111 Indium CHX-A DTPA Trastuzumab (Indium-Herceptin) for Imaging Breast Cancer

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2013 by National Institutes of Health Clinical Center (CC)
Sponsor:
Information provided by:
National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:
NCT01445054
First received: September 30, 2011
Last updated: March 14, 2014
Last verified: July 2013

September 30, 2011
March 14, 2014
February 2007
Not Provided
Correlation of uptake with HER2/neu status of tumor. [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01445054 on ClinicalTrials.gov Archive Site
Establish safety of 111 Indium Trastuzumab, determine the optimal timing of imaging as a function of HER2 status and correlate uptake with traditional IHC assessment of HER2 status, biodistribution.
Same as current
Not Provided
Not Provided
 
111 Indium CHX-A DTPA Trastuzumab (Indium-Herceptin) for Imaging Breast Cancer
A Phase 0 Trial of (111)Indium CHX-A DTPA Trastuzumab Imaging in Cancer

Background:

  • Some breast cancer cells have specific proteins (receptors) on their surface that make the tumor grow faster than normal cells. One of these receptors is called HER2/neu.
  • An FDA-approved drug called Herceptin attaches to HER2/neu if it is present on the cancer cell.
  • Indium-Herceptin is an agent in which a tiny amount of radioactivity called Indium has been attached to a tiny amount of Herceptin.

Objectives:

-To see if Indium-Herceptin provides information about the characteristics of the breast cancer in women whose tumors express HER2/neu and those whose tumors do not.

Eligibility:

-Women 18 years or older with primary or metastatic breast cancer who have not received treatment with herceptin for at least 6 months before enrollment into the study.

Design:

  • Tissue from the patient s original breast or tumor biopsy is analyzed for HER2/neu status.
  • Patients have a physical examination and review of medical records.
  • Patients receive an injection of Indium-Herceptin, followed by scanning with a gamma camera that detects the radioactivity in the Indium-Herceptin.
  • Patients return to the clinic 1, 2, 3 and 7 days later for repeat imaging to determine the best time to image after injection of Indium-Herceptin.
  • Blood samples are obtained every day of scanning to monitor the effects, if any, of the Indium-Herceptin and to see how fast the agent leaves the body.

Background:

  • Trastuzumab (Herceptin ), targets HER2 (aka: neu, ErbB2, c-erb-B2) on the surface of cancer cells and is used in the treatment of breast cancers that overexpress HER2/Neu (Erb2). It has also been demonstrated that other malignancies express HER2/Neu (Erb2).
  • Radiolabeling trastuzumab could allow human biodistribution studies, noninvasive assessment of HER2/Neu (Erb2) expression, identification of HER2/Neu (Erb2) positive metastases, monitoring of treatment response and establishment of dosimetry for future radioimmunotherapy.
  • We have developed a chelated form of trastuzumab, CHX-A DTPA-trastuzumab, that can bind a number of radioisotopes including (111)In, (212), (213)Bi, (212)Pb (86), (90)Y and (177)Lu which have alpha, beta and gamma emissions for imaging and therapy.
  • We believe that the agent will be safe based on the low dose of trastuzumab (up to a maximum of 200 mcg of protein or less than1% of the typical loading dose of trastuzumab in a 70 Kg human) and the low dose of radioactivity (5mCi).
  • Whereas trastuzumab therapy is generally only useful in tumors that highly express HER2/Neu (Erb2), (111)In-CHX-A DTPA trastuzumab (henceforth (111)Indium-trastuzumab ) will image tumors that are not only highly expressing HER2/Neu (Erb2) but also tumors that are poorly expressing HER2/Neu (Erb2) as documented by preclinical data.

Objectives:

  • The primary objective is to compare uptake of 111Indium trastuzumab with HER2/Neu (Erb2) status of the tumor as determined by IHC
  • Secondary objectives will be to establish safety of (111)Indium trastuzumab, determine the optimal timing of imaging as a function of HER2/Neu (Erb2) status, and determine biodistribution of the agent in normal organs and pharmacokinetics of serum clearance.

Eligibility:

  • Participants with a history of primary or metastatic cancer (other than melanoma, basal cell carcinoma, sarcoma or lymphoma) with known solid tumor size greater than or equal to 1.5 cm.
  • Availability of HER2/Neu (Erb2) expression by immunohistochemistry (IHC) or pathology or biopsy specimen can be provided on which such an analysis can be made.

Design:

  • The design of this pilot trial follows the concept of a Phase 0 or Exploratory IND (xIND) study.
  • Participants with known malignancy greater than or equal to 1.5cm and known HER2/Neu(ErbB2) tumor status (0, 1+, 2+ or 3+) by IHC or FISH.
  • After receiving 5 mCi of (111)Indium-trastuzumab, all participants will undergo gamma camera scans at approximately 24-72 hours after injection. In some subjects, an additional imaging session may be required 24 hours after the first set of images as physiologic bowel clearance is variable and may obscure the lesion of interest on the initial scan.
  • We will accrue 20 participants to this study.
  • A total of 8 blood samples (4 lab tests and up to 4 for pharmacokinetics) will be obtained from each participant to establish toxicity and the pharmacokinetics of clearance.
  • Images will be correlated with IHC status using tumor to background ratios and the optimal scanning strategy with regard to HER2/neu(ErbB2) expression will be determined.
  • Participants who undergo a therapy thought to target or effect HER2 will have the option of undergoing repeat imaging following therapy.
Interventional
Phase 0
Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Breast Cancer
  • Radiation: 111 Indium CHX-A DTPA-Trastuzumab
    N/A
  • Drug: 111Indium Trastuzumab
    N/A
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
20
Not Provided
Not Provided
  • INCLUSION CRITERIA:

Participant must have histological confirmation of primary or metastatic cancer other than melanoma, basal cell carcinoma, sarcoma, or lymphoma.

  • Primary tumor or metastatic focus must be 1.5cm or greater in diameter as established by palpation, ultrasound, mammography, CT or MRI.
  • Participant must be 18 years or older.
  • Availability of tumor tissue (either from the initial primary tumor or from current tumor lesion) for performing IHC or FISH analysis for HER2/Neu (Erb2)
  • Chemistry and CBC parameters: serum creatinine less than or equal to 1.4mg/dl. SGOT and SGPT less than or equal to 3 times of the upper limits of normal; total bilirubin, of less than or equal to 2 times the upper limits of normal or 3.0 mg/dl in patients with Gilbert s syndrome; platelet count must be greater than 100,00.
  • ECOG Performance score of 0 or 1.
  • Ability to provide informed consent.
  • Negative serum pregnancy test (within 48 hours of imaging agent injection) in women of child bearing age and willingness to use contraception (barrier, abstinence, non-hormonal) for 3 weeks after injection of (111)Indium trastuzumab if participant is of child bearing age.

EXCLUSION CRITERIA:

  • Known allergy to trastuzumab.
  • Pregnant or lactating women.
  • Participants for whom enrollment would significantly delay (greater than 2 weeks) the scheduled standard of care therapy.
  • Participants with an active second malignancy (excluding treated basal cell skin carcinoma).
  • History of cardiac disease (myocardial infarction, arrhythmias requiring therapy, symptomatic valvular disease, cardiomyopathy, or pericarditis).
  • Participants with any coexisting medical or psychiatric condition that is likely to interfere with study procedures and/or results.
  • Participants with severe claustrophobia.
  • A participant who needs a nuclear medicine scan other than a PET scan as part of their work-up cannot enroll until these scans have been completed.
  • Gamma-camera table restrictions preclude scanning participants greater than 350 lbs (160 Kg)
  • With the exception of AT13387 and PU-H71, and Ad5f35HER2ECTM transduced autologous dendritic cell vaccine participants cannot have received another experimental drug within 14 days prior to or during study enrollment.
Female
18 Years and older
No
Contact: Yolanda McKinney, R.N. (301) 443-6913 ymckinney@mail.nih.gov
Contact: Peter L Choyke, M.D. (301) 402-8409 pchoyke@mail.nih.gov
United States
 
NCT01445054
070101, 07-C-0101
Not Provided
Not Provided
National Cancer Institute (NCI)
Not Provided
Principal Investigator: Peter L Choyke, M.D. National Cancer Institute (NCI)
National Institutes of Health Clinical Center (CC)
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP