Evidence map›Paper›PMID 34525181›Full record

ArticleBlood advances2021

Do age, fitness, and concomitant medications influence management and outcomes of patients with CLL treated with ibrutinib?

Alessandra Tedeschi, Anna Maria Frustaci, Francesca Romana Mauro, Annalisa Chiarenza, Marta Coscia, Stefania Ciolli, Gianluigi Reda, Luca Laurenti, Marzia Varettoni, Roberta Murru and 21 more

Abstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Trial
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  4. Fitness in CLL.Cancers · 2026
    Review
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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

31 authors.

Alessandra TedeschiDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Anna Maria FrustaciDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Francesca Romana MauroHematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
Annalisa ChiarenzaDivision of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
Marta CosciaDivision of Hematology, AOU Città della Salute e della Scienza di Torino, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Stefania CiolliDepartment of Hematology, Università degli Studi di Firenze, Firenze, Italy.
Gianluigi RedaDepartment of Hematology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.
Luca LaurentiHematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Roma, Italy.ORCID 0000-0002-8327-1396
Marzia VarettoniDivision of Hematology Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Roberta MurruHematology and Stem Cell Transplantation Unit, Ospedale A. Businco, ARNAS "G. Brotzu," Cagliari, Italy.
Claudia BaratèDepartment of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Paolo SportolettiDivision of Hematology and Clinical Immunology, Department of Medicine, University of Perugia, Perugia, Italy.
Antonino GrecoDepartment of Hematology, Azienda Ospedaliera Giovanni Panìco, Tricase, Italy.
Chiara BorellaDepartment of Hematology, Ospedale San Gerardo, Monza, Italy.
Valentina RossiHematology & Transfusion Medicine L. Sacco University Hospital and School of Medicine, Milano, Italy; and.
Marina DeodatoDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Annalisa BiagiHematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.
Giulia ZamprognaDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Angelo Curto PelleDivision of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
Gianfranco LapietraHematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
Candida VitaleDivision of Hematology, AOU Città della Salute e della Scienza di Torino, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.ORCID 0000-0002-2592-8724
Francesca MorelliDepartment of Hematology, Università degli Studi di Firenze, Firenze, Italy.
Ramona CassinDepartment of Hematology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.
Alberto FresaHematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Roma, Italy.
Chiara CavalloniDivision of Hematology Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Massimiliano PostorinoHematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.
Claudia IeloHematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
Roberto CairoliDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Francesco Di RaimondoDivision of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
Marco MontilloDepartment of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Giovanni Del PoetaHematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional reserve of organs and systems is known to be relevant in predicting immunochemotherapy tolerance. Age and comorbidities, assessed by the cumulative illness rating scale (CIRS), have been used to address chemotherapy intensity. In the ibrutinib era, it is still unclear whether age, CIRS, and Eastern Cooperative Oncology Group performance status (ECOG-PS) retain their predictive role on treatment vulnerability. In this series of 712 patients with chronic lymphocytic leukemia (CLL) treated with ibrutinib outside clinical trials, baseline ECOG-PS and neutropenia resulted as the most accurate predictors of treatment feasibility and outcomes. Age did not independently influence survival and ibrutinib tolerance, indicating that not age per se, but age-related conditions, may affect drug management. We confirmed the role of CIRS > 6 as a predictor of a poorer progression- and event-free survival (PFS, EFS). The presence of a severe comorbidity was significantly associated with permanent dose reductions (PDRs), not translating into worse outcomes. As expected, del(17p) and/or TP53mut and previous therapies affected PFS, EFS, and overall survival. No study so far has analyzed the influence of concomitant medications and CYP3A inhibitors with ibrutinib. In our series, these factors had no impact, although CYP3A4 inhibitors use correlated with Cox regression analysis, with an increased risk of PDR. Despite the limitation of its retrospective nature, this large study confirmed the role of ECOG-PS as the most accurate predictor of ibrutinib feasibility and outcomes, and importantly, neutropenia emerged as a relevant tool influencing patients' vulnerability. Although CIRS > 6 retained a significant impact on PFS and EFS, its value should be confirmed by prospective studies.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellPharmaceutical PreparationsAdenineHumansPiperidinesProspective StudiesRetrospective StudiesAdenineibrutinibPharmaceutical PreparationsPiperidines

Identifiers

PMID34525181
PMCPMC8714729

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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.