Evidence map›Paper›PMID 35766303›Full record

ArticleThe Prostate2022

Elevated serum CEA is associated with liver metastasis and distinctive circulating tumor DNA alterations in patients with castration-resistant prostate cancer.

Alexander W Bray, Rong Duan, Pannaga Malalur, Leylah M Drusbosky, Theodore S Gourdin, Elizabeth G Hill, Michael B Lilly

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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  11. Polygenic anti-cancer activity ofToxicology reports · 2024
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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

7 authors at 3 institutions in 1 country.

Alexander W BrayDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.ORCID 0000-0002-1849-2555
Rong DuanDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Pannaga MalalurThe Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Leylah M DrusboskyGuardant Health, Inc, Redwood City, California, USA.
Theodore S GourdinDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Elizabeth G HillDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Michael B LillyDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Medical University of South Carolina · USGuardant (United States) · USThe Ohio State University Wexner Medical Center · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI John J Lemasters · 2009 to 2026
$42.7M
Sociobiological Responses to Stress in Prostate Cancer SurvivorsU54MD010706 · NIMHD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LENERT, LESLIE A. · 2016 to 2020
$8.0M
NCI NIH HHS P30 CA138313NIMHD NIH HHS U54 MD010706
6 · The paper itself

Abstract

backgroundElevated serum carcinoembryonic antigen (CEA) is used to identify "treatment emergent" forms of castration-resistant prostate cancer (CRPC) such as aggressive variant prostate cancer (AVPC). However, its individual utility as a prognostic marker and the genetic alterations associated with its expression have not been extensively studied in CRPC.

methodsThis study retrospectively analyzed clinical outcomes and circulating tumor DNA profiles in 163 patients with CRPC and elevated or normal serum CEA. These same patients were then classified as AVPC or non-AVPC and compared to determine the uniqueness of CEA-associated gene alterations.

resultsPatients with elevated CEA demonstrated higher rates of liver metastasis (37.5% vs. 19.1%, p = 0.02) and decreased median overall survival from CRPC diagnosis (28.7 vs. 73.2 mo, p < 0.0001). In addition, patients with elevated CEA were more likely to harbor copy number amplifications (CNAs) in AR, PIK3CA, MYC, BRAF, CDK6, MET, CCNE1, KIT, RAF1, and KRAS. Based on variant allele frequency we also defined "clonal" single-nucleotide variants (SNVs) thought to be driving disease progression in each patient and found that CEA expression was negatively correlated with clonal AR SNVs and positively correlated with clonal TP53 SNVs. Of these genetic associations, only the increases in clonal TP53 SNVs and KRAS amplifications were recapitulated among patients with AVPC when compared to patients without AVPC.

conclusionsTogether these findings suggest that CEA expression in CRPC is associated with aggressive clinical behavior and gene alterations distinct from those in AVPC.

Indexed as

Carcinoembryonic AntigenCirculating Tumor DNALiver NeoplasmsProstatic Neoplasms, Castration-ResistantHumansMaleProto-Oncogene Proteins p21(ras)Receptors, AndrogenRetrospective StudiesCarcinoembryonic AntigenCirculating Tumor DNAProto-Oncogene Proteins p21(ras)Receptors, Androgenaggressive variant prostate cancercarcinoembryonic antigencastration resistant prostate cancercirculating tumor DNAgene amplificationsliver metastasis

Identifiers

PMID35766303
PMCPMC9388585
OpenAlexW4283706249

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.