Evidence map›Paper›PMID 34338966›Full record

ArticleTargeted oncology2021

Cabozantinib in Pretreated Patients with Metastatic Renal Cell Carcinoma with Sarcomatoid Differentiation: A Real-World Study.

Matteo Santoni, Francesco Massari, Enrique Grande, Giuseppe Procopio, Marc R Matrana, Mimma Rizzo, Ugo De Giorgi, Umberto Basso, Michele Milella, Roberto Iacovelli and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Targeted oncology, 2021. 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
1.2field-weighted citation impact, top 20% 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, 11 citations in OpenAlex.

  1. Review
  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

21 authors at 17 institutions in 3 countries.

Matteo SantoniOncology Unit, Macerata Hospital, Macerata, Italy. mattymo@alice.it.ORCID http://orcid.org/0000-0001-7340-6173
Francesco MassariMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Enrique GrandeDepartment of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain.
Giuseppe ProcopioDepartment of Medical Oncology, Istituto Nazionale dei Tumori IRCCS, Milan, Italy.
Marc R MatranaDepartment of Internal Medicine, Hematology/Oncology, Ochsner Medical Center, New Orleans, LA, USA.
Mimma RizzoMedical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Pavia, Italy.
Ugo De GiorgiDepartment of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.
Umberto BassoDepartment of Medical Oncology, Istituto Oncologico Veneto (IOV) IRCCS, Padua, Italy.
Michele MilellaU.O.C. Oncology, Azienda Ospedaliera Universitaria Integrata, University and Hospital Trust of Verona, Verona, Italy.
Roberto IacovelliMedical Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Gaetano AurilioMedical Oncology Division of Urogenital and Head and Neck Tumours, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Lorena IncorvaiaDepartment of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy.
Sebastiano ButiMedical Oncology Unit, University Hospital of Parma, Parma, Italy.
Orazio CaffoMedical Oncology Department, Santa Chiara Hospital, Trento, Italy.
Giuseppe FornariniMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Francesco CarrozzaOncology Unit, City Hospital, Faenza, Italy.
Veronica MollicaMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Alessandro RizzoMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Fady FaragDepartment of Internal Medicine, Hematology/Oncology, Ochsner Medical Center, New Orleans, LA, USA.
Javier Molina-CerrilloDepartment of MedicalOncology, Hospital Ramón y Cajal, Madrid, Spain.
Nicola BattelliOncology Unit, Macerata Hospital, Macerata, Italy.
Azienda USL di Bologna · ITOchsner Medical Center · USOspedale di MacerataAgostino Gemelli University Polyclinic · ITAzienda Ospedaliera Universitaria Integrata Verona · ITEuropean Institute of Oncology · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITHospital Universitario Ramón y Cajal · ESIstituto Oncologico Veneto · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITMD Anderson Cancer Center Madrid · ESOspedale per gli Infermi · ITOspedale Policlinico San Martino · ITOspedale Santa Chiara · ITUniversity of Palermo · ITUniversity of Parma · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal cell carcinoma with sarcomatoid differentiation is a highly aggressive form of kidney cancer.

objectiveWe aimed to analyze the outcomes of patients treated with cabozantinib for metastatic renal cell carcinoma with sarcomatoid features.

methodsWe retrospectively collected data from 16 worldwide centers. Overall survival and progression-free survival were analyzed using Kaplan-Meier curves. Cox proportional models were used for univariate and multivariate analyses.

resultsWe collected data from 66 patients with metastatic sarcomatoid renal cell carcinoma receiving cabozantinib as second-line (51%) or third-line (49%) therapy. The median progression-free survival from the start of cabozantinib was 7.59 months (95% confidence interval [CI] 5.75-17.49) and was longer in male patients (8.81 vs 5.95 months, p = 0.042) and in patients without bone metastases (7.59 vs 5.11 months, p = 0.010); the median overall survival was 9.11 months (95% CI 7.13-23.80). At the multivariate analysis, female sex (hazard ratio = 1.81; 95% CI 1.02-3.37, p = 0.046), bone metastases (hazard ratio = 2.62; 95% CI 1.34-5.10, p = 0.005), and International Metastatic Renal Cell Carcinoma Database Consortium criteria (hazard ratio = 3.04; 95% CI 1.54-5.99, p = 0.001) were significant predictors of worse overall survival.

conclusionsOur data show that cabozantinib is active in pretreated patients with sarcomatoid renal cell carcinoma. Biomarkers are needed in this field to select patients for multi-kinase inhibitors or other options.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAnilidesCell DifferentiationFemaleHumansMalePyridinesRetrospective StudiesAnilidescabozantinibPyridines

Identifiers

PMID34338966
OpenAlexW3189550989

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.