Palbociclib: Randomized Studies and Real-world Evidence as the Basis for Therapeutic Planning in Metastatic Breast Cancer

Endocrine-based combination therapy with an inhibitor of the cyclin-dependent kinases 4 and 6 (CDK4/6 inhibitors) is currently the first-line therapy of choice for patients with hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-), locally advanced or metastatic breast cancer (mBC). The efficacy and safety of the treatment with palbociclib, the first CDK4/6 inhibitor approved for this indication, have been confirmed in large randomized controlled clinical trials (RCTs) with strictly defined patient cohorts. Since then, many relevant questions about CDK4/6 inhibition with palbociclib for mBC have been investigated in RCTs and real-world studies. Based on this evidence, palbociclib is widely used in clinical practice since many years because of its efficacy and good tolerability. The aim of this review is to summarize findings from RCTs and RWE considering clinically relevant aspects such as safety, tolerability, quality of life and efficacy with a focus on specific questions and patient characteristics. A critical discussion and review of the overall evidence for endocrine-based therapy with the CDK4/6 inhibitor palbociclib can contribute to support therapy decisions in daily clinical practice.

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Publication Details

Journal
Geburtshilfe und Frauenheilkunde
Published
2024-09-01
DOI
https://doi.org/10.1055/a-2344-5269
Citations
3
Primary Topic
Advanced Breast Cancer Therapies
Type
article
Field-Weighted Citation Impact
1.26

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article

Palbociclib: Randomized Studies and Real-world Evidence as the Basis for Therapeutic Planning in Metastatic Breast Cancer

Michael Untch, Oleg Gluz, Nadia Harbeck, Anja Welt et al.
3 citations
Geburtshilfe und Frauenheilkunde
Advanced Breast Cancer Therapies
1.26
article

Palbociclib: Randomized Studies and Real-world Evidence as the Basis for Therapeutic Planning in Metastatic Breast Cancer

Michael Untch, Oleg Gluz, Nadia Harbeck, Anja Welt, Eugen Ruckhäberle, Achim Wöckel, Michael P. Lux, Marcus Schmidt, Tjoung‐Won Park‐Simon
article en
3 citations

Abstract

Endocrine-based combination therapy with an inhibitor of the cyclin-dependent kinases 4 and 6 (CDK4/6 inhibitors) is currently the first-line therapy of choice for patients with hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-), locally advanced or metastatic breast cancer (mBC). The efficacy and safety of the treatment with palbociclib, the first CDK4/6 inhibitor approved for this indication, have been confirmed in large randomized controlled clinical trials (RCTs) with strictly defined patient cohorts. Since then, many relevant questions about CDK4/6 inhibition with palbociclib for mBC have been investigated in RCTs and real-world studies. Based on this evidence, palbociclib is widely used in clinical practice since many years because of its efficacy and good tolerability. The aim of this review is to summarize findings from RCTs and RWE considering clinically relevant aspects such as safety, tolerability, quality of life and efficacy with a focus on specific questions and patient characteristics. A critical discussion and review of the overall evidence for endocrine-based therapy with the CDK4/6 inhibitor palbociclib can contribute to support therapy decisions in daily clinical practice.

Geburtshilfe und FrauenheilkundeVol. 84(09)
Johannes Gutenberg University Mainz (DE), LMU Klinikum (DE), Medizinische Hochschule Hannover (DE), Düsseldorf University Hospital (DE), Klinik für Frauenheilkunde (DE), Essen University Hospital (DE), Universitätsklinikum Würzburg (DE), Brüderkrankenhaus St. Josef Paderborn (DE), Evangelisches Krankenhaus Bethesda Mönchengladbach (DE), Helios Hospital Berlin-Buch (DE), Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe, Heinrich Heine University Düsseldorf (DE), Ludwig-Maximilians-Universität München (DE)
Pfizer
Good health and well-being
Openalex Percentile: Top 19%
Advanced Breast Cancer Therapies
1.26
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