Evidence map›Paper›PMID 34077597›Full record

Observational studyThe oncologist2021

Prognostic Role of Circulating Tumor Cells in Metastatic Renal Cell Carcinoma: A Large, Multicenter, Prospective Trial.

Umberto Basso, Antonella Facchinetti, Elisabetta Rossi, Marco Maruzzo, Vincenza Conteduca, Michele Aieta, Francesco Massari, Anna Paola Fraccon, Claudia Mucciarini, Teodoro Sava and 13 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Trial
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  8. Article
  9. Article
  10. Review
  11. Review
  12. Management of Renal Cell Carcinoma: Promising Biomarkers and the Challenges to Reach the Clinic.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Review
  13. Article
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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

23 authors.

Umberto BassoOncology Unit 1, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0002-5075-2177
Antonella FacchinettiImmunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0002-5628-5899
Elisabetta RossiImmunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0002-5242-9568
Marco MaruzzoOncology Unit 1, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0002-6256-9249
Vincenza ConteducaDepartment of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.ORCID 0000-0002-6921-714X
Michele AietaDepartment of Onco-Hematology, Division of Medical Oncology, Centro di Riferimento Oncologico della Basilicata IRCCS, Rionero in Vulture, Italy.ORCID 0000-0001-9487-6238
Francesco MassariDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.ORCID 0000-0001-6476-6871
Anna Paola FracconMedical Oncology, Ospedale P. Pederzoli, Peschiera Del Garda, Peschiera Del Garda (VR), Italy.
Claudia MucciariniMedical Oncology Unit, Ramazzini Hospital, Carpi-AUSL Modena, Modena, Italy.
Teodoro SavaMedical Oncology, Ospedale Borgo Trento, Verona, Italy.
Matteo SantoniMedical Oncology, Polytechnic University of the Marche Region, Azienda Ospedaliero-Universitaria, Ospedali Riuniti Umberto I-GM Lancisi and G Salesi, Ancona, Italy.ORCID 0000-0001-7340-6173
Cristina PegoraroMedical Oncology Ospedale di Montecchio Maggiore, Azienda ULSS 8 Berica, Berica, Italy.
Emilia DuranteDepartment of Medical Oncology, Ospedale di Legnago, Azienda ULSS 9 Scaligera, Scaligera, Italy.
Maurizio NicodemoDepartment of Medical Oncology, Sacro Cuore - Don Calabria Hospital, Negrar, Italy.
Alessandra PerinMedical Oncology, Polo Unico Ospedale Santorso, Santorso, Azienda ULSS 7 Pedemontana, Pedemontana, Italy.
Alessandra BearzDepartment of Medical Oncology, Centro Riferimento Oncologico CRO IRCCS, Aviano, Italy.ORCID 0000-0003-1020-2338
Carlo GattiMedical Oncology, Ospedale di Chioggia, Azienda ULSS 3 Serenissima, Chioggia, Italy.
Pasquale FiducciaClinical Research Unit, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
Alberto DiminuttoOncology Unit 1, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
Carmen BarileMedical Oncology, Ospedale di Rovigo, Azienda ULSS 5 Polesana, Rovigo, Italy.
Ugo De GiorgiDepartment of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.ORCID 0000-0001-7520-2908
Rita Zamarchi *Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0001-6435-2257
Vittorina Zagonel *Oncology Unit 1, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.ORCID 0000-0002-0829-2525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCirculating tumor cells (CTCs) correlate with adverse prognosis in patients with breast, colorectal, lung, and prostate cancer. Little data are available for renal cell carcinoma (RCC). MATERIALS AND

methodsWe designed a multicenter prospective observational study to assess the correlation between CTC counts and progression-free survival (PFS) in patients with metastatic RCC treated with an antiangiogenic tyrosine kinase inhibitor as a first-line regimen; overall survival (OS) and response were secondary objectives. CTC counts were enumerated by the CellSearch system at four time points: day 0 of treatment, day 28, day 56 and then at progression, or at 12 months in the absence of progression.

resultsOne hundred ninety-five eligible patients with a median age of 69 years were treated with sunitinib (77.5%) or pazopanib (21%). At baseline, 46.7% of patients had one or more CTCs per milliliter (range, 1 to 263). Thirty patients had at least three CTCs, with a median PFS of 5.8 versus 15 months in the remaining patients (p = .002; hazard ratio [HR], 1.99), independently of the International Metastatic RCC Database Consortium score at multivariate analysis (HR, 1.91; 95% confidence interval [CI], 1.16-3.14). Patients with at least three CTCs had a shorter estimated OS of 13.8 months versus 52.8 months in those with fewer than three CTCs (p = .003; HR, 1.99; multivariate analysis HR, 1.67; 95% CI, 0.95-2.93). Baseline CTC counts did not correlate with response; neither did having CTC sequencing counts greater than or equal to one, two, three, four, or five.

conclusionWe provide prospective evidence that the presence of three or more CTCs at baseline is associated with a significantly shorter PFS and OS in patients with metastatic RCC. IMPLICATIONS FOR PRACTICE: This prospective study evaluated whether the presence of circulating tumor cells (CTCs) in the peripheral blood correlates with activity of first-line tyrosine kinase inhibitors in metastatic renal cell carcinoma (RCC). This study demonstrated that almost half of patients with metastatic RCC have at least one CTC in their blood and that those patients with at least three CTCs are at increased risk of early progressive disease and early death due to RCC. Studies incorporating CTC counts in the prognostic algorithms of metastatic RCC are warranted.

Indexed as

Breast NeoplasmsCarcinoma, Renal CellKidney NeoplasmsNeoplastic Cells, CirculatingAgedBiomarkers, TumorHumansMalePrognosisProspective StudiesBiomarkers, TumorBiomarkerCirculating tumor cellsMetastasesPazopanibRenal cell carcinomaSunitinib

Identifiers

PMID34077597
PMCPMC8417856

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.