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Trial · Interventional

Active, not recruitingPhase 2Results postedRegistry data

Neoadjuvant Study Chemotherapy vs Letrozole + Abemaciclib in HR+/HER2- High/Intermediate Risk Breast Cancer Patients

Short name CARABELA

NCTNCT04293393 (opens ClinicalTrials.gov in a new tab)Other idGEICAM/2019-01Other id2019-002123-15Other id2019

Overview

Status
Active, not recruiting
Phase
Phase 2
Enrollment
200 participants (actual)
Sponsor
Spanish Breast Cancer Research Group · Other
Design
Randomized · Open label (no masking)
Countries
1 country

Spain

Start
2 Oct 2020
Primary completion
21 Jun 2023
Completion
28 Feb 2033 (estimated)
First posted
3 Mar 2020
Last update posted
12 Mar 2026
Conditions
Early Breast Cancer

Timeline

1 trial · 1 ongoing · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202020252030
  1. Ph 2

    CARABELA

    NCT04293393

    2 Oct 2020 to est. 28 Feb 2033

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Phase II, randomized, open-label, international, multicenter study to compare efficacy of standard chemotherapy vs. letrozole plus abemaciclib as neoadjuvant therapy in HR-positive/HER2-negative high/intermediate risk breast cancer patients

Interventions

  • DoxorubicinDrug
  • CyclophosphamideDrug
  • TaxaneDrug
  • LetrozoleDrug
  • AbemaciclibDrug
  • LHRH AnalogueDrug

Arms2

  • Active comparator

    Arm A: Doxorubicin plus cyclophosphamide and taxane

    Doxorubicin 60mg/m2 and cyclophosphamide 600mg/m2 (AC) every 21 days for 4 cycles followed by weekly paclitaxel 80mg/m2 for 12 weeks or 3-weekly docetaxel 100mg/m2 for 4 cycles. Approximately duration of 24 weeks (6 months).

  • Experimental

    Arm B: Letrozole plus abemaciclib +/- LHRH

    Letrozole 2.5mg orally daily + abemaciclib 150mg orally every 12 hours on a continuous dosing schedule, +/- luteinizing hormone-releasing hormone (LHRH) analogs in premenopausal women, up to 12 months, in 28-day cycles.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Residual Cancer Burden (RCB) 0-I Rate

    Time frame · Through study treatment, and average of 12 months

    Registry description

    Evaluation of the number of patients with a RCB 0-I index as a measure of efficacy. RCB is a continuous variable derived from the primary tumor dimensions, cellularity of the tumor bed, and axillary nodal burden. It is estimated from routine pathological sections of the primary breast tumor site and the regional lymph nodes after the completion of Neoadjuvant therapy. The pathological variables include bidimensional diameters of the primary tumor bed, the proportion of primary tumor area containing invasive carcinoma, the number of positive lymph nodes, and the diameter of the largest nodal metastasis

Secondary outcomes(8)
  1. Changes in Percentage of KI67 Dyed Cells

    Time frame · 2 weeks of treatment

    Registry description

    The percentage of decrease in the geometric mean of Ki67 after 2 weeks of treatment in both treatments arms. Number of patients with cell cycle arrest (Ki67 \< 2.7%) after 2 weeks of treatment in both treatment arms.

  2. RCB 0+I Versus RCB-II Versus RCB-III

    Time frame · 24 weeks

    Registry description

    RCB is classified in four classes based on the residual disease (RD): * RCB-0 defined as pathological complete response. * RCB-I defined as minimal RD. * RCB-II defined as moderate RD. * RCB-III defined as extensive RD.

  3. Number of Participants With Preoperative Endocrine Prognostic Index (PEPI) Score of 0 at Surgery

    Time frame · 24 weeks

    Registry description

    PEPI requires pathological stage (tumor size and nodal status), level of Ki67 protein, and Allred ER score measured on the surgical specimen. PEPI score 0 includes pT1 or pT2, pN0, Ki67 ≤ 2.7%, Allred score \> 2. Patients with a PEPI score of 0 are found to have a low risk of recurrence.

  4. Clinical Response Measured by Magnetic Resonance Imaging (MRI)

    Time frame · 24 weeks

    Registry description

    According to RECIST v1.1 in both treatment arms. Clinical Response Rate (CRR) is defined as the proportion of subjects with complete or partial radiographic response. Complete Response (CR) and Partial Response (PR) definitions are assessed by MRI at baseline and prior to breast surgery, with or without regional lymph nodes surgery, and categorized according to percent reduction in tumor size.

  5. Rate of Breast Conservative Surgery (BCS) in Both Treatment Arms.

    Time frame · 24 weeks

    Registry description

    Rate of BCS: defined as the proportion of patients who achieved breast-conserving surgery between both treatment arms.

  6. iEFS (Invasive Event Free Survival) in Both Treatment Arms.

    Time frame · Up to 10 years

    Registry description

    Invasive event free survival (iEFS): defined as time from randomization to progressive disease or invasive disease recurrence (local, regional, distant, or contralateral), or death from any cause. Invasive disease recurrence is defined as: * Ipsilateral invasive breast tumor recurrence (including second primary invasive breast cancer): an invasive breast cancer involving the same breast parenchyma as the original primary lesion. * Ipsilateral regional invasive breast cancer recurrence (i.e., an invasive breast cancer in the axilla, other regional lymph nodes, chest wall, and/or skin of the ipsilateral breast). * Distant recurrence (i.e., evidence of breast cancer in any anatomic site outside local and/or regional location and that has been either histologically confirmed or clinically diagnosed as recurrent invasive breast cancer) * Contralateral invasive breast cancer * Second primary invasive cancer of non-breast origin.

  7. The Number of Participants Who Experienced Adverse Events (AE) Related to Study Treatment

    Time frame · Through study treatment, and average of 12 months

    Registry description

    Safety assessments were performed at baseline and during the study: Vital signs assessments (blood pressure, pulse and body temperature), measurement of left ventricular ejection fraction, standard 12-lead electrocardiogram, laboratory assessments (hemoglobin, White Blood Cell, Absolute Neutrophil Count, Lymphocytes, platelet count, fasting glucose, alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, total bilirubin, serum creatinine, sodium, potassium, total calcium, blood urea nitrogen (or urea), pregnancy test , ophthalmologic assessments (visual acuity testing, slit lamp examination, fundoscopy), Viral serology. AEs will be graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0. The toxicity of study treatments will be evaluated in the safety population.

  8. To Assess Molecular Downstaging for High Risk Genomic Groups Defined by a Multigene Expression Panel.

    Time frame · 24 weeks

    Registry description

    Gene expression data provided by a multigene expression panel in sequential tumor biopsies.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeCount of participants· Through study treatment, and average of 12 months

Residual Cancer Burden (RCB) 0-I Rate

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane18
Arm B: Letrozole Plus Abemaciclib +/- LHRH13
Secondary and other outcome results(7)
Secondary outcomeMean· 2 weeks of treatment

Changes in Percentage of KI67 Dyed Cells

GroupValue (% KI67 dyed cells)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane22.8
Arm B: Letrozole Plus Abemaciclib +/- LHRH6
Secondary outcomeCount of participants· 24 weeks

RCB 0+I Versus RCB-II Versus RCB-III

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane18
Arm B: Letrozole Plus Abemaciclib +/- LHRH13
Secondary outcomeCount of participants· 24 weeks

Number of Participants With Preoperative Endocrine Prognostic Index (PEPI) Score of 0 at Surgery

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane26
Arm B: Letrozole Plus Abemaciclib +/- LHRH14
Secondary outcomeCount of participants· 24 weeks

Clinical Response Measured by Magnetic Resonance Imaging (MRI)

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane71
Arm B: Letrozole Plus Abemaciclib +/- LHRH78
Secondary outcomeCount of participants· 24 weeks

Rate of Breast Conservative Surgery (BCS) in Both Treatment Arms.

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane81
Arm B: Letrozole Plus Abemaciclib +/- LHRH64
Secondary outcome· Up to 10 years

iEFS (Invasive Event Free Survival) in Both Treatment Arms.

GroupValue
Secondary outcomeCount of participants· Through study treatment, and average of 12 months

The Number of Participants Who Experienced Adverse Events (AE) Related to Study Treatment

GroupValue (Participants)
Arm A: Doxorubicin Plus Cyclophosphamide and Taxane97
Arm B: Letrozole Plus Abemaciclib +/- LHRH94

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Arm A: Doxorubicin Plus Cyclophosphamide and TaxaneDoxorubicin 60mg/m2 and cyclophosphamide 600mg/m2 (AC) every 21 days for 4 cycles followed by weekly paclitaxel 80mg/m2 for 12 weeks or 3-weekly docetaxel 100mg/m2 for 4 cycles. Approximately duration of 24 weeks (6 months). Doxorubicin: Doxorubicin 60mg/m2 and cyclophosphamide 600mg/m2 (AC) every 21 days for 4 cycles followed by weekly paclitaxel 80mg/m2 for 12 weeks or 3-weekly docetaxel 100mg/m2 for 4 cycles. Cyclophosphamide: Doxorubicin 60mg/m2 and cyclophosphamide 600mg/m2 (AC) every 21 days for 4 cycles followed by weekly paclitaxel 80mg/m2 for 12 weeks or 3-weekly docetaxel 100mg/m2 for 4 cycles. Taxane: Doxorubicin 60mg/m2 and cyclophosphamide 600mg/m2 (AC) every 21 days for 4 cycles followed by weekly paclitaxel 80mg/m2 for 12 weeks or 3-weekly docetaxel 100mg/m2 for 4 cycles.1 / 1007 / 10097 / 100
Arm B: Letrozole Plus Abemaciclib +/- LHRHLetrozole 2.5mg orally daily + abemaciclib 150mg orally every 12 hours on a continuous dosing schedule, +/- luteinizing hormone-releasing hormone (LHRH) analogs in premenopausal women, up to 12 months, in 28-day cycles. Letrozole: Letrozole 2.5mg orally daily + abemaciclib 150mg orally every 12 hours on a continuous dosing schedule, +/- LHRH analogs in premenopausal women, up to 12 months, in 28-day cycles Abemaciclib: Letrozole 2.5mg orally daily + abemaciclib 150mg orally every 12 hours on a continuous dosing schedule, +/- LHRH analogs in premenopausal women, up to 12 months, in 28-day cycles LHRH Analogue: Letrozole 2.5mg orally daily + abemaciclib 150mg orally every 12 hours on a continuous dosing schedule, +/- LHRH analogs in premenopausal women, up to 12 months, in 28-day cycles4 / 998 / 9994 / 99

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
Female
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: Patients are eligible to be enrolled in the study only if they meet all of the following criteria: 1. Written informed consent prior to any specific study procedures. 2. Women ≥ 18 years of age. 3. Documentation of histologically confirmed primary invasive adenocarcinoma of the breast. 4. Availability of a primary tumor tissue sample obtained during the diagnostic process before treatment for the central assessment of Ki67 index. 5. Documentation of Hormone Receptor (HR) positive and Human Epidermal Growth Factor Receptor 2 (HER2) negative Breast Cancer (BC) based on local laboratory determination. * HR positive is defined as more than or equal to 10% positive cells by Immunohistochemistry (IHC) for ER and/or progesterone receptor (PgR). * HER2 negative tumor is determined according to recommendations of American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) 2018 guidelines. 6. Intermediate and high risk patients based on Ki67 index value (≥ 20%) determined at a central laboratory. 7. Patients should be in the following clinical stages of disease according to the 8th edition of the TNM Classification of Breast Cancer by the Union for International Cancer Control (UICC): T2 (\> 2cm) - T3, T4b, N0 - N2, M0 (stages IIA, IIB, IIIA or IIIB). Subpopulation with tumors T2 N0 M0 will include high risk patients based on Ki67 index \> 30% or Ki67 index between 20-30% and PgR negative with or without histological grade 3. 8. Patients diagnosed with multifocal or multicentric breast cancer will be eligible for the study if only 2 tumor lesions have been confirmed in the clinical evaluation and both lesions comply with the characteristics required by the protocol (please, refer to previous inclusion criteria). 9. Indication of neoadjuvant treatment. 10. At the time of presentation, patients must be candidates for potentially curative surgery by surgeon's assessment. 11. Sentinel lymph node biopsy (SLNB) will be preferable after the neoadjuvant treatment. Those patients with SLNB before the neoadjuvant treatment will be eligible for the study only if the SLNB has a negative result (N0). One Step Nucleic Acid Amplification (OSNA) method is not allowed. 12. Premenopausal and postmenopausal women. Postmenopausal status is defined as: * Patient underwent bilateral oophorectomy, or * Age ≥ 60 years, or * Age \< 60 years and amenorrhea for 12 or more months (in the absence of chemotherapy, tamoxifen, toremifene or ovarian suppression) and Folliculostimulating hormone (FSH) and plasma estradiol are in the postmenopausal ranges per local normal ranges. All women who do not meet the criteria for postmenopausal status are considered premenopausal for the purpose of this trial. 13. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1. 14. Patients are able to swallow oral medications. 15. Adequate organ and bone marrow function: * Absolute neutrophil count (ANC) ≥ 1,500/mm3 (1.5x109/L); * Platelets ≥ 100,000/mm3 (100x109/L); * Hemoglobin (Hgb) ≥ 8g/dL (80g/L) (erythrocyte transfusions are permitted; initial treatment must not begin earlier than the day after the erythrocyte transfusion); * Total serum bilirubin ≤ 1.5x Upper Limit of Normal (ULN) (≤ 2x ULN and direct bilirubin within normal limits if Gilbert´s disease); * Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 3x ULN. 16. Left ventricular ejection fraction (LVEF) ≥ 50% measured by multiple-gated acquisition scan (MUGA) or echocardiogram (ECHO). 17. For premenopausal women: agreement to remain abstinent or use single or combined non-hormonal contraceptive methods that result in a failure rate of \< 1% per year during the treatment period and for at least 3 weeks after the last dose of study treatment. Abstinence is only acceptable if it is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or post-ovulation methods) and withdrawal are not acceptable methods of contraception. Examples of non-hormonal contraceptive methods with a failure rate of \< 1% per year include tubal ligation, male sterilization, and certain intrauterine devices. Alternatively, two methods (e.g., two barrier methods such as a condom and a cervical cap) may be combined to achieve a failure rate of \< 1% per year. Barrier methods must always be supplemented with the use of a spermicide. 18. Negative serum pregnancy test within 7 days of the first dose of abemaciclib for premenopausal women, and for women who have experienced menopause onset \< 12 months prior to first dose of therapy. 19. Patients consent to biological sample provision for biomarker exploratory analyses. 20. Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures. Exclusion Criteria: Patients will be excluded from the study if they meet any of the following criteria: 1. Previous anti-cancer treatment with therapeutic intent for current breast cancer is not allowed. 2. Inflammatory breast cancer, multifocal/multicentric breast cancer with ≥ 3 tumor lesions or synchronous bilateral invasive breast cancers are not eligible. 3. Serious and/or uncontrolled preexisting medical condition(s) that, in the judgment of the investigator, would preclude participation in this study (for example, interstitial lung disease, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment \[e.g. estimated creatinine clearance \< 30ml/min\], history of major surgical resection involving the stomach or small bowel, or preexisting Crohn's disease or ulcerative colitis or a preexisting chronic condition resulting in baseline Grade 2 or higher diarrhea). 4. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose- galactose malabsorption. 5. Females who are pregnant or lactating. 6. Active systemic bacterial infection (requiring intravenous \[IV\] antibiotics at time of initiating study treatment), fungal infection, or detectable viral infection (such as known human immunodeficiency virus positivity or with known active hepatitis B or C \[for example, hepatitis B surface antigen positive\]. Screening is not required for enrollment. 7. Personal history of any of the following conditions: syncope of cardiovascular etiology, ventricular arrhythmia of pathological origin (including, but not limited to, ventricular tachycardia and ventricular fibrillation), or sudden cardiac arrest. 8. Diagnosis of any other malignancy within 5 years prior to randomization, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix or colorectal. 9. Prior hematopoietic stem cell or bone marrow transplantation. 10. Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.

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