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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02072720
Other study ID # 2013/340
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date February 2014
Est. completion date May 1, 2021

Study information

Verified date October 2019
Source VU University Medical Center
Contact Henk Verheul, MD/ PhD
Email h.verheul@vumc.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main question of this study is if and when VEGF (vascular endothelial growth factor) expression in the tumor is upregulated during chemoradiation and if bevacizumab inhibits subsequent vessel growth in the tumor.

- Therefore the first aim of this study is to identify the time point of induction of VEGF in the tumor tissue of esophagus carcinoma during chemoradiation (after 1,2,3 or 4 weeks of chemoradiation).

- If we identify increased expression of VEGF at a certain time point, our second aim is to determine if we can inhibit the subsequent tumor vessel growth by administration of bevacizumab.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date May 1, 2021
Est. primary completion date March 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients that will receive chemoradiation following CROSS-schedule before surgery for esophageal carcinoma

- ability to give informed consent

- age 18 years or older

Exclusion Criteria:

- pregnancy

- evidence of bleeding diathesis, coagulopathy

- inflammation of the GI-tract

- brain metastases

- diastolic/ systolic hypertension, not responding to treatment

- arterial thromboembolism in medical history

- surgery within the month prior to start of bevacizumab treatment

Study Design


Intervention

Drug:
Bevacizumab
patients will receive bevacizumab (3mg/kg/wk) starting from the identified induction time point of VEGF expression

Locations

Country Name City State
Netherlands Noordwest Ziekenhuisgroep Alkmaar
Netherlands Academisch Medisch Centrum Amsterdam
Netherlands VU university medical center Amsterdam Noord-Holland

Sponsors (3)

Lead Sponsor Collaborator
VU University Medical Center Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Noordwest Ziekenhuisgroep

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of VEGF mRNA expression in tumor biopsies To compare the VEGF mRNA expression in the pre-treatment and on-treatment tumor biopsies, to measure the change in VEGF expression from baseline. 5 weeks
Primary Change of VEGFR2 phosphorylation with IHC To determine the level of pVEGFR2 expression in tumor biopsies of patients that received bevacizumab, and to compare that to their pre-treatment expression levels, to identify the changes in expression from baseline. 8 weeks
Secondary Changes of mRNA expression of other pro-angiogenic factors To identify the expression of other pro-angiogenic factors in the tumor, and to measure the changes from baseline expression (pre-treatment vs on-treatment biopsies). 5 weeks
Secondary Changes in protein expression of pro-angiogenic factors To identify the protein expression of other pro-angiogenic factors in the tumor, and to measure the changes from baseline expression (pre-treatment vs on-treatment biopsies). 5 weeks
Secondary Changes in vascular parameters in the tumor tissue to asses ongoing angiogenesis To identify the expression of CD31+ and pericyte markers with IHC staining in the tumor, and to measure the changes from baseline expression (pre-treatment vs on-treatment biopsies). 5 weeks