TY - JOUR
T1 - Development of Pericardial Effusion in Non-small Cell Lung Cancer Is Associated with the Presence of EGFR/ALK Mutations
AU - Nardi-Agmon, Inbar
AU - Zer, Alona
AU - Peysakhovich, Yuri
AU - Margalit, Ili
AU - Kornowski, Ran
AU - Peled, Nir
AU - Lakobishvili, Zaza
N1 - Publisher Copyright:
© 2022 Israel Medical Association. All rights reserved.
PY - 2022/3
Y1 - 2022/3
N2 - Background: No specific clinical or histological factors are recognized to be associated with the development of pericardial effusion in non-small cell lung cancer (NSCLC) other than a metastatic disease. Objectives: To assess whether specific clinical and histological features are associated with development of pericardial effusion in patients with NSCLC. Methods: A consecutive cohort of patients with NSCLC who presented with symptomatic pericardial effusion 2014-2017 was compared to a control group of patients with advanced NSCLC without pericardial effusion. Results: The 27 patients in the effusion group were generally younger, more often female, and with a higher percentage of never-smokers, compared to the 54 patients of the control group. Epidermal growth factor receptor/anaplastic lymphoma kinase (EGFR/ALK) mutation tumors were found in 48% of patients in the effusion group vs. 25% in the control group. In the multivariate analysis, the unadjusted odds ratio (OR) for the development of pericardial effusion in patients with somatic mutations was significantly higher compared to wild type tumors (OR 2.65,95% confidence interval 1.00-7.00). However, a suspected association between pericardial effusion and mutation status was found to be confounded by age. While a high rate of recurrence was observed when pericardiocentesis was initially performed (9/17,53%), no recurrence was documented when pericardial window procedure was performed (total of 17 patients). Conclusions: Patients with EGFR/ALK mutations may be at higher risk for the development of pericardial effusion; therefore, attending physicians need to be aware and have a high index of clinical suspicion.
AB - Background: No specific clinical or histological factors are recognized to be associated with the development of pericardial effusion in non-small cell lung cancer (NSCLC) other than a metastatic disease. Objectives: To assess whether specific clinical and histological features are associated with development of pericardial effusion in patients with NSCLC. Methods: A consecutive cohort of patients with NSCLC who presented with symptomatic pericardial effusion 2014-2017 was compared to a control group of patients with advanced NSCLC without pericardial effusion. Results: The 27 patients in the effusion group were generally younger, more often female, and with a higher percentage of never-smokers, compared to the 54 patients of the control group. Epidermal growth factor receptor/anaplastic lymphoma kinase (EGFR/ALK) mutation tumors were found in 48% of patients in the effusion group vs. 25% in the control group. In the multivariate analysis, the unadjusted odds ratio (OR) for the development of pericardial effusion in patients with somatic mutations was significantly higher compared to wild type tumors (OR 2.65,95% confidence interval 1.00-7.00). However, a suspected association between pericardial effusion and mutation status was found to be confounded by age. While a high rate of recurrence was observed when pericardiocentesis was initially performed (9/17,53%), no recurrence was documented when pericardial window procedure was performed (total of 17 patients). Conclusions: Patients with EGFR/ALK mutations may be at higher risk for the development of pericardial effusion; therefore, attending physicians need to be aware and have a high index of clinical suspicion.
KW - cardio-oncology
KW - cardiotoxicity
KW - lung cancer
KW - pericardial effusion
UR - http://www.scopus.com/inward/record.url?scp=85128000205&partnerID=8YFLogxK
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C2 - 35347923
AN - SCOPUS:85128000205
SN - 1565-1088
VL - 24
SP - 135
EP - 139
JO - Israel Medical Association Journal
JF - Israel Medical Association Journal
IS - 3
ER -