Prevalence and risk factors of dry eye disease in patients treated with aromatase inhibitors for breast cancer.

Aromatase inhibitors OSDI Schirmer test TBUT breast cancer dry eye disease

Journal

Clinical & experimental optometry
ISSN: 1444-0938
Titre abrégé: Clin Exp Optom
Pays: United States
ID NLM: 8703442

Informations de publication

Date de publication:
12 Sep 2023
Historique:
medline: 13 9 2023
pubmed: 13 9 2023
entrez: 12 9 2023
Statut: aheadofprint

Résumé

Treatment with aromatase inhibitors (AIs) in patients with breast cancer can lead to dry eye disease (DED). The purpose of the study is to determine the prevalence and risk factors of DED in patients treated with AIs for breast cancer. Participants in this cross-sectional study were patients with breast cancer treated with AIs. Demographic and clinical data, including age, sex, type of cancer, stage, grade, duration of treatment and adjuvant chemotherapy and/or radiotherapy were collected. All patients underwent a detailed ophthalmic examination, as well as Tear Break up Time (TBUT) and Schirmer test, while Ocular Surface Disease Index (OSDI) questionnaires were administered. Based on the clinical findings, a diagnosis of DED was made, and prevalence was calculated. Univariate analysis of the association of different variables with DED was performed. A logistic regression analysis was done to identify risk factors for DED among study population. A total of 102 participants were included in the study. The mean age of patients was 62.4 ± 10.8 years. A total of 77 out of 102 patients (75.5%) had ductal, 16 (15.7%) lobular and 9 (8.8%) other types of breast cancer. A total of 83 patients (81.4%) received chemotherapy and 70 patients (68.6%) received radiotherapy. The mean duration of treatment was 24.4 ± 18.9 months. The prevalence of DED in the study sample was 69.6%. Patients who received radiotherapy (OR = 3.31, 95%CI = 1.30-7.82, There was a high prevalence of DED among the study population. Radiotherapy and duration of treatment with AIs were independently associated with DED.

Sections du résumé

CLINICAL RELEVANCE UNASSIGNED
Treatment with aromatase inhibitors (AIs) in patients with breast cancer can lead to dry eye disease (DED).
BACKGROUND UNASSIGNED
The purpose of the study is to determine the prevalence and risk factors of DED in patients treated with AIs for breast cancer.
METHODS UNASSIGNED
Participants in this cross-sectional study were patients with breast cancer treated with AIs. Demographic and clinical data, including age, sex, type of cancer, stage, grade, duration of treatment and adjuvant chemotherapy and/or radiotherapy were collected. All patients underwent a detailed ophthalmic examination, as well as Tear Break up Time (TBUT) and Schirmer test, while Ocular Surface Disease Index (OSDI) questionnaires were administered. Based on the clinical findings, a diagnosis of DED was made, and prevalence was calculated. Univariate analysis of the association of different variables with DED was performed. A logistic regression analysis was done to identify risk factors for DED among study population.
RESULTS UNASSIGNED
A total of 102 participants were included in the study. The mean age of patients was 62.4 ± 10.8 years. A total of 77 out of 102 patients (75.5%) had ductal, 16 (15.7%) lobular and 9 (8.8%) other types of breast cancer. A total of 83 patients (81.4%) received chemotherapy and 70 patients (68.6%) received radiotherapy. The mean duration of treatment was 24.4 ± 18.9 months. The prevalence of DED in the study sample was 69.6%. Patients who received radiotherapy (OR = 3.31, 95%CI = 1.30-7.82,
CONCLUSION UNASSIGNED
There was a high prevalence of DED among the study population. Radiotherapy and duration of treatment with AIs were independently associated with DED.

Identifiants

pubmed: 37699786
doi: 10.1080/08164622.2023.2239247
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-5

Auteurs

Genovefa Machairoudia (G)

2nd Department of Ophthalmology, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Dimitrios Kazantzis (D)

2 Department of Ophthalmology, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Irini Chatziralli (I)

2 Department of Ophthalmology, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Katerina Kampoli (K)

Hematology Oncology Unit, 4th Department of Internal Medicine, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Anastasios Ntavatzikos (A)

Hematology Oncology Unit, 4 Department of Internal Medicine, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Panagiotis Theodossiadis (P)

2 Department of Ophthalmology, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Anna Koumarianou (A)

Hematology Oncology Unit, 4 Department of Internal Medicine, School of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Classifications MeSH