Evidence map›Paper›PMID 33061448›Full record

ReviewOncoTargets and therapy2020

Lights and Shade of Next-Generation Pi3k Inhibitors in Chronic Lymphocytic Leukemia.

Andrea Visentin, Federica Frezzato, Filippo Severin, Silvia Imbergamo, Stefano Pravato, Leila Romano Gargarella, Sabrina Manni, Serena Pizzo, Edoardo Ruggieri, Monica Facco and 4 more

Abstract readReview
In one paragraph

Review in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  3. Article
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  5. Review
  6. Therapeutic Monoclonal Antibody Therapies in Chronic Autoimmune Demyelinating Neuropathies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Targeting Protein Kinases in Blood Cancer: Focusing on CK1α and CK2.International journal of molecular sciences · 2021
    Review
  16. 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

14 authors.

Andrea VisentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0003-0271-7200
Federica FrezzatoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0001-7093-2493
Filippo SeverinHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0001-8712-9656
Silvia ImbergamoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.
Stefano PravatoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.
Leila Romano GargarellaHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.
Sabrina ManniHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0001-6804-0680
Serena PizzoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0002-8936-2248
Edoardo RuggieriHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0002-9439-4121
Monica FaccoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0003-0100-5789
Anna Maria BrunatiDepartment of Molecular Medicine, University of Padua, Padua, Italy.ORCID 0000-0002-3481-9503
Gianpietro SemenzatoHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.
Francesco PiazzaHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0002-2831-623X
Livio TrentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padua, Padua, Italy.ORCID 0000-0003-1222-6149

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment (i.e. therapy and management) of chronic lymphocytic leukemia (i.e. the disease) has been improved thanks to the introduction (i.e. approval) of kinase inhibitors during the last years. PI3K is one of the most important kinases at the crossroad to the B-cell receptor and cytokine receptor which play a key role in CLL cell survival, proliferation and migration. Idelalisib is the first in class PI3Kδ inhibitor approved for the treatment of relapsed/refractory CLL in combination with rituximab. Idelalisib activity in heavily treated patients is balanced by recurrent adverse events which limit its long-term use. These limitations prompt the investigation on novel PI3K inhibitors, also targeting different protein isoforms, and alternative schedule strategies. In this regard, duvelisib is the only PI3K γ and δ inhibitor approved as single agent for relapsed CLL. In this review, we will address novel insights on PI3K structure, isoforms, regulating signaling and the most updated data of next-generation PI3K inhibitors in CLL.

Indexed as

chronic lymphocytic leukemiacopanlisibduvelisibPI3K inhibitorumbralisib

Identifiers

PMID33061448
PMCPMC7532889

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.