Safety Study of Radiation and CP-675,206 Infusion for Breast Cancer Patients

Phase 1

Terminated

• Conditions: Metastatic Breast Cancer

• Registration Number: NCT01334099
• Lead Sponsor: University Health Network, Toronto

Brief Summary

The purpose of this study is to determine the maximum dose of CP-675,206 when given in combination with radiation. Patients will be given local radiation to one tumor site and an intravenous infusion of CP-675,206.

Detailed Description

Breast cancer is the most common cancer in Canadian women. In 2007 an estimated 22,300 women will be diagnosed and 5300 will die of the disease. Despite advances in therapy, metastatic disease remains an incurable illness, with a median survival of only 2 years. Standard systemic treatment options for metastatic disease include chemotherapy or hormonal therapy. Radiation is frequently used in the metastatic setting for palliation of symptoms, with the most frequent site of radiation being bone. Response rates to first line chemotherapy are in the range of 30%, however these responses are not durable. Currently there are no curative options for metastatic disease, underscoring the need for novel therapeutic approaches.

CTLA4 is a receptor expressed on the surface of activated T cells and regulatory T cells. CTLA-blockade has been tested in clinical trials using humanized monoclonal antibodies, and some biological responses have been reported. The anti-tumor immune response may be further augmented by the combination of CTLA4-blockade with radiation, with the potential to mediate regression of metastases outside of the field of radiation. The primary goal of this study therefore is to establish the safety of CTLA4-blockade using the antibody CP-675, 206 in combination with radiation. This trial is being conducted as a prelude to a planned phase II trial of CP-675,206 in combination with radiation in metastatic breast cancer.

Study Timeline

• Study Start: 2010-07
• Study First Submitted: 2011-01-18
• Study First Submitted QC: 2011-04-11
• Study First Posted: 2011-04-12
• Primary Completion: 2013-03
• Status Verified: 2015-06
• Last Update Submitted: 2015-06-19
• Last Update Posted: 2015-06-22

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

• Inoperable locally recurrent or metastatic breast cancer
• Performance status 0-1
• Adequate organ function as determined by lab tests
• Greater than 3 weeks since any chemotherapy treatment
• Greater than 2 weeks since last dose of hormonal therapy

Exclusion Criteria

• Previous treatment with any anti-CTLA4 agent
• Patients with active diarrhea
• Patients who will receive radiation to pelvic lesions
• History of chronic inflammatory or autoimmune disorder
• History of insulin-dependent diabetes
• History in the last 5 years of any chronic gastrointestinal conditions
• History within the last year of congestive heart failure, stroke, myocardial infarction or thromboembolic event
• Patients with known brain metastasis
• Concurrent treatment with immunosuppressive medication for longer than 10 days within 4 weeks of enrollment or while on trial
• Patients of reproductive potential not using effective contraception, breast-feeding, or patients who test positive for pregnancy at enrollment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Assessing safety through toxicities observed using CTCAE version 3.0	At each study visit for the duration of the 12-week cycle

Secondary Outcome Measures

Name	Time	Method
Evaluating lesions using Response Evaluation Criteria in Solid Tumors (RECIST 1.0)	Every 8 weeks after treatment
Immunological responses to the treatment measured through analysis of blood draws	At the end of the 12-week cycle

Trial Locations

Locations (1)

Princess Margaret Hospital; 🇨🇦 Toronto, Ontario, Canada