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Spots Global Cancer Trial Database for Nivolumab and Ipilimumab Plus Chemotherapy for Patients With Stage IV Lung Cancer With Brain Metastases

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Trial Identification

Brief Title: Nivolumab and Ipilimumab Plus Chemotherapy for Patients With Stage IV Lung Cancer With Brain Metastases

Official Title: Nivolumab Plus Ipilimumab Plus Two Cycles of Platinum-based Chemotherapy as First Line Treatment for Stage IV/Recurrent Non-small Cell Lung Cancer (NSCLC) Patients With Synchronous Brain Metastases

Study ID: NCT05012254

Study Description

Brief Summary: This is an open-label, non-randomised, phase II, multicenter clinical trial. 71 stage IV or recurrent, non-small cell lung cancer patients with synchronous brain metastases will be enrolled in this trial to evaluate the efficacy of Nivolumab plus Ipilimumab plus two cycles of platinum-based chemotherapy as first line treatment.

Detailed Description: This is an open-label, non-randomised, phase II, multicenter clinical trial. The total sample size is 71 patients. The population to be included are stage IV or recurrent, non-small cell lung cancer patients with synchronous brain metastases. Patients randomised will receive induction treatment with two cycles of platinum-based chemotherapy plus Nivolumab and Ipilimumab. At the end of induction treatment the patient with start maintenance with Nivolumab and Ipilimumab until disease progression, unacceptable toxicity, loss of clinical benefit as judged by the investigator or up to a maximum of 2 years of treatment The primary objective of this trial is to determine the rate of intracranial clinical benefit, defined as the percentage of patients who had lack of radiological or clinical progression for at least 6 months according to RANO-BM assessment criteria. Patient accrual is expected to be completed within 1.5 years, treatment is planned to extend for 1 year and the patients will be followed up for 2 years. The study will end once survival follow-up has concluded.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

ICO Badalona, Hospital Germans Trias i Pujol, Badalona, Barcelona, Spain

ICO Hospitalet, Hospitalet de Llobregat, Barcelona, Spain

Hospital Provincial de Castellón, Castelló de la Plana, Castellon, Spain

Hospital Universitario Insular de Gran canaria, Las Palmas De Gran Canaria, Gran Canaria, Spain

Hospitalario Universitario A Coruña, A Coruña, La Coruña, Spain

Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain

Hospital Universitari Vall d' Hebron, Barcelona, , Spain

Hospital de la Santa Creu i Sant Pau, Barcelona, , Spain

Hospital Universitario de Jaén, Jaén, , Spain

Hospital Universitario de León, León, , Spain

Hospital Universitario Lucus Augusti, Lugo, , Spain

Hospital Universitario Fundación Jiménez Díaz, Madrid, , Spain

Hospital 12 De Octubre, Madrid, , Spain

Hospital Universitario Regional de Málaga, Málaga, , Spain

Hospital Universitari Son Llatzer, Palma De Mallorca, , Spain

Hospital General Universitario de Valencia, Valencia, , Spain

Hospital Universitario La Fe, Valencia, , Spain

Hospital Clínico Universitario de Valladolid, Valladolid, , Spain

Contact Details

Name: Ernest Nadal, MD

Affiliation: Fundación GECP Investigator

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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