Etude : BYLIEVE /

ATTENTION : pour chaque essai clinique, les éléments affichés ci-dessous ne sont pas exhaustifs, et le protocole fourni par le promoteur reste l’unique document à consulter pour mener à bien un essai clinique sur centre. Pour plus d'informations, contactez le référent du territoire concerné.

Acronyme / Nom
Situation thérapeutique
Cadre réglementaire
Présentation de l'étude
Acronyme / Nom : BYLIEVE

Situation thérapeutique : Métastatique ou localement avancé

Traitement :

Cadre réglementaire : RIPH1

Dernière MÀJ : 30/04/2021
CIM10 - Localisation(s)
Informations principales
Titre : Étude de phase II non comparative, multicentrique, en ouvert, à deux bras de traitement, évaluant l’efficacité et l’innocuité de l’alpelisib associé au fulvestrant ou au létrozole chez des patients atteints de cancer du sein à un stade avancé avec mutation du gène PIK3CA, récepteurs hormonaux positifs (RH+) et HER2 négatif, ayant progressé pendant ou après un traitement par inhibiteur de CDK 4/6

Spécialité : Seins, organes génitaux de la femme
Localisation : C50 - Tumeur maligne du sein
Informations complémentaires
Schéma : This is a phase II, multicenter, open-label, two-cohort, non-comparative study of alpelisib plus endocrine therapy (either fulvestrant or letrozole) in patients with HR+, HER2-negative aBC harboring PIK3CA mutation(s) in the tumor whose disease has progressed on or after CDK 4/6 inhibitor containing treatments

3 cohorts:
- Cohort A: Prior CDK 4/6 + aromatase
Patients who received any CDK 4/6 inhibitor plus aromatase inhibitor as treatment (immediately prior) will receive alpelisib 500 mg oral.+ fulvestrant 500 mg intramuscular (i.m)
- Cohort B: Prior CDK 4/6 + fulvestrant
Patients who received any CDK 4/6 inhibitor plus fulvestrant as treatment (immediately prior) will receive alpelisib 300 mg oral + letrozole 2.5 mg oral
- Cohort C: Prior systemic chemo or ET
Patients who received systemic chemotherapy or endrocrine therapy (ET) as immediate prior treatment will receive alpelisib 300 mg oral + fulvestrant 500 mg i.m.

Phase : II

Stade : Localement avancé à Métastatique

2, 3, 4, X
Critères d'inclusion
Critères de non-inclusion
Critères d'inclusion et de non-inclusion
Critères d'inclusion : - Patient is male or female 18 years or older
- Males or females with advanced (locoregionally recurrent or metatstatic) breast cancer not amenable to curative therapy
- In case of women, both premenopausal and postmenopausal patients are allowed to be included in study; menopausal status is relevant for the requirement of LHRH agonist (examples for use in this study include but not limited to goserelin, leuprolide or locally available treatment) to be used concomitantly with alpelisib and letrozole/fulvestrant
-> Patient is postmenopausal woman defined as either:
- Prior bilateral oophorectomy or
- Age ≥60 or
- Age <60 and amenorrhea for 12 or more months (in the absence of chemotherapy, tamoxifen, toremifene, or ovarian suppression) and FSH and/or estradiol in the postmenopausal range per local normal range.
If patient is taking tamoxifen or toremifene and age <60, then FSH and plasma estradiol levels should be in post-menopausal range per local normal range.
Note: For women using therapy-induced amenorrhea other than ovarian radiation, goserelin or leuprolide, etc., serial measurements of FSH and/or estradiol are needed to ensure menopausal status
-> Patient is premenopausal defined as either:
- Patient had last menstrual period within the last 12 months or
- If on tamoxifen or toremifene with in the past 14 days, plasma estradiol and FSH must be in the premenopausal range per local normal range, or
- In case of therapy induced amenorrhea, plasma estradiol and/or FSH must be in the premenopausal range per local normal range
- Patient has histological and/or cytological confirmed ER+ and/or PgR+ aBC
- Patient has confirmed HER2-negative advanced breast cancer (aBC)
- Patient has a PIK3CA mutation confirmed by Novartis designated central lab or patient has a pathology report confirming PIK3CA mutant status by certified laboratory (using validated PI3KCA mutation assay) either from tissue or blood and must (mandatory) send tumor tissue to Novartis designated central lab for confirmation of mutational status
- Patient must have:
-> Documented evidence of tumor progression on or after CDK 4/ 6 inhibitor combination treatment; CDK 4/6 inhibitor must be the last treatment regimen prior to study entry,
-> No more than two (2) prior anti-cancer therapies for aBC
-> Received no more than one prior regimen of chemotherapy in the metastatic setting
- Patient has either measurable disease per RECIST v1.1 or at least one predominantly lytic bone lesion must be present
- ECOG performance status ≤ 2
- Patient has fasting plasma glucose (FPG) ≤140 mg/dL (7.7 mmol/L) and glycosylated hemoglobin (HbA1c) ≤ 6.4% (both criteria have to be met)
- Patient has adequate bone marrow, coagulation, liver and renal function

Critères de non-inclusion : - Patient has known hypersensitivity to alpelisib, fulvestrant or letrozole
- Patient has received prior treatment with any PI3K inhibitors
- Patient with an established diagnosis of diabetes mellitus type I or uncontrolled type II
- Patient has a concurrent malignancy or malignancy within 3 years of study screening period, with the exception of adequately treated, basal or squamous cell carcinoma, non-melanoma skin cancer or curatively resected cervical cancer
- Patient has received radiotherapy ≤ 4 weeks or limited field radiation for palliation ≤ 2 weeks prior to enrollment, and who has not recovered to grade 1 or better from related side effects of such therapy
- History of acute pancreatitis within 1 year of screening or past medical history of pancreatitis
- Patients with central nervous system (CNS) involvement unless they meet ALL of the following criteria:
-> At least 4 weeks from prior therapy completion (including radiation and/or surgery) to starting the study treatment
-> Clinically stable CNS tumor at the time of screening untreated or without evidence of progressions for at least 4 weeks after treatment as determined by clinical examination and brain imaging (MRI or CT) during screening period and stable low dose of steroids for 2 weeks prior to initiating study treatment
- Patient with severe liver impairment (Child Pugh score B/C)
- Patient has impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the study drugs
- Patient has documented pneumonitis which is active and requiring treatment
- Patient has a history of Stevens-Johnson-Syndrome (SJS) or Toxic Epidermal Necroloysis (TEN)
- Patient is concurrently using other anti-cancer therapy. All anti-cancer therapy must be discontinued prior to day one of study treatment.
Informations relatives au promoteur
Promoteur :
Novartis Pharmaceuticals
Type de sponsor : Industriel

Coordonnateur :
Centre investigateur
Informations relatives aux investigateurs
Centre investigateur :
Centre François BACLESSE - 3 avenue du Général Harris - 14000 CAEN
Apicrypt :

Investigateur :
Christelle LEVY


Statut de l'essai : CLOS

MAJ : 03/11/2020