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Spots Global Cancer Trial Database for 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

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Trial Identification

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

Interventions

Alpelisib
Ribociclib

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Fabrice ANDRE

Affiliation: Gustave Roussy, Cancer Campus, Grand Paris

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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