Literature DB >> 29147869

Hematological adverse effects in breast cancer patients treated with cyclin-dependent kinase 4 and 6 inhibitors: a systematic review and meta-analysis.

Loay Kassem1, Kyrillus S Shohdy2, Shaimaa Lasheen1, Omar Abdel-Rahman3, Thomas Bachelot4.   

Abstract

BACKGROUND: The introduction of specific cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors significantly improved progression-free survival in hormone receptor-positive metastatic breast cancer. CDK 4/6 inhibitors induce cell cycle arrest via liberating the tumor suppressor retinoblastoma protein from CDK4/6 inhibitory effect. Preliminary studies suggested an increase in the hematological toxicities which might affect the quality of life in such palliative setting.
METHODS: We searched PubMed, ASCO, ESMO and San Antonio meeting databases for randomized phase II/III trials in metastatic breast cancer receiving CDK4/6 inhibitors with safety data provided on the incidence of hematological adverse effects.
RESULTS: Our search identified 1012 citations that were screened for relevance. Thirty-six studies were found to be potentially eligible. After excluding the ineligible studies, six studies were deemed to be eligible for meta-analysis. The risk ratio (RR) was 11.31 [95% confidence interval (CI) 8.06-15.87; p < 0.0001] for all-grade leucopenia, 14.86 (95% CI 11.37-19.41; p < 0.0001) for all-grade neutropenia, 9.04 (95% CI 3.78-21.63; p < 0.0001) for all-grade thrombocytopenia and 3.57 (95% CI 2.65-4.81; p < 0.0001) for all-grade anemia. The RR for grade 3/4 leucopenia was 33.86 (95% CI 14.59-78.57; p < 0.0001), for grade 3/4 neutropenia was 44.00 (95% CI 24.72-78.33; p < 0.0001), for grade 3/4 thrombocytopenia was 5.70 (95% CI 2.03-16.01; p = 0.001) and for grade 3/4 anemia was 2.80 (95% CI 1.45-5.41; p = 0.002). There was no significant increase in the RR of febrile neutropenia with RR of 3.29 (95% CI 0.93-11.57; p = 0.06).
CONCLUSION: Our analysis provides evidence that the use of CDK 4/6 inhibitors is associated with an increased risk of all-grade and high-grade hematological adverse events, which seems to be a class-effect, but not of febrile neutropenia compared with hormonal therapy alone.

Entities:  

Keywords:  Abemaciclib; Breast cancer; Hematological toxicity; Palbociclib; Ribociclib

Mesh:

Substances:

Year:  2017        PMID: 29147869     DOI: 10.1007/s12282-017-0818-4

Source DB:  PubMed          Journal:  Breast Cancer        ISSN: 1340-6868            Impact factor:   4.239


  3 in total

Review 1.  Mechanisms of resistance to cyclin-dependent kinase 4/6 inhibitors.

Authors:  Georgia Gomatou; Ioannis Trontzas; Stephanie Ioannou; Maria Drizou; Nikolaos Syrigos; Elias Kotteas
Journal:  Mol Biol Rep       Date:  2021-01-07       Impact factor: 2.316

2.  Targeting cyclin-dependent kinases for the treatment of pulmonary arterial hypertension.

Authors:  Astrid Weiss; Moritz Christian Neubauer; Dinesh Yerabolu; Baktybek Kojonazarov; Beate Christiane Schlueter; Lavinia Neubert; Danny Jonigk; Nelli Baal; Clemens Ruppert; Peter Dorfmuller; Soni Savai Pullamsetti; Norbert Weissmann; Hossein-Ardeschir Ghofrani; Friedrich Grimminger; Werner Seeger; Ralph Theo Schermuly
Journal:  Nat Commun       Date:  2019-05-17       Impact factor: 14.919

3.  Management of Abemaciclib-Associated Adverse Events in Patients with Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer: Safety Analysis of MONARCH 2 and MONARCH 3.

Authors:  Hope S Rugo; Jens Huober; José A García-Sáenz; Norikazu Masuda; Joo Hyuk Sohn; Valerie A M Andre; Susana Barriga; Joanne Cox; Matthew Goetz
Journal:  Oncologist       Date:  2020-10-09
  3 in total

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