CP-724,714 in Treating Patients With Metastatic Breast Cancer

A Phase I Safety and Pharmacokinetic/Pharmacodynamic Study of CP-724, 714 In Patients With Metastatic HER2-Overexpressing Breast Cancer

RATIONALE: CP-724,714 may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth.

PURPOSE: Phase I trial to study the effectiveness of CP-724,714 in treating patients who have metastatic HER2-overexpressing breast cancer.

Study Overview

• Status: Completed
• Conditions: Breast Cancer
• Intervention / Treatment: Drug: CP-724,714

Detailed Description

OBJECTIVES:

• Determine the safety and tolerability of CP-724,714 in patients with metastatic HER2-overexpressing breast cancer.
• Determine the maximum tolerated dose of this drug in these patients.
• Determine, preliminarily, any antitumor activity of this drug in these patients.
• Determine the pharmacokinetics of this drug in these patients.
• Determine the relationship of drug-related adverse events to pharmacokinetic exposure parameters in these patients.
• Determine the relationship of changes in serum HER2 extracellular domain and HER2 receptor tyrosine kinase phosphorylation to pharmacokinetic exposure parameters and clinical outcome in patients treated with this drug.

OUTLINE: This is an open-label, dose-escalation, multicenter study.

Patients receive oral CP-724,714 on days 1 and 3-21 during course 1 and then daily during subsequent courses. Courses repeat every 3 weeks for up to 1 year in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of CP-724,714 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients are followed for at least 30 days.

PROJECTED ACCRUAL: A total of 3-20 patients will be accrued for this study within 6 months.

• Study Type: Interventional
• Enrollment (Actual): 9
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • California
    • Los Angeles, California, United States, 90095-1781
      • Jonsson Comprehensive Cancer Center, UCLA

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Histologically or cytologically confirmed HER2-overexpressing breast cancer
• Prior or newly documented HER2 amplification by fluorescence in situ hybridization (FISH)
• Progressive metastatic disease
• Must have received at least one prior chemotherapy regimen for metastatic breast cancer
• At least 1 measurable or evaluable lesion
• At least 1 lesion accessible for 2 separate core biopsies for pharmacodynamic evaluation
• 18 and over
• Male or female
• ECOG 0-1
• Life expectancy, More than 3 months

• Hematopoietic

  • Absolute neutrophil count at least 1,500/mm^3*
  • Platelet count at least 100,000/mm^3* NOTE: *Without hematopoietic growth factors or transfusions

• Hepatic

  • Bilirubin no greater than 1.5 mg/dL
  • AST/ALT no greater than 2.5 times upper limit of normal (ULN) (5 times ULN if liver metastases are present)

• Renal

  • Creatinine no greater than 1.5 times ULN OR
  • Creatinine clearance at least 60 mL/min

• Cardiovascular

  • 12-lead ECG with normal tracing
• history of cardiovascular disease (i.e., ischemic heart disease, arrhythmia, or congestive heart failure) unless asymptomatic for the past year with no requirement for antiarrhythmics or a clinically significant medical management change

• Gastrointestinal

  • Able to take oral medication* Negative pregnancy test
  • Fertile patients must use effective contraception
• At least 4 weeks since prior trastuzumab (Herceptin)
• At least 4 weeks since other prior biologic therapy or immunotherapy
• At least 4 weeks since prior chemotherapy (6 weeks for mitomycin or nitrosoureas)
• At least 6 months since prior doxorubicin or doxorubicin equivalents without any prior or developing signs or symptoms of cardiomyopathy
• No cumulative doses of more than 300 mg/m^2
• At least 2 weeks since prior hormonal therapy for the primary disease
• Concurrent hormone replacement therapy or luteinizing hormone-releasing hormone agonists allowed
• At least 4 weeks since prior radiotherapy
• At least 3 weeks since prior major surgery (2 weeks for minor surgery)
• Recovered from prior therapy
• At least 4 weeks since prior investigational treatment
• Coumarin or heparin derivatives allowed for the prevention of deep vein thrombosis or port patency

Exclusion Criteria:

• known or clinically suspected brain metastases or leptomeningeal disease
• symptomatic edema or third-space fluid (e.g., ascites or pleural effusions)
• known hepatitis B or C infection
• significant ECG changes that require medical intervention
• QTc interval less than 460 msec
• No history of torsade or other symptomatic QTc abnormality
• LVEF greater than 50% by MUGA
• gastrointestinal abnormality that would require medications (including all antacids)
• persistent symptoms of an esophageal or digestive disorder
• pregnant or nursing
• known HIV infection
• active infection
• concurrent uncontrolled systemic disorders or laboratory abnormalities that would preclude study drug safety evaluation
• mental disorder that would preclude study compliance or ability to give informed consent
• No more than 2 prior trastuzumab-based regimens for advanced disease
• concurrent immunotherapy
• more than 1 prior anthracycline- or anthracenedione-containing regimen (except with approval of the sponsor)
• prior high-dose chemotherapy with hematopoietic stem cell transplantation
• concurrent anticancer chemotherapy
• No concurrent anticancer hormonal therapy, including tamoxifen
• prior radiotherapy to the only disease site that would be assessed for response
• concurrent radiotherapy
• prior partial or complete gastrectomy
• concurrent antiarrhythmics
• concurrent antacids
• concurrent anticoagulant at therapeutic doses
• other concurrent experimental anticancer medications for breast cancer

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Masking: None (Open Label)

Collaborators and Investigators

• Sponsor: Jonsson Comprehensive Cancer Center
• Collaborators: Pfizer

Study record dates

Study Major Dates

• Study Start: January 1, 2003
• Primary Completion (Actual): December 1, 2004
• Study Completion (Actual): May 1, 2005

Study Registration Dates

• First Submitted: March 6, 2003
• First Submitted That Met QC Criteria: March 6, 2003
• First Posted (Estimate): March 7, 2003

Study Record Updates

• Last Update Posted (Actual): August 3, 2020
• Last Update Submitted That Met QC Criteria: July 30, 2020
• Last Verified: August 1, 2012

More Information

Terms related to this study

• Keywords: stage IV breast cancer; recurrent breast cancer; male breast cancer
• Additional Relevant MeSH Terms: Skin Diseases; Neoplasms; Neoplasms by Site; Breast Diseases; Breast Neoplasms
• Other Study ID Numbers: CDR0000271533; UCLA-0209105; PFIZER-A4031001