Evidence map›Paper›PMID 38416491›Full record

ArticleJAMA network open2024

Serum Tumor Markers and Outcomes in Patients With Appendiceal Adenocarcinoma.

Abdelrahman Yousef, Mahmoud Yousef, Mohammad A Zeineddine, Aditya More, Mohammad Fanaeian, Saikat Chowdhury, Mark Knafl, Paul Edelkamp, Ichiaki Ito, Yue Gu and 25 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
15.5field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 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

35 authors at 4 institutions in 3 countries.

Abdelrahman YousefDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Mahmoud YousefDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Mohammad A ZeineddineDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Aditya MoreDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Mohammad FanaeianDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Saikat ChowdhuryDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Mark KnaflDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
Paul EdelkampDepartment of Data Engineering and Analytics, University of Texas MD Anderson Cancer Center, Houston.
Ichiaki ItoDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Yue GuDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Vinay PattalachintiDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Zahra Alavi NainiDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Fadl A ZeineddineDepartment of Internal Medicine, Houston Methodist Hospital, Houston, Texas.
Jennifer PetersonDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Kristin AlfaroDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Wai Chin FooDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston.
Jeff JinDepartment of Enterprise Development and Integration, University of Texas MD Anderson Cancer Center, Houston.
Neal BhutianiDepartment of Colon and Rectal Surgery, University of Texas MD Anderson Cancer Center, Houston.
Victoria HigbieDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Christopher P ScallyDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Bryan KeeDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Scott KopetzDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Drew GoldsteinPalantir Technologies, Denver, Colorado.
Madeleine StrachColorectal and Peritoneal Oncology Centre, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Andrew WilliamsonDepartment of Medical Oncology, The Christie National Health Service Foundation Trust, Manchester, United Kingdom.
Omer AzizColorectal and Peritoneal Oncology Centre, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Jorge BarriusoColorectal and Peritoneal Oncology Centre, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Abhineet UppalDepartment of Colon and Rectal Surgery, University of Texas MD Anderson Cancer Center, Houston.
Michael G WhiteDepartment of Colon and Rectal Surgery, University of Texas MD Anderson Cancer Center, Houston.
Beth HelminkDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Keith F FournierDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Kanwal P RaghavDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
Melissa W TaggartDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston.
Michael J OvermanDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
John Paul ShenDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
The University of Texas MD Anderson Cancer Center · USThe Christie NHS Foundation Trust · GBMethodist Hospital · USUniversity of Manchester · GB

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
High-Throughput Functional Genomics to Guide Precision Oncology in Gastrointestinal TumorsK22CA234406 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHEN, JOHN PAUL YING CHING · 2019 to 2021
$577k
NCI NIH HHS K22 CA234406NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Importance: Serum tumor markers carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), and cancer antigen 125 (CA125) have been useful in the management of gastrointestinal and gynecological cancers; however, there is limited information regarding their utility in patients with appendiceal adenocarcinoma. Objective: To assess the association of serum tumor markers (CEA, CA19-9, and CA125) with clinical outcomes and pathologic and molecular features in patients with appendiceal adenocarcinoma. Design, Setting, and Participants: This is a retrospective cohort study at a single tertiary care comprehensive cancer center. The median (IQR) follow-up time was 52 (21-101) months. Software was used to query the MD Anderson internal patient database to identify patients with a diagnosis of appendiceal adenocarcinoma and at least 1 tumor marker measured at MD Anderson between March 2016 and May 2023. Data were analyzed from January to December 2023. Main Outcomes and Measures: Association of serum tumor markers with survival in patients with appendiceal adenocarcinoma. Cox proportional hazards regression analyses were also performed to assess associations between clinical factors (serum tumor marker levels, demographics, and patient and disease characteristics) and patient outcomes (overall survival). Results: A total of 1338 patients with appendiceal adenocarcinoma were included, with a median (range) age at diagnosis of 56.5 (22.3-89.6) years. The majority of the patients had metastatic disease (1080 patients [80.7%]). CEA was elevated in 742 of the patients tested (56%), while CA19-9 and CA125 were elevated in 381 patients (34%) and 312 patients (27%), respectively. Individually, elevation of CEA, CA19-9, or CA125 were associated with worse 5-year survival; elevated vs normal was 81% vs 95% for CEA (hazard ratio [HR], 4.0; 95% CI, 2.9-5.6), 84% vs 92% for CA19-9 (HR, 2.2; 95% CI, 1.4-3.4), and 69% vs 93% for CA125 (HR, 4.6; 95% CI, 2.7-7.8) (P < .001 for all). Quantitative evaluation of tumor markers was associated with outcomes. Patients with highly elevated (top 10th percentile) CEA, CA19-9, or CA125 had markedly worse survival, with 5-year survival rates of 59% for CEA (HR, 9.8; 95% CI, 5.3-18.0), 64% for CA19-9 (HR, 6.0; 95% CI, 3.0-11.7), and 57% for CA125 (HR, 7.6; 95% CI, 3.5-16.5) (P < .001 for all). Although metastatic tumors had higher levels of all tumor markers, when restricting survival analysis to 1080 patients with metastatic disease, elevated CEA, CA19-9, or CA125 were all still associated worse survival (HR for CEA, 3.4; 95% CI, 2.5-4.8; P < .001; HR for CA19-9, 1.8; 95% CI, 1.2-2.7; P = .002; and HR for CA125, 3.9; 95% CI, 2.4-6.4; P < .001). Interestingly, tumor grade was not associated with CEA or CA19-9 level, while CA-125 was slightly higher in high-grade tumors relative to low-grade tumors (mean value, 18.3 vs 15.0; difference, 3.3; 95% CI, 0.9-3.7; P < .001). Multivariable analysis identified an incremental increase in the risk of death with an increase in the number of elevated tumor markers, with an 11-fold increased risk of death in patients with all 3 tumor markers elevated relative to those with none elevated. Somatic mutations in KRAS and GNAS were associated with significantly higher levels of CEA and CA19-9. Conclusions and Relevance: In this retrospective study of serum tumor markers in patients with appendiceal adenocarcinoma, CEA, CA19-9, and CA125 were associated with overall survival in appendiceal adenocarcinoma. Given their value, all 3 biomarkers should be included in the initial workup of patients with a diagnosis of appendiceal adenocarcinoma.

Indexed as

AdenocarcinomaAppendiceal NeoplasmsNeoplasms, Second PrimaryAgedAged, 80 and overBiomarkers, TumorCA-125 AntigenCA-19-9 AntigenCarcinoembryonic AntigenHumansMiddle AgedRetrospective StudiesBiomarkers, TumorCA-125 AntigenCA-19-9 AntigenCarcinoembryonic Antigen

Identifiers

PMID38416491
PMCPMC10902735
OpenAlexW4392231659

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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.