Evidence map›Paper›PMID 36765527›Full record

ArticleCancers2023

Multi-Parameter Analysis of Disseminated Tumor Cells (DTCs) in Early Breast Cancer Patients with Hormone-Receptor-Positive Tumors.

Theresa König, Senol Dogan, Anne Kathrin Höhn, Laura Weydandt, Bahriye Aktas, Ivonne Nel

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Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Theresa KönigDepartment of Gynecology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.
Senol DoganDepartment of Gynecology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0001-7358-4850
Anne Kathrin HöhnDepartment of Pathology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.
Laura WeydandtDepartment of Gynecology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0001-5216-3547
Bahriye AktasDepartment of Gynecology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0002-5474-051X
Ivonne NelDepartment of Gynecology, Medical Center, University of Leipzig, 04103 Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with hormone-receptor-positive (HR+) breast cancer are at increased risk for late recurrence. One reason might be disseminated tumor cells (DTCs), which split off in the early stages of the disease and metastasize into the bone marrow (BM).

methodsWe developed a novel multi-parameter immunofluorescence staining protocol using releasable and bleachable antibody-fluorochrome-conjugates. This sequential procedure enabled us to analyze six distinct phenotypical and therapy-related markers on the same DTC. We characterized BM aspirates from 29 patients with a HR+ tumor and a known positive DTC status-based on the standardized detection of epithelial cells in BM.

resultsUsing the immunofluorescence staining, a total of 153 DTCs were detected. Luminal A patients revealed a higher DTC count compared with luminal B. The majority of the detected DTCs were CK-positive (128/153). However, in 16 of 17 luminal A patients we found HER2-positive DTCs. We detected CK-negative DTCs (25/153) in 12 of 29 patients. Of those cells, 76% were Ki67-positive and 68% were HER2-positive. Moreover, we detected DTC clusters consisting of mixed characteristics in 6 of 29 patients.

conclusionsUsing sequential multi-parameter imaging made it possible to identify distinct DTC profiles not solely based on epithelial features. Our findings indicate that characterization rather than quantification of DTCs might be relevant for treatment decisions.

Indexed as

bone marrowbreast cancerdisseminated tumor cellsdormancyHER2hormone receptorproliferation

Identifiers

PMID36765527
PMCPMC9913363

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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.