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Eribulin Mesylate in Treating Patients With Previously Treated Metastatic Breast Cancer

Complete title: Phase II Trial of Metronomic Eribulin (Halaven) in Pretreated Metastatic Breast Cancer (MBC)

Research Study Number       8093
    
Principal Investigator       Hannah Linden, MD
    
Phase       II

Look up trial at NIH

Research Study Description

This phase II trial studies how well eribulin mesylate works in treating patients with previously treated metastatic breast cancer. Drugs used in chemotherapy, such as eribulin mesylate, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

Eligibility Criteria (must meet the following to participate in this study)

Ages Eligible for Study: 18 Years and older

Genders Eligible for Study: Both

- Ability to provide written informed consent

- Prior exposure to taxane in the adjuvant, neoadjuvant or metastatic setting

- At least one prior regimen of chemotherapy in the setting of metastatic breast cancer; no upper limit on the number of prior endocrine regimens for metastatic breast cancer, however no more than 6 chemotherapeutic regimens may have been given in the metastatic setting

- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2

- Patients with measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria

- ** At least one non-lymph node lesion of >= 1.0 cm or lymph node > 1.5 cm in short axis by computerized tomography (CT) scan (CT scan thickness no greater than 5 mm which is serially measurable according to RECIST 1.1 using either computerized tomography (CT) or magnetic resonance imaging (MRI)

- ** Lesions that have had radiotherapy must show evidence of progressive disease (PD) based on RECIST 1.1 to be deemed a target lesion

- Absolute neutrophil count >= 1,500/mm^3

- Hemoglobin >= 10 g/dL

- Platelets >= 100,000/mm^3

- Creatinine =< 1.5 x upper limit of normal (ULN)

- Total bilirubin =< 1.5 x ULN

- Alkaline phosphatase =< 2.5 x ULN

- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 2.5 x institutional upper limit of normal, unless due to liver metastases (=< 5 x ULN)

- Women of child-bearing potential (WOCBP) and men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for the duration of study participation

- Life expectancy of > 12 weeks

Other eligibility criteria may apply.

Exclusions (conditions that would prevent participation in this study)

- Plan to administer any other systemic antitumor including endocrine therapy except for following standard of care treatment:

- ** Trastuzumab at standard dosing human epidermal growth factor receptor 2 (HER2) positive tumors;

- ** Denosumab or bisphosphonates to treat metastatic bone disease

- Plan to administer concurrent radiation therapy now or for progressive symptoms during treatment

- Patients with known central nervous system (CNS) metastases must have stable disease off steroids after treatment with surgery or radiation therapy

- Second primary malignancy that is clinically detectable or clinically significant at the time of consideration for study enrollment

- Patients with mild (Child-Pugh A) or moderate (Child-Pugh B) hepatic and/or moderate (creatinine clearance [CrCl] 30-50 mL/min) renal impairment

- Radiotherapy within 14 days of study treatment

- Major surgery within 21 days of study treatment; minor surgery within 2 weeks of study treatment; placement of vascular access device and biopsies allowed and is not considered major or minor surgery

- Treatment with any chemotherapy or investigational agents within 3 weeks of the start of study treatment; endocrine treatment must be stopped prior to initiating study treatment; subjects must have recovered from toxicities of prior therapy

- Patients with peripheral neuropathy > grade 2 regardless of etiology

- Significant cardiovascular impairment: congestive heart failure > class II according to the New York Heart Association (NYHA), unstable angina or myocardial infarction within 6 months of enrollment, or serious cardiac arrhythmia (> grade 2)

- Concomitant severe or uncontrolled medical disease

- Significant psychiatric or neurologic disorder which would compromise participation in the study

- Pregnant or breast-feeding females

Other exclusion criteria may apply.



Research Study Number       8093
    
Contact       Seattle Cancer Care Alliance Intake Office
    
Telephone       800-804-8824 / 206-288-1024
    
   

Keywords
Breast Cancer; Solid Tumors

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  • Talk to your health care providers first before making decisions about your health care.
  • Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each study.

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