Neoadjuvant Chemotherapy Docetaxel With or Without SELUMETINIB in Patients With Triple Negative Breast Cancer
A Phase II Randomized Multicenter Open Label Prospective Study of Neoadjuvant Chemotherapy Docetaxel With or Without MEK Inhibitor SELUMETINIB in Patients With Early and Locally Advanced Triple Negative Breast Cancer
1 other identifier
interventional
164
0 countries
N/A
Brief Summary
The purpose of this study is to increase survival of patients with early and locally advanced triple-negative breast cancer adding selumatinib to standard preoperative chemotherapy regimen.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 13, 2016
CompletedFirst Posted
Study publicly available on registry
February 19, 2016
CompletedStudy Start
First participant enrolled
September 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2018
CompletedFebruary 22, 2016
February 1, 2016
1.3 years
February 13, 2016
February 18, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
• Pathological complete response rate
After 24 weeks of neoadjuvant chemotherapy and surgery
Secondary Outcomes (2)
• Overall clinical response rate
After 24 weeks of neoadjuvant chemotherapy
• Adverse events rate in both treatment groups
After 24 weeks of neoadjuvant chemotherapy
Other Outcomes (1)
Association between RAS-ERK signal pathway activity in tumor and pathological complete response rate in patients who were receiving or not receiving SELUMETINIB
After 24 weeks of neoadjuvant chemotherapy
Study Arms (2)
AC followed by Docetaxel with Selumetinib
EXPERIMENTALDoxorubicin 60 mg/m2 and Cyclophosphamide 600 mg/m2 as a single IV infusion on day 1 of every 3 week cycle then 75 mg/m2 of Docetaxel given as a single IV infusion on day 1 of every 3 week cycle, 75 mg of SELUMETINIB twice a day PO on days 1-21 of every 3 week cycle
AC followed by Docetaxel
ACTIVE COMPARATORDoxorubicin 60 mg/m2 and Cyclophosphamide 600 mg/m2 as a single IV infusion on day 1 of every 3 week cycle then 75 mg/m2 of Docetaxel given as a single IV infusion on day 1 of every 3 week cycle
Interventions
Eligibility Criteria
You may qualify if:
- Written informed consent;
- Women with early and locally advanced breast cancer ( Stage IIB-IIIB: T2N1-2, T3-4/N0-2 or any T/N2)
- Triple negative breast cancer (absence of estrogen receptor (0-2 points), progesterone receptor (0-2 points), and HER2/neu receptor (IHC 0-1+ or IHC 2+ in the absence of her2/neu gene amplification as evidenced by FISH);
- Age: over 18 years;
- Eastern Cooperative Oncology Group (ECOG) score: 0-1 points;
- Left ventricular ejection fraction (LVEF) based on Echocardiogram (ECHO) or Multigated radionuclide angiography (MUGA scan): \>55%
- Laboratory values before the study start must meet the following criteria:
- Absolute neutrophil count \> 1500/microlitre Platelet count \> 100000/microlitre Hemoglobin level \> 9.0 g/dl Albumin \> 2,5 g/dl Normal plasma creatinine level or estimated glomerular filtration rate (eGFR) \>60 ml/minute Total bilirubin level \< 1.25 upper limit of normal (ULN) Aspartate aminotransferase (AST), alanine aminotransferase (ALT) \< 3 x ULN;
- Patient is able to abide by the protocol requirements (in the opinion of the Investigator)
- Patient's and her sexual partner's willing to use reliable methods of contraception (condoms with spermicidal foams/gels, intrauterine device) during the study and for at least 4 weeks after discontinuation of study treatment.
- Negative serum pregnancy test for women with childbearing potential or evidence of a post-menopausal status (total cessation of menses for more than 1 year. The following age-specific requirements must also apply:
- Women \< 60 years old: they would be considered post-menopausal if they have been amenorrheic for the past 12 months or more. The levels of Follicle-Stimulating Hormone (FSH) and estradiol must also be in the post-menopausal range (as per the institution).
- Women ≥ 60 years;
- Bilateral oophorectomy.
You may not qualify if:
- Prior treatment (chemo-, hormone, radiation or immunotherapy) of breast cancer
- Major surgery within 28 days prior to enrollment;
- Known hypersensitivity to Docetaxel, SELUMETINIB or to the components of the investigational product;
- Cardiac conditions as follows:
- a. Uncontrolled hypertension (BP ≥ 150/95 mmHg despite medical therapy) b. Acute coronary syndrome within 6 months prior to starting treatment c. Uncontrolled Angina - Canadian Cardiovascular Society grade II-IV despite medical therapy (Appendix 3) d. Symptomatic heart failure New York Heart Association (NYHA) Class II-IV, prior or current cardiomyopathy (Appendix 4) e. Prior or current cardiomyopathy including but not limited to the following: i. Known hypertrophic cardiomyopathy ii. Known arrhythmogenic right ventricular cardiomyopathy iii. Previous moderate or severe impairment of left ventricular systolic function (Left ventricular ejection fraction (LVEF) \<45% on echocardiography or equivalent on MuGA) even if full recovery has occurred.
- f. Severe valvular heart disease g. Baseline Left ventricular ejection fraction (LVEF) below the lower limit of normal (LLN) or \<55% measured by echocardiography or institution's LLN for MUGA h. Atrial fibrillation with a ventricular rate \>100 bpm on ECG at rest i. QTcF \>450ms or other factors that increase the risk of QT prolongation
- Pregnancy or lactation;
- Conditions (dementia, psychiatric or neurological disorders, drug addiction, alcoholism etc.) that limit patient's ability to undergo study procedures;
- Simultaneous participation in other clinical studies;
- Presence of acute or active chronic infections or other conditions (e.g. unstable or uncompensated respiratory, cardiac, hepatic, or renal disease, active bleeding diatheses or renal transplant), that in investigator's opinion may interfere with the treatment described in the study protocol;
- Have refractory nausea and vomiting, chronic gastrointestinal diseases (e.g., inflammatory bowel disease), or significant bowel resection that would adversely affect the absorption / bioavailability of the orally administered study medication
- History of another neoplasm (with the exception of adequately treated basal cell or cervical cancer in situ and cases when a cancer has been in remission for 5 years of more)
- Ophthalmological conditions as follows:
- Intra-ocular pressure \>21 mmHg, or uncontrolled glaucoma (irrespective of intra-ocular pressure)
- Current or past history of retinal pigment epithelial detachment / central serous retinopathy
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mona Frolova
Russian Cancer Research Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Research Associate, Russian Cancer Research Center
Study Record Dates
First Submitted
February 13, 2016
First Posted
February 19, 2016
Study Start
September 1, 2016
Primary Completion
January 1, 2018
Last Updated
February 22, 2016
Record last verified: 2016-02
Data Sharing
- IPD Sharing
- Will not share