Residual Cancer Burden (RCB) 0-I Rate
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 18 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 13 |
Trial · Interventional
Active, not recruitingPhase 2Results postedRegistry dataShort name CARABELA
Spain
1 trial · 1 ongoing · 1 with posted results
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
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.
Outcomes the sponsor listed as primary.
Residual Cancer Burden (RCB) 0-I Rate
Time frame · Through study treatment, and average of 12 months
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
Changes in Percentage of KI67 Dyed Cells
Time frame · 2 weeks of treatment
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.
RCB 0+I Versus RCB-II Versus RCB-III
Time frame · 24 weeks
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.
Number of Participants With Preoperative Endocrine Prognostic Index (PEPI) Score of 0 at Surgery
Time frame · 24 weeks
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.
Clinical Response Measured by Magnetic Resonance Imaging (MRI)
Time frame · 24 weeks
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.
Rate of Breast Conservative Surgery (BCS) in Both Treatment Arms.
Time frame · 24 weeks
Rate of BCS: defined as the proportion of patients who achieved breast-conserving surgery between both treatment arms.
iEFS (Invasive Event Free Survival) in Both Treatment Arms.
Time frame · Up to 10 years
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.
The Number of Participants Who Experienced Adverse Events (AE) Related to Study Treatment
Time frame · Through study treatment, and average of 12 months
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.
To Assess Molecular Downstaging for High Risk Genomic Groups Defined by a Multigene Expression Panel.
Time frame · 24 weeks
Gene expression data provided by a multigene expression panel in sequential tumor biopsies.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 18 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 13 |
| Group | Value (% KI67 dyed cells) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 22.8 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 6 |
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 18 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 13 |
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 26 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 14 |
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 71 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 78 |
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 81 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 64 |
| Group | Value |
|---|
| Group | Value (Participants) |
|---|---|
| Arm A: Doxorubicin Plus Cyclophosphamide and Taxane | 97 |
| Arm B: Letrozole Plus Abemaciclib +/- LHRH | 94 |
| Group | Deaths | Serious events | Other 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 / 100 | 7 / 100 | 97 / 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 cycles | 4 / 99 | 8 / 99 | 94 / 99 |
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