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Molecular Determinants for Therapy Response on Renal Cell Carcinoma (MORE)

Primary Purpose

Renal Cell Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Sunitinib, Pazopanib, Bevacizumab, Everolimus...
Sponsored by
Heidelberg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Cell Carcinoma focused on measuring Renal cell carcinoma, Biomarkers, Molecular modifications

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Minimum Age: 18 Years Maximum Age: no maximum age

  • metastatic lesions easy of access for puncture for specimen storage
  • histological subtype: clear-cell renal cancer
  • no contraindications against systemic therapy
  • indication for systemic therapy given

Exclusion Criteria:

  • preexisting mental illness
  • further active malignancy
  • patients with increased risk of bleeding and/or wound healing disorder
  • patients who are not legally competent or unable to consent
  • contraindication for surgical intervention

Sites / Locations

  • Urological Department of the University Hospital HeidelbergRecruiting

Arms of the Study

Arm 1

Arm Type

No Intervention

Arm Label

Receptor-Tyrosinkinase-Inhibitor

Arm Description

Guidelines-oriented therapy with approved systemic medications for renal cell carcinoma individually for each patient (Receptor-Tyrosinkinase-Inhibitor) (e.g.Sunitinib, Pazopanib, Bevacizumab, Everolimus, Axitinib, Temsirolimus). With 1.progression turning to second line treatment with one of the upper mentioned medications. Third line therapy due to the individual molecular modifications for each patient.

Outcomes

Primary Outcome Measures

Time to disease progression in third line therapy
Progression free survival in third-line therapy ( defined as the time from beginning of the third-line therapy to the date of the first documented progression as determined by the investigator using Response Evaluation Criteria in Solid Tumors criteria assessed by CT/MRI every 12 weeks).

Secondary Outcome Measures

Identification of preventive biomarkers.
Identification of preventive biomarkers.

Full Information

First Posted
June 2, 2014
Last Updated
July 31, 2014
Sponsor
Heidelberg University
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1. Study Identification

Unique Protocol Identification Number
NCT02208128
Brief Title
Molecular Determinants for Therapy Response on Renal Cell Carcinoma
Acronym
MORE
Official Title
Molecular Determinants for Therapy Response on Renal Cell Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2014 (undefined)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
February 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Heidelberg University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Aim of the scientific analysis is to find biological factors (biomarkers) allowing a prediction of disease progression and a better choice of therapy. After diagnosis the kidney and the tumor will be removed by standard surgery followed by drug therapy. Within surgery remaining tumor tissue will be used for the scientific analysis. In case of disease progression during the drug treatment the drug therapy will be changed. Before therapy change a small tissue sample will be collected for molecular diagnostics. This will be done by puncture through the skin under local anesthesia. Blood samples taken before surgery and at the time of first and second disease progression will also be used for molecular-biological analysis. As there is no clear recommendation for drug therapy after disease progression this study should serve to determine an individual therapy on the basis of the molecular profile and the molecular changes. As the tumor disease changes and developes resistance to drugs, analysis at the time of disease progression shall identify biological factors which will predict a likelihood response to a specific drugs. This shall allow to give the patient an individual therapy.
Detailed Description
Aim of this study is to perform a profound molecular analysis of the tumor before beginning therapy and after failure of the approved targeted first-and second line therapy (standard therapy). The tumor sample will be analyzed by using profound molecular analysis to identify target structures which will predict the efficacy of a specific therapy (substance group)and therefore have a predictive value. The analysis of molecular biomarkers include the genomic sequencing of targeted areas or of the entire DNA of the tumor tissue comparative to the DNA of healthy cells, the measurement of DNA-regulatory elements (methylation, mi-RNA expression, protein expression analytics, functional tumorcell analysis in-vitro, efficacy analysis in cell culture or in animal model) who are supposed to inspect the biological influence of the molecular biomarkers and measurements of free tumor DNA out of the blood. The response to the established standard therapy in the first and second line will be acquired due to all clinical and radiological established standard parameters. The clinical-radiological response will be correlated with the molecular changes and their changes in therapy process to allow predictive prognosis for a further therapy. There is no approved clinical standard for third line therapy. However there are further medications approved without any scientific evidence of their efficacy in this therapy situation (third line treatment after failure of first and second line treatment) and for which a response of under 6 weeks is expected. For these patients the third line therapy will be adjusted to the molecular profiles of the previous therapies. Therefore the oncological history of the noticed marker profiles and the presence of target structures (from whom it is known that they are influenced by certain substances) will be considered. The therapy will use substances which are approved in general for the treatment of metastatic renal cell cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma
Keywords
Renal cell carcinoma, Biomarkers, Molecular modifications

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Receptor-Tyrosinkinase-Inhibitor
Arm Type
No Intervention
Arm Description
Guidelines-oriented therapy with approved systemic medications for renal cell carcinoma individually for each patient (Receptor-Tyrosinkinase-Inhibitor) (e.g.Sunitinib, Pazopanib, Bevacizumab, Everolimus, Axitinib, Temsirolimus). With 1.progression turning to second line treatment with one of the upper mentioned medications. Third line therapy due to the individual molecular modifications for each patient.
Intervention Type
Drug
Intervention Name(s)
Sunitinib, Pazopanib, Bevacizumab, Everolimus...
Other Intervention Name(s)
e.g.Sunitinib, Pazopanib, Bevacizumab, Everolimus...
Intervention Description
Clinical standard
Primary Outcome Measure Information:
Title
Time to disease progression in third line therapy
Description
Progression free survival in third-line therapy ( defined as the time from beginning of the third-line therapy to the date of the first documented progression as determined by the investigator using Response Evaluation Criteria in Solid Tumors criteria assessed by CT/MRI every 12 weeks).
Time Frame
Approximately 2 years depending on when the failure in third line therapy happens
Secondary Outcome Measure Information:
Title
Identification of preventive biomarkers.
Description
Identification of preventive biomarkers.
Time Frame
2weeks in average before surgery and 4 weeks in average after surgery before starting first line treatment
Other Pre-specified Outcome Measures:
Title
Identification of preventive biomarkers
Time Frame
2years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Minimum Age: 18 Years Maximum Age: no maximum age metastatic lesions easy of access for puncture for specimen storage histological subtype: clear-cell renal cancer no contraindications against systemic therapy indication for systemic therapy given Exclusion Criteria: preexisting mental illness further active malignancy patients with increased risk of bleeding and/or wound healing disorder patients who are not legally competent or unable to consent contraindication for surgical intervention
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sascha Pahernik, PD Dr.
Phone
+49 6221 5639689
Email
sascha.pahernik@med.uni-heidelberg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Carsten Grüllich, PD Dr.
Phone
+49 6221 5637125
Email
carsten.gruellich@med.uni-heidelberg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sascha Pahernil, PD Dr.
Organizational Affiliation
University of Heidelberg, Urological Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
Urological Department of the University Hospital Heidelberg
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sascha Pahernik, PD Dr.
Phone
+49 6221 56 39689
Email
sascha.pahernik@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Sascha Pahernik, PD Dr.

12. IPD Sharing Statement

Learn more about this trial

Molecular Determinants for Therapy Response on Renal Cell Carcinoma

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