Sunitinib Treatment on Tissue Sodium Accumulation (TSS2)

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Completed
CT.gov ID
NCT04368546
Collaborator
German Heart Institute (Other)
6
1
52
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Study Details

Study Description

Brief Summary

Here, it is investigated how sunitinib, a tyrosine kinase-inhibitor targeting vascular endothelial growth factor receptors, might influence sodium homeostasis in the skin and if this is related to a well-described treatment side-effect of sunitinib, hypertension.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Tyrosine kinases-inhibitors targeting vascular endothelial growth factor (VEGF)-receptors (RTKIs) are increasingly used in oncology in several metastatic tumor types. These agents are featured by toxicities including hypertension. According to a new insight, sodium in response to a high dietary sodium intake, is accumulated in a hyperosmolar way in the interstitial compartment. In response to this high sodium concentration cells of the mononuclear phagocytic system (MPS) are activated resulting in an increased production of VEGF-C, activation of VEGF type 3 receptors and formation of a lymphatic capillary network, involved in clearance of interstitial sodium. Blockade of stimulation of VEGF-C receptors or depletion of MPS cells in rodents has been associated with salt-sensitive hypertension.

Sunitinib is an orally-active, multitarget RTKI mainly used for the treatment of patients with metastatic renal cancer and imatinib-resistant gastrointestinal stromal tumors. Sunitinib blocks all three VEGF receptors subtypes, including VEGF-receptor type 3.

The investigators hypothesize that treatment of patients with sunitinib is associated with tissue sodium accumulation and this accumulation contributes to the rise in blood pressure. Tissue sodium is measured by using a newly developed 23Na magnetic resonance-imaging (MRI) technique which allows a non-invasive and contrast agent-free sodium content measurement in the muscle and skin of the lower leg.

Study Design

Study Type:
Observational
Actual Enrollment :
6 participants
Observational Model:
Case-Crossover
Time Perspective:
Prospective
Official Title:
Effect of Sunitinib Treatment on Tissue Sodium Accumulation in Patients With Renal Cancer: a Pilot Study
Actual Study Start Date :
Nov 1, 2015
Actual Primary Completion Date :
Feb 1, 2019
Actual Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Patients

Metastatic cell carcinoma patients before sunitinib treatment, after 4 week on, after 2 week off and finally again 4 week on medication.

Drug: Sunitinib
Other Names:
  • Diagnostic test: 23Na-MRI
  • Healthy controls

    Age-matched subjects without known disease.

    Outcome Measures

    Primary Outcome Measures

    1. Skin sodium [3 months (before, 4 weeks on, 2 weeks off and 4 weeks on medication)]

      Changes in sodium content measured by 23Na magnetic resonance-imaging (MRI) technique

    Secondary Outcome Measures

    1. Plasma VEGF-C [3 months (before, 4 weeks on, 2 weeks off and 4 weeks on medication)]

      Concentration of VEGF-C in patients plasma

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age men > 18 years

    • Life-expectation > 3 months

    • Stable weight

    • Blood pressure below 140/90 mmHg at baseline

    • Estimated glomerular filtration rate > 45 ml/min/1.73m2

    • Willingness to give written informed consent

    Exclusion Criteria:
    • Heart failure

    • Liver disease with ascites

    • Nephrotic syndrome

    • Gastrointestinal complaints, preventing normal daily food intake or diarrhea

    • Any form of diabetes mellitus

    • Known autoimmune diseases

    • Acute or chronic infection

    • Alcohol or substance abuse

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Experimental and Clinical Research Center, Clinical Research Unit Berlin Germany 13125

    Sponsors and Collaborators

    • Charite University, Berlin, Germany
    • German Heart Institute

    Investigators

    • Study Director: Dominik Müller, PhD, Group leader at the Max Delbruck Center for Molecular Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Dr. Lajos Marko, MD, PhD, Charite University, Berlin, Germany
    ClinicalTrials.gov Identifier:
    NCT04368546
    Other Study ID Numbers:
    • ChariteU-ECRC-TSS2
    • EA1/044/15
    First Posted:
    Apr 29, 2020
    Last Update Posted:
    Jan 27, 2021
    Last Verified:
    Jan 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Dr. Lajos Marko, MD, PhD, Charite University, Berlin, Germany
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 27, 2021