Evidence map›Paper›PMID 32646060›Full record

ArticleInternational journal of molecular sciences2020

A Pilot Study of the Predictive Potential of Chemosensitivity and Gene Expression Assays Using Circulating Tumour Cells from Patients with Recurrent Ovarian Cancer.

Stefano Guadagni, Marco Clementi, Francesco Masedu, Giammaria Fiorentini, Donatella Sarti, Marcello Deraco, Shigeki Kusamura, Ioannis Papasotiriou, Panagiotis Apostolou, Karl Reinhard Aigner and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 20 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

15 authors at 5 institutions in 2 countries.

Stefano GuadagniDepartment of Applied Clinical Sciences and Biotechnology, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0001-8525-084X
Marco ClementiDepartment of Applied Clinical Sciences and Biotechnology, University of L'Aquila, 67100 L'Aquila, Italy.
Francesco MaseduDepartment of Applied Clinical Sciences and Biotechnology, University of L'Aquila, 67100 L'Aquila, Italy.
Giammaria FiorentiniDepartment of Oncology and Hematology, Ospedali Riuniti Marche Nord, 61121 Pesaro, Italy.
Donatella SartiDepartment of Oncology and Hematology, Ospedali Riuniti Marche Nord, 61121 Pesaro, Italy.
Marcello DeracoPeritoneal Surface Malignancies Unit, Colon and Rectal Surgery, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, Italy.
Shigeki KusamuraPeritoneal Surface Malignancies Unit, Colon and Rectal Surgery, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, Italy.
Ioannis PapasotiriouResearch Genetic Cancer Centre International GmbH, 6300 Zug, Switzerland.
Panagiotis ApostolouResearch Genetic Cancer Centre S.A, 53100 Florina, Greece.
Karl Reinhard AignerDepartment of Surgical Oncology, Medias Klinikum GmbH & Co KG, Krankenhausstr. 3a, 84489 Burghausen, Germany.ORCID 0000-0003-2952-6180
Giuseppe ZavattieriDepartment of Surgical Oncology, Medias Klinikum GmbH & Co KG, Krankenhausstr. 3a, 84489 Burghausen, Germany.
Antonietta Rossella FarinaDepartment of Applied Clinical Sciences and Biotechnology, University of L'Aquila, 67100 L'Aquila, Italy.
Giuseppe VizzielliFondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Roma, Italy.
Giovanni ScambiaFondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Roma, Italy.
Andrew Reay MackayDepartment of Applied Clinical Sciences and Biotechnology, University of L'Aquila, 67100 L'Aquila, Italy.
University of L'Aquila · ITAgostino Gemelli University Polyclinic · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITMedias Klinikum · DEOspedali Riuniti Marche Nord · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumour cells (CTCs) from liquid biopsies are under current investigation in several cancers, including epithelial ovarian cancer (EOC) but face significant drawbacks in terms of non-standardised methodology, low viable cell numbers and accuracy of CTC identification. In this pilot study, we report that chemosensitivity assays using liquid biopsy-derived metastatic EOC CTCs, from 10 patients, nine with stage IIIC and one with stage IV disease, in progression after systemic chemotherapy, submitted for hypoxic isolated abdominal perfusion (HAP), are both feasible and useful in predicting response to therapy. Viable metastatic EOC CTCs (>5 cells/mL for all 10 blood samples), enriched by transient culture and identified by reverse transcription polymerase chain reaction (RT-PCR) and indirect immunofluorescence (IF), were subjected to flow cytometry-based Annexin V-PE assays for chemosensitivity to several chemotherapeutic agents and by RT-PCR for tumour gene expression profiling. Using a cut-off value of >80% cell death, CTC chemosensitivity tests were predictive of patient RECIST 1.1 responses to HAP therapy associated with 100% sensitivity, 50% specificity, 33% positive predictive, 100% negative predictive and 60% accuracy values. We propose that the methodology employed in this study is feasible and has the potential to predict response to therapy, setting the stage for a larger study.

Indexed as

AdultAgedAntineoplastic AgentsCarcinoma, Ovarian EpithelialFemaleGene ExpressionGene Expression ProfilingHumansLiquid BiopsyMiddle AgedNeoplasm Recurrence, LocalNeoplastic Cells, CirculatingOvarian NeoplasmsPilot ProjectsAntineoplastic Agentscirculating tumour cellshypoxic isolated abdominal perfusionliquid biopsiesprecision oncotherapyrecurrent ovarian cancer

Identifiers

PMID32646060
PMCPMC7370156
OpenAlexW3040171315

What OpenQuestion holds

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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.