89Zr-atezolizumab PET Scan and Lobular Breast Cancer

  • STATUS
    Recruiting
  • participants needed
    10
  • sponsor
    University Medical Center Groningen
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Updated on 19 February 2024
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Summary

The exploratory single center feasibility ImaGelato study is conducted as an imaging side study to the Dutch GELATO trial (Assessing efficacy of carboplatin and atezolizumab in metastatic lobular breast cancer). Ten patients with lobular metastatic breast cancer, who are included in the GELATO trial at the UMCG, are eligible for the ImaGelato study.

All patients will undergo two Zirconium-89 (89Zr)-atezolizumab positron emission tomography (PET) scans, one at baseline and one after two doses carboplatin induction treatment. The 89Zr-atezolizumab PET scan will be performed 4 days after tracer injection. Procedures within the ImaGelato study will be completed after the two 89Zr-atezolizumab PET scans, but patients will continue treatment with carboplatin combined with atezolizumab in the GELATO trial.

Details
Condition Lobular Metastatic Breast Cancer
Age 18years - 100years
Treatment 89Zr-atezolizumab PET scans
Clinical Study IdentifierNCT04222426
SponsorUniversity Medical Center Groningen
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

A patient must meet the inclusion criteria of the GELATO trial
Able to give written informed consent and to comply with the ImaGelato protocol

Exclusion Criteria

Contra-indication for 89Zr-atezolizumab PET scan
Any approved anti-cancer therapy, including chemotherapy or hormonal therapy within 14 days prior to the first 89Zr-atezolizumab injection. Treatment with any other investigational agent or participation in another clinical trial with therapeutic intent within 28 days prior to the first 89Zr-atezolizumab injection
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    University Medical Center Groningen

    Netherlands

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University Medical Center Groningen

Netherlands

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Investigator Avatar
C. P. Schröder, MD, PhD

Primary Contact

University Medical Center Groningen

Netherlands

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