HER2-Peptide Vaccination of Patients With Solid Tumors

Technical University of Munich

Status and phase

Completed

Phase 1

Conditions

Breast Cancer

Gastric Cancer

Treatments

Drug: Cyclophosphamide

Drug: HER2-Peptid-Vakzine

Drug: Imiquimod

Drug: Sargramostim

Study type

Interventional

Funder types

Other

Identifiers

NCT02276300

ATZ-1068-KRA-20I

Details and patient eligibility

About

Investigation of peptide vaccination targeting HER2/neu in patients with metastasized breast or gastric cancer with moderate HER2/neu expression.

Full description

This is an interventional phase I clinical study to investigate the safety, tolerability and efficacy of HER2-derived peptide vaccination. HLA-A2+ patients with stage IV metastasized breast or gastric cancer with HER2 expression (IHC Score 2+) without gene amplification proved by FISH analysis, with documented stable disease or objective response after at least first line systemic chemotherapy/radiotherapy for advanced disease who have not been treated for the underlying malignant disease for 4 weeks with chemo-, radio- or immunotherapy will be included into the study. The aim of the study is to show safety and tolerability of this immunotherapeutic approach and to investigate efficacy of the immunotherapy.

Enrollment

2 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with stage IV metastasized breast or gastric cancer with documented stable disease or objective response after at least first line chemo/ radiotherapy for advanced disease
HER2 IHC score 2+ on tumor cells, negative FISH result
HLA-A2 expression
Female or male patients aged >= 18 years
Measurable disease according to RECIST criteria
ECOG 0-1
Neutrophile count > 1,5x10^9/l
WBC > 2,5x10^9/l
Lymphocyte count > 1x10^9/l
Hemoglobin > 10g/dl
Platelets > 100x10^9/l
Normal renal function (creatinine < 150% ULN)
Normal liver function (Bilirubin < 150% ULN; ALAT/SGPT and ASAT/SGOT < 300% ULN, except proven metastases)
Expected survival of at least 6 months
Concomitant anti-hormonal treatment is allowed
Female patients within child bearing age must have a negative pregnancy test performed not earlier than 21 days before administration of investigational product. Male and female patients with reproductive potential must agree to employ an effective method of birth control throughout the study and for 6 months discontinuation of investigational product. Postmenopausal women must be amenorrheal for at least 12 months to be considered of non-childbearing potential.
Men and women of childbearing potential must agree to use a highly effective method of birth control which results in a low failure rate (less than 1% per year) when used consistently and correctly.
Written informed consent that the patient or a legally authorized representative has been informed about all aspects of the study prior to enrollment and is willing to participate and to be included in the study
Ability to understand and comply with study and follow-up procedures

Exclusion criteria

Treatment with any other investigational drug within 4 weeks prior to the start of the study medication
Known hypersensitivity to any components of the study product
Any severe concomitant disease
Any disease (including psychotic disorders, drug abuse, active infection, uncontrolled hypertension, unstable angina, heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal or metabolic disease, obstructive or restrictive lung disease) metabolic dysfunction) and physical examination finding likely (in the investigator's opinion) to affect the evaluation of the study or to put patient at risk associated to treatment with the study medication.
Any heart disease
Any serious infection or sepsis
Any autoimmune disorder
Infection with HIV, chronic infection with Hepatitis B or C
Any immunodeficiency syndrome
Surgery within 4 weeks before study entry
Prior splenectomy
Brain metastasis or leptomeningeal involvement
Systemic application of immunosuppressive drugs including systemic corticosteroids within three weeks before study entry
Patients eligible or treated with any aproved HER2-targeted therapy as Trastuzumab, Pertzuzumab, T-DM1 or Lapatinib
Radio-, chemo- or immunotherapy other than study medication in parallel or within 4 weeks prior study start
Active drug abuse or chronic alcoholism
Pregnancy or breast feeding
Female and male patients of reproductive potential unwilling or unable to practice a highly effective method of birth control
History of non-compliance with medical regimens
Patients unwilling or unable to comply with the protocol