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Spots Global Cancer Trial Database for T790M Mutation Positive 2nd Line STandard of cAre Registry

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Trial Identification

Brief Title: T790M Mutation Positive 2nd Line STandard of cAre Registry

Official Title: T-STAR - T790M Mutation Positive 2nd Line STandard of cAre Registry

Study ID: NCT02368990

Interventions

Study Description

Brief Summary: The aim of the study is to collect real world information on patients with locally advanced or metastatic non small cell lung cancer (NSCLC) who progressed after first line treatment with an approved Tyrosine-Kinase Inhibitor (TKI), who are known to be T790M positive and have been prescribed second line platinum-based chemotherapy (Pemetrexed + Cisplatin /Carboplatin).

Detailed Description: The study is an observational prospective cohort study that plans to enroll approximately 200 patients worldwide. There are Epidermal Growth Factor Receptor (EGFR) mutations known to be associated with EGFR-targeted TKI sensitivity ( Ex19Del, L858R, L861Q, and G719X). Further tests on biopsied tissue or cytology at progression after treatment with an approved EGFR targeted TKI are used to determine positivity to T790M mutation. Primary objectives of the study are : * To estimate overall survival * To estimate disease progression (as assessed and defined by physician) * To estimate time on treatment by line of therapy * To describe time to subsequent therapies (or death) * To describe healthcare resource utilization patterns * To capture patient reported symptoms, functioning, and health-related quality of life (HRQoL) data using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 items (EORTC QLQ-C30) and European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Lung Cancer 13 items (EORTC QLQ-LC13) * To describe the use of pemetrexed + cisplatin/carboplatin as the 2nd line treatment * To describe treatment patterns for 3rd line treatment and beyond

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Kentucky, Kentucky, United States

Research Site, Maryland, Maryland, United States

Research Site, Langhorne, Pennsylvania, United States

Research Site, Beijing, , China

Research Site, Changsha, , China

Research Site, Guangzhou, , China

Research Site, Jiangsu, , China

Research Site, Jilin, , China

Research Site, Shanghai Ruijin Hospital, , China

Research Site, Shanghai, , China

Research Site, Sichuan Cancer Hospital, , China

Research Site, Xian, , China

Research Site, Boulogne Billancourt, , France

Research Site, Bretagne, , France

Research Site, La Chaussee-Saint-Victor, , France

Research Site, Lille, , France

Research Site, Pontoise, , France

Research Site, Rhone-Alpes, , France

Research Site, Saint Quentin, , France

Research Site, Esslingen, , Germany

Research Site, Catania, , Italy

Research Site, Ferrara, , Italy

Research Site, Messina, , Italy

Research Site, Modena, , Italy

Research Site, Napoli, , Italy

Research Site, Padova, , Italy

Research Site, Parma, , Italy

Research Site, Perugia, , Italy

Research Site, Rome, , Italy

Research Site, Torino, , Italy

Research Site, Groningen, , Netherlands

Research Site, Barnaul, , Russian Federation

Research Site, Saint Petersburg, , Russian Federation

Research Site, Saint- Petersburg, , Russian Federation

Research Site, Alicante, , Spain

Research Site, Badalona, , Spain

Research Site, Barcelona, , Spain

Research Site, La Coruna, , Spain

Research Site, Leon, , Spain

Research Site, Lugo, , Spain

Research Site, Madrid, , Spain

Research Site, Ourense, , Spain

Research Site, Pamplona, , Spain

Research Site, Santander, , Spain

Research Site, Sevilla, , Spain

Research Site, Valencia, , Spain

Research Site, Vizcaya, , Spain

Research Site, LinKou, , Taiwan

Research Site, Taichung, , Taiwan

Research Site, Taipei, , Taiwan

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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