Evidence map›Paper›PMID 32883002›Full record

ReviewInternational journal of molecular sciences2020

CDK4/6 Inhibitors in Breast Cancer Treatment: Potential Interactions with Drug, Gene, and Pathophysiological Conditions.

Rossana Roncato, Jacopo Angelini, Arianna Pani, Erika Cecchin, Andrea Sartore-Bianchi, Salvatore Siena, Elena De Mattia, Francesco Scaglione, Giuseppe Toffoli

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 6 pooled it
–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

48 citing papers in PubMed, 6 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Pooled it
  4. Association of germlineFrontiers in pharmacology · 2026
    Pooled it
  5. Pooled it
  6. Pooled it
  7. Observational
  8. Assessment and Density Functional Theory of Bioactive Compounds ofPharmaceuticals (Basel, Switzerland) · 2026
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
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  15. Review
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  19. Retrospective registry of patients with locally advanced/metastatic HRClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  20. 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

9 authors.

Rossana RoncatoExperimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.ORCID 0000-0002-4219-6182
Jacopo AngeliniDepartment of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Arianna PaniDepartment of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Erika CecchinExperimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.ORCID 0000-0001-7517-7490
Andrea Sartore-BianchiDepartment of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.ORCID 0000-0003-0780-0409
Salvatore SienaDepartment of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Elena De MattiaExperimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.ORCID 0000-0003-4948-8767
Francesco ScaglioneDepartment of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.ORCID 0000-0002-8554-2401
Giuseppe ToffoliExperimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.ORCID 0000-0002-5323-4762

Funding

Ministero della Salute [no grant number provided]
6 · The paper itself

Abstract

Palbociclib, ribociclib, and abemaciclib belong to the third generation of cyclin-dependent kinases inhibitors (CDKis), an established therapeutic class for advanced and metastatic breast cancer. Interindividual variability in the therapeutic response of CDKis has been reported and some individuals may experience increased and unexpected toxicity. This narrative review aims at identifying the factors potentially concurring at this variability for driving the most appropriate and tailored use of CDKis in the clinic. Specifically, concomitant medications, pharmacogenetic profile, and pathophysiological conditions could influence absorption, distribution, metabolism, and elimination pharmacokinetics. A personalized therapeutic approach taking into consideration all factors potentially contributing to an altered pharmacokinetic/pharmacodynamic profile could better drive safe and effective clinical use.

Indexed as

Molecular Targeted TherapyAnimalsBreast NeoplasmsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6FemaleHumansProtein Kinase InhibitorsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Protein Kinase Inhibitorsbreast cancercyclin-dependent kinases inhibitorspersonalized medicine

Identifiers

PMID32883002
PMCPMC7504705

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.