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Brief Title: Detection of Tumor DNA in the Blood of Patients Receiving Standard Therapy for Hormone Receptor-positive (HR+) Non-HER2 Expressing (HER2-) Metastatic Breast Cancer as a Tool to Select Those Who May Benefit From the Next Course of Fulvestrant in Combination With Alpelisib or Ribociclib
Official Title: A ctDNA Screening Program in Patients With HR+, HER2- Metastatic Breast Cancer for Detection of High-risk Relapse Patients on Any CDK4/6 Inhibitor and a Randomised Phase II Study Comparing Alpelisib Combined With Fulvestrant to Ribociclib Combined With Fulvestrant, in Patients With Persistent Targetable PIK3CA Mutations
Study ID: NCT05625087
Brief Summary: After an initial screening phase (SAFIR 03 - SCREENING) to identify patients with blood circulating mutated-PIK3CA tumours persistent, patients will be enrolled in the treatment phase of SAFIR 03 (SAFIR 03 - ARRIBA) that was designed as a randomised, open-label, multicentre, phase II study, for comparison of alpelisib to ribociclib in combination with fulvestrant (as the continuation of the CDK4/6 inhibitor-fulvestrant strategy) in terms of progression-free survival (PFS).
Detailed Description: INDICATION The population eligible to the screening phase is composed of all women or men with HR+, HER2- metastatic breast cancer who are eligible for first-line treatment with a cyclin-dependent kinases (CDK) 4/6 inhibitor combined with fulvestrant (and a luteinizing hormone realeasing hormone (LH-RH) analogue in men and premenopausal women) in the context of the standard healthcare management. The screening will identify patients with high risk of relapse on any CDK4/6 inhibitor thanks to ctDNA kinetic between baseline and 4 weeks of treatment. The purpose is to early adapt the therapeutic intervention for ctDNA no drop patient to prevent from relapse. This study will propose an intervention for PIK3CA mutated patients with alpelisib vs. ribociclib. Other therapeutic approaches might be proposed to patients with wild type PIK3CA through other protocols. The randomised study phase will include patients with persistent mutations on exons 4, 9 or 20\* of PIK3CA ctDNA after 4 weeks of treatment with any CDK4/6 inhibitor-fulvestrant in first-line setting.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
CHU Amiens Picardie, Amiens Cedex 1, , France
Clinique de l'Europe Amiens - CTHE, Amiens, , France
Centre Hospitalier d'Auxerre, Auxerre, , France
Sainte Catherine Institut du Cancer Avignon Provence, Avignon, , France
Centre Hospitalier de Beauvais, Beauvais, , France
Hôpital Simone Veil de Blois, Blois, , France
Institut Bergonié, Bordeaux, , France
Centre Hospitalier de Boulogne-sur-Mer, Boulogne-sur-Mer, , France
CHRU Morvan, Brest, , France
Clinique Pasteur Lanroze - CFRO - Groupe Vivalto Santé, Brest, , France
Centre François Baclesse, Caen, , France
Hôpital NOVO, Cergy-Pontoise Cedex, , France
Centre Hospitalier William Morey, Chalon-sur-Saône, , France
Centre Hospitalier de Cholet, Cholet, , France
Pôle Santé République (ELSAN), Clermont-Ferrand, , France
Centre Jean Perrin, Clermont-Ferrand, , France
Centre Hospitalier Alpes Léman, Contamine-sur-Arve, , France
CHI Fréjus-Saint-Raphaël, Fréjus, , France
Groupe Hospitalier Mutualiste de Grenoble (GHMG), Grenoble Cedex 1, , France
CHD Vendée, La Roche-sur-Yon, , France
Centre Hospitalier de Versailles - Hôpital André Mignot, Le Chesnay, , France
Polyclinique de Limoges - Site François Chénieux, Limoges, , France
Centre Léon Bérard, Lyon, , France
Hôpital privé Jean Mermoz, Lyon, , France
Clinique de la Sauvegarde, Lyon, , France
Institut Paoli Calmettes, Marseille, , France
ICM Val d'Aurelle, Montpellier, , France
Medipôle de Nancy - COG-ILC (Polyclinique de Gentilly), Nancy, , France
Clinique Hartmann, Neuilly-sur-Seine, , France
Centre Antoine Lacassagne, Nice, , France
Hôpital Saint-Louis, Paris, , France
Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, , France
Centre Hospitalier de Pau, Pau, , France
Hôpital Privé des Côtes-d'Armor (HPCA) - Cario, Plérin, , France
Institut Godinot, Reims, , France
Centre Eugène Marquis, Rennes Cedex, , France
CHP Saint-Grégoire - Groupe Vivalto Santé, Saint-Grégoire, , France
Clinique Sainte-Anne - GH Saint-Vincent, Strasbourg, , France
Hôpitaux du Léman, Thonon-les-Bains, , France
Institut Claudius Regaud - IUCT-O, Toulouse, , France
Institut de Cancérologie de Lorraine, Vandœuvre-lès-Nancy, , France
Gustave Roussy, Villejuif, , France
Name: Fabrice ANDRE
Affiliation: Gustave Roussy, Cancer Campus, Grand Paris
Role: PRINCIPAL_INVESTIGATOR