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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Series: | Therapeutic Advances in Medical Oncology |
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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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