Evidence map›Paper›PMID 36479077›Full record

ArticleFrontiers in oncology2022

Obinutuzumab plus chlorambucil versus ibrutinib in previously untreated chronic lymphocytic leukemia patients without TP53 disruptions: A real-life CLL campus study.

Andrea Visentin, Francesca Romana Mauro, Gioachino Catania, Alberto Fresa, Candida Vitale, Alessandro Sanna, Veronica Mattiello, Francesca Cibien, Paolo Sportoletti, Massimo Gentile and 17 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 13 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

27 authors at 16 institutions in 1 country.

Andrea VisentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padova, Italy.
Francesca Romana MauroHematology, Department of Translational and Precision Medicine, "Sapienza" University, Rome, Italy.
Gioachino CataniaDivision of Hematology, Hospital Saints (A. O. SS) Antonio e Biagio and Cesare Arrigo, Alessandria, Italy.
Alberto FresaHematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.
Candida VitaleDepartment of Molecular Biotechnology and health Sciences, University of Torino and Division of Hematology, University Hospital (A.O.U.) Città della Salute e della Scienza di Torino, Torino, Italy.
Alessandro SannaHematology Unit, Careggi Hospital, Florence, Italy.
Veronica MattielloHematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore, University of Milan, Milan, Italy.
Francesca CibienHematology Unit, Ca' Foncello Hospital, Treviso, Italy.
Paolo SportolettiHematology and Clinical Immunology Unit, University of Perugia, Perugia, Italy.
Massimo GentileHematology Section, Cosenza Hospital, Cosenza, Italy.
Gian Matteo RigolinHematology Section, Department of Medical Sciences, Azienda Ospedaliera-Universitaria, Arcispedale S. Anna, University of Ferrara, Ferrara, Italy.
Francesca Maria QuagliaDepartment of Medicine, Section of Hematology, University of Verona and Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Roberta MurruHematology and Stem Cell Transplantation Unit, Ospedale A. Businco ARNAS "G. Brotzu", Cagliari, Italy.
Alessandro GozzettiHematology Unit, University of Siena, Siena, Italy.
Stefano MolicaDepartment Hematology-Oncology, Azienda Ospedaliera Pugliese-Ciaccio, Catanzaro, Italy.
Monia MarchettiDivision of Hematology, Hospital Saints (A. O. SS) Antonio e Biagio and Cesare Arrigo, Alessandria, Italy.
Stefano PravatoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padova, Italy.
Francesco AngotziHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padova, Italy.
Alessandro CelliniHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padova, Italy.
Lydia ScarfòStrategic Program on CLL, University Health and Science "San Raffaele", Milan, Italy.
Gianluigi RedaHematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore, University of Milan, Milan, Italy.
Marta CosciaDepartment of Molecular Biotechnology and health Sciences, University of Torino and Division of Hematology, University Hospital (A.O.U.) Città della Salute e della Scienza di Torino, Torino, Italy.
Luca LaurentiHematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.
Paolo GhiaStrategic Program on CLL, University Health and Science "San Raffaele", Milan, Italy.
Robin FoàHematology, Department of Translational and Precision Medicine, "Sapienza" University, Rome, Italy.
Antonio CuneoHematology Section, Department of Medical Sciences, Azienda Ospedaliera-Universitaria, Arcispedale S. Anna, University of Ferrara, Ferrara, Italy.
Livio TrentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padova, Italy.
University of Padua · ITAgostino Gemelli University Polyclinic · ITAzienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITSapienza University of Rome · ITUniversity of Ferrara · ITUniversity of Turin · ITAzienda Ospedaliera di Cosenza · ITAzienda Ospedaliera G. Brotzu · ITAzienda Ospedaliera Pugliese Ciaccio · ITAzienda Ospedaliero-Universitaria Careggi · ITCa' Foncello Hospital · ITUniversity of Perugia · ITUniversity of Siena · ITUniversity of Verona · ITVeneto Institute of Molecular Medicine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the main issues in the treatment of patients with chronic lymphocytic leukemia (CLL) deals with the choice between continuous or fixed-duration therapy. Continuous ibrutinib (IB), the first-in-class BTK inhibitor, and obinutuzumab-chlorambucil (G-CHL) are commonly used therapies for elderly and/or comorbid patients. No head-to-head comparison has been carried out. Within the Italian campus CLL network, we performed a retrospective study on CLL patients without TP53 disruption treated with IB or G-CHL as first-line therapy. Patients in the G-CHL arm had a higher CIRS score and the worst renal function. The overall response rates between the G-CHL and IB arms were similar, but more complete remissions (CRs) were achieved with G-CHL (

Indexed as

economic impactibrutinibMRDobinutizumabtreatment-naive

Identifiers

PMID36479077
PMCPMC9719965
OpenAlexW4309787431

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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.