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OpenTrials
Completed

NCT Number: NCT00162929

Her-2/Neu in Patients With Metastatic Breast Cancer (AdHERe)

The purpose of this study is to determine the maximum tolerated dose and/or maximum attainable dose of a vaccine consisting of human autologous dendritic cells transduced by an adenovector expressing rat Her-2/neu (AdHer-2/neu) in patients with metastatic breast cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Metastatic or locally recurrent breast cancer
  • 18 years of age or older
  • Her-2/neu positive (3+ by immunohistochemistry or fluorescence in-situ hybridization [FISH] +)
  • One of the following:
  • currently receiving hormonal therapy or are candidates for such, or
  • being considered for trastuzumab, or
  • cancer has progressed on trastuzumab.

Exclusion criteria

  • Pregnant or lactating women.
  • Prior or concurrent malignancies except for treated basal cell or squamous cell carcinoma of the skin or in situ cancer of the cervix or any other cancer treated and presumed cured for more than five years prior to study entry.
  • Currently receiving chemotherapy, immunotherapy, adenoviral gene therapy or biological cancer therapy. [Note: concurrent hormonal therapy (tamoxifen, aromatase inhibitors, or megace) is permitted.]
  • Treatment with trastuzumab within 4 weeks prior to first dose of vaccine therapy.
  • Hemoglobin < 80 g/L or granulocytes < 1.5 × 10^9/L or lymphocytes < 1.0 × 10^9/L or platelets < 100 × 10^9/L.
  • Baseline liver enzymes (AST or ALT) greater than 3 times the upper limit of normal or greater than 5 times the upper limit of normal if liver metastases are present and/or bilirubin is greater than 50 mmol.
  • CD4 cells < 0.5 ×10^9/L
  • Patients with documented brain metastases.
  • Patients with any acute illness that would interfere with the collection of CD34+ cells or administration of vaccination cellular therapy (i.e. unstable angina, renal or liver failure, or severe chronic obstructive airway disease).
  • Any patients requiring concurrent immunosuppressive therapy (e.g. corticosteroids).
  • Eastern Cooperative Oncology Group (ECOG) performance status of > 2.
  • Patients with a life expectancy of less than 6 months.
  • Geographic inaccessibility which would preclude follow-up. Patients registered on the trial must be treated and followed at the Juravinski Cancer Center and the Henderson site of the Hamilton Health Sciences.
  • Failure to give written informed consent.
  • Baseline left ventricular ejection fraction (LVEF) < 55% by echocardiography or multigated acquisition (MUGA) scan.

Treatment and study plan

AdHer-2/neu transduced dendritic cells

Biological

Group 1 1 ×10'7 expanded cells (2.5 ×106 DCs per injection site) Group 2 5 ×10'7 expanded cells (1.25 ×107 DCs per injection site) Group 3 1 ×10'8 expanded cells (2.5 ×107 DCs per injection site)

Primary outcomes

  1. toxicity

    Time frame: weeks 4, 6, 7, 10, 14, 18, 22, 26

Secondary outcomes

  1. tumour response

    Time frame: Weeks 6, 18

Sponsors and collaborators

Lead sponsor

Ontario Clinical Oncology Group (OCOG)

Other

Collaborators

  • Canadian Breast Cancer Research Alliance
  • Ontario Cancer Research Network

Registry information

Official study title

A Phase I Study Investigating Multiple Injections of Autologous CD34+ Derived Dendritic Cells Transduced With an Adenovirus Expressing Rat Her-2/Neu in Patients With Metastatic or Locally Recurrent Breast Cancer

Acronym: AdHERe

Important dates

Study start
2005
Primary completion
2009
Study completion
2012
First posted
Sep 13, 2005
Registry last updated
Jun 4, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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