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Brief Title: The EPIC Trial The Elderly Patient Individualized Chemotherapy Trial
Official Title: Randomized Phase III Multicenter Trial of Customized Chemotherapy Versus Standard of Care for1st Line Treatment of Elderly Patients With Advanced Non-Small-Cell Lung Cancer
Study ID: NCT03402048
Brief Summary: This is a randomized phase III trial that will randomize elderly patients(70 years of age and older) who are not considered eligible for standard doublet or triplet regimens. In a 2:1 fashion, patients will be randomized to the customization arm or the standard arm, respectively. This trial will be offered to patients who are previously untreated for stage IV NSCLC. The primary objective is to evaluate if chemotherapy selection based on histology and tumoral molecular determinants ERCC1, RRM1 and TS (arm A, the experimental arm) results in superior outcome in elderly patients with untreated, advanced NSCLC compared to standard of care treatments (arm B, the standard arm).
Detailed Description: The study population will consist of patients with histologically or cytologically proven stage IV NSCLC, who have not been previously treated with chemotherapy for stage IV and are either elderly (70 years of age and older). Patients must fulfill all the inclusion/exclusion criteria to be eligible. Tissue will be obtained, and gene expression analysis will be performed at the University of Turin. The tissue sample used for this analysis will be obtained from the biopsy procedure performed as standard of care procedures during the patient's diagnosis and staging. Patients will be randomized to either Arm A: Experimental or Arm B: Standard of Care in a 2:1 fashion. Tissue will be obtained for gene analysis for ALL patients. However, ONLY patients randomized to Arm A will receive the genetic analysis results. Genetic results will not be disclosed to the registering center for those patients randomized to Arm B: Standard of Care. For patients randomized to Arm A: Experimental arm, the chemotherapy treatment prescription will be based on the gene analysis according to the protocol. For patients randomized to Arm B: Standard of Care arm, the chemotherapy treatment will be at the discretion of the care provider.
Minimum Age: 70 Years
Eligible Ages: OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
IRCSSIstituto Scientifico Romagnolo per lo studio e la cura dei tumori IRST, Meldola, Forlì, Italy
Istituto Nazionale Tumori, Aviano, Pordenone, Italy
Ospedale di Faenza, Faenza, Ravenna, Italy
Ospedale di Lugo, Lugo, Ravenna, Italy
AUSL Rimini-Oncologia Medica Cattolica, Cattolica, Rimini, Italy
AOU San Luigi Gonzaga, Department of Oncology, University of Turin, Orbassano, Turin, Italy
Ospedale Giovanni Paolo II, Bari, , Italy
AO Cannizzaro, Catania, , Italy
AOU Santa Croce e Carle, Cuneo, , Italy
Azienda Ospedaliera Careggi, Firenze, , Italy
Istituto Nazionale per la Ricerca sul Cancro, Genova, , Italy
Ospedale Galliera, Genova, , Italy
Azienda Ospedaliera Fatebenefratelli, Milano, , Italy
Ospedale S. Raffaele, Milano, , Italy
AO San Gerardo, Monza, , Italy
Istituto Oncologico Veneto, Padova, , Italy
Ospedale Santa MAria della Misericordia, Perugia, , Italy
Ospedale S MAria delle Croci, Ravenna, , Italy
Arcispedale Santa Maria Nuova, Reggio Emilia, , Italy
AUSL Rimini-Oncologia medica, Rimini, , Italy
Istituto Nazionale Tumori Regina Elena, Roma, , Italy
Ospedale S. Giovanni Addolorata, Roma, , Italy
Policlinico Umberto I- Università la Sapienza, Roma, , Italy
AOU Sassari, Sassari, , Italy
Azienda Ospedaliera Sondalo, Sondalo, , Italy
Ospedale Santa Chiara, Trento, , Italy
AOU S.M. Misericordia, Udine, , Italy
AOU Verona, Verona, , Italy
Name: Silvia Novello, MD, PhD
Affiliation: University of Turin, Italy
Role: PRINCIPAL_INVESTIGATOR
Name: Giorgio Vittorio Scagliotti, MD, PhD
Affiliation: Univerisity of Turin
Role: PRINCIPAL_INVESTIGATOR
Name: Tiziana Vavalà, MD
Affiliation: University of Turin, Italy
Role: PRINCIPAL_INVESTIGATOR