Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01788163
Other study ID # D7913C00074
Secondary ID
Status Completed
Phase N/A
First received February 7, 2013
Last updated May 16, 2017
Start date February 27, 2013
Est. completion date June 20, 2016

Study information

Verified date May 2017
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Interventional diagnostic, international, multicenter and non-comparative study of EGFR mutation status in aNSCLC patients (locally advanced and/or metastatic disease) with adenocarcinoma and non-adenocarcinoma histologies. It will be conducted in Asia Pacific and Russia and will assess the current status of EGFR mutation testing, and the concordance of EGFR mutation status derived from tumour samples and blood based circulating free DNA.


Description:

A diagnostic study to determine the prevalence of EGFR mutations in Asian and Russian patients with advanced NSCLC of Adenocarcinoma and Non-adenocarcinoma histologies


Recruitment information / eligibility

Status Completed
Enrollment 3500
Est. completion date June 20, 2016
Est. primary completion date August 25, 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histological or cytological confirmed locally advanced NSCLC (stage IIIA/B) not suitable for curative treatment or metastatic (stage IV) NSCLC

- Newly diagnosed patients with locally advanced and/or metastatic NSCLC who are systemic treatment Naive (i.e. no chemotherapy or EGFR-TKI) or patients with recurrent disease who have previously received adjuvant chemotherapy (not including EGFR-TKI)

- Provision of diagnostic cancer tissue or cytology sample upon inclusion (surgical specimen, biopsy sample, or cytology sample is acceptable) and Provision of a routine blood (plasma) sample in China, Russia, Taiwan and Korea

- Patients aged 18 years and older

Exclusion Criteria:

- As judged by the investigator, any evidence of severe or uncontrolled systemic disease (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease)

- Evidence of any other significant clinical disorder or laboratory finding that made it undesirable for the patient to participate in the study

- Pregnancy or breast-feeding

Study Design


Related Conditions & MeSH terms

  • EGFR Mutation Status in aNSCLC Patients

Intervention

Genetic:
EGFR mutation test
EGFR mutation being tested in tissue and blood

Locations

Country Name City State
Australia Research Site Brisbane Queensland
Australia Research Site Campbelltown New South Wales
Australia Research Site Coffs Harbour New South Wales
Australia Research Site Concord New South Wales
Australia Research Site Murdoch Western Australia
Australia Research Site Tamworth New South Wales
Australia Research Site Tweed Heads New South Wales
Australia Research Site Wahroonga New South Wales
Australia Research Site Woolloongabba Queensland
China Research Site Beijing
China Research Site Changsha
China Research Site Changzhou
China Research Site Chengdu
China Research Site Chengdu City
China Research Site Chongqing
China Research Site Foshan City
China Research Site Guangzhou
China Research Site Hangzhou
China Research Site Hangzhou City
China Research Site Nanjing
China Research Site Shanghai
China Research Site Suzhou City
China Research Site Taiyuan
China Research Site Wuhan City
China Research Site Zhengzhou
Indonesia Research Site Jakarta
Indonesia Research Site Surabaya
Korea, Republic of Research Site Cheongju
Korea, Republic of Research Site Daegu
Korea, Republic of Research Site Seoul
Malaysia Research Site Kuala Lumpur
Russian Federation Research Site Arkhangelsk
Russian Federation Research Site Barnaul
Russian Federation Research Site Belgorod
Russian Federation Research Site Birobidzhan
Russian Federation Research Site Chelyabinsk
Russian Federation Research Site Chita
Russian Federation Research Site Irkutsk
Russian Federation Research Site Izhevsk
Russian Federation Research Site Kazan
Russian Federation Research Site Kemerovo
Russian Federation Research Site Khabarovsk
Russian Federation Research Site Khanty-Mansisk
Russian Federation Research Site Krasnodar
Russian Federation Research Site Krasnoyarsk
Russian Federation Research Site Lipetsk
Russian Federation Research Site Moscow
Russian Federation Research Site Novosibirsk
Russian Federation Research Site Obninsk
Russian Federation Research Site Omsk
Russian Federation Research Site Orel
Russian Federation Research Site Perm
Russian Federation Research Site Pyatigorsk
Russian Federation Research Site Rostov-on-Don
Russian Federation Research Site Ryazan
Russian Federation Research Site Samara
Russian Federation Research Site St. Petersburg
Russian Federation Research Site Surgut
Russian Federation Research Site Tula
Russian Federation Research Site Ufa
Russian Federation Research Site Velikiy Novgorod
Russian Federation Research Site Vladivostok
Russian Federation Research Site Volgograd
Russian Federation Research Site Yakutsk
Russian Federation Research Site Yaroslavl
Russian Federation Research Site Yuzhno-Sakhalinsk
Singapore Research Site Singapore
Taiwan Research Site Kaohsiung
Taiwan Research Site Tainan
Taiwan Research Site Tainan City
Taiwan Research Site Taipei
Thailand Research Site Chiang Mai
Thailand Research Site Khon Kaen
Thailand Research Site Patumwan Bangkok

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

Australia,  China,  Indonesia,  Korea, Republic of,  Malaysia,  Russian Federation,  Singapore,  Taiwan,  Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Tumour Epidermal Growth Factor Receptor (EGFR) Mutation Status The 95% Confidence intervals were calculated using Clopper Pearson method for each country. At Screening
Primary Tumour EGFR Mutation by Subtype Frequency distribution of subjects with a positive mutation status by the mutation subtype and country. At Screening
Primary Tumour EGFR Mutation Status by Histology Only subjects who had a recorded Histological Type of Adenocarcinoma or Non-adenocarcinoma are included. Confidence intervals were calculated using Clopper Pearson method for each country. At Screening
Primary Overall Plasma EGFR Mutation Status Plasma samples were only performed in China, Taiwan, South Korea and Russia. The Confidence intervals were calculated using Clopper Pearson method for each country. At Screening
Primary Plasma EGFR Mutation by Subtype Plasma samples were only performed in China, Taiwan, South Korea and Russia. Frequency distribution of subjects with a positive mutation status by the mutation subtype and country. At Screening
Primary Plasma EGFR Mutation Status by Histology Only subjects who had a recorded Histological Type of Adenocarcinoma or Non-adenocarcinoma are included. Confidence intervals were calculated using Clopper Pearson method for each country At Screening
Secondary Concordance Rate of Comparison of Mutation Status Between Tumour and Plasma Samples Plasma samples were only performed in China, Taiwan, South Korea and Russia. At Screening
Secondary Sensitivity and Specificity of Comparison of Mutation Status Between Tumour and Plasma Samples Plasma samples were only performed in China, Taiwan, South Korea, and Russia. Participants only include those who had sensitivity and specificity tests performed. At Screening
Secondary Predictive Values of Comparison of Mutation Status Between Tumour and Plasma Samples Plasma samples were only performed in China, Taiwan, South Korea, and Russia. Participants include only those who had Positive and Negative Predictive tests performed. At Screening
Secondary Tumour EGFR Mutation Testing Frequencies of tumour EGFR mutation testing practices parameters. At Screening
Secondary Tumour EGFR Mutation Testing Rates Testing Success rate is the percentage of subjects with a non-missing test result. Mutation Detection Rate is the percentage of subjects with successful test that detects a mutation. At Screening
Secondary Tumour EGFR Mutation Testing Turnaround Time Tumour EGFR mutation testing turnaround time is the number of days from the test request to getting the test result. At Screening
Secondary Plasma EGFR Mutation Testing Plasma samples were only performed in China, Taiwan, South Korea and Russia. Frequencies of plasma EGFR mutation testing practices parameters. At Screening
Secondary Plasma EGFR Mutation Testing Rates Testing Success rate is the percentage of subjects with a non-missing test result. Mutation Detection Rate is the percentage of subjects with successful test that detects a mutation. Plasma samples were only performed in China, Taiwan, South Korea and Russia. At Screening
Secondary Plasma EGFR Mutation Testing Turnaround Time Plasma samples were only performed in China, Taiwan, South Korea and Russia. Plasma EGFR mutation testing turnaround time is the number of days from the test request to getting the test result. At Screening
Secondary Demographics and Disease Characteristics by Tumour EGFR Mutation Status Correlation of demographic and disease characteristics are summarized by EGFR mutation status with results from a multivariate logistic regression using stepwise forward selection with a 10% significance level for model entry. At Screening
Secondary Time Since First Non-small-cell Lung Carcinoma (NSCLC) Diagnosis by Tumor EGFR Mutation Number of months since the first diagnosis of NSCLC from informed consent date. At Screening
Secondary Number of Organs With Metastasis by Tumour EGFR Mutation Status Summary of number of organs with metastasis. Only participants with at least 1 organ with metastasis are included. At Screening
Secondary Demographics and Disease Characteristics by Plasma EGFR Mutation Status Correlation of demographic and disease characteristics are summarized by EGFR mutation status with results from a multivariate logistic regression using stepwise forward selection with a 10% significance level for model entry. At Screening
Secondary Time Since First NSCLC Diagnosis by Plasma EGFR Mutation Number of months since the first diagnosis of NSCLC from informed consent date. At Screening
Secondary Number of Organs With Metastasis by Plasma EGFR Mutation Status Summary of number of organs with metastasis. Only participants with at least 1 organ with metastasis are included. At Screening
Secondary First Line Treatment Choice by Asia Pacific Country At Screening
Secondary First Line Treatment Choice by Asia Pacific Country by Tumour EGFR Mutation Status At Screening

External Links