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Imaging the effect of HSP90 inhibitor AUY922 on VEGF by means of 89Zr-bevacizumab PET. A side study to the phase I-II study with AUY922 in adult patients with advanced solid malignancies, or either HER2 or ER positive locally advanced or metastatic breast cancer: protocol CAUY922A2101.

Imaging the effect of HSP90 inhibitor AUY922 on VEGF by means of 89Zr-bevacizumab PET. A side study to the phase I-II study with AUY922 in adult patients with advanced solid malignancies, or either HER2 or ER positive locally advanced or metastatic breast cancer: protocol CAUY922A2101. - 89Zr-bevacizumab PET for imaging the effect of HSP90 inhibition

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33855
Enrollment
11
Registered
2009-07-29
Start date
2010-02-08
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer mammary carcinoma

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - patients with ER positive, hormone therapy refractory breast cancer - participation in the phase I-II trial with HSP90 inhibitor AUY922 (in- and exclusion criteria for the study with AUY922 are described in protocol CAUY922A2101 -METc 2008.237-, section 5.1 and 5.2 (p 37-40).

Exclusion criteria

Exclusion criteria: - no participation in the phase I-II trial with HSP90 inhibitor AUY922

Design outcomes

Primary

MeasureTime frame
Measurement of decreased VEGF-levels compared to baseline, as a reflection of response to HSP90 inhibitor AUY922. A decline is defined as at least a 30% decrease of the mean SUV in a maximum of three lesions. These lesions will have a size of at least 2 cm (on the baseline CT), and will show the highest uptake on baseline 89Zr-bevacizumab scan (on which they are predefined).

Secondary

MeasureTime frame
Not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)