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CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience
Background: Aromatase inhibitors (AIs) are associated with musculoskeletal pain in one third (20–47%) of breast cancer patients. Recently, CDK4/6 inhibitors have emerged as a new therapeutic approach in hormone receptor (HR)-positive breast cancer. While hematological and gastrointestinal toxicities...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293403/ https://www.ncbi.nlm.nih.gov/pubmed/34198899 http://dx.doi.org/10.3390/medsci9020042 |
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author | Andrikopoulou, Angeliki Fiste, Oraianthi Apostolidou, Kleoniki Skafida, Efthymia Markellos, Christos Liontos, Michalis Kyriazoglou, Anastasios Dimopoulos, Meletios-Athanasios Zagouri, Flora |
author_facet | Andrikopoulou, Angeliki Fiste, Oraianthi Apostolidou, Kleoniki Skafida, Efthymia Markellos, Christos Liontos, Michalis Kyriazoglou, Anastasios Dimopoulos, Meletios-Athanasios Zagouri, Flora |
author_sort | Andrikopoulou, Angeliki |
collection | PubMed |
description | Background: Aromatase inhibitors (AIs) are associated with musculoskeletal pain in one third (20–47%) of breast cancer patients. Recently, CDK4/6 inhibitors have emerged as a new therapeutic approach in hormone receptor (HR)-positive breast cancer. While hematological and gastrointestinal toxicities are frequently reported during treatment with CDK4/6 inhibitors, musculoskeletal symptoms are less commonly encountered. Methods: Herein, we present a retrospective study of 47 breast cancer patients who received CDK4/6 inhibitors along with endocrine therapy in our department between 01/01/2018 and 01/09/2020. Results: Median age at diagnosis was 58 years (29–81). Median duration of treatment was 8.76 months (SD: 7.68; 0.47–30.13 months). Median PFS was 24.33 months (95% CI; 1.71–46.96). Overall, toxicity was reported in 61.7% of the cases (29/47). Arthralgia was reported in 6.4% (3/47) of the patients. Hematological toxicity was reported in 51.1% (24/47) of the patients. Neutropenia was the main hematological toxicity observed (86.8%; 22/47) along with anemia (4.3%; 2/47), thrombocytopenia (2.1%; 1/47), and leukopenia (4.2%; 1/24). Conclusions: Though our data reflect a small sample size, we report a reduced arthralgia rate (6.4%) during treatment with CDK4/6 inhibitors compared with that reported in studies of AIs (20–47%). |
format | Online Article Text |
id | pubmed-8293403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82934032021-07-22 CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience Andrikopoulou, Angeliki Fiste, Oraianthi Apostolidou, Kleoniki Skafida, Efthymia Markellos, Christos Liontos, Michalis Kyriazoglou, Anastasios Dimopoulos, Meletios-Athanasios Zagouri, Flora Med Sci (Basel) Article Background: Aromatase inhibitors (AIs) are associated with musculoskeletal pain in one third (20–47%) of breast cancer patients. Recently, CDK4/6 inhibitors have emerged as a new therapeutic approach in hormone receptor (HR)-positive breast cancer. While hematological and gastrointestinal toxicities are frequently reported during treatment with CDK4/6 inhibitors, musculoskeletal symptoms are less commonly encountered. Methods: Herein, we present a retrospective study of 47 breast cancer patients who received CDK4/6 inhibitors along with endocrine therapy in our department between 01/01/2018 and 01/09/2020. Results: Median age at diagnosis was 58 years (29–81). Median duration of treatment was 8.76 months (SD: 7.68; 0.47–30.13 months). Median PFS was 24.33 months (95% CI; 1.71–46.96). Overall, toxicity was reported in 61.7% of the cases (29/47). Arthralgia was reported in 6.4% (3/47) of the patients. Hematological toxicity was reported in 51.1% (24/47) of the patients. Neutropenia was the main hematological toxicity observed (86.8%; 22/47) along with anemia (4.3%; 2/47), thrombocytopenia (2.1%; 1/47), and leukopenia (4.2%; 1/24). Conclusions: Though our data reflect a small sample size, we report a reduced arthralgia rate (6.4%) during treatment with CDK4/6 inhibitors compared with that reported in studies of AIs (20–47%). MDPI 2021-06-05 /pmc/articles/PMC8293403/ /pubmed/34198899 http://dx.doi.org/10.3390/medsci9020042 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Andrikopoulou, Angeliki Fiste, Oraianthi Apostolidou, Kleoniki Skafida, Efthymia Markellos, Christos Liontos, Michalis Kyriazoglou, Anastasios Dimopoulos, Meletios-Athanasios Zagouri, Flora CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title | CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title_full | CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title_fullStr | CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title_full_unstemmed | CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title_short | CDK4/6 Inhibitors and Arthralgia: A Single Institution Experience |
title_sort | cdk4/6 inhibitors and arthralgia: a single institution experience |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293403/ https://www.ncbi.nlm.nih.gov/pubmed/34198899 http://dx.doi.org/10.3390/medsci9020042 |
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