Effect of Sorafenib on ccRCC Uptake of Radiolabeled Bevacizumab or cG250

Radboud University Medical Center

Status: Completed

Conditions: Clear Cell Renal Cell Carcinoma

Treatments: Drug: 111Indium-cG250; Drug: Sorafenib; Drug: 111Indium-bevacizumab

Study type: Interventional

Funder types: Other

Identifiers

NCT00602862

Sorafenib-mAbs

Details and patient eligibility

About

Sorafenib is a tyrosine kinase inhibitor that is registered for the treatment of metastasized clear cell Renal Cell Carcinoma (ccRCC). It inhibits signal transduction of the Vascular Endothelial Growth Factor Receptor (VEGFR) and the Platelet Derived Growth Factor Receptor (PDGFR). In the tumorigenesis of ccRCC, VEGF and PDGF are upregulated due to the defective Von-Hippel-Lindau (VHL) gene. CcRCC has a high Interstitial Fluid Pressure (IFP) and Tumor Microvascular Density (TMD), hampering the delivery of chemotherapeutics and monoclonal antibodies (mAbs). It was hypothesized that antiangiogenic compounds decrease tumor IFP and TMD, thus normalizing tumor vasculature, before diminishing tumor vasculature. Bevacizumab is an anti-VEGF mAb which depletes soluble VEGF from plasma, depriving VEGFR of its ligand. Chimeric monoclonal antibody cG250 recognizes carbonic anhydrase IX (CAIX), an antigen that is abundantly expressed in Renal Cell Carcinoma (RCC) and has limited expression in normal tissue. The aim of this study was to investigate the effect of Sorafenib on ccRCC physiology, by determining tumor uptake of 111In labeled cG250 or 111In labeled Bevacizumab.

Enrollment: 26 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Renal cell carcinoma patients planned for surgery (nephrectomy/metastasectomy)

• Karnofsky > 70 %

• Laboratory values within 14 days prior to start:

  • White blood cells (WBC) > 3.5 x 109/L
  • Platelets > 100 x 109/L
  • Hemoglobin > 6 mmol/L
  • Total bilirubin < 1.5 upper limit of normal (ULN)
  • ASAT, ALAT < 2.5 x ULN (<5 x in case of liver metastases)
  • Lactate dehydrogenase (LDH) > 1.5. ULN
  • Serum creatinine < 2 x ULN
  • Amylase and Lipase < 1.5 ULN

• Negative pregnancy test in premenopausal women

• Age over 18 years

• Signed informed consent

• Life expectancy > 24 weeks

• PT/APTT/ INR < 1.5 ULN

• No current use of coumarin derivatives

Exclusion criteria

• Known subtype other than clear cell RCC
• Pre-exposure to murine/chimeric antibody therapy
• Known brain metastases
• Untreated hypercalcemia
• Uncontrolled hypertension
• Concurrent therapeutic anticoagulation
• Chemotherapy, immunotherapy or radiation therapy within 4 weeks prior to start of study. Palliative limited field external radiation for fracture prevention is allowed
• Cardiac arrhythmias requiring antiarrhythmics (beta-blockers, digoxin), symptomatic coronary artery disease and congestive heart failure New York Heart Association III or IV.
• Previous malignancy < 2 years prior to the study (except for cervical carcinoma in situ, basal cell carcinoma, or superficial bladder tumours (Ta, Tis, T1)
• Any medical condition present that in the opinion of the investigator will affect patients' clinical status. No other concurrent malignancy except nonmetastatic nonmelanoma skin cancer or carcinoma in situ of the cervix.
• Active clinically serious bacterial or fungal infections (< grade 2 NCI-CTC version 3)
• Known history of Human Immunodeficiency virus (HIV) infection or chronic hepatitis B/C.
• Prior use of Raf-kinase inhibitors, MEK and Farnesyl transferase inhibitors
• Prior use of Bevacizumab and all other drugs that target VEGF/ VEGF-receptors
• Use of antiepileptic drugs
• Pregnancy and lactation

Trial design

Primary purpose: Basic Science

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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26 participants in 3 patient groups

1

Experimental group

Description:

10 Patients planned to undergo (partial) nephrectomy or metastasectomy receive an iv injection of 100 MBq/1mg 111In-Bevacizumab. Patients are then treated with Sorafenib 200 mg 2dd2 po for 4 weeks. In the last week of treatment, the same injection is given to determine tumor accumulation of the radiolabeled mAb after Sorafenib treatment. Whole-body scintigraphic images are recorded 1 week after both injections to calculate tumor uptake. After Sorafenib treatment, patients will undergo surgery.

Treatment:

Drug: 111Indium-bevacizumab

Drug: Sorafenib

2

Experimental group

Description:

10 Patients planned to undergo (partial) nephrectomy or metastasectomy receive an iv injection of 100 MBq/10mg 111In-cG250. Patients are then treated with Sorafenib 200 mg 2dd2 po for 4 weeks. In the last week of treatment, the same injection is given to determine tumor accumulation of the radiolabeled mAb after Sorafenib treatment. Whole-body scintigraphic images are recorded 1 week after both injections to calculate tumor uptake. After Sorafenib treatment, patients will undergo surgery.

Treatment:

Drug: Sorafenib

Drug: 111Indium-cG250

3

Active Comparator group

Description:

5 Patients planned to undergo (partial) nephrectomy or metastasectomy receive an iv injection of 100 MBq/1mg 111In-Bevacizumab. Whole-body scintigraphic images are recorded 1 week after the injection to calculate tumor uptake. Hereafter, patients will undergo surgery.

Treatment:

Drug: 111Indium-bevacizumab