Purpose

To examine whether rapamycin can reduce malignant markers and aberrant mammary stem/progenitor cells (MaSCs) number in surgical specimens

Category

IRB Number
20150556HU
NCT Number
NCT02642094
Open to Enrollment
No
Sponsor
LuZhe Sun -



Study Contact

Principal Investigator
Ismail Jatoi

Frances Crawford
(210) 450-5037
crawfordf1@uthscsa.edu

Sonia Creighton
(210) 450-1366
creighton@uthscsa.edu

Ismail Jatoi
(210) 567-5759
jatoi@uthscsa.edu

Myrna Montenegro
(210) 450-5954
montenegro@uthscsa.edu

Courtney Nichols
(210) 450-1794
nicholsc2@uthscsa.edu

Mailbox Ctrc Regulatory Affairs
regaffapp@uthscsa.edu

Regulatory Staff
regaffstaff@uthscsa.edu

Kathleen Rodriguez
(210) 450-1365
rodriguezk3@uthscsa.edu

Benjamin Schleif
(210) 450-1366
schleifb@uthscsa.edu

Morgan Seekatz
(210) 450-1133
seekatz@uthscsa.edu



Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Genders
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

    • Women with confirmed menopausal status. All patients who have NOT had a prior bilateral oophorectomy and/or are younger than age 60, will require menopausal status verified by FSH and estradiol local labs.
    • Women diagnosed with DCIS/LCIS, Atypical lobular hyperplasia (ALH) or ADH lesions detected by pathology
    • Women scheduled for mastectomy or lumpectomy after DCIS/LCIS, ALH or ADH diagnosis
    • Women consented to the UT Health Cancer Center MD Anderson Cancer Center tissue biorepository (HSC20070684H)
    • Women of child-bearing potential willing to practice 2 forms of contraception, one of which must be a barrier method until at least 30 days after the last dose of rapamycin.
    • Women of child-bearing potential must have a negative serum pregnancy test at time of enrollment.
    • Patients must be able to swallow and retain oral medication.
    • All patients must have given signed informed consent prior to registration on study.
    • Patients must have normal organ and marrow function as defined below:

      1. Leukocytes ≥ 3,000/uL
      2. Absolute neutrophil count ≥ 1,500/uL
      3. Platelets ≥ 100,000/uL
      4. AST ≤ 2.5 X ULN
      5. ALT ≤ 2.5 X ULN
      6. Total bili ≤ 1.5 X ULN or Direct bili ≤ 1 X ULN

Exclusion Criteria

    • Women who are pregnant.
    • Women who are receiving any other concomitant treatment for their DCIS/LCIS, ALH or ADH
    • Women who are taking rapamycin for another diagnosis.
    • Women with an allergy to rapamycin or its derivatives.
    • Active infection requiring systemic therapy.
    • Patients who are taking any pills containing herbal (alternative) medicines are NOT eligible for participation. Patients must be off any such medications by the time of registration.
    • Immunocompromised subjects, including patients with human immunodeficiency virus
    • Women currently taking strong CYP3A4 inducers or inhibitors. Drugs that cannot be coadministered with rapamycin include but are not limited to: Calcium channel blockers: nicardipine, Antifungal agents: clotrimazole, fluconazole, Antibiotics: troleandomycin, Gastrointestinal prokinetic agents: cisapride, metoclopramide, Other drugs: bromocriptine, cimetidine, danazol, HIV-protease inhibitors (e.g., ritonavir, indinavir), Anticonvulsants: carbamazepine, phenobarbital, phenytoin, Antibiotics: rifapentine. The research team can provide a full list of these medications.
    • Patients with any of the following conditions or complications are NOT eligible for participation:

      1. GI tract disease resulting in an inability to take oral medication
      2. Malabsorption syndrome
      3. Require IV alimentation
      4. History of prior surgical procedures affecting absorption
      5. Uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis)

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Basic Science
Masking
None (Open Label)
Condition
  • Cancer of Breast
  • Arm Groups

    ArmDescriptionIntervention
    Experimental

    The effect of short-term rapamycin treatment

    Subjects will be given a low dose of rapamycin at 2 mg/day for 5-7 days of treatment. A surgical specimen will be taken 3-7 days after the last dose of rapamycin. The specimens will be evaluated for lesion size, nuclear grade, presence of necrosis in each patient's core biopsy and surgical specimens, as well as IHC (ImmunoHistoChemistry) for biomarkers including p16, COX2 (cyclooxygenase-2), and Ki-67. Specimens will also be tested for rapamycin treatment on the properties of mammary stem/progenitor cells as another biomarker for gauging the efficacy of rapamycin treatment.
  • Drug: Rapamycin

    Low dose of rapamycin at 2 mg/day for -5-7 days of treatment

    Other names:

    • Sirolimus