Pharmacogenomic Study of Neoadjuvant Eribulin for HER2 Non-overexpressing Breast Cancer

• Status: Completed
• Trial end date: 2015-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a prospective, non-randomized, open-label, multicenter, single-arm exploratory pharmacogenomic study of single agent eribulin as neoadjuvant therapy in patients with operable Stage III HER2 non-overexpressing breast cancer.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: SOLTI Breast Cancer Research Group
• Collaborator: Eisai Inc.

Criteria

Inclusion Criteria:

• Written informed consent, specifically highlighting the molecular characterization of tumor and genomic samples

• Age ≥18 years

• Histologically confirmed invasive breast carcinoma, with all of the following characteristics:

• Primary tumor ≥2cm in largest diameter (cT1-3)

• cN0-1

• No evidence of distant metastasis (M0)

• Breast cancer (BC) eligible for primary surgery

• Available pre-treatment core (Tru-cut) biopsy or possibility of performing one

• HER2-negative BC (as per local assessment), defined as either of the following:

• 0-1+ expression by IHC

• 2+ expression by IHC and in situ hybridization (FISH/CISH) without HER2 gene amplification (<4 HER2 gene copies per nucleus, or a FISH ratio [HER2 gene copies to Cr17 signals] of <1.8)

• Is situ hybridization (FISH/CISH) without HER2 gene amplification, independently of IHC

• Known hormone receptor (ER/PgR) status (as per local assessment) or the possibility of performing the tests

• Known percentage of hormone receptor (ER/PgR) and Ki67-positive tumor cells (as per local assessment), or possibility of performing the tests

• In the case of a multifocal tumor, the largest lesion must be ≥2 cm and designated the "target" lesion for all subsequent tumor evaluations and HER2-negative status must be documented in all the tumor foci

• ECOG performance status of 0 or 1

• Laboratory values as follows:

• Absolute neutrophil count (ANC) ≥1.5 x 109/L

• Platelets count ≥100 x 109/L

• Hemoglobin ≥9 g/dL

• Serum bilirubin ≤1.5 time the upper limit of normal (ULN)

• Alanine aminotransferase and aspartate aminotransferase (AST) ≤2.5 x ULN

• Alkaline phosphatase ≤2.5 x ULN

• Serum creatinine ≤1.5 mg/dL or calculated creatinine clearance ≥60 mL/m

• Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule

• Ability and willingness to comply with study visits, treatment, testing, and to comply with the protocol

• Availability of genomic DNA (via whole blood)

Exclusion Criteria:

• Any prior treatment for primary invasive BC

• Metastatic, locally advanced or inflammatory (i.e., Stage III-IV) BC

• Bilateral invasive BC

• Multicentric BC, defined as the presence of two or more foci of cancer in different quadrants of the same breast

• Pre-existing peripheral neuropathy of any grade

• Uncontrolled hypertension (systolic >150 mmHg and/or diastolic >100 mmHg)

• Clinically significant (i.e., active) cardiovascular disease

• Long QT syndrome

• Concomitant use of inhibitors of hepatic transport proteins such as organic anion-transporting proteins, P-glycoprotein, multidrug resistant proteins etc

• Major medical conditions that might affect study participation (e.g., uncontrolled seizure disorder, uncontrolled pulmonary, renal or hepatic dysfunction, or uncontrolled infection)

• Other primary malignant tumors within the previous 5 years, except for adequately controlled limited basal cell carcinoma of the skin or carcinoma in situ of the cervix

• Known human immunodeficiency virus(HIV) infection or other active or serious infection requiring IV antibiotics at randomization

• Pregnancy or breastfeeding women

• Women of childbearing potential(<2 years after the last menstruation) not using effective, non-hormonal means of contraception during the study and for a period of 6 months following the last administration of study drug

• Administration of any live virus vaccine within 8 weeks preceding study entry

• Use of any investigational agent within 30 days of administration of the first dose of study drug or concurrent treatment on another clinical study

• Requirement for radiation therapy concurrent with study anticancer treatment

• Known hypersensitivity to any of the study drugs or excipients

• Inability or unwillingness to abide by the study protocol or cooperate fully with the investigator or designee