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Clinical Trials/NCT01159288
NCT01159288
Completed
Phase 2

Phase II Trial of a Vaccination With Tumor Antigen-loaded Dendritic Cell-derived Exosomes on Patients With Unresectable Non Small Cell Lung Cancer Responding to Induction Chemotherapy

Gustave Roussy, Cancer Campus, Grand Paris1 site in 1 country41 target enrollmentMay 19, 2010

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Non Small Cell Lung Cancer
Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Enrollment
41
Locations
1
Primary Endpoint
Progression free survival
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Lung cancer is the worldwide leading cause of cancer death. In France, with 28,000 new cases per year, lung cancer is the 4th in terms of incidence but remains the leading cause of cancer death. The 5-year survival of lung cancer, all stages and all types, is very low, estimated at 12% among men and 16% among women in France. In advanced unresectable non small cell lung cancer, standard treatment relies on platinum-based induction chemotherapy. The median progression-free survival (PFS) in patients responding or stabilized after 4 chemotherapy cycles ranges from 2 to 2.8 months. Gustave Roussy and Curie institutes have developed an immunotherapy involving metronomic cyclophosphamide (mCTX) followed by vaccinations with tumor antigen-loaded dendritic cell-derived exosomes (Dex). mCTX inhibits Treg functions restoring T and NK cell effector functions and Dex are able to activate the innate and adaptive immunity. Phase I trials showed the safety and feasibility of Dex vaccines but no induction of T cells could be monitored in patients. Since 2007, we validated a new process for isolation of second generation Dex with improved immune stimulatory capacities. We propose a maintenance immunotherapy in 47 advanced unresectable NSCLC patients responding or stabilized after induction chemotherapy with Dex-based treatment to improve PFS rate at 4 months in these patients.

Registry
clinicaltrials.gov
Start Date
May 19, 2010
End Date
December 19, 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • advanced unresectable non small cell lung cancer
  • responding or stabilizer after induction chemotherapy

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Progression free survival

Time Frame: 4 months

Study Sites (1)

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