Breast Cancer
Conditions
Keywords
Breast Cancer, Neoadjuvant, Luminal B tumors, Ribociclib
Brief summary
CORALLEEN is a two-arm, randomized, multicentric study in postmenopausal women with primary HR+/HER2 negative Luminal B breast cancer that will explore if the combination of ribociclib with letrozole offers clinical benefit at least comparable to that of standard chemotherapy.
Detailed description
This is a parallel, two-arm, randomized 1:1, stratified by tumor size and nodal involvement, open-label, multicenter, exploratory study in postmenopausal women with primary operable HR+/HER2-negative Luminal B breast cancer according to PAM50 intrinsic subtype to evaluate the clinical benefit and biological effects of ribociclib combined with letrozole. The primary trial objective is to evaluate the ability of each treatment strategy to provide ROR-low score at surgery. Luminal B patients will be randomized 1:1 to either letrozole plus ribociclib or chemotherapy.Two weeks after the first administration of the assigned treatment, patients will undergo a biopsy to assess early biological response to treatment, at Ki67 protein and gene expression level. After finalization of the assigned neoadjuvant treatment, patients will undergo surgery. The primary endpoint, Rate of ROR-low (at surgery) after neoadjuvant treatment, according to the Prosigna test will be centrally assessed. Baseline, Day 15 and post-treatment (surgical) primary breast tumor tissue samples should be available for each patient for molecular characterization A post-surgery visit will be performed within 28 days (7 days) from surgery, and will mark the end of the study for that patient
Interventions
DRUGRibociclib
Ribociclib flat-fixed dose of 600 mg daily (three 200-mg capsules), days 1 to 21 of a 28-days cycle.
DRUGLetrozole 2.5mg
Daily continuous
DRUGDoxorubicin
60 mg/m2 as a continuous IV perfusion
DRUGCyclophosphamide
600 MG/M2 in a 30 minutes IV infusion
DRUGPaclitaxel
80 mg/m2, in one hour IV infusion
Sponsors
Novartis
SOLTI Breast Cancer Research Group
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Signed Informed Consent Form prior to any study-specific procedure. 2. Female patients. 3. Post-menopausal status and age ≥18 years. 4. Histologically confirmed invasive breast carcinoma, with all the following characteristics: * Primary tumor ≥ 2cm in largest diameter as measured by breast MRI * Stage I to stage IIIA breast cancer * No evidence of distant metastasis (M0) 5. Breast cancer eligible for primary surgery. 6. Available pre-treatment FFPE core (Tru-cut) biopsy evaluable for PAM50 or possibility to obtain one. Minimal sample requirements are to have at least 2 tumor cylinders with a minimal tissue surface of 10 mm2 tissue, containing at least 10% tumor cells and having enough tissue to do at least 2 cuts of 10 micrometers each. 7. Luminal B subtype as per PAM50 analysis of pre-treatment sample. 8. ER-positive and/or PgR-positive and HER2-negative tumor by ASCO/CAP guidelines assessed locally. 9. In the case of a multifocal tumor (defined as the presence of two or more foci of cancer within the same breast quadrant), the largest lesion must be ≥ 2 cm and designated the target lesion for all subsequent tumor evaluations and HR+/HER2-negative status must be documented in all the tumor foci. 10. ECOG performance status of 0 or 1. 11. Adequate hematological, renal and hepatic function. 12. Ability and willingness to comply with study visits, treatment, testing and to comply with the protocol.
Exclusion criteria
1. Any prior treatment for primary invasive breast cancer. 2. Inoperable locally advanced or inflammatory (i.e., inoperable Stage III) breast cancer. 3. Metastatic (Stage IV) breast cancer. 4. Bilateral invasive breast cancer. 5. Multicentric breast cancer, defined as the presence of two or more foci of cancer in different quadrants of the same breast. 6. Patients who have undergone sentinel lymph node biopsy prior to study treatment. 7. Inability or unwillingness to swallow pills. 8. Malabsorption syndrome or other condition that would interfere with enteric absorption of study drugs. 9. Participation in a prior investigational study within 30 days prior to enrollment or within 5 half-lives of the investigational product, whichever is longer. 10. Patient with a Child-Pugh score B or C. 11. Patient has active cardiac disease or a history of cardiac dysfunction including any of the following: * History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty or stenting) or symptomatic pericarditis within 12 months prior to screening. * History of documented congestive heart failure (New York Heart Association functional classification III-IV). * Documented cardiomyopathy. * Patient has a Left Ventricular Ejection Fraction (LVEF) \< 50% as determined by Multiple Gated acquisition (MUGA) scan or echocardiogram (ECHO). * Clinical significant cardiac arrhythmias (e.g. ventricular tachycardia), complete left bundle branch block, high-grade AV block (e.g. bifascicular block, Mobitz type II and third-degree AV block) * Long QT Syndrome or family history of idiopathic sudden death or congenital long QT syndrome. * On screening 12-lead ECG, any of the following cardiac parameters (defined as the mean of triplicate ECGs: bradycardia (resting heart rate \< 50), tachycardia (resting heart rate \> 90), PR interval \> 220 msec, QRS interval \>109 msec, or QTcF interval ≥450 msec (using Fridericia's correction). 12. Uncontrolled hypertension (Systolic blood pressure \>160 mmHg or \<90 mmHg and/or diastolic \>100 mmHg). 13. Active infection requiring intravenous (IV) antibiotics. 14. Symptomatic hypercalcemia despite adequate management. 15. Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis. 16. Known human immunodeficiency virus (HIV) infection. 17. Any other diseases, active or uncontrolled pulmonary dysfunction, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug, that may compromise compliance with the protocol, that may affect the interpretation of the results, or renders the patients at high risk from treatment complications. 18. Significant traumatic injury within 3 weeks prior to initiation of study treatment. 19. Major surgical procedure (not including minor procedures such as lymph node biopsy, tumor core biopsy, fine needle aspiration) within 4 weeks prior to initiation of study treatment or not fully recovered from any side effects of previous procedures. 20. Any psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule. 21. History of other malignancy within 5 years prior to screening, except for appropriately treated basal or squamous cell carcinoma, carcinoma in situ of the cervix, non-melanoma skin carcinoma, or Stage I uterine cancer. 22. Hormone replacement therapy stopped less than 2 weeks before treatment start. 23. Currently receiving or has received systemic corticosteroids until 2 weeks before treatment start or who have not fully recovered from side effects of such treatment. Following corticosteroid uses are permitted: single doses, topical applications (e.g. for rash), inhaled sprays (e.g. for obstructive airways diseases), eye drops or local injections (e.g. intra-articular) 24. Known hypersensitivity to any of the excipients of ribociclib, letrozole, doxorubicin, cyclophosphamide or paclitaxel. 25. Patients currently on following medications, which cannot be interrupted 7 days prior treatment start: * Any prohibited medication as per letrozole, doxorubicin, cyclophosphamide, or paclitaxel label. * Herbal preparations/medications, dietary supplements. * Medications that have a known risk to prolong the QT interval or cause Torsades de Pointe. * Medications with a narrow therapeutic window and predominantly metabolized through CYP3A4/5. * Strong inducers or inhibitors of CYP3A4/5, including grapefruit, grapefruit hybrids, pummelos, star-fruit and Seville oranges. * Warfarin or other coumarin-derived anticoagulant for treatment, prophylaxis or otherwise. Therapy with heparin, low molecular weight heparin or fondaparinux is allowed.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of ROR-low according to the Prosigna test. | 24 weeks | Rate of ROR-low after neoadjuvant treatment at surgery, according to the Prosigna test,as per central assessment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| pCR in the breast and axillary lymph nodes | 24 weeks | pCR is defined as the complete absence of invasive carcinoma in the breast and axillary lymph nodes on histological examination. |
| PEPI Score | 24 weeks | Preoperative endocrine prognostic index (PEPI) score in the ribociclib plus letrozole treatment arm compared to historical values |
| Residual Cancer Burden (RCB) | 24 weeks | Rate of residual cancer burden (RCB) score 0 or 1 (RCB0/1) after neoadjuvant treatment, according to the MD Anderson Cancer Center procedures, as per central assessment. |
| Tumor Overall response rate (ORR) | 24 weeks | Tumor overall objective response rate (ORR), defined as the sum of Partial Responses (PR) and Complete Responses (CR) according to RECIST v1.1, as per Investigator's assessments by breast MRI. |
| Decrease in Ki67 in both treatment arms. | At baseline, in week 2, and pre-surgery | Decrease in Ki67 in both treatment arms. |
| Incidence, duration and severity of Adverse Events (AEs) | Up to 24 weeks | Incidence, duration and severity of Adverse Events (AEs) assessed by the NCI Common Terminology for Classification of Adverse Events (CTCAE) version 4. |
| Rate of breast conserving surgery (BCS) | 24 weeks | Rate of breast conserving surgery |
Countries
Spain
Outcome results
None listed