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Phase IB & II Study of Ribociclib With Trastuzumab Plus Letrozole in Postmenopausal HR+, HER2+ Advanced Breast Cancer Patients

Primary Purpose

HER2-positive Breast Cancer, Postmenopausal, Metastatic Breast Cancer

Status
Recruiting
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Ribociclib, Trastuzumab, Letrozole
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HER2-positive Breast Cancer focused on measuring HR-positive, HER2-positive, Breast Cancer, Hormone-positive, CDK4/6 inhibitor

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged ≥19 years
  • Women with advanced (loco-regionally recurrent or metastatic) breast cancer not amenable for curative therapy
  • Histologically and/or cytologically confirmed estrogen receptor positive and/or progesterone receptor positive breast cancer
  • HER2 positive breast cancer (IHC 3+ or IHC 2+ and FISH, SISH or CISH+)
  • Postmenopausal patient defined as either one of the following.

    • Prior bilateral ovariectomy
    • Age ≥ 60 years old
    • Age <60 years and amenorrhea over 12 months (without chemotherapy, tamoxifen, toremifene or ovarian inhibition), FSH and estradiol are in the postmenopausal range according to local normal range
  • Patients who were not previously treated with systemic treatment for advanced / metastatic breast cancer
  • ECOG performance status 0 or 1
  • Measurable or evaluable lesion according to RECIST v1.1
  • Normal organ function defined as

    • ANC (absolute neutrophil count) ≥ 1.5 × 109/L
    • Platelet ≥ 100 × 109/L
    • Serum Hb ≥ 9.0 g/dL
    • INR ≤1.5
    • Serum creatinine ≤ 1.5 X ULN
    • ALT & ALT < 2.5 X ULN (in the absence of liver metastasis) or ALT & ALT < 5 X ULN (with liver metastasis)
    • Total serum bilirubin < 1.5 X ULN
  • Left Ventricular Ejection Fraction (LVEF) within normal range
  • Voluntary agreement on clinical trials

Exclusion Criteria:

- Patients who have previously received CDK4 / 6 inhibitors or who have received other systemic treatments for advanced / metastatic breast cancer (Previous neo-adjuvant of adjuvant trastuzumab or aromatase inhibitor is not allowed, unless

  1. Disease free interval was more than 12 months from the last dose of adjuvant trastuzumab or
  2. Adjuvant aromatase inhibitor was administered more than 2 years)

    • Inflammatory breast cancer
    • Central nervous system metastasis
    • Active cardiac disease or a history of cardiac dysfunction including any of the following (Congestive heart failure within 6 months, history of myocardial infarction, unstable angina pectoris, or QTc prolongation on electrocardiogram)
    • Gastrointestinal absorption disorders that interfere with drug absorption
    • Patients who is currently receiving medications that can prolong QT intervals (QTc>450msec) on ECG or that can cause torsades de pointes
    • Patients with severe visceral metastasis on enrolment who are not indicated with hormone treatment
    • Serious surgical treatment within 14 days prior to study treatment
    • Radiotherapy within 21 days prior to study treatment
    • Serious medical comorbidities
    • Concurrent malignancy or malignancy within 3 years of study participation, with the exception of adequately treated, basal or squamous cell carcinoma, non-melanomatous skin cancer or curatively resected cervical cancer.

Sites / Locations

  • Yonsei Cancer Center at Yonsei University Health SystemRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Combination of Letrozole, Trastuzumab with Ribociclib

Arm Description

Phase IB (dose escalation of ribociclib with fixed dose of letrozole and Ribociclib) Phase II (ribociclib of RPIID with fixed dose of letrozole and ribociclib)

Outcomes

Primary Outcome Measures

Progression free survival
Progression free survival is defined as the time from the start of investigational drug to disease progression or patient's death whichever occurred first

Secondary Outcome Measures

Overall survival
Overall survival is the time from the start of investigational drug to patient's death.
Response rate
Response rate is defined as the response to the drug according to RECIST v1.1 criteria.
Quality of life
Overall survival is the time from the start of investigational drug to patient's death Response rate is defined as the response to the drug according to RECIST v1.1 criteria Quality of life will be measured using EORTC-QLQ C30 questionaire. (Purpose of EORTC-QLQ C30 is to measure the quality of life of the subjects who participated in the clinical study. It consists of 30 questions and each question will be answered by 4 scale answers "Not at all", "A little", "Quite a bit", and "Very much".)

Full Information

First Posted
April 10, 2019
Last Updated
May 9, 2022
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT03913234
Brief Title
Phase IB & II Study of Ribociclib With Trastuzumab Plus Letrozole in Postmenopausal HR+, HER2+ Advanced Breast Cancer Patients
Official Title
Phase IB & II Study of Ribociclib With Trastuzumab Plus Letrozole in Postmenopausal HR+, HER2+ Advanced Breast Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 10, 2019 (Actual)
Primary Completion Date
October 30, 2023 (Anticipated)
Study Completion Date
October 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Survival benefit and quality of life are two key elements that should be kept in mind in the treatment of metastatic breast cancer. In this regards, endocrine therapy (ET) is strongly recommended in hormone receptor (HR) positive patients unless there is visceral crisis even though there is no concrete evidence that it is better than chemotherapy in terms of survival. HER2 positive breast cancer is a subtype of breast cancer that showed the greatest improvement in terms of survival during the last decade due to trastuzumab based therapy. Recently, taxane and HER2 directed doublet including trastuzumab and pertuzumab (THP) is considered as standard of therapy based upon randomized phase 3 clinical trial (CLEOTATRA). HER2 positive breast cancer can be divided into HER2 enriched subgroup (HR-HER2+) and luminal B subgroup (HR+HER2+) in biologic viewpoint because they are distinctly different subgroups in gene expression analysis. Accordingly, we are currently treating biologically different subtypes in a same way, which is CTx and anti-HER2 combination therapy (THP). Luminal HER2+ subgroup has actually been tested with endocrine therapy (ET) and anti-HER2 therapy showed better PFS than ET alone (TAnDEM trial and trial comparing lapatinib plus letrozole versus letrozole alone) [2],[3] confirming existence of cross talk between ER and HER2 pathways in clinical setting. However, the combination regimen between ET and anti-HER2 therapy is not widely used in current practice in ER+HER2+ MBC patients because PFS seemed to be relatively shorter compared with chemotherapy based combination with anti-HER2 therapy even though several guidelines recommend it to be used as an initial treatment unless there is visceral crisis as they recommended ET alone first in ER+HER2- MBC (NCCN 2018). Recently, various CDK4/6 inhibitors including palbociclib, abemaciclib, and ribociclib were approved by FDA based on the clinical trial results demonstrating prolonged PFS over ET alone when it was combined with ET in ER+ advanced breast cancer [4]. In PALOMA 2 biomarker study, it was beneficial regardless of ER and Ki67 expression status. Reflecting quite durable PFS prolongation (10 month in PALOMA2) shown in ER+ disease (luminal A and luminal B subtype except HR+HER2+ patients) with CDK4/6 inhibitor on top of ET, the hypothesis of this trial is whether CDK4/6 inhibitor could prolong survival in luminal HER2 breast cancer as it did in ER+HER2-patients. In preclinical study, palbociclib showed activity in not only ER+ cell lines but also HER2 positive cell lines [5]. Also, in phase Ib trial, a CDK4/6 inhibitor from Lilly, abemaciclib showed acceptable toxicity with endocrine therapy or trastuzumab with response rate of around 20%. Hence, as of today, it could be justified and warranted to conduct a prospective trial of ribocicib+letrozole+trastuzumab in order to take a look at its efficacy and toxicity in HR+HER2 + advanced breast cancer.
Detailed Description
This trial is performed in a multicenter, single-group, and phases IB and II clinical trial. This is a single-group clinical trial of the effects of ribociclib, letrozole and trastuzumab in postmenopausal women with HR+, HER2+ advanced breast cancer. This trial consists of two parts. The first part is a phase IB study of increasing the dose of ribociclib from 200mg to 600mg in combination with letrozole 2.5mg and trastuzumab (8mg/kg followed by 6mg/kg every 3 weeks). In phase IB study, three to six patients will be enrolled for each dose group. When the IB phase ends, patient enrollment will be discontinued for intermediate safety analysis, and after DLT analysis will determine recommended phase II phase II part will be started. The recommended phase II dose of ribocicib determined in phase IB part with ribociclib and trastuzumab (8mg/kg followed by 6mg/kg every 3 weeks) will be administered. Treatment is discontinued in the following cases. Progression of disease Uncontrolled toxicity Patient's death Withdrawal of consent In phase II part, 61 patients will be enrolled and the first 20 patients will be analyzed for run-in phase to confirm the safety of the therapy. Regardless of treatment cycle, the disease will be evaluated in the same manner as the method used at the time of registration at intervals of 8 weeks for the first 18 months and at intervals of 12 weeks after that. If the progress of the disease is clinically suspected, additional tests can be performed

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HER2-positive Breast Cancer, Postmenopausal, Metastatic Breast Cancer
Keywords
HR-positive, HER2-positive, Breast Cancer, Hormone-positive, CDK4/6 inhibitor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
95 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Combination of Letrozole, Trastuzumab with Ribociclib
Arm Type
Experimental
Arm Description
Phase IB (dose escalation of ribociclib with fixed dose of letrozole and Ribociclib) Phase II (ribociclib of RPIID with fixed dose of letrozole and ribociclib)
Intervention Type
Drug
Intervention Name(s)
Ribociclib, Trastuzumab, Letrozole
Intervention Description
Phase IB: letrozole 2.5mg (fixed dose), trastuzumab (8mg/kg loading followed by 6mg/kg q 3weeks, fixed dose) plus ribociclib (dose escalation from 200mg to 600mg) to identify recommended phase iI dose (RPIID) Phase II: letrozole, trastuzumab (same as phase IB) plus ribocicilb RPIID
Primary Outcome Measure Information:
Title
Progression free survival
Description
Progression free survival is defined as the time from the start of investigational drug to disease progression or patient's death whichever occurred first
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall survival
Description
Overall survival is the time from the start of investigational drug to patient's death.
Time Frame
1 year
Title
Response rate
Description
Response rate is defined as the response to the drug according to RECIST v1.1 criteria.
Time Frame
1 year
Title
Quality of life
Description
Overall survival is the time from the start of investigational drug to patient's death Response rate is defined as the response to the drug according to RECIST v1.1 criteria Quality of life will be measured using EORTC-QLQ C30 questionaire. (Purpose of EORTC-QLQ C30 is to measure the quality of life of the subjects who participated in the clinical study. It consists of 30 questions and each question will be answered by 4 scale answers "Not at all", "A little", "Quite a bit", and "Very much".)
Time Frame
1 year

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged ≥19 years Women with advanced (loco-regionally recurrent or metastatic) breast cancer not amenable for curative therapy Histologically and/or cytologically confirmed estrogen receptor positive and/or progesterone receptor positive breast cancer HER2 positive breast cancer (IHC 3+ or IHC 2+ and FISH, SISH or CISH+) Postmenopausal patient defined as either one of the following. Prior bilateral ovariectomy Age ≥ 60 years old Age <60 years and amenorrhea over 12 months (without chemotherapy, tamoxifen, toremifene or ovarian inhibition), FSH and estradiol are in the postmenopausal range according to local normal range Patients who were not previously treated with systemic treatment for advanced / metastatic breast cancer ECOG performance status 0 or 1 Measurable or evaluable lesion according to RECIST v1.1 Normal organ function defined as ANC (absolute neutrophil count) ≥ 1.5 × 109/L Platelet ≥ 100 × 109/L Serum Hb ≥ 9.0 g/dL INR ≤1.5 Serum creatinine ≤ 1.5 X ULN ALT & ALT < 2.5 X ULN (in the absence of liver metastasis) or ALT & ALT < 5 X ULN (with liver metastasis) Total serum bilirubin < 1.5 X ULN Left Ventricular Ejection Fraction (LVEF) within normal range Voluntary agreement on clinical trials Exclusion Criteria: - Patients who have previously received CDK4 / 6 inhibitors or who have received other systemic treatments for advanced / metastatic breast cancer (Previous neo-adjuvant of adjuvant trastuzumab or aromatase inhibitor is not allowed, unless Disease free interval was more than 12 months from the last dose of adjuvant trastuzumab or Adjuvant aromatase inhibitor was administered more than 2 years) Inflammatory breast cancer Central nervous system metastasis Active cardiac disease or a history of cardiac dysfunction including any of the following (Congestive heart failure within 6 months, history of myocardial infarction, unstable angina pectoris, or QTc prolongation on electrocardiogram) Gastrointestinal absorption disorders that interfere with drug absorption Patients who is currently receiving medications that can prolong QT intervals (QTc>450msec) on ECG or that can cause torsades de pointes Patients with severe visceral metastasis on enrolment who are not indicated with hormone treatment Serious surgical treatment within 14 days prior to study treatment Radiotherapy within 21 days prior to study treatment Serious medical comorbidities Concurrent malignancy or malignancy within 3 years of study participation, with the exception of adequately treated, basal or squamous cell carcinoma, non-melanomatous skin cancer or curatively resected cervical cancer.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joo Hyuk Sohn, Md, PhD
Phone
82-2-2228-8135
Email
oncosohn@yuhs.ac
Facility Information:
Facility Name
Yonsei Cancer Center at Yonsei University Health System
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joo Hyuk Sohn, MD, PhD
Phone
82-2-2228-8135
Email
oncosohn@yuhs.ac

12. IPD Sharing Statement

Learn more about this trial

Phase IB & II Study of Ribociclib With Trastuzumab Plus Letrozole in Postmenopausal HR+, HER2+ Advanced Breast Cancer Patients

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