Evidence map›Paper›PMID 38096474›Full record

ArticleJCO precision oncology2023

Prospective Characterization of Circulating Tumor Cell Kinetics in Patients With Oligometastatic Disease Receiving Definitive Intent Radiation Therapy.

Shivani Sud, Michael J Poellmann, Jacob Hall, Xianming Tan, Jiyoon Bu, Ja Hye Myung, Andrew Z Wang, Seungpyo Hong, Dana L Casey

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 8 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

9 authors at 3 institutions in 1 country.

Shivani SudDepartment of Radiation Oncology University of North Carolina-Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-7713-3771
Michael J PoellmannPharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-0085-3957
Jacob HallDepartment of Radiation Oncology University of North Carolina-Chapel Hill, Chapel Hill, NC.
Xianming TanDepartment of Radiation Oncology University of North Carolina-Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-5478-2269
Jiyoon BuPharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0002-0153-5109
Ja Hye MyungDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Illinois at Chicago, Chicago, IL.ORCID 0000-0001-5726-7302
Andrew Z WangDepartment of Radiation Oncology University of North Carolina-Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-9781-4494
Seungpyo HongPharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0001-9870-031X
Dana L CaseyDepartment of Radiation Oncology University of North Carolina-Chapel Hill, Chapel Hill, NC.ORCID 0000-0001-6851-7653
University of North Carolina at Chapel Hill · USUniversity of Wisconsin–Madison · USUniversity of Illinois Chicago · US

Funding

Project 3: Modulation of the head and neck tumor immune microenvironment by targeting the TAM family of receptorsP50CA278595 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Zachary Scott Morris · 2022 to 2026
$12.5M
Translational Nanosystems for Improved Lung Cancer Treatment with Small MoleculesU54CA151652 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESIMONE, JOSEPH M. · 2010 to 2014
$12.1M
Cooperation of the TAM and Abl family kinases in therapeutic resistance in HNCR01CA262292 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Ravi Salgia, DERIC L WHEELER · 2022 to 2026
$2.9M
Nanoparticle formulations of DNA repair inhibitors to improve chemoradiotherapyR01CA178748 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WANG, ANDREW ZHUANG · 2013 to 2017
$1.6M
NCI NIH HHS P50 CA278595NCI NIH HHS R01 CA178748NCI NIH HHS R01 CA262292NCI NIH HHS U54 CA151652
6 · The paper itself

Abstract

purposeThere are currently no predictive molecular biomarkers to identify patients with oligometastatic disease (OMD) who will benefit from definitive-intent radiation therapy (RT). We prospectively characterized circulating tumor cell (CTC) kinetics in patients with OMD undergoing definitive-intent RT.

methodsThis prospective correlative biomarker study included patients with any solid malignancy ≤5 metastatic sites in ≤3 anatomic organ systems undergoing definitive-intent RT to all disease sites. Circulating tumor cells (CTCs) were captured and enumerated using a biomimetic cell rolling and nanotechnology-based assay functionalized with antibodies against epithelial cell adhesion molecule, against human epidermal growth factor receptor 2, and against epidermal growth factor receptor before and during RT and at follow-up visits up to 2 years post-RT.

resultsWe enrolled 43 patients with a median follow-up of 14.3 months. The pretreatment CTC level (cells captured/mL) was not associated with the number of disease sites (median one metastatic site/patient, range 1-5) or metastasis location (bone, brain, visceral) on Wilcoxon signed-rank test,

conclusionCTCs may serve as a biomarker for disease control in OMD and may predict disease progression before standard assessments for patients receiving diverse cancer-directed therapies.

Indexed as

Neoplastic Cells, CirculatingBiomarkers, TumorDisease ProgressionHumansProspective StudiesBiomarkers, Tumor

Identifiers

PMID38096474
PMCPMC10730071
OpenAlexW4389745625

What OpenQuestion holds

Textmetadata
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.