Back to resultsPhase 2 Trial of AEZS-108 in Chemotherapy Refractory in Triple Negative Breast Cancer
Primary Purpose
Breast Cancer
Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
AEZS-108
SCCC
Dexamethasone
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Women ≥ 18 years of age
- Histologically documented breast cancer (either primary or metastatic site) that is (i) ER-negative (0), (ii) PR-negative (0), and (iii) HER2-negative, defined by IHC (immunohistochemistry; IHC 0/1, non-overexpressing) or FISH (fluorescence in situ hybridization; FISH negative) or CISH (chromogen in situ hybridization; CISH negative).
- Expression of LHRH receptor confirmed by IHC on archival (or current biopsy of breast tumor or metastatic site) breast cancer tissue
- Progressive disease after failure of 1 to 3 prior chemotherapy regimens for recurrent or metastatic (Stage IV) disease (prior adjuvant/neoadjuvant therapy is allowed)
- Measurable disease by RECIST 1.1 criteria; at least one target lesion that has not been previously irradiated.
Exclusion Criteria:
- Eastern Cooperative Oncology Group (ECOG) performance status > 2
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or recent myocardial infarction (within 6 months of enrollment)
- Leptomeningeal disease or brain metastases requiring steroids or other therapeutic intervention
- Left ventricular ejection fraction (LVEF) < 50 %, determined by echocardiogram or MUGA scan
Compromised organ or marrow function as evidenced by any of the following:
- thrombocyte count: < 100x109/L
- absolute neutrophil count (ANC): < 1.5x109/L
- hemoglobin: < 6.0 mmol/L (< 9 g/100 mL)
- AS(A)T, AL(A)T: > 2.5 times upper limit of normal range (ULN) (> 5x ULN if clearly related to liver metastases)
- bilirubin: > 1.5 mg/dL
- creatinine: > 1.5 mg/dL or creatinine clearance < 40 mL/min.
Systemic anticancer therapy or radiotherapy within 21 calendar days of the first dose of study drug*)
* also excluded are patients with anticipated ongoing concomitant anticancer therapy during the study
- Prior exposure to anthracyclines or anthracenediones for the treatment of metastatic breast cancer including liposomal doxorubicin (Doxil), doxorubicin, daunorubicin, or mitoxantrone
- Prior adjuvant anthracyclines with a cumulative anthracycline dose ≥ 300 mg/m2
- Ongoing therapeutic anticoagulation
Patients who are not surgically sterile or post-menopausal must agree to use for the duration of the study reliable methods of birth control defined as:
- complete abstinence
- any intrauterine device (IUD) with published data showing that the lowest expected failure rate is < 1 % per year, or
- any other methods with published data showing that the lowest expected failure rate is less than 1 % per year
- Investigational therapy within 30 calendar days of the first scheduled day of protocol treatment (investigational therapy is defined as treatment for which there is currently no regulatory authority approved indication).
Sites / Locations
- University of Miami
- Universitäts-Frauenklinik
- Klinik für Frauenheilkunde und Geburtshilfe
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Arm A: AEZS-108
Arm B: Standard (SCCC)
Arm Description
Intervention: AEZS-108 (267 mg/m^2, 2-hour IV infusion every Day 1 of a 21-day (3-week) cycle). Recommended prophylactic anti-emetic for AEZS-108: 8 mg dexamethasone
commercially available standard single agent cytotoxic chemotherapy (SSCC): - doses below the recommended package insert at the discretion of treating oncologist; - on a 21-day cycle (although weekly administration is allowed; note: pegylated liposomal doxorubicin will be administered on a 28-day cycle).
Outcomes
Primary Outcome Measures
Efficacy of AEZS-108 compared to SSCC as measured by the median time of progression-free survival (PFS).
PFS is defined as the time elapsed from randomization to the date of documented progression or death, whichever comes first. For surviving patients without progression who begin alternative treatment, PFS will be censored at the last date of documented progression-free status prior to starting alternative treatment. Similarly, losses to follow up will be censored at the last date of documented progression-free status.
Secondary Outcome Measures
Efficacy of AEZS-108: overall response
Overall response per RECIST 1.1 (i.e. complete response (CR) + partial response (PR).
Efficacy of AEZS-108: clinical benefit
Overall clinical benefit = complete response (CR) + partial response (PR) + stable disease (SD)
Efficacy of AEZS-108: duration of response
The duration of overall response is measured from the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented (taking as reference for progressive disease the smallest measurements recorded since the treatment started). The duration of overall CR is measured from the time measurement criteria are first met for CR until the first date that progressive disease is objectively documented.
Efficacy of AEZS-108: time to progression (TTP)
TTP is defined as the time elapsed from randomization to the earliest date of documented disease progression. For surviving patients without progression of breast cancer who begin alternative treatment, TTP will be censored at the last date of documented progression-free status prior to starting alternative treatment. This is expected to be negligible and, if the actual data suggest otherwise, competing risk methods will be used instead of Kaplan-Meier estimates. Similarly, losses to follow up will be censored at the last date of documented progression free status.
Efficacy of AEZS-108: overall survival
Overall survival (OS) is defined as the elapsed time from start of therapy to death from any cause. For surviving patients, follow-up will be censored at the date of last contact.
Toxicity of AEZS-108 in this patient population
All patients will be evaluable for toxicity from the time of their first treatment with the study drug.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01698281
Brief Title
Phase 2 Trial of AEZS-108 in Chemotherapy Refractory in Triple Negative Breast Cancer
Official Title
A Randomized Phase 2 Trial of AEZS-108 in Chemotherapy Refractory Triple Negative, LHRH-positive Metastatic Breast Cancer.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2013
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment
Study Start Date
December 2012 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AEterna Zentaris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a therapeutic exploratory Phase 2 study evaluating AEZS-108 compared to standard single agent cytotoxic chemotherapy (SSCC) as measured by the median time of progression-free survival (PFS) in patients with chemotherapy refractory triple negative (ER/PR/HER2-negative) LHRH-R positive metastatic breast cancer.
Detailed Description
The study will be conducted as an open-label randomized two-arm multicenter Phase II study. Patients will be randomized in a 1:1 ratio into one of the two treatment arms within each stratum: AEZS-108 (267 mg/m2 every 21 calendar days) (Arm A) OR SSCC (Arm B) at discretion of treating oncologist cycled every 21 calendar days.
Stratified randomization will be used with number of prior lines of therapies (1-2 versus >2). Tumor assessment will be repeated every 2 cycles. At the time of disease progression, Arm B patients may be crossed over to AEZS-108 as long as none of the exclusion criteria for study entry apply. Particularly, LVEF ≥50% is required, and patients failing on liposomal doxorubicin cannot be crossed over to AEZS-108.
Analysis of the main study endpoint, PFS, will follow a group sequential design with one interim and one final analysis utilizing the O'Brien-Fleming stopping boundaries procedure. The study will be terminated for futility if the lower bound is crossed and for superiority if the upper bound is crossed. The sponsor may also terminate the study for futility based on other considerations such as safety.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm A: AEZS-108
Arm Type
Experimental
Arm Description
Intervention: AEZS-108 (267 mg/m^2, 2-hour IV infusion every Day 1 of a 21-day (3-week) cycle). Recommended prophylactic anti-emetic for AEZS-108: 8 mg dexamethasone
Arm Title
Arm B: Standard (SCCC)
Arm Type
Active Comparator
Arm Description
commercially available standard single agent cytotoxic chemotherapy (SSCC): - doses below the recommended package insert at the discretion of treating oncologist;
- on a 21-day cycle (although weekly administration is allowed; note: pegylated liposomal doxorubicin will be administered on a 28-day cycle).
Intervention Type
Drug
Intervention Name(s)
AEZS-108
Other Intervention Name(s)
Zoptarelin doxorubicin
Intervention Description
AEZS-108 (267 mg/m2, 2-hour IV infusion every Day 1 of a 21-day (3-week) cycle. Allowed delay of re-treatment: up to 2 weeks.
Dose reduction: to 210 mg/m2 and 160 mg/m2, if dose limiting toxicity.
Intervention Type
Drug
Intervention Name(s)
SCCC
Other Intervention Name(s)
Standard single agent cytotoxic chemotherapy
Intervention Description
commercially available SSCC (doses below the recommended package insert at the discretion of treating oncologist), on a 21-day cycle (although weekly administration is allowed; note: pegylated liposomal doxorubicin will be administered on a 28-day cycle).
Drugs considered acceptable as SSCC: paclitaxel; nab-paclitaxel; eribulin; pegylated liposomal doxorubicin (PLD); vinorelbine; gemcitabine; capecitabine.
Related to PLD: Per notification from EMA (dated 22-Nov-2011) "no new patients should be started on treatment with Caelyx until further notice." Accordingly, this drug may be selected as SSCC treatment option only after such written notice is available.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Recommended prophylactic anti-emetic for AEZS-108: 8 mg dexamethasone.
Primary Outcome Measure Information:
Title
Efficacy of AEZS-108 compared to SSCC as measured by the median time of progression-free survival (PFS).
Description
PFS is defined as the time elapsed from randomization to the date of documented progression or death, whichever comes first. For surviving patients without progression who begin alternative treatment, PFS will be censored at the last date of documented progression-free status prior to starting alternative treatment. Similarly, losses to follow up will be censored at the last date of documented progression-free status.
Time Frame
Up to two years
Secondary Outcome Measure Information:
Title
Efficacy of AEZS-108: overall response
Description
Overall response per RECIST 1.1 (i.e. complete response (CR) + partial response (PR).
Time Frame
Up to two years
Title
Efficacy of AEZS-108: clinical benefit
Description
Overall clinical benefit = complete response (CR) + partial response (PR) + stable disease (SD)
Time Frame
up to 2 years
Title
Efficacy of AEZS-108: duration of response
Description
The duration of overall response is measured from the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented (taking as reference for progressive disease the smallest measurements recorded since the treatment started). The duration of overall CR is measured from the time measurement criteria are first met for CR until the first date that progressive disease is objectively documented.
Time Frame
up to 2 years
Title
Efficacy of AEZS-108: time to progression (TTP)
Description
TTP is defined as the time elapsed from randomization to the earliest date of documented disease progression. For surviving patients without progression of breast cancer who begin alternative treatment, TTP will be censored at the last date of documented progression-free status prior to starting alternative treatment. This is expected to be negligible and, if the actual data suggest otherwise, competing risk methods will be used instead of Kaplan-Meier estimates. Similarly, losses to follow up will be censored at the last date of documented progression free status.
Time Frame
up to 2 years
Title
Efficacy of AEZS-108: overall survival
Description
Overall survival (OS) is defined as the elapsed time from start of therapy to death from any cause. For surviving patients, follow-up will be censored at the date of last contact.
Time Frame
up to 2 years
Title
Toxicity of AEZS-108 in this patient population
Description
All patients will be evaluable for toxicity from the time of their first treatment with the study drug.
Time Frame
up to 2 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women ≥ 18 years of age
Histologically documented breast cancer (either primary or metastatic site) that is (i) ER-negative (0), (ii) PR-negative (0), and (iii) HER2-negative, defined by IHC (immunohistochemistry; IHC 0/1, non-overexpressing) or FISH (fluorescence in situ hybridization; FISH negative) or CISH (chromogen in situ hybridization; CISH negative).
Expression of LHRH receptor confirmed by IHC on archival (or current biopsy of breast tumor or metastatic site) breast cancer tissue
Progressive disease after failure of 1 to 3 prior chemotherapy regimens for recurrent or metastatic (Stage IV) disease (prior adjuvant/neoadjuvant therapy is allowed)
Measurable disease by RECIST 1.1 criteria; at least one target lesion that has not been previously irradiated.
Exclusion Criteria:
Eastern Cooperative Oncology Group (ECOG) performance status > 2
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or recent myocardial infarction (within 6 months of enrollment)
Leptomeningeal disease or brain metastases requiring steroids or other therapeutic intervention
Left ventricular ejection fraction (LVEF) < 50 %, determined by echocardiogram or MUGA scan
Compromised organ or marrow function as evidenced by any of the following:
thrombocyte count: < 100x109/L
absolute neutrophil count (ANC): < 1.5x109/L
hemoglobin: < 6.0 mmol/L (< 9 g/100 mL)
AS(A)T, AL(A)T: > 2.5 times upper limit of normal range (ULN) (> 5x ULN if clearly related to liver metastases)
bilirubin: > 1.5 mg/dL
creatinine: > 1.5 mg/dL or creatinine clearance < 40 mL/min.
Systemic anticancer therapy or radiotherapy within 21 calendar days of the first dose of study drug*)
* also excluded are patients with anticipated ongoing concomitant anticancer therapy during the study
Prior exposure to anthracyclines or anthracenediones for the treatment of metastatic breast cancer including liposomal doxorubicin (Doxil), doxorubicin, daunorubicin, or mitoxantrone
Prior adjuvant anthracyclines with a cumulative anthracycline dose ≥ 300 mg/m2
Ongoing therapeutic anticoagulation
Patients who are not surgically sterile or post-menopausal must agree to use for the duration of the study reliable methods of birth control defined as:
complete abstinence
any intrauterine device (IUD) with published data showing that the lowest expected failure rate is < 1 % per year, or
any other methods with published data showing that the lowest expected failure rate is less than 1 % per year
Investigational therapy within 30 calendar days of the first scheduled day of protocol treatment (investigational therapy is defined as treatment for which there is currently no regulatory authority approved indication).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alberto J. Montero, MD
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Universitäts-Frauenklinik
City
Göttingen
Country
Germany
Facility Name
Klinik für Frauenheilkunde und Geburtshilfe
City
Regensburg
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
Phase 2 Trial of AEZS-108 in Chemotherapy Refractory in Triple Negative Breast Cancer
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