Evidence map›Paper›PMID 34885114›Full record

ArticleCancers2021

Multiparametric Circulating Tumor Cell Analysis to Select Targeted Therapies for Breast Cancer Patients.

André Franken, Bianca Behrens, Florian Reinhardt, Liwen Yang, Mahdi Rivandi, Francesco Marass, Bernadette Jaeger, Natalia Krawczyk, Jan-Philipp Cieslik, Ellen Honisch and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 14 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

21 authors at 4 institutions in 3 countries.

André FrankenDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Bianca BehrensGeneral, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Florian ReinhardtDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Liwen YangDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Mahdi RivandiDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Francesco MarassDepartment of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland.
Bernadette JaegerDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Natalia KrawczykDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Jan-Philipp CieslikDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0001-5102-5919
Ellen HonischDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Hannah AspergerDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0003-3253-7016
Emmanuelle JeannotCirculating Tumor Biomarkers Laboratory, SiRIC, Institut Curie, PSL Research University, 75005 Paris, France.ORCID 0000-0002-4851-7450
Charlotte ProudhonInstitut Curie, INSERM U934/CNRS UMR3215, PSL Research University, 75248 Paris, France.ORCID 0000-0002-4649-4574
Niko BeerenwinkelDepartment of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland.ORCID 0000-0002-0573-6119
Natali SchölermannFrauenarztpraxis Dr. med. Natali Schölermann, 42781 Haan, Germany.
Irene EspositoInstitute of Pathology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0002-0554-2402
Frederic DietzelDepartment of Diagnostic and Interventional Radiology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0002-0005-1700
Nikolas H StoeckleinGeneral, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Dieter NiederacherDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Tanja FehmDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.
Hans NeubauerDepartment of Obstetrics and Gynecology, University Hospital and Medical Faculty of the Heinrich-Heine University Duesseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0002-3467-4105
Düsseldorf University Hospital · DESIB Swiss Institute of Bioinformatics · CHCentre National de la Recherche Scientifique · FRUniversité Paris Sciences et Lettres · FR

Funding

Brigitte and Dr. Konstanze Wegener Foundation 67German Cancer Aid 70112504
6 · The paper itself

Abstract

backgroundThe analysis of liquid biopsies, e.g., circulating tumor cells (CTCs) is an appealing diagnostic concept for targeted therapy selection. In this proof-of-concept study, we aimed to perform multiparametric analyses of CTCs to select targeted therapies for metastatic breast cancer patients.

methodsFirst, CTCs of five metastatic breast cancer patients were analyzed by whole exome sequencing (WES). Based on the results, one patient was selected and monitored by longitudinal and multiparametric liquid biopsy analyses over more than three years, including WES, RNA profiling, and in vitro drug testing of CTCs.

resultsMutations addressable by targeted therapies were detected in all patients, including mutations that were not detected in biopsies of the primary tumor. For the index patient, the clonal evolution of the tumor cells was retraced and resistance mechanisms were identified. The AKT1 E17K mutation was uncovered as the driver of the metastatic process. Drug testing on the patient's CTCs confirmed the efficacy of drugs targeting the AKT1 pathway. During a targeted therapy chosen based on the CTC characterization and including the mTOR inhibitor everolimus, CTC numbers dropped by 97.3% and the disease remained stable as determined by computer tomography/magnetic resonance imaging.

conclusionThese results illustrate the strength of a multiparametric CTC analysis to choose and validate targeted therapies to optimize cancer treatment in the future. Furthermore, from a scientific point of view, such studies promote the understanding of the biology of CTCs during different treatment regimens.

Indexed as

AKT1breast cancercirculating tumor cellstargeted therapywhole exome sequencing

Identifiers

PMID34885114
PMCPMC8657376
OpenAlexW3215991548

What OpenQuestion holds

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Registered trials

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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.