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Palbociclib (PD-0332991) Combined With Fulvestrant In Hormone Receptor+ HER2-Negative Metastatic Breast Cancer After Endocrine Failure (PALOMA-3)

Phase 3
Completed
Conditions
HR+/HER2 advanced breast cancer
Registration Number
JPRN-jRCT2080222543
Lead Sponsor
Pfizer R&D Japan G.K.
Brief Summary

The addition of palbociclib to fulvestrant resulted in a statistically significant, and clinically meaningful improvement in PFS as compared with placebo plus fulvestrant. The results across response-based analyses, including supportive PFS analyses, OR, DR, and CBR, are consistent and support the robustness of the primary PFS analysis at the time of the data cutoff. The magnitude of treatment effect of the palbociclib combination observed in PFS continued and was maintained for OS at the later cutoff.

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
Female
Target Recruitment
521
Inclusion Criteria

Inclusion Criteria:
*Women 18 years or older with metastatic or locally advanced disease, not amenable to curative therapy
*Confirmed diagnosis of HR+/HER2- breast cancer
*Any menopausal status
*Progressed within 12 months from prior adjuvant or progressed within 1 month from prior advanced/metastatic endocrine breast cancer therapy
*On an LHRH agonist for at least 28 days, if pre-/peri-menopausal, and willing to switch to goserelin (Zoladex) at time of randomization.
*Measurable disease defined by RECIST version 1.1, or bone-only disease
*Eastern Cooperative Oncology Group (ECOG) PS 0-1
*Adequate organ and marrow function, resolution of all toxic effects of prior therapy or surgical procedures
*Patient must agree to provide tumor tissue from metastatic tissue at baseline

Exclusion Criteria

Exclusion Criteria:
*Prior treatment with any CDK inhibitor, fulvestrant, everolimus, or agent that inhibits the PI3K-mTOR pathway
*Patients with extensive advanced/metastatic, symptomatic visceral disease, or known uncontrolled or symptomatic CNS metastases
*Major surgery or any anti-cancer therapy within 2 weeks of randomization
*Prior stem cell or bone marrow transplantation
*Use of potent CYP3A4 inhibitors or inducers

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
efficacy<br>Progression Free Survival (PFS) as assessed by the Investigator
Secondary Outcome Measures
NameTimeMethod
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