Evidence map›Paper›PMID 36212433›Full record

ArticleFrontiers in oncology2022

The prognostic value of baseline and early variations of peripheral blood inflammatory ratios and their cellular components in patients with metastatic renal cell carcinoma treated with nivolumab: The Δ-Meet-URO analysis.

Sara Elena Rebuzzi, Alessio Signori, Marco Stellato, Daniele Santini, Marco Maruzzo, Ugo De Giorgi, Paolo Pedrazzoli, Luca Galli, Paolo Andrea Zucali, Emanuela Fantinel and 29 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 4 pooled it
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

19 citing papers in PubMed, 4 syntheses or guidelines pooled it, 14 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

39 authors at 20 institutions in 2 countries.

Sara Elena RebuzziMedical Oncology Unit, Ospedale San Paolo, Savona, Italy.
Alessio SignoriDepartment of Health Sciences, Section of Biostatistics, University of Genova, Genova, Italy.
Marco StellatoSS Oncologia Medica Genitourinaria, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Daniele SantiniDepartment of Medical Oncology, Università Campus Bio-Medico of Roma, Rome, Italy.
Marco MaruzzoOncology Unit 1, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
Ugo De GiorgiDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Paolo PedrazzoliDepartment of Internal Medicine and Medical Therapy, University of Pavia, Pavia, Italy.
Luca GalliMedical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
Paolo Andrea ZucaliDepartment of Biomedical Sciences, Humanitas University, Milano, Italy.
Emanuela FantinelDepartment of Oncology, Azienda Ospedaliera Universitaria Integrata di Verona, University of Verona, Verona, Italy.
Claudia CarellaDivision of Medical Oncology, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
Giuseppe ProcopioSS Oncologia Medica Genitourinaria, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Michele MilellaDepartment of Oncology, Azienda Ospedaliera Universitaria Integrata di Verona, University of Verona, Verona, Italy.
Francesco BoccardoAcademic Unit of Medical Oncology, IRCCS Ospedale Policlinico San Martino of Genova, Genova, Italy.
Lucia FratinoDepartment of Medical Oncology, Centro di Riferimento Oncologico di Aviano CRO-IRCCS, Aviano, Italy.
Roberto SabbatiniMedical Oncology Unit, Department of Oncology and Hemathology, University Hospital of Modena, Modena, Italy.
Riccardo RicottaOncology Unit, IRCCS MultiMedica, Milan, Italy.
Stefano PanniMedical Oncology Unit, ASSTl- Istituti Ospitalieri Cremona Hospital, Cremona, Italy.
Francesco MassariMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Mariella SorarùU. O. Oncologia, Ospedale di Camposampiero, Padova, Italy.
Matteo SantoniOncology Unit, Macerata Hospital, Macerata, Italy.
Alessio CortelliniDepartment of Surgery and Cancer, Imperial College London, Faculty of Medicine, Hammersmith Hospital, London, United Kingdom.
Veronica PratiDepartment of Medical Oncology, Ospedale Michele e Pietro Ferrero, Verduno, Italy.
Hector Josè Soto ParraDepartment of Oncology, Medical Oncology, University Hospital Policlinico-San Marco, Catania, Italy.
Francesco AtzoriMedical Oncology Department, University Hospital, University of Cagliari, Cagliari, Italy.
Marilena Di NapoliDepartment of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.
Orazio CaffoMedical Oncology Department, Santa Chiara Hospital, Trento, Italy.
Marco MessinaUOC Oncologia Medica, Istituto Fondazione G. Giglio, Cefalù, Italy.
Franco MorelliOncology Department, Gemelli Molise, Campobasso, Italy.
Giuseppe PratiDepartment of Oncology and Advanced Technologies AUSL - IRCCS, Reggio Emilia, Italy.
Franco NolèMedical Oncology Division of Urogenital and Head and Neck Tumors, IEO, European Institute of Oncology IRCCS, Milano, Italy.
Francesca VignaniDivision of Medical Oncology, Ordine Mauriziano Hospital, Torino, Italy.
Alessia CavoOncology Unit, Villa Scassi Hospital, Genova, Italy.
Giandomenico RovielloDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Firenze, Firenze, Italy.
Miguel Angel Llaja ObispoMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Camillo PortaInterdisciplinary Department of Medicine, University of Bari "A. Moro", Bari, Italy.
Sebastiano ButiMedical Oncology Unit, University Hospital of Parma, Parma, Italy.
Giuseppe FornariniMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Giuseppe Luigi BannaDepartment of Oncology, Portsmouth Hospitals University NHS Trust, Portsmouth, United Kingdom.
Ospedale Policlinico San Martino · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Verona · ITA. O. Ordine Mauriziano di Torino · ITAzienda Ospedaliera Universitaria Pisana · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITCentro di Riferimento Oncologico · ITEuropean Institute of Oncology · ITFondazione Istituto G. Giglio di Cefalù · ITHumanitas University · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITIstituti Ospitalieri di Cremona · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITIstituto Oncologico Veneto · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITIstituto Tumori Bari · ITMultiMedica · ITOspedale di MacerataOspedale San Paolo · ITOspedale San Pietro Fatebenefratelli · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Treatment choice for metastatic renal cell carcinoma (mRCC) patients is still based on baseline clinical and laboratory factors. Methods: By a pre-specified analysis of the Meet-URO 15 multicentric retrospective study enrolling 571 pretreated mRCC patients receiving nivolumab, baseline and early dynamic variations (Δ) of neutrophil, lymphocyte, and platelet absolute cell counts (ACC) and their inflammatory ratios (IR) were evaluated alongside their association with the best disease response and overall (OS) and progression-free survival (PFS). Multivariable analyses on OS and PFS between baseline and Δ ACC and IR values were investigated with receiving operating curves-based cut-offs. Results: The analysis included 422 mRCC patients. Neutrophil-to-lymphocyte ratio (NLR) increased over time due to consistent neutrophil increase (p < 0.001). Higher baseline platelets (p = 0.044) and lower lymphocytes (p = 0.018), increasing neutrophil Δ (p for time-group interaction <0.001), higher baseline IR values (NLR: p = 0.012, SII: p = 0.003, PLR: p = 0.003), increasing NLR and systemic immune-inflammatory index (SII) (i.e., NLR x platelets) Δ (p for interaction time-group = 0.0053 and 0.0435, respectively) were associated with disease progression. OS and PFS were significantly shorter in patients with baseline lower lymphocytes (p < 0.001 for both) and higher platelets (p = 0.004 and p < 0.001, respectively) alongside early neutrophils Δ (p = 0.046 and p = 0.033, respectively). Early neutrophils and NLR Δ were independent prognostic factors for both OS (p = 0.014 and p = 0.011, respectively) and PFS (p = 0.023 and p = 0.001, respectively), alongside baseline NLR (p < 0.001 for both) and other known prognostic variables. Conclusions: Early neutrophils and NLR Δ may represent new dynamic prognostic factors with clinical utility for on-treatment decisions.

Indexed as

dynamicsimmunotherapyinflammatoryNLRprognosticrenal cell carcinoma

Identifiers

PMID36212433
PMCPMC9541611
OpenAlexW4296844629

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