The role of abemaciclib in treatment of advanced breast cancer

Until recently, the mainstay of treatment in the majority of hormone receptor (HR)-positive, human epidermal growth factor 2 receptor (HER2)-negative advanced breast cancer (ABC) has consisted of single-agent endocrine therapy (ET). However, as understanding of endocrine resistance has grown, newer...

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Main Authors: Amelia McCartney, Erica Moretti, Giuseppina Sanna, Marta Pestrin, Emanuela Risi, Luca Malorni, Laura Biganzoli, Angelo Di Leo
Format: Article
Language:English
Published: SAGE Publishing 2018-05-01
Series:Therapeutic Advances in Medical Oncology
Online Access:https://doi.org/10.1177/1758835918776925
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spelling doaj-2f7758a47ae14bc5a4b374ea27837cd72020-11-25T03:24:02ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83592018-05-011010.1177/1758835918776925The role of abemaciclib in treatment of advanced breast cancerAmelia McCartneyErica MorettiGiuseppina SannaMarta PestrinEmanuela RisiLuca MalorniLaura BiganzoliAngelo Di LeoUntil recently, the mainstay of treatment in the majority of hormone receptor (HR)-positive, human epidermal growth factor 2 receptor (HER2)-negative advanced breast cancer (ABC) has consisted of single-agent endocrine therapy (ET). However, as understanding of endocrine resistance has grown, newer targeted agents have come to the fore. Inhibition of cyclin-dependent kinase complexes 4 and 6 (CDK4/6) combined with ET has shown significant activity in HR+ HER2− ABC, with impressive results in terms of progression-free survival (PFS) when compared with ET alone. This review summarizes the seminal findings pertaining to CDK4/6 inhibition in this population, specifically focusing on abemaciclib, contrasted with palbociclib and ribociclib. Potential directions for future studies are discussed, as a way of addressing outstanding issues such as establishing optimal treatment sequencing and agent combinations, appropriate patient selection to derive maximal benefits, predictive biomarkers and the employment of CDK4/6 inhibition beyond the ABC setting.https://doi.org/10.1177/1758835918776925
collection DOAJ
language English
format Article
sources DOAJ
author Amelia McCartney
Erica Moretti
Giuseppina Sanna
Marta Pestrin
Emanuela Risi
Luca Malorni
Laura Biganzoli
Angelo Di Leo
spellingShingle Amelia McCartney
Erica Moretti
Giuseppina Sanna
Marta Pestrin
Emanuela Risi
Luca Malorni
Laura Biganzoli
Angelo Di Leo
The role of abemaciclib in treatment of advanced breast cancer
Therapeutic Advances in Medical Oncology
author_facet Amelia McCartney
Erica Moretti
Giuseppina Sanna
Marta Pestrin
Emanuela Risi
Luca Malorni
Laura Biganzoli
Angelo Di Leo
author_sort Amelia McCartney
title The role of abemaciclib in treatment of advanced breast cancer
title_short The role of abemaciclib in treatment of advanced breast cancer
title_full The role of abemaciclib in treatment of advanced breast cancer
title_fullStr The role of abemaciclib in treatment of advanced breast cancer
title_full_unstemmed The role of abemaciclib in treatment of advanced breast cancer
title_sort role of abemaciclib in treatment of advanced breast cancer
publisher SAGE Publishing
series Therapeutic Advances in Medical Oncology
issn 1758-8359
publishDate 2018-05-01
description Until recently, the mainstay of treatment in the majority of hormone receptor (HR)-positive, human epidermal growth factor 2 receptor (HER2)-negative advanced breast cancer (ABC) has consisted of single-agent endocrine therapy (ET). However, as understanding of endocrine resistance has grown, newer targeted agents have come to the fore. Inhibition of cyclin-dependent kinase complexes 4 and 6 (CDK4/6) combined with ET has shown significant activity in HR+ HER2− ABC, with impressive results in terms of progression-free survival (PFS) when compared with ET alone. This review summarizes the seminal findings pertaining to CDK4/6 inhibition in this population, specifically focusing on abemaciclib, contrasted with palbociclib and ribociclib. Potential directions for future studies are discussed, as a way of addressing outstanding issues such as establishing optimal treatment sequencing and agent combinations, appropriate patient selection to derive maximal benefits, predictive biomarkers and the employment of CDK4/6 inhibition beyond the ABC setting.
url https://doi.org/10.1177/1758835918776925
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