Circulating Tumor Cells Enumerated by a Centrifugal Microfluidic Device as a Predictive Marker for Monitoring Ovarian Cancer Treatment: A Pilot Study.

CA125 centrifugal microfluidic device circulating tumor cells fluid-assisted separation technology ovarian cancer

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
23 Apr 2020
Historique:
received: 17 03 2020
revised: 21 04 2020
accepted: 21 04 2020
entrez: 29 4 2020
pubmed: 29 4 2020
medline: 29 4 2020
Statut: epublish

Résumé

We investigated the size-based isolation and enumeration of circulating tumor cells (CTCs) using a centrifugal microfluidic device equipped with a fluid-assisted separation technology (FAST) disc. We further assessed the correlations among CTCs, cancer antigen-125 (CA125) levels, and clinical course of the disease in a prospective analysis of 47 serial blood samples collected at multiple time-points from 13 ovarian cancer patients. CTCs were isolated from whole blood using the FAST disc and were classified as epithelial cell adhesion molecule (EpCAM)/cytokeratin+, CD45-, and 4',6-diamidino-2-phenylindole (DAPI)+. Mean CTC count at baseline was 20.2; 84.62% of patients had more than one CTC at baseline and had decreased CTCs counts after surgery and chemotherapy. The CTC counts in eight patients with complete responses were <3. CTC counts were correlated with CA125 levels in three patients without recurrence; they were elevated in three patients with recurrence and normal CA125 concentrations. CTC counts and CA125 levels showed high concordance with directional changes (increasing 71.4%; non-increasing 75.0%). CTC counts showed higher associations with clinical status, sensitivity (100.0% vs. 60.0%), positive predictive value (55.6% vs. 42.9%), and negative predictive value (100.0% vs. 87.5%) than CA125 levels. CTC counts were better associated with treatment response and recurrence than CA125 levels.

Identifiants

pubmed: 32340330
pii: diagnostics10040249
doi: 10.3390/diagnostics10040249
pmc: PMC7236001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Korean government
ID : IBS-R020-D1
Organisme : Ministry of Health & Welfare, Republic of Korea
ID : A121994

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Auteurs

Hyera Kim (H)

Division of Hematology/Oncology, Department of Internal Medicine, Keimyung University Dongsan Hospital, Daegu 42601, Korea.

Minji Lim (M)

Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan 44919, Korea.
Department of Biomedical Engineering, School of Life Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.

Jin Young Kim (JY)

Division of Hematology/Oncology, Department of Internal Medicine, Keimyung University Dongsan Hospital, Daegu 42601, Korea.

So-Jin Shin (SJ)

Department of Obstetrics and Gynecology, Keimyung University Dongsan Hospital, Daegu 42601, Korea.

Yoon-Kyoung Cho (YK)

Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan 44919, Korea.
Department of Biomedical Engineering, School of Life Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.

Chi Heum Cho (CH)

Department of Obstetrics and Gynecology, Keimyung University Dongsan Hospital, Daegu 42601, Korea.

Classifications MeSH