Evidence map›Paper›PMID 32098246›Full record

Trial reportInternational journal of molecular sciences2020

Analysis of Single Circulating Tumor Cells in Renal Cell Carcinoma Reveals Phenotypic Heterogeneity and Genomic Alterations Related to Progression.

Vera Cappelletti, Elena Verzoni, Raffaele Ratta, Marta Vismara, Marco Silvestri, Rosanna Montone, Patrizia Miodini, Carolina Reduzzi, Melanie Claps, Pierangela Sepe and 2 more

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-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

21 citing papers in PubMed, 45 citations in OpenAlex.

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  14. Combinatorial Power of cfDNA, CTCs and EVs in Oncology.Diagnostics (Basel, Switzerland) · 2022
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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 1 institution in 1 country.

Vera CappellettiBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.ORCID 0000-0002-9709-0676
Elena VerzoniDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Raffaele RattaDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Marta VismaraBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.
Marco SilvestriBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.ORCID 0000-0001-8283-9130
Rosanna MontoneClinical Trial Center, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Patrizia MiodiniBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.
Carolina ReduzziBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.
Melanie ClapsDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Pierangela SepeDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Maria Grazia DaidoneBiomarker Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale Tumori di Milano, 20133 Milano, Italy.ORCID 0000-0002-4786-1321
Giuseppe ProcopioDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG2014 Id.15792 and IG2018 Id.21694
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) are promising biomarkers for prognosis, therapeutic response prediction, and treatment monitoring in cancer patients. Despite its epithelial origin, renal cell carcinoma (RCC) shows low expression of epithelial markers hindering CTC-enrichment approaches exploiting epithelial cell surface proteins. In 21 blood samples serially collected from 10 patients with metastatic RCC entering the TARIBO trial, we overcame this limitation using the marker-independent Parsortix™ approach for CTC-enrichment coupled with positive and negative selection with the DEPArray™ with single cell recovery and analysis for copy number alterations (CNA) by next generation sequencing NGS. Two CTC subpopulations were identified: epithelial CTC (eCTC) and non-conventional CTC (ncCTC) lacking epithelial and leukocyte markers. With a threshold ≥1CTC/10 mL of blood, the positivity rates were 28% for eCTC, 62% for ncCTCs, and 71% considering both CTC types. In two patients with detectable eCTCs at baseline, progression free survival was less than 5 months. In an index case, hierarchical structure by translational oncology (TRONCO) identified three clones among 14 CTCs collected at progression and at baseline, each containing cells with a 9p21.3loss, a well-known metastasis driving subclonal alteration. CTCs detection in RCC can be increased by marker-independent approaches, and CTC molecular characterization can allow detection of subclonal events possibly related to tumor progression.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellChromosome DeletionKidney NeoplasmsNeoplastic Cells, CirculatingSingle-Cell AnalysisChromosomes, Human, Pair 9FemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedBiomarkers, Tumorcancer evolutioncirculating tumor cellscopy number alterationsheterogeneityrenal cell cancersingle-cell analysis

Identifiers

PMID32098246
PMCPMC7073151
OpenAlexW3007155651

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.