Evidence map›Paper›PMID 35565422›Full record

ArticleCancers2022

Compassionate Use Program of Ipilimumab and Nivolumab in Intermediate or Poor Risk Metastatic Renal Cell Carcinoma: A Large Multicenter Italian Study.

Umberto Basso, Federico Paolieri, Mimma Rizzo, Ugo De Giorgi, Sergio Bracarda, Lorenzo Antonuzzo, Francesco Atzori, Giacomo Cartenì, Giuseppe Procopio, Lucia Fratino and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Article
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 18 institutions in 1 country.

Umberto BassoOncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, 35128 Padova, Italy.ORCID 0000-0002-5075-2177
Federico PaolieriMedical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, 43126 Pisa, Italy.
Mimma RizzoDivision of Translational Oncology, IRCCS Istituti Clinici Scientifici Maugeri, 27100 Pavia, Italy.
Ugo De GiorgiDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", 47014 Meldola, Italy.ORCID 0000-0001-7520-2908
Sergio BracardaMedical and Translational Oncology Unit, Azienda Ospedaliera Santa Maria, 05100 Terni, Italy.
Lorenzo AntonuzzoClinical Oncology Unit, Careggi University Hospital, 50135 Florence, Italy.
Francesco AtzoriMedical Oncology, Azienda Ospedaliero-Universitaria, 09124 Cagliari, Italy.ORCID 0000-0002-8211-0363
Giacomo CartenìOncology Unit, Azienda Ospedaliera di Rilievo Nazionale "Antonio Cardarelli"-AORN A. Cardarelli, 80131 Napoli, Italy.
Giuseppe ProcopioDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Lucia FratinoMedical Oncology Unit, Centro di Riferimento Oncologico CRO IRCCS, 33081 Aviano (PN), Italy.ORCID 0000-0002-5550-0868
Manolo D'ArcangeloDepartment of Oncology and Hematology, Azienda Unità Sanitaria Locale della Romagna, 48121 Ravenna, Italy.ORCID 0000-0003-0409-7762
Giuseppe FornariniMedical Oncology Unit 1, Ospedale Policlinico San Martino IRCCS, 16132 Genova, Italy.ORCID 0000-0003-4754-6572
Paolo ZucaliDepartment of Biomedical Sciences, Humanitas University, 20090 Milan, Italy.
Antonio CusmaiDon Tonino Bello Oncology, Istituto Tumori IRCCS Giovanni Paolo II, 70124 Bari, Italy.
Matteo SantoniOncology Unit, Macerata Hospital, 62100 Macerata, Italy.
Stefania PipitoneDepartment of Oncology and Hematology, University of Modena and Reggio Emilia, Azienda Ospedaliero Universitaria of Modena, 41125 Modena, Italy.
Claudia CarellaMedical Oncology Unit, Istituto Tumori IRCCS Giovanni Paolo II, 70124 Bari, Italy.
Stefano PanniMedical Oncology Unit, ASST di Cremona, 26100 Cremona, Italy.
Filippo Maria DeppieriOncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, 35128 Padova, Italy.ORCID 0000-0001-5959-2432
Vittorina ZagonelOncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, 35128 Padova, Italy.
Giampaolo TortoraUniversità Cattolica del Sacro Cuore, 00168 Rome, Italy.
Istituto Oncologico Veneto · ITIstituto Tumori Bari · ITAzienda Ospedaliera S.Maria · ITAzienda Ospedaliera Universitaria Pisana · ITAzienda Ospedaliero-Universitaria Cagliari · ITAzienda Ospedaliero-Universitaria Careggi · ITAzienda Unità Sanitaria Locale Della Romagna · ITCentro di Riferimento Oncologico · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITHumanitas University · ITIstituti Clinici Scientifici Maugeri · ITIstituti Ospitalieri di Cremona · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITOspedale Antonio Cardarelli · ITOspedale di MacerataOspedale Policlinico San Martino · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This is a retrospective analysis on the safety and activity of compassionate Ipilimumab and Nivolumab (IPI-NIVO) administered to patients with metastatic Renal Cell Carcinoma (mRCC) with intermediate or poor International Metastatic RCC Database Consortium (IMDC) score as a first-line regimen. IPI was infused at 1 mg/kg in combination with Nivolumab 3 mg/kg every three weeks for four doses, followed by maintenance Nivolumab (240 or 480 mg flat dose every two or four weeks, respectively) until disease progression or unacceptable toxicity. A total of 324 patients started IPI-NIVO at 86 Italian centers. Median age was 62 years, 68.2% IMDC intermediate risk. Primary tumor had been removed in 65.1% of patients. Two hundred and twenty patients (67.9%) completed the four IPI-NIVO doses. Investigator-assessed overall response rate was 37.6% (2.8% complete). Twelve-month survival rate was 66.8%, median progression-free survival was 8.3 months. Grade 3 or 4 treatment-related adverse events occurred in 67 patients (26.9%). IMDC intermediate risk, nephrectomy, BMI ≥ 25 kg/m2, and steroid use for toxicities correlated with improved survival, while age < 70 years did not. IPI-NIVO combination is a feasible and effective regimen for the first-line treatment of intermediate-poor IMDC risk mRCC patients in routine clinical practice.

Indexed as

immune-related adverse eventsipilimumabmetastatic Renal Cell Carcinomanivolumabprogressionretrospectivesurvivaltoxicity

Identifiers

PMID35565422
PMCPMC9105283
OpenAlexW4225397957

What OpenQuestion holds

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LicenceCC BY
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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.