Evidence map›Paper›PMID 40221735›Full record

ArticleWorld journal of surgical oncology2025

The combination of CA125, CA199, CEA, and AFP is an effective diagnostic biomarker for gastric cancer in elderly individuals.

Xiao-Wen Yuan, Jia-Hao Feng, De Bing Huang, Zhan-Tao Lu, Hui-Ling Ye, Ping Chen, Lv Deng

Abstract read
In one paragraph

Article in World journal of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
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.

Xiao-Wen YuanDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China. 499963979@qq.com.
Jia-Hao FengDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China.
De Bing HuangDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China.
Zhan-Tao LuDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China.
Hui-Ling YeDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China.
Ping ChenDepartment of Laboratory Medicine of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528200, Guangdong, China.
Lv DengDepartment of Gastroenterology of Eighth People's Hospital of Nanhai District, Foshan City, 528216, Guangdong, China. 183027228@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum tumour markers (TMs) such as alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), carbohydrate antigen 199 (CA199) and CA125 have been established as prognostic indicators for gastric cancer (GC); however, the diagnostic value of these markers for GC in older adults has yet to be examined. Therefore, this study aimed to explore the diagnostic and prognostic significance of AFP, CEA, CA199 and CA125 for GC in elderly individuals.

methodsA total of 188 patients who visited The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, from May 2021 to March 2024 were selected for this study. TMs, namely, CA199, CA125, CEA, and AFP, were examined in all patients. Comparisons of these TMs were conducted among the three groups, and TM levels were compared in patients with GC at various TNM stages. The diagnostic value of these TMs for GC was evaluated by calculating the area under the curve (AUC).

resultsWe selected 89 patients diagnosed with GC: 52 patients with benign gastric diseases and 47 healthy individuals for our study. The positivity rates of AFP, CA125, CEA and CA199 were significantly greater in the GC group (31.46%, 31.46%, 43.82% and 23.60%, respectively) than in the benign gastric disease group and healthy control group. The diagnostic sensitivities of CEA, CA125, CA199 and AFP for GC were 31.46%, 29.21%, 44.90% and 24.72%, respectively. The combination of these markers yielded a sensitivity of 65.17%, which was significantly greater than the sensitivity of each marker alone (P < 0.05). Additionally, patients with stage I-II disease had significantly lower serum levels of CEA, CA199, CA125, and AFP than did those with stage III-IV disease.

conclusionsThe levels of serum TMs, including CA12-5, CEA, CA199 and AFP, are elevated in elderly individuals with GC, indicating a higher TNM stage. The combination of CEA, CA12-5, CA199 and AFP has enhanced diagnostic value for GC, thereby offering significant clinical guidance. However, this study is limited by its retrospective design and lack of external validation, which should be addressed in future prospective trials.

Indexed as

alpha-FetoproteinsAntigens, Tumor-Associated, CarbohydrateBiomarkers, TumorCA-125 AntigenCarcinoembryonic AntigenStomach NeoplasmsAgedAged, 80 and overCase-Control StudiesFemaleFollow-Up StudiesHumansMaleMembrane ProteinsMiddle AgedNeoplasm StagingAFP protein, humanalpha-FetoproteinsAntigens, Tumor-Associated, CarbohydrateBiomarkers, TumorCA-125 Antigencarbohydrate antigen 199, humanCarcinoembryonic AntigenMembrane ProteinsMUC16 protein, humanElderly individualsGastric cancerTumour marker

Identifiers

PMID40221735
PMCPMC11992887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.