Phase I/II Trial of Palbociclib in Combination With Bicalutamide for the Treatment of AR(+) Metastatic Breast Cancer (MBC)
Overview
- Phase
- Phase 1
- Intervention
- Palbociclib
- Conditions
- Metastatic Breast Cancer (MBC)
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Enrollment
- 46
- Locations
- 5
- Primary Endpoint
- recommended phase II dose (RP2D) (phase I)
- Status
- Active, Not Recruiting
- Last Updated
- 10 months ago
Overview
Brief Summary
The purpose of this study is to test the safety and effectiveness of the investigational drug, palbociclib with bicalutamide for the treatment of triple negative, androgen receptor positive breast cancer.
Detailed Description
The study therapy is to be self administered on an outpatient basis. Patients who meet eligibility criteria and sign informed consent to Step 2 may begin treatment on study. Treatment consists of bicalutamide orally once daily and palbociclib will be given orally daily for 3 weeks on followed by 1 week off. A treatment cycle is considered to be 4 weeks. Eligible patients will be evaluated for toxicity every 2 weeks during Cycle #1 and 2, followed by every 4 weeks in subsequent cycles. Toxicity assessment will include history, physical examination including vital signs, and laboratories including complete blood count and comprehensive metabolic panel. Patients will keep a drug diary to document adherence to oral therapy. Radiographic response evaluation per RECIST will occur every 8 weeks (2 cycles) for cycles 1-6 and then every 12 weeks thereafter with high-resolution CT scan. Patients with suspected bone-only lesions must have bone lesions assessed by CT with bone windows or by bone scan at screening. Phase I: We will use a standard 3+3 design for the dose finding lead in to establish the recommended phase II doses for the combination of palbociclib and bicalutamide. The doses for Phase I will be determined based on the dose level to which the patient is accrued. Phase II: Treatment consists of bicalutamide orally once daily and palbociclib will be given orally daily for 3 weeks on followed by 1 week off at the doses determined in phase I.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A patient will be eligible for androgen receptor expression testing (STEP 1) if the following criteria are met:
- •Pathologically confirmed invasive cancer of the breast
- •ER/PR status (ER or PR defined as positive if ≥1%; ER/PR is defined as negative if \<1%):
- •Phase I: Patients may have ER/PR(-) breast cancer.
- •HER2 normal (IHC 0-1; FISH \< 2.0)
- •Non-measurable or measurable, metastatic disease
- •Available tissue for AR testing for research purposes
- •A patient will be eligible for participation in the therapeutic trial (STEP 2) if the following criteria are met:
- •Androgen receptor expression testing confirms that the patient's tumor is AR (+). AR is considered positive if ≥1% of cell nuclei are immunoreactive using the Dako antibody (clone AR441). Receptor testing may be performed on either primary tumor specimen or tissue from a metastatic site. Local testing permitted for eligibility but will require confirmation at MSKCC.
- •There is no limit to the number of prior chemotherapy or endocrine therapy regimens allowed. Patients with ER(+) AR(+) breast cancer must have had at least 1 prior line of endocrine therapy to be eligible for the phase I portion of the trial.
Exclusion Criteria
- •Patients who have not recovered from adverse events of prior therapy to ≤ NCI CTCAEv4.0 Grade
- •Patients receiving any other investigational anti-cancer agents.
- •Patients who have received prior treatment with a selective CDK4/6 inhibitor
- •Patients who have received prior anti-androgen therapy
- •History of allergic reactions attributed to compounds of similar chemical or biologic composition to palbociclib.
- •Uncontrolled intercurrent illness including, but not limited to, known ongoing or active infection, including HIV, active hepatitis B or C, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia (specifically, uncontrolled atrial fibrillation or ventricular dysrhythmias except ventricular premature contractions), or psychiatric illness/social situations that would limit compliance with study requirements.
- •Pregnant women and women who are breast-feeding.
- •Patients with a history of long-QT syndrome or documented family history of long-QT syndrome. Patients who must remain on drugs that prolong the QT interval.
- •Palbociclib is a substrate of CYP3A. Caution should be exercised when dosing palbociclib concurrently with CYP3A inducers or inhibitors. Furthermore, patients who are taking concurrent medications that are strong inducers/inhibitors or substrates of CYP3A4 should be switched to alternative medications to minimize any potential risk.
Arms & Interventions
Palbociclib in Combination with Bicalutamide
This is a non-randomized, open-label, phase I/II trial for patients with AR(+) MBC . There will be a dose finding phase I portion of the study to establish the recommended phase II dose (R2PD). This will be followed by a phase II where efficacy is evaluated. Patients with AR(+)ER(-) breast cancer treated on the phase I at the recommended phase II dose will be counted towards the primary endpoint analysis for the phase II study.
Intervention: Palbociclib
Palbociclib in Combination with Bicalutamide
This is a non-randomized, open-label, phase I/II trial for patients with AR(+) MBC . There will be a dose finding phase I portion of the study to establish the recommended phase II dose (R2PD). This will be followed by a phase II where efficacy is evaluated. Patients with AR(+)ER(-) breast cancer treated on the phase I at the recommended phase II dose will be counted towards the primary endpoint analysis for the phase II study.
Intervention: Bicalutamide
Outcomes
Primary Outcomes
recommended phase II dose (RP2D) (phase I)
Time Frame: 1 year
We will use a standard 3+3 design for the dose finding lead in to establish the recommended phase II doses for the combination of palbociclib and bicalutamide.
progression free survival (phase II)
Time Frame: 6 monthis
Evaluation Criteria in Solid Tumors (RECIST) Committee. Changes in only the largest diameter (unidimensional measurement) of the tumor lesions are used in the RECIST v 1.1 criteria.
Secondary Outcomes
- Progression-free survival(1 year)
- Objective response rate (CR+PR)(1 year)
- Clinical benefit rate (CBR)(≥24 weeks)
- Safety and Tolerability by assessing the number of subjects with adverse events(1 year)