Evidence map›Paper›PMID 27197300›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2016

Circulating Cancer-Associated Macrophage-Like Cells Differentiate Malignant Breast Cancer and Benign Breast Conditions.

Daniel L Adams, Diane K Adams, R Katherine Alpaugh, Massimo Cristofanilli, Stuart S Martin, Saranya Chumsri, Cha-Mei Tang, Jeffrey R Marks

Open access · bronzeAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 74 citations in OpenAlex.

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  8. Circulating tumor cellsTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2024
    Review
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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

8 authors at 3 institutions in 1 country.

Daniel L AdamsCreatv MicroTech, Inc., Monmouth Junction, New Jersey. dan@creatvmicrotech.com.
Diane K AdamsRutgers, The State University of New Jersey, New Brunswick, New Jersey.
R Katherine AlpaughFox Chase Cancer Center, Philadelphia, Pennsylvania.
Massimo CristofanilliRobert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.
Stuart S MartinUniversity of Maryland School of Medicine, Baltimore, Maryland.
Saranya ChumsriUniversity of Maryland School of Medicine, Baltimore, Maryland. Mayo Clinic Cancer Center, Jacksonville, Florida.
Cha-Mei TangCreatv MicroTech, Inc., Rockville, Maryland.
Jeffrey R MarksDuke University Medical Center, Durham, North Carolina.
Duke Medical Center · USFox Chase Cancer Center · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
EXPRESSION BASED MARKERS FOR BREAST CANCER DETECTIONU01CA084955 · NCI · DUKE UNIVERSITY · PI MARKS, JEFFREY R. · 1999 to 2015
$6.5M
Targeting microtubule stabilization to reduce breast tumor metastasisR01CA154624 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI MARTIN, STUART S · 2012 to 2023
$3.4M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA154624NCI NIH HHS U01 CA084955
6 · The paper itself

Abstract

backgroundBlood-based testing can be used as a noninvasive method to recover and analyze circulating tumor-derived cells for clinical use. Circulating cancer-associated macrophage-like cells (CAML) are specialized myeloid cells found in peripheral blood and associated with the presence of solid malignancies. We measured CAMLs prospectively in peripheral blood to ascertain their prevalence, specificity, and sensitivity in relation to breast disease status at clinical presentation.

methodsWe report on two related but separate studies: 1) CellSieve microfilters were used to isolate CAMLs from blood samples of patients with known malignant disease (n = 41). Prevalence and specificity was compared against healthy volunteers (n = 16). 2) A follow-up double-blind pilot study was conducted on women (n = 41) undergoing core-needle biopsy to diagnose suspicious breast masses.

resultsCAMLs were found in 93% of known malignant patients (n = 38/41), averaging 19.4 cells per sample, but none in the healthy controls. In subjects undergoing core biopsy for initial diagnosis, CAMLs were found in 88% of subjects with invasive carcinoma (n = 15/17) and 26% with benign breast conditions (n = 5/19).

conclusionThese preliminary pilot studies suggest that the presence of CAMLs may differentiate patients with malignant disease, benign breast conditions, and healthy individuals. IMPACT: We supply evidence that this previously unidentified circulating stromal cell may have utility as a screening tool to detect breast cancer in various malignancies, irrespective of disease stage. Cancer Epidemiol Biomarkers Prev; 25(7); 1037-42. ©2016 AACR.

Indexed as

Neoplastic Cells, CirculatingBiomarkers, TumorBiopsyBreast DiseasesBreast NeoplasmsCase-Control StudiesDouble-Blind MethodEarly Detection of CancerFemaleHumansMacrophagesMiddle AgedPilot ProjectsProspective StudiesROC CurveSensitivity and SpecificityBiomarkers, Tumor

Identifiers

PMID27197300
PMCPMC4930681
OpenAlexW2395483593

What OpenQuestion holds

Textmetadata
LicenceTDM
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.