Evidence map›Paper›PMID 37492625›Full record

ArticleTherapeutic advances in urology

The role of mean corpuscular volume and red cell distribution width in patients with metastatic renal cell carcinoma treated with tyrosine kinase inhibitors: the MARECAP retrospective study.

Chiara Tommasi, Giulia Scartabellati, Diana Giannarelli, Ugo De Giorgi, Nicole Brighi, Giuseppe Fornarini, Sara Elena Rebuzzi, Silvia Puglisi, Orazio Caffo, Stefania Kinspergher and 10 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in urology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Observational
  2. Observational
  3. Article
  4. Review
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

20 authors at 12 institutions in 1 country.

Chiara TommasiMedical Oncology Unit, University Hospital of Parma, Via Gramsci 14, Parma 43126, Italy.ORCID https://orcid.org/0000-0002-9230-9288
Giulia ScartabellatiDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Diana GiannarelliFacility Epidemiology and Biostatistic, G-Step, Fondazione Policlinico Universitario A. Gemelli, Scientific Direction, IRCCS, Rome, Italy.
Ugo De GiorgiIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.
Nicole BrighiIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.
Giuseppe FornariniMedical Oncology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Sara Elena RebuzziMedical Oncology Unit, Ospedale San Paolo, Savona, Italy.
Silvia PuglisiMedical Oncology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Orazio CaffoDepartment of Medical Oncology, Santa Chiara Hospital, Trento, Italy.
Stefania KinspergherDepartment of Medical Oncology, Santa Chiara Hospital, Trento, Italy.
Alessia MennittoDivision of Oncology, University Hospital 'Maggiore della Carità', Novara, Italy.
Carlo CattriniDivision of Oncology, University Hospital 'Maggiore della Carità', Novara, Italy.ORCID https://orcid.org/0000-0003-4785-9480
Matteo SantoniOncology Unit, Macerata Hospital, Macerata, Italy.
Elena VerzoniDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Alessandro RamettaDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Marco StellatoDepartment of Medical Oncology, Università Campus Bio-Medico di Roma, Rome, Italy.ORCID https://orcid.org/0000-0002-0993-7540
Andrea MalgeriDepartment of Medical Oncology, Università Campus Bio-Medico di Roma, Rome, Italy.
Giandomenico RovielloDepartment of Health Sciences, University of Florence, Florence, Italy.
Matteo BrunelliDepartment of Diagnostic and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Sebastiano ButiMedical Oncology Unit, University Hospital of Parma, Parma, Italy.ORCID https://orcid.org/0000-0003-0876-0226
University of Parma · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITOspedale Policlinico San Martino · ITOspedale Santa Chiara · ITUniversità Campus Bio-Medico · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITAgostino Gemelli University Polyclinic · ITOspedale di MacerataOspedale San Paolo · ITUniversity of Florence · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tyrosine-kinase inhibitors (TKIs) and immunotherapy represent the backbone treatment for metastatic renal cell carcinoma (mRCC) patients. The aim of the present study was to describe mean corpuscular volume (MCV) and red cell distribution width (RDW) in mRCC patients treated with pazopanib or cabozantinib, and to explore their potential impact on oncological outcomes. Materials and methods: We conducted a multicenter retrospective observational study in mRCC patients treated with pazopanib or cabozantinib between January 2012 and December 2020 in nine Italian centers. Descriptive statistics, univariate, and multivariate analyses were performed. Objectives: The primary endpoints were the incidence and trend over time of anemia, macrocytosis (elevated MCV), and anisocytosis (elevated RDW). The secondary endpoints were the correlations of MCV and RDW with objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Results: A total of 301 patients were enrolled; mean Hb value was 12.5 g/dl, a mean increase of 1 g/dl was observed at day 15 and maintained at 3 months. Most patients had baseline macrocytosis (MCV levels > 87 fl), with a significant mean increase after 3 months of treatment. At univariate analysis patients with macrocytosis had better ORR, longer PFS, and OS. About one third of patients had baseline anisocytosis (RDW > 16%), with a significant mean increase after 3 months of treatment. At univariate analysis, patients with RDW values ⩽ 16% had higher ORR, longer PFS, and OS. At multivariate analysis, baseline macrocytosis was significantly associated with better PFS in patients treated with pazopanib and baseline anisocytosis with shorter OS in all patients. Conclusions: mRCC patients treated with pazopanib or cabozantinib may have baseline macrocytosis and anisocytosis. A significant increase of Hb, MCV, and RDW after TKIs start was observed. Baseline macrocytosis is positively correlated with PFS in patients treated with pazopanib and baseline anisocytosis affects survival of patients treated with TKIs.

Indexed as

anisocytosiscabozantinibmacrocytosismetastatic renal cell carcinomapazopanibprognostic

Identifiers

PMID37492625
PMCPMC10363886
OpenAlexW4385142864

What OpenQuestion holds

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LicenceCC BY-NC
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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.