Assessing Everolimus in Fist Line Treatment on Patients With Metastatic Kidney Cancer (POORTOR)
Primary Purpose
Kidney Cancer
Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Everolimus
Sponsored by
About this trial
This is an interventional treatment trial for Kidney Cancer
Eligibility Criteria
Inclusion Criteria:
- Metastatic kidney cancer, regardless of histology (except Bellini carcinomas), with measurable or evaluable disease
- Age >= 18 years
- With Karnofsky ≥ 60
- Without prior treatment for metastatic cancer (chemotherapy, targeted therapy, or mTOR inhibitor)
Bad prognosis, defined as follows: at least three of the following six criteria of poor prognosis:
- Karnofsky <80
- LDH> 1.5 ULN
- hemoglobin <LLN
- corrected calcium> 2.5 mmol / l (10 mg / dl)
- Time frame between initial diagnostic and treatment <1 year
- More than one metastatic site
- medullary function: neutrophils ≥ 1.5 x 109 / L, Platelets ≥ 100 x 109 / L, Hb> 8g/dL
- Hepatic function: bilirubin: ≤ 1.5 x ULN, ALT and AST ≤ 2.5x ULN in the absence of hepatic metastasis ≤ 5x ULN if hepatic metastasis documented
- Renal function: creatinine <1.5 x ULN
- Life expectancy> 3 months,
- Patient signed informed consent and agreeing to comply with the requirements of the trial
Exclusion Criteria:
- Previous treatment with chemotherapy, targeted therapy, or mTOR inhibitor
- Previous radiotherapy in the last 2 weeks
- Chronic treatment with corticoids or immunosuppressive agents except substitutive opotherapy.. A washout period of at least 8 days must be respected before the patient inclusion.
- Patients with brain metastases untreated or uncontrolled by prior treatment. The non-progression of the metastases must be proved by comparing two brain scans separated by a minimum interval of 6 weeks.
- Active bleeding
- Patient with positive serology HBs (Ag HBs (+) and AC anti-HBc (+)
- Hypersensitivity to everolimus, sirolimus, to other rapamycin derivatives or to any of the excipients
Severe or uncontrolled medical pathology:
- unstable angina, symptomatic heart failure, myocardial infarction ≤ 6 months before randomization, severe rhythm disorder,
- Uncontrolled diabetes with glycaemia> 1.5X ULN.
- Active or uncontrolled infection.
- cirrhosis or chronic active hepatitis,
- severe alteration in lung function (> 50% decrease in FEV or vital capacity)
- Other cancer within the past 3 years, with the exception of basal cell carcinoma and carcinoma in situ of the cervix
- Pregnant or lactating woman, and adults refusing an effective contraceptive method
- Participation in another clinical trial with an investigational drug
- Refusal of the patient to comply with the rules of the clinical trial
- Person deprived of liberty or person under guardianship, inability to submit to medical treatment test for geographical, social or psychological reasons.
Sites / Locations
- Gustave Roussy
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Everolimus
Arm Description
Everolimus will be administered per os every day at the same hour immediately after a meal with a glass of water 10 mg (1 tablet of 10 mg)
Outcomes
Primary Outcome Measures
Overall Survival (OS)
Secondary Outcome Measures
Response rate
Response rate based on RECIST 1.1 criteria
Toxicity of Everolimus
Progression Free Survival (PFS)
Full Information
NCT ID
NCT01888042
First Posted
June 25, 2013
Last Updated
February 9, 2016
Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
1. Study Identification
Unique Protocol Identification Number
NCT01888042
Brief Title
Assessing Everolimus in Fist Line Treatment on Patients With Metastatic Kidney Cancer
Acronym
POORTOR
Official Title
Phase II Study Assessing Everolimus as Fist Line Treatment in Patients With Metastatic Kidney Cancer of Bad Prognosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Study Start Date
July 2011 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
It is a an open label, multicentric, phase II study assessing the efficacy of everolimus (given per os) as a first line treatment in kidney cancer of bad prognosis.
92 patients will be included (anticipated). The treatment by everolimus will continue until progression, significant toxicity or withdraw of consent
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
61 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Everolimus
Arm Type
Experimental
Arm Description
Everolimus will be administered per os every day at the same hour immediately after a meal with a glass of water 10 mg (1 tablet of 10 mg)
Intervention Type
Drug
Intervention Name(s)
Everolimus
Intervention Description
10 mg (1 tablet of 10 mg)
Primary Outcome Measure Information:
Title
Overall Survival (OS)
Time Frame
From inclusion to progression, significant toxicity or death wichever come first up to 56 months
Secondary Outcome Measure Information:
Title
Response rate
Description
Response rate based on RECIST 1.1 criteria
Time Frame
From inclusion to progression, significant toxicity or death whichever come first up to 56 months
Title
Toxicity of Everolimus
Time Frame
From inclusion to progression, significant toxicity or death whichever come first up to 56 months
Title
Progression Free Survival (PFS)
Time Frame
From inclusion to progression, significant toxicity or death whichever come first up to 56 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Metastatic kidney cancer, regardless of histology (except Bellini carcinomas), with measurable or evaluable disease
Age >= 18 years
With Karnofsky ≥ 60
Without prior treatment for metastatic cancer (chemotherapy, targeted therapy, or mTOR inhibitor)
Bad prognosis, defined as follows: at least three of the following six criteria of poor prognosis:
Karnofsky <80
LDH> 1.5 ULN
hemoglobin <LLN
corrected calcium> 2.5 mmol / l (10 mg / dl)
Time frame between initial diagnostic and treatment <1 year
More than one metastatic site
medullary function: neutrophils ≥ 1.5 x 109 / L, Platelets ≥ 100 x 109 / L, Hb> 8g/dL
Hepatic function: bilirubin: ≤ 1.5 x ULN, ALT and AST ≤ 2.5x ULN in the absence of hepatic metastasis ≤ 5x ULN if hepatic metastasis documented
Renal function: creatinine <1.5 x ULN
Life expectancy> 3 months,
Patient signed informed consent and agreeing to comply with the requirements of the trial
Exclusion Criteria:
Previous treatment with chemotherapy, targeted therapy, or mTOR inhibitor
Previous radiotherapy in the last 2 weeks
Chronic treatment with corticoids or immunosuppressive agents except substitutive opotherapy.. A washout period of at least 8 days must be respected before the patient inclusion.
Patients with brain metastases untreated or uncontrolled by prior treatment. The non-progression of the metastases must be proved by comparing two brain scans separated by a minimum interval of 6 weeks.
Active bleeding
Patient with positive serology HBs (Ag HBs (+) and AC anti-HBc (+)
Hypersensitivity to everolimus, sirolimus, to other rapamycin derivatives or to any of the excipients
Severe or uncontrolled medical pathology:
unstable angina, symptomatic heart failure, myocardial infarction ≤ 6 months before randomization, severe rhythm disorder,
Uncontrolled diabetes with glycaemia> 1.5X ULN.
Active or uncontrolled infection.
cirrhosis or chronic active hepatitis,
severe alteration in lung function (> 50% decrease in FEV or vital capacity)
Other cancer within the past 3 years, with the exception of basal cell carcinoma and carcinoma in situ of the cervix
Pregnant or lactating woman, and adults refusing an effective contraceptive method
Participation in another clinical trial with an investigational drug
Refusal of the patient to comply with the rules of the clinical trial
Person deprived of liberty or person under guardianship, inability to submit to medical treatment test for geographical, social or psychological reasons.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernard ESCUDIER
Organizational Affiliation
Gustave Roussy, Cancer Campus, Grand Paris
Official's Role
Study Chair
Facility Information:
Facility Name
Gustave Roussy
City
Villejuif
State/Province
Val de Marne
ZIP/Postal Code
94805
Country
France
12. IPD Sharing Statement
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Assessing Everolimus in Fist Line Treatment on Patients With Metastatic Kidney Cancer
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