VEGF Trap in Treating Patients With Metastatic Breast Cancer

Metastatic Breast Cancer Clinical Trial

Official title:

Phase II Trial of VEGF Trap in Patients With Metastatic Breast Cancer Previously Treated With Anthracycline and/or Taxane

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00369655
• Other study ID #: NCI-2012-01827
• Secondary ID: NCCTG-N0537U10CA
• Status: Completed
• Phase: Phase 2
• First received: August 24, 2006
• Last updated: April 2, 2014
• Start date: January 2007
• Est. completion date: January 2011

Study information

• Verified date: November 2013
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This phase II trial is studying how well VEGF Trap works in treating patients with metastatic breast cancer. VEGF Trap may stop the growth of tumor cells by blocking blood flow to the tumor

Description:

PRIMARY OBJECTIVES:

I. Assess the antitumor activity of VEGF Trap, in terms of tumor response rate, in patients with metastatic breast cancer who have received =< 2 prior chemotherapy regimens for metastatic disease, including a taxane and/or anthracycline.

II. Assess the 6-month progression-free survival rate in patients treated with VEGF Trap.

SECONDARY OBJECTIVES:

I. Describe the adverse event profile (grade using the NCI CTCAE version 3.0) of VEGF Trap in these patients.

II. Describe the progression-free survival times in patients treated with VEGF Trap.

III. Describe the overall survival of patients treated with VEGF Trap. IV. Describe the duration of response in patients treated with VEGF Trap.

OUTLINE: This is a multicenter study.

Patients receive VEGF Trap IV over 1 hour on day 1. Courses repeat every 14 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3-6 months for up to 5 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: January 2011
• Est. primary completion date: March 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically confirmed adenocarcinoma of the breast

• Clinical evidence of metastatic disease

• No more than 2 prior chemotherapy regimens for metastatic disease

• Prior neoadjuvant or adjuvant chemotherapy allowed*

• At least 1 prior regimen (in any setting) must have included a taxane and/or an anthracycline

• Measurable disease, defined as = 1 lesion whose longest diameter can be accurately measured per RECIST criteria

• No nonmeasurable disease, defined as all other lesions, including small lesions(longest diameter < 20 mm) and truly nonmeasurable lesions, including the following:

• Bone lesions

• Leptomeningeal disease

• Ascites

• Pleural/pericardial effusion

• Inflammatory breast disease

• Lymphangitis cutis/pulmonis

• Abdominal masses that are not confirmed and followed by imaging techniques

• Cystic lesions

• Patients with HER2-positive tumors (3+ by immunohistochemistry or amplified by fluorescent in situ hybridization [FISH]) must have received = 1 prior trastuzumab (Herceptin®)-containing regimen in either the adjuvant or metastatic setting, unless there was a contraindication

• No known CNS metastases

• No evidence of leptomeningeal involvement

• Hormone receptor status not specified

• Male or female

• Menopausal status not specified

• ECOG performance status 0-1

• Life expectancy > 3 months

• WBC = 3,000/mm³

• Absolute neutrophil count = 1,500/mm³

• Platelet count = 75,000/mm³

• Hemoglobin > 8.0 g/dL

• Bilirubin = 1.5 times upper limit of normal (ULN)

• Alkaline phosphatase = 3 times ULN

• AST and ALT = 2.5 times ULN

• Creatinine = 1.5 times ULN

• Urine protein:creatinine ratio < 1 OR urine protein < 500 mg by 24-hour urine collection

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 6 months after completion of study treatment

• No significant traumatic injury within the past 4 weeks

• No history of allergy or hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies, drug product excipients, or agents chemically or biologically similar to VEGF Trap

• No abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 28 days

• No nonhealing wound, fracture, or ulcer

• No stage III or IV invasive, nonbreast malignancy within the past 5 years

• No history of lung carcinoma of squamous cell type

• No clinically significant cardiovascular disease, including any of the following:

• Cerebrovascular accident or stroke within the past 6 months

• Uncontrolled hypertension, defined as blood pressure (BP) > 150/100 mm Hg OR systolic BP > 180 mm Hg if diastolic blood pressure < 90 mm Hg on = 2 separate occasions within the past 3 months

• Myocardial infarction, coronary artery bypass graft, or unstable angina within the past 6 months

• New York Heart Association class III or IV cardiovascular disease

• Serious cardiac arrhythmia requiring medication

• Peripheral vascular disease = grade 2 within the past 6 months

• Pulmonary embolism, deep vein thrombosis, or other thromboembolic event within the past 6 months

• No evidence of bleeding diathesis or uncontrolled coagulopathy

• No active, unresolved infection

• No serious concurrent medical condition that would preclude study participation

• No other condition or circumstance that would preclude compliance with study requirements

• See Disease Characteristics

• Prior hormonal therapy in the neoadjuvant, adjuvant, or metastatic setting allowed

• No prior bevacizumab

• More than 4 weeks since prior chemotherapy, endocrine therapy, experimental drug therapy, or immunotherapy and recovered

• More than 4 weeks since prior major surgery or open biopsy

• More than 7 days since prior core biopsy

• More than 2 weeks since prior radiotherapy, except if to a nontarget lesion only

• Prior radiotherapy to a target lesion allowed only if there has been clear progression of the lesion since radiotherapy was completed

• Prior single-dose palliative radiotherapy within the past 2 weeks allowed

• No concurrent major surgery

• No concurrent trastuzumab

• Concurrent full-dose anticoagulants (e.g., warfarin) with PT INR > 1.5 allowed provided the following criteria are met:

• INR in-range (usually between 2 and 3) on a stable dose of oral anticoagulant or on a stable dose of low molecular weight heparin

• No active bleeding or pathological condition that carries a high risk of bleeding (e.g., tumor involving major vessels or known varices)

• No concurrent combination antiretroviral therapy for HIV-positive patients

• No concurrent participation in another investigational clinical trial

• No other concurrent chemotherapeutic agents, endocrine therapy, biologic agents, radiotherapy, or other nonprotocol antitumor therapy

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Neoplasms
• Metastatic Breast Cancer
• Recurrent Breast Cancer
• Stage IV Breast Cancer

Intervention

Biological:
• ziv-aflibercept

Locations

Country	Name	City	State
United States	North Central Cancer Treatment Group	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of Patients With Confirmed Tumor Response	Confirmed tumor response was defined as the total number of efficacy-evaluable patients who achieved a complete or partial response according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria on 2 consecutive evaluations at least 8 weeks apart.	Up to 5 years	No
Primary	Proportion of Patients Receiving Vascular Endothelial Growth Factor (VEGF) Trap With 6-month Progression-free Survival	The 6-month progression free survival rate was defined as the proportion of efficacy-evaluable patients on study treatment and progression-free 6 months from registration. Patients who died without documentation of progression will be considered to have progressed on the date of their death.	6 months	No
Secondary	Progression Free Survival	Progression-free survival was defined as the number of months from registration to the date of disease progression or death, with patients who died without documentation of progression being considered to have progressed on the date of their death.	Time from registration to disease progression or death (up to 5 years)	No
Secondary	Overall Survival	Overall survival time was defined as the number of months from registration to the date of death or last follow-up	Time from registration to death or last follow up (up to 5 years)	No
Secondary	Median Duration of Response	Duration of response was defined as for all evaluable patients who have achieved an objective response as the date at which the patient's objective status is first noted to be either a complete response or partial response to the date progression is documented.	Up to 5 years	No
Secondary	Number of Participant With Previous Treatment of Anti-HER2 With Cardiac Events		Up to 5 years	Yes