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Prediction of Everolimus-induced Interstitial Lung Disease — PREVENT  

Breast Neoplasms Clinical Trial

Official title:
Prediction of Everolimus-induced Interstitial Lung Disease in Breast Cancer Patients; Maximizing Efficacy by Reducing Toxicity

Clinical Trial Summary

The investigators will determine which factors are predictive for the development and severity of everolimus-induced interstitial lung disease and will develop a prediction model based on these risk factors.

Clinical Trial Description

In this study the investigators will prospectively investigate pulmonary adverse events during treatment with everolimus. The investigators will distinguish the following everolimus-induced pulmonary adverse events: pulmonary infection, everolimus-induced airway disease and everolimus-induced interstitial lung disease (ILD). The investigators will investigate the predictive value of pneumoproteins, everolimus exposure, pulmonary function tests, four distinct radiological patterns, baseline patient characteristics and the development of skin toxicity or oral mucositis for the development and severity of everolimus-induced ILD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01978171
Study type Observational
Source Radboud University
Contact
Status Completed
Phase
Start date May 2014
Completion date January 15, 2018
View Details
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