Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01795352
Other study ID # NIS-OES-XXX-2012/1
Secondary ID
Status Completed
Phase N/A
First received February 18, 2013
Last updated October 29, 2013
Start date March 2013
Est. completion date October 2013

Study information

Verified date October 2013
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Spain: Spanish Agency of MedicinesSpain: Ethics Committee
Study type Observational

Clinical Trial Summary

This is a national, multicentre, non-interventional, retrospective study to be carried out in the oncology settings of approximately 15-20 Spanish hospitals.

At each participant hospital, all patients recently diagnosed with advanced EGFR mutated NSCLC (both newly or with recurrent disease , without previous treatment for metastatic disease) from April 2010 to December 2011 will be included as study population. Information about the follow-up of the patients during a minimum of 12 months after diagnosis will be collected.


Description:

Observational retrospective study to describe the management of advanced or metastatic EGFR mutated non-small cell lung cancer patients in Spain


Recruitment information / eligibility

Status Completed
Enrollment 187
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histologically or cytologically confirmed newly locally advanced or metastatic NSCLC (stage IIIB/IV)

- Confirmed EGFR mutation by a validated test

- Availability of medical record

Exclusion Criteria:

- Participating on a blinded randomized clinical trial at any time during the study period

- Pregnant women (due to they do not reflect daily clinical practice)

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Research Site Barcelona
Spain Research Site Cordoba
Spain Research Site Donostia
Spain Research Site Granada
Spain Research Site Leon
Spain Research Site Madrid
Spain Research Site Malaga
Spain Research Site Navarra
Spain Research Site Sevilla
Spain Research Site Toledo
Spain Research Site Valencia
Spain Research Site Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of management patterns (clinical and diagnostic) of advanced/metastatic EGFR M+ NSCLC patients in Spain. 32 months No
Secondary Description of use of resources related with the management of advanced/metastatic EGFR M+ NSCLC patients in Spain. 32 months No
Secondary Evaluation of overall response rate (ORR). 32 months No
Secondary Evaluation of disease control rate (DCR). 32 months No
Secondary Evaluation of progression free survival (PFS: median PFS and 1 year PFS rate). 32 months No
Secondary Evaluation of overall survival (OS: median OS and 1 year OS rate). 32 months No
Secondary Description of clinical outcome data in all EGFR M+ patients by regimen, type of EGFR TK mutation, line of therapy and other relevant demographics or clinic pathologic characteristics. TK- Tyrosine Kinase 32 months No