Evidence map›Paper›PMID 38450313›Full record

ArticleFrontiers in oncology2023

Genomic amplifications identified by circulating tumor DNA analysis guide prognosis in metastatic castration-resistant prostate cancer.

Toros A Dincman, Joseph A Q Karam, Antonio Giordano, Hong Li, Leylah M Drusbosky, Theodore S Gourdin, Philip H Howe, Michael B Lilly

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. 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

8 authors at 4 institutions in 1 country.

Toros A DincmanDepartment of Medicine, Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC, United States.
Joseph A Q KaramDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States.
Antonio GiordanoDepartment of Medicine, Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC, United States.
Hong LiHollings Cancer Center, Medical University of South Carolina, Charleston, SC, United States.
Leylah M DrusboskyGuardant Health, Redwood City, CA, United States.
Theodore S GourdinDepartment of Medicine, Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC, United States.
Philip H HoweDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States.
Michael B LillyDepartment of Medicine, Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC, United States.
Medical University of South Carolina · USMUSC Hollings Cancer Center · USGuardant (United States) · USUniversity of California, Davis · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
South Carolina Clinical & Translational Research Institute (SCTR)KL2TR001452 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MCRAE-CLARK, AIMEE L · 2015 to 2024
$5.9M
NCATS NIH HHS KL2 TR001452NCATS NIH HHS UL1 TR001450
6 · The paper itself

Abstract

Purpose: Analysis of circulating tumor DNA (ctDNA) in patients with metastatic prostate cancer (mPC) provides an opportunity to identify and monitor genomic alterations during a patient's treatment course. We evaluated whether the presence of specific gene amplifications (GAs) and plasma copy number (PCN) alterations are associated with disease features. Methods: This is a single-institution retrospective study of patients with mPC who underwent ctDNA profiling using Guardant360 Results: The presence of liver and/or lung metastases was associated with GAs of Conclusions: The association of select GAs with survival provides an additional tool for assessing mCRPC prognosis and informing management. Serial monitoring of ctDNA GAs is also useful to guide prognosis and therapeutic response.

Indexed as

androgen receptoraneuploidycastration-resistant prostate cancercirculating tumor DNAgenomic amplificationmetastasisPIK3CAprostate cancer

Identifiers

PMID38450313
PMCPMC10915757
OpenAlexW4392013607

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.