Evidence map›Paper›PMID 38914928›Full record

Observational studyBMC cancer2024

International multicenter real-world REGistry for patients with metastatic renAL cell carcinoma - Meet-URO 33 study (REGAL study).

Sara Elena Rebuzzi, Giuseppe Fornarini, Alessio Signori, Sebastiano Buti, Giuseppe Procopio, Ugo De Giorgi, Sandro Pignata, Emanuele Naglieri, Marco Maruzzo, Giuseppe Luigi Banna and 5 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

15 authors.

Sara Elena Rebuzzi *Medical Oncology Unit, Ospedale San Paolo, Savona, Italy.
Giuseppe Fornarini *Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Alessio SignoriDepartment of Health Sciences (DISSAL), Section of Biostatistics, University of Genova, Genova, Italy.
Sebastiano ButiMedical Oncology Unit, University Hospital of Parma, Parma, Italy. sebabuti@libero.it.
Giuseppe ProcopioMedical Oncology, Fondazione IRCCS - Istituto Nazionale dei Tumori, Milano, Italy.
Ugo De GiorgiMedical Oncology Department, IRCCS Istituto Romagnolo per lo studio dei tumori (IRST) "Dino Amadori", Meldola, Italy.
Sandro PignataDepartment of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.
Emanuele NaglieriU.O. Oncologia, IRCCS Istituto Tumori Giovanni Paolo II, Bari, Italy.
Marco MaruzzoIOV - IRCCS, Oncologia 1, Istituto Oncologico Veneto, Padova, Italy.
Giuseppe Luigi BannaPortsmouth Hospitals University NHS Trust, Portsmouth, PO6 3LY, UK.
Pasquale RescignoTranslational and Clinical Research Institute, Centre for Cancer, Newcastle University, Newcastle Upon Tyne, UK.
Carlo MessinaOncology Unit, ARNAS Civico, Palermo, Italy.
Alvise MattanaIOV - IRCCS, Oncologia 1, Istituto Oncologico Veneto, Padova, Italy.
Umberto Basso *IOV - IRCCS, Oncologia 1, Istituto Oncologico Veneto, Padova, Italy.
Davide Bimbatti *IOV - IRCCS, Oncologia 1, Istituto Oncologico Veneto, Padova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNowadays, different therapeutic options are available for the first-line treatment of metastatic renal cell carcinoma (mRCC). Immuno-combinations are the standard first-line therapy in all mRCC patients regardless of the International Metastatic RCC Database Consortium (IMDC) risk category, even though TKI monotherapy is still a therapeutic option in selected patients. However, comparisons between the different first-line treatment strategies are lacking and few real-world data are available in this setting. For this reason, the regimen choice represents an important issue in clinical practice and the optimal treatment sequence remains unclear.

methodsThe REGAL study is a multicentric prospective observational study enrolling mRCC patients treated with first-line systemic therapy according to clinical practice in a real-world setting. A retrospective cohort of mRCC patients who received first-line systemic therapy from the 1st of January 2021 will also be included. The primary objective is to identify potential prognostic and predictive factors that could help guide the treatment choice; secondary objectives included the assessment of the prognostic performance of the novel prognostic Meet-URO score (IMDC score + neutrophil-to-lymphocyte ratio + bone metastases) compared with the IMDC score and the comparison between treatment strategies according to response and survival outcomes and toxicity profile. DISCUSSION: Considering the high number of therapeutic first-line strategies available for mRCC, the identification of clinical prognostic and predictive factors to candidate patients to a preferable systemic therapy is still an unmet clinical need. The Meet-URO 33 study aims to provide a large-scale real-world database on mRCC patients, to identify the clinical predictive and prognostic factors and the different performances between the ICI-based combinations according to response, survival and toxicity.

trial registrationCESC IOV 2023-78.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsRegistriesAgedFemaleHumansMaleMiddle AgedPrognosisProspective StudiesRetrospective StudiesClinical practiceIMDC scoreImmune checkpoint inhibitorImmunotherapyMeet-URO scoreMetastatic renal cell carcinomaProspectiveReal-worldRetrospective

Identifiers

PMID38914928
PMCPMC11194925

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.