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Spots Global Cancer Trial Database for Personalized Maintenance Therapy for m-PDAC Using Olaparib or Selumetinib + Durvalumab, Based on BRCAness and KRAS Status.

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Trial Identification

Brief Title: Personalized Maintenance Therapy for m-PDAC Using Olaparib or Selumetinib + Durvalumab, Based on BRCAness and KRAS Status.

Official Title: MAZEPPA: Phase II PRODIGE-GERCOR Study to Evaluate MAintenance Therapy With Olaparib or Selumetinib Plus Durvalumab According to BRCAness and KRAS Somatic Status Personalized in Metastatic Pancreatic Adenocarcinoma Patients

Study ID: NCT04348045

Study Description

Brief Summary: MAZEPPA is open-label, phase II study to assess the efficacy of a genomic-driven maintenance therapy in terms of PFS in Pancreatic ductal adenocarcinoma (PDAC) patients with disease controlled after 4 months of mFOLFIRINOX chemotherapy as following: Patients with a BRCAness somatic profile: olaparib Arm A. Patients with no BRCAness profile and with KRAS mutation randomization between durvalumab plus selumetinib Arm B, versus FOLFIRI Arm C.

Detailed Description: Searching for efficient maintenance therapies in metastatic PDAC patients whose disease has been controlled using an induction chemotherapy is crucial for two main reasons: 1. Patients may stop IV toxic chemotherapy while their tumor remains under control. Although up to 70% of PDAC patients achieve tumor control when treated during induction with mFOLFIRINOX, toxicity of this regimen, particularly neuropathy and fatigue, remains a key concern. 2. Tumor control may be extended, which might improve quality of life (QoL) and survival. Patients are included in MAZEPPA study based on the genetic profile of their tumor. * If a BRCA gene mutation is present in the tumor, treatment with the drug olaparib will be proposed (arm A), regardless of the status of the other genes analyzed. * In the absence of a mutation in the BRCA gene and in the presence of a mutation in the KRAS gene, a treatment combining immunotherapy and targeted therapy (durvalumab and selumetinib - Arm B) or chemotherapy by FOLFIRI (arm C) will be proposed.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Institut Sainte Catherine, Avignon, , France

CHRU Jean Minjoz, Besançon, , France

Polyclinique Bordeaux Nord Aquitaine, Bordeaux, , France

Centre François Baclesse, Caen, , France

Hôpital Beaujon, Clichy, , France

GHPSO Site de Creil, Creil, , France

Centre Georges François Leclerc, Dijon, , France

CHU Dijon, Dijon, , France

CHU Grenoble Alpes Hôpital Michallon, Grenoble, , France

Hôpital Franco-Britannique, Levallois-Perret, , France

CHRU Lille, Lille, , France

centre Léon Bérard, Lyon, , France

Hôpital Privé Jean Mermoz, Lyon, , France

Hôpital Saint Joseph Saint Luc, Lyon, , France

CHU La Timone, Marseille, , France

Hôpital Européen, Marseille, , France

Institut Paoli Calmette, Marseille, , France

Hôpital Nord Franche Comté, Montbéliard, , France

GH Diaconesses Croix Saint Simon, Paris, , France

Hôpital Européen Georges Pompidou, Paris, , France

Hôpital Pitié Salpêtrière, Paris, , France

Hôpital Saint Antoine, Paris, , France

Institut Mutualiste Montsouris, Paris, , France

CHU Poitiers, Poitiers, , France

CHU Robert Debré, Reims, , France

ICO Site de Saint Herblain, Saint-Herblain, , France

Centre Paul Strauss, Strasbourg, , France

CHU Toulouse IUCT Rangueil, Toulouse, , France

Hôpital Trousseau, Tours, , France

Contact Details

Name: Pascal HAMMEL, MD

Affiliation: Hôpital Beaujon

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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