A Study of Trastuzumab-MCC-DM1 Administered Intravenously to Patients With HER2-Positive Metastatic Breast Cancer Who Have Previously Received a Trastuzumab-Containing Regimen

Metastatic Breast Cancer Clinical Trial

Official title:

A Phase I, Open-Label, Dose-Escalation Study of the Safety and Pharmacokinetics of Trastuzumab-MCC-DM1 (PRO132365) Administered Intravenously to Patients With HER2-Positive Metastatic Breast Cancer Who Have Previously Received a Trastuzumab-Containing Regimen

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00932373
• Other study ID #: TDM3569g
• Status: Completed
• Phase: Phase 1
• First received: June 30, 2009
• Last updated: August 13, 2015
• Start date: April 2006
• Est. completion date: June 2009

Study information

• Verified date: August 2015
• Source: Genentech, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a phase I, multicenter, open-label, dose-escalation study of single-agent trastuzumab-MCC-DM1 administered by intravenous (IV) infusion in patients with HER2-positive metastatic breast cancer (MBC) who have previously received trastuzumab. The study will assess the safety, tolerability, and pharmacokinetics of trastuzumab-MCC-DM1 and determine the dose and schedule to be used in Phase II.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 54
• Est. completion date: June 2009
• Est. primary completion date: June 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Histologically documented, incurable, locally advanced or metastatic breast cancer

• Evaluable or measurable HER2-positive disease

• History of progression during or within 60 days after treatment with any prior trastuzumab-containing chemotherapy regimen for HER2-positive breast cancer

• Previous treatment with chemotherapy for MBC

• Granulocyte count = 1,500/µL, platelet count = 100,000/µL, and hemoglobin = 9 g/dL

• Serum bilirubin = 1.5 mg/dL; AST, ALT, and alkaline phosphatase = 2.5 × upper limit of normal (ULN) except for: Patients with hepatic metastases: ALT and AST = 5 × ULN Patients with hepatic and/or bone metastases: alkaline phosphatase = 5 × ULN

• Serum creatinine = 1.5 mg/dL or creatinine clearance of = 60 mL/min based on a 24-hour urine collection

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2

• Women of childbearing potential and men must agree to use an effective method of birth control (e.g., hormonal, barrier) while receiving study treatment

Exclusion Criteria:

• History of significant cardiac disease, unstable angina, CHF, myocardial infarction, or ventricular arrhythmia requiring medication

• History of Grade = 3 hypersensitivity reaction to trastuzumab

• History of any toxicity to trastuzumab that resulted in trastuzumab being permanently discontinued

• Symptomatic brain metastases or any radiation or surgery for brain metastases within 3 months of first study treatment

• Require supplemental oxygen for daily activities

• Grade = 2 peripheral neuropathy

• Bisphosphonate therapy for symptomatic hypercalcemia

• Any chemotherapy, hormonal therapy, radiotherapy, immunotherapy, or biologic therapy for the treatment of breast cancer within 4 weeks of first study treatment

• Any experimental therapy within 4 weeks of first study treatment

• Any major surgical procedure within 4 weeks of first study treatment

• History of clinically symptomatic liver disease, including viral or other hepatitis, current or history of alcoholism, or cirrhosis

• Pregnancy or lactation

• Cardiac troponin I = 0.2 ng/mL

• Ejection fraction < 50% or below the lower limit of normal determined by echocardiogram or MUGA scan

• Prior cumulative doxorubicin dose of > 360 mg/m2 or equivalent

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Neoplasms
• Metastatic Breast Cancer

Intervention

Drug:
• trastuzumab-MCC-DM1
Intravenous escalating dose

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Genentech, Inc.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants With Adverse Events (AE), Serious Adverse Events (SAE), AEs With Grade >=3, and AEs Related To Treatment	The time frame for AEs is study treatment initiation until 30 days after last administration of study treatment or at the time of initiation of another anti-cancer therapy, which ever occurs first.; The time frame for SAEs is study treatment initiation until 90 days after last administration of study treatment or at the time of initiation of another anti-cancer therapy, which ever occurs first.	Study treatment initiation until 30 or 90 days after last administration of study treatment	Yes
Primary	Number of Patients With Dose Limiting Toxicities (DLTs)	DLT is defined as one of the following as per investigator related to study drug: Grade = 3 non-hematologic, non-hepatic major organ toxicity; Grade = 3 cardiac toxicity, including cardiac troponin I elevation or any new segmental wall abnormality as determined by non-invasive cardiac imaging; Grade = 4 thrombocytopenia; Grade = 4 neutropenia (absolute neutrophil count < 500/µ L) lasting > 4 days or accompanied by fever; Grade = 4 anemia; Grade = 3 serum bilirubin, hepatic transaminase (alanine aminotransferase or aspartate aminotransferase), or alkaline phosphatase For patients with Grade 2 hepatic transaminase or alkaline phosphatase levels at baseline as a result of liver metastases or bone metastases, a hepatic transaminase or alkaline phosphatase level = 10 times the upper limit of normal will be considered a DLT.; Weekly cohorts only: Toxicity preventing retreatment on Cycle 1, Day 8 or toxicity preventing re-treatment on Cycle 1, Days 15 and Day 22	A minimum of 21 days after first dose of trastuzumab-MCC-DM1	Yes
Primary	Maximum Tolerated Dose (MTD)	The highest dose level resulting in a DLT in = 1 of 6 patients was declared the MTD.	A minimum of 21 days after first dose of trastuzumab-MCC-DM1	Yes
Primary	Pharmacokinetic (PK) Parameters After the First Dose: Maximum Observed Plasma Concentration Cmax for T-DM1 Concentrations		3-Week and Weekly Cohorts: Cycle 1 Day 1 Pre-dose 30 minutes and 4 hours after the end of infusion; Cycle 1 Day 2, 3, 4, 8 (Pre-dose 30 minutes after the end of infusion) 11, 15 (Pre-dose 30 minutes after the end of infusion) and 18	No
Primary	PK Parameters After the First Dose: Area Under the Plasma Concentration-time Curve From 0 to Infinity (AUC[0-8] for T-DM1 Concentrations		3-Week and Weekly Cohorts: Cycle 1 Day 1 Pre-dose 30 minutes and 4 hours after the end of infusion; Cycle 1 Day 2, 3, 4, 8 (Pre-dose 30 minutes after the end of infusion) 11, 15 (Pre-dose 30 minutes after the end of infusion) and 18	No
Primary	PK Parameters After the First Dose: Terminal Half-life (t½) for T-DM1 Concentrations	Terminal phase elimination half-life (T1/2) is the time required for half of the drug to be eliminated from the plasma.	3-Week and Weekly Cohorts: Cycle 1 Day 1 Pre-dose 30 minutes and 4 hours after the end of infusion; Cycle 1 Day 2, 3, 4, 8 (Pre-dose 30 minutes after the end of infusion) 11, 15 (Pre-dose 30 minutes after the end of infusion) and 18	No
Secondary	Percentage of Participants With an Objective Response	The occurrence of an objective response was determined by the investigator according to Response Evaluation Criteria in Solid Tumors (RECIST). An objective response was defined as a complete response or a partial response as determined on 2 consecutive occasions = 4 weeks apart. A complete response was defined as the disappearance of all target lesions or the disappearance of all non-target lesions and normalization of tumor marker level. A partial response was defined as at least a 30% decrease in the sum of the longest diameter of target lesions, taking as reference the baseline sum of the longest diameter of target lesions.	Baseline to the end of the study (up to 3 years 2 months)	No
Secondary	Duration of Objective Response	Duration of objective response was defined as the time from the initial response to disease progression or death from any cause within 30 days of the last dose of trastuzumab emtansine.	Baseline to the end of the study (up to 3 years 2 months)	No
Secondary	Progression-free Survival	Progression-free survival was defined as the time from first dose of trastuzumab emtansine to documented disease progression or death from any cause within 30 days of the last dose of trastuzumab emtansine, whichever occurred earlier. Progressive disease was defined as at least a 20% increase in the sum of the longest diameter of target lesions, taking as reference the smallest sum of the longest diameter of target lesions recorded since treatment started or the appearance of one or more new lesions and/or unequivocal progression of existing non-target lesions.	Baseline to the end of the study (up to 3 years 2 months)	No
Secondary	Percentage of Participants With Anti-therapeutic Antibodies to Trastuzumab Emtansine	After the start of trastuzumab emtansine treatment, serum samples were collected every 3 weeks prior to trastuzumab emtansine dosing for detection of anti-therapeutic antibodies using a validated assay. A bridging antibody electrochemiluminescence assay (ECLA) was used to detect antibodies to trastuzumab emtansine. The assay utilized trastuzumab emtansine conjugated to biotin and a ruthenium label to form a complex with anti-trastuzumab emtansine antibodies. The antibody complex was captured by streptavidin-coated paramagnetic beads.	Baseline to the end of the study (up to 3 years 2 months)	No