. In addition, PFS and OS were decreased in ANA+ patients compared with the ANA- group (median PFS, 2.8 months vs. 4.2 months, P = 0.043; median OS, 21.1 months vs. not reached, P = 0.041). IrAEs occur at higher frequency in ANA+ liver cancer patients undergoing anti-PD-1 therapy. ANA titer could help predict irAE development and treatment outcome in these patients.

Indexed as

Antineoplastic Agents, ImmunologicalImmune System DiseasesLiver NeoplasmsAntibodies, AntinuclearHumansNivolumabRetrospective StudiesAntibodies, AntinuclearAntineoplastic Agents, ImmunologicalNivolumabantinuclear antibodycommon terminology criteria for adverse eventsimmune-related adverse eventPD-1primary liver cancer

Identifiers

PMID36966354
PMCPMC10243869
OpenAlexW4360976984

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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.