Evidence map›Paper›PMID 33569295›Full record

ArticleTranslational lung cancer research2021

A fully automated assay to detect the expression of pan-cytokeratins and of EML4-ALK fusion protein in circulating tumour cells (CTCs) predicts outcome of non-small cell lung cancer (NSCLC) patients.

Elisabetta Rossi, Michele Aieta, Alfredo Tartarone, Aldo Pezzuto, Antonella Facchinetti, Daniele Santini, Paola Ulivi, Vienna Ludovini, Luciana Possidente, Pasquale Fiduccia and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 27 citations in OpenAlex.

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  12. ES-SCLC Patients with PD-L1Biomedicines · 2024
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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

12 authors at 8 institutions in 1 country.

Elisabetta RossiDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Michele AietaCROB-IRCCS - Rionero in Vulture (PZ), Italy.
Alfredo TartaroneCROB-IRCCS - Rionero in Vulture (PZ), Italy.
Aldo PezzutoDepartment of Cardiopulmonary and Vascular Science, S. Andrea Hospital-Sapienza University, Roma, Italy.
Antonella FacchinettiDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Daniele SantiniMedical Oncology Unit, Campus Bio-Medico University, Rome, Italy.
Paola UliviBiosciences Laboratory, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola (FC), Italy.
Vienna LudoviniDepartment of Medical Oncology, Santa Maria della Misericordia Hospital, Perugia, Italy.
Luciana PossidenteCROB-IRCCS - Rionero in Vulture (PZ), Italy.
Pasquale FiducciaVeneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Nadia MinicuciCNR, Neuroscience Institute, Padua, Italy.
Rita ZamarchiVeneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Centro di Riferimento Oncologico della Basilicata · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Oncologico Veneto · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITNeuroscience Institute · ITOspedale Santa Maria · ITUniversità Campus Bio-Medico · ITUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn advanced non-small cell lung cancer (NSCLC) a recent meta-analysis confirms circulating tumour cells (CTCs) as an independent prognostic indicator of progression-free survival (PFS) and overall survival (OS). However, further investigations are necessary to predict and dynamically monitor the therapy in NSCLC patients using CTCs. To this aim, we combined the classical standard assay (SA) with an expanded cytokeratins profile (EA) and quantified the expression of EML4-ALK fusion protein in CTCs.

methodsThe CellSearch (CS) platform-first marked

resultsEA identified a significantly much more number of CTC-positive patients (115 out of 180) than SA (103 out of 192; Chi-square =4.0179, with 1 degrees of freedom, P=0.04502). Similar to SA, EA levels were still associated with patient' outcomes. Furthermore, the expression of EML4-ALK on CTCs allowed stratifying NSCLC patients according to a statistically significant difference in PFS.

conclusionsWe proposed here two novel automated tests, to characterize the expression of specific molecules on CTCs. We demonstrated that these integrated assays are robust and actionable in prospective clinical studies, and in the future could allow clinicians to improve both choice and length of treatment in individual NSCLC patient.

Indexed as

circulating tumour cells (CTCs)cytokeratins (CK)EML4-ALKliquid biopsyNon-small cell lung cancer (NSCLC)

Identifiers

PMID33569295
PMCPMC7867748
OpenAlexW3124198549

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.