Overview

This trial is active, not recruiting.

Condition breast cancer
Treatments palbociclib, anastrozole, letrozole, exemestane, fulvestrant
Phase phase 2
Target CDK4
Sponsor Fondazione Sandro Pitigliani
Start date October 2012
End date June 2017
Trial size 115 participants
Trial identifier NCT02549430, 2011-005637-38, TREnd

Summary

This study aims to assess the activity of PD0332991 in monotherapy and in combination with the endocrine therapy (anastrozole, letrozole, exemestane or fulvestrant) on which the patient has progressed in the previous line for advanced breast cancer in order to reverse endocrine resistance.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
Palbociclib monoterapy
palbociclib PD0332991
Palbociclib 125 mg/day orally in an ongoing 3:1 schedule (3 weeks on/1 week off)
(Experimental)
Palbociclib + HT (Anastrozole, Letrozole, Exemestane, Fulvestrant)
palbociclib PD0332991
Palbociclib 125 mg/day orally in an ongoing 3:1 schedule (3 weeks on/1 week off)
anastrozole
Continuation of prior anastrozole 1mg/day orally in a continuous regimen
letrozole
Continuation of prior letrozole 2.5mg/day orally in a continuous regimen
exemestane
Continuation of prior exemestane 25mg/day orally in a continuous regimen
fulvestrant
Continuation of prior fulvestrant 500mg intramuscular injection every 4 weeks in a continuous regimen

Primary Outcomes

Measure
Incidence of complete response (CR), partial response (PR) or stable disease (SD) ≥24 weeks (clinical benefit)
time frame: Baseline up to 3 years

Secondary Outcomes

Measure
Progression free survival (PFS)
time frame: Baseline up to 3 years
Objective Response (OR)
time frame: Baseline up to 3 years
Overall Survival (OS)
time frame: Baseline up to 6 years
Time to Progression (TTP)
time frame: Baseline up to 3 years
Duration of Response (DR)
time frame: Baseline up to 3 years

Eligibility Criteria

Female participants at least 18 years old.

Inclusion Criteria: - Histologically proven diagnosis of adenocarcinoma of the breast with evidence of metastatic disease - ER positive tumor ≥ 10% - HER2 negative breast cancer by FISH or IHC - Progression of advanced breast cancer on first or second line endocrine therapy for advanced breast cancer - Paraffin-embedded tumor available for centralized assessment of biomarkers - Measurable disease according to RECIST 1.1 (bone only disease is allowed only if measurable). - Postmenopausal status - Eastern Cooperative Oncology Group (ECOG) Performance status 0 -2 - Resolution of all acute toxic effects of prior therapy or surgical procedures to CTCAE grade >1 - Adequate organ function Exclusion Criteria: - Unstable brain metastases - Prior treatment with more than one line of CT or more than two lines of HT advanced breast cancer or any CDK inhibitor - Current treatment with therapeutic doses of anticoagulant - Current use or anticipated need for food or drugs that are known strong CYP3A4 inhibitors / inducers, drugs that are predominantly metabolized by CYP3A with narrow therapeutic indices, drugs with the potential of prolonging QT interval - Diagnosis of any secondary malignancy within the last 3 years - Active inflammatory bowel disease or chronic diarrhea - Known human immunodeficiency virus infection; active hepatitis C, active hepatitis B

Additional Information

Official title Phase 2,Open-label,Multicenter,Randomized Study of PD0332991 (Oral CDK4/6 Inhibitor) Monotherapy and in Combination With the HT to Which the pt Has Progressed in the Previous Line for ER+,Her2- Post-menopausal Advanced Breast Cancer Pts
Principal investigator LUCA MALORNI, MD
Description In a clinical context, there is a lack of molecular compounds with demonstrated clinical activity in delaying/reversing resistance to endocrine agents. CDK 4/6 inhibitors may represent a biologically-driven option in this context. With the present study investigators aim to complement the ongoing trial on PD0332991 by acquiring information on its clinical activity in post-menopausal patients with ER positive, Her2 negative advanced breast cancer patients already pretreated with a first-line or second line endocrine therapy.
Trial information was received from ClinicalTrials.gov and was last updated in August 2016.
Information provided to ClinicalTrials.gov by Fondazione Sandro Pitigliani.