Sequential Therapy in Metastatic Renal Cell Carinoma

Metastatic Renal Cell Carcinoma Clinical Trial

— BERAT  

Official title:

A Prospective, Open-label, Multicenter, Randomized Phase II Trial: Sequential Therapy With BEvacizumab, RAd001 (Everolimus) and Tyrosinekinase Inhibitors (TKI) in Metastatic Renal Cell Carcinoma (mRCC) (BERAT Study)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01731158
• Other study ID #: C-II-008
• Secondary ID: 2011-005939-78
• Status: Completed
• Phase: Phase 2
• Start date: October 2012
• Est. completion date: September 2016

Study information

• Verified date: February 2019
• Source: Central European Society for Anticancer Drug Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Sequential therapy with BEvacizumab, RAd001 (everolimus) and Tyrosinekinase inhibitors (TKI) in metastatic renal cell carcinoma (mRCC)

Description:

This will be a prospective, open label, randomized multicenter phase-II study to evaluate progression free survival (PFS) in 2nd line treatment in patients with locally advanced or metastatic clear-cell renal cell cancer (cc-RCC) receiving everolimus (arm A) in comparison to a tyrosine-kinase inhibitor (TKI) (arm B). Following 2nd line treatment, patients will be switched to a TKI in arm A and everolimus in arm B. All patients will receive bevacizumab as standardized first-line treatment.

Another key element of the study is the analysis of predictive biomarkers, which will be performed in serum and tumor tissue, respectively. Serum samples will be collected at prespecified timepoints throughout the study and analysed by SELDI-TOF-MS and DIGE. Candidate proteins are thought to predict therapeutic outcome and candidates are subject for target validation by Western Blot or ELISA. In addition, formalin-fixed paraffin-embedded (FFPE) tumor tissue will be collected prospectively and analysed for micro RNA (miRNA). Candidate miRNAs that predict therapeutic outcome will be validated by quantitative RT-PCR. Furthermore, circulating tumor cells (CTCs) will be generated from blood drawings during routine visits. The primary objective is to correlate the marker profile defined from the FFPE tissue with the profile obtained from CTCs in order to validate expression based markers ant their change during different treatment lines.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: September 2016
• Est. primary completion date: September 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed Informed Consent

• Documented progressive disease prior to study inclusion.

• Adult males and females: = 18 years of age.

• Metastatic or locally advanced RCC, not amendable to surgery with curative intention.

• ECOG performance status 0-1.

• Patients with measurable disease (at least one uni-dimensionally measurable target lesion by CT-scan or MRI) according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1) If prior palliative radiotherapy to metastatic lesions: = 1 measurable lesion that has not been irradiated. Patients with bone lesions as the only measurable lesion are eligible, provided that lesions consist of soft tissue, which is assessed via CT or MRI.

• Prior radiotherapy and surgery are allowed if completed 4 weeks (for minor surgery 2 weeks) prior to start of treatment and patient recovered from toxic effects.

• Modified MSKCC risk (according to Heng): good or intermediate.

• White blood cell count (WBC) = 4x10*9/L with neutrophils = 1.5 x 10*9/L, platelet count = 100x10*9/L, hemoglobin = 9 g/dL.

• Total bilirubin = 2 x upper limit of normal.

• AST and ALT = 2.5 x upper limit of normal, or = 5 x upper limit of normal in case of liver metastases.

• Serum creatinine = 2 x upper limit of normal or calculated creatinine clearance >30 ml/min.

• International Normalized Ratio (INR) =1.5 except for patients on stable anticoagulant therapy. Activated partial thromboplastin time (aPTT) =1.5 times upper limit of normal (ULN) or greater than the lower limit of the therapeutic range. Note: The use of full-dose oral or parenteral anticoagulants is permitted as long as the INR or aPTT is within therapeutic limits (according to the medical standard in the institution) and the patient has been on a stable dose of anticoagulants for at least two weeks at the treatment start.

• Adequate cardiac function (left ventricular ejection fraction =50% as assessed by ECHO)

Exclusion Criteria:

• Any investigational drug within the 30 days before inclusion.

• Known or suspected allergy or hypersensitivity reaction to any of the components of study treatments or their excipients.

• Pregnancy (absence to be confirmed by beta-hCG test) or lactation period.

• Men or women of child-bearing potential who are sexually active and unwilling to use a highly effective method of contraception (Pearl index < 1%) during the trial. Oral contraceptives are acceptable if a barrier method is applied in conjunction.

• Clinically symptomatic brain or meningeal metastasis (known or suspected), unless completion of local therapy for at least 3 months with discontinuation of steroids prior to start of treatment.

• Cardiac arrhythmias requiring anti-arrhythmics (excluding beta blockers, digoxin or digitoxin).

• History of any of the following cardiac events within the past 6 months:

1. myocardial infarction (including severe/unstable angina),

2. coronary/peripheral artery bypass graft,

3. congestive heart failure (CHF) (NYHA Class III, or IV),

4. cerebrovascular accident,

5. transient ischemic attack,

6. pulmonary embolism, abdominal or tracheo-oesophageal fistula, gastrointestinal perforation, or intra-abdominal abscess

• Hemorrhage = grade 3 or clinically significant hemoptysis within the past 4 weeks

• Uncontrolled severe hypertension (failure of diastolic blood pressure to fall below 90 mm Hg despite the use of = 3 anti-hypertensive drugs).

• History of relevant pulmonary hypertension or interstitial lung disease or severely impaired lung function.

• Acute or sub-acute intestinal occlusion or history of inflammatory bowel disease or chronic diarrhea.

• Previous malignancy (other than renal cell cancer) in the last 3 years, except basal cell cancer of the skin, pre-invasive cancer of the cervix, T1a prostate carcinoma or superficial bladder tumor [Ta, Tis and T1].

• History of organ allograft.

• Significant disease which, in the investigator's opinion would exclude the patient from the study.

• Medication that is known to interfere with any of the agents applied in the trial.

• Patients with a serious non-healing wound, ulcer or bone fracture.

• Patients with a history of seizure(s) not controlled with standard medical therapy.

• Patients receiving chronic systemic treatment with corticosteroids (dose of > 20 mg/day methylprednisone equivalent) or another immune-suppressive agent. Inhaled and topical steroids are acceptable.

• Legal incapacity or limited legal capacity.

• Medical or psychological conditions that would not permit the patient to complete the study or sign informed consent.

• Significant vascular disease (e.g. aortic aneurysm, aortic dissection), or symptomatic peripheral vascular disease.

• Evidence or history of recurrent thromboembolism (>1 episode of deep venous thrombosis/peripheral embolism = CTCAE Grade 3) during the past 2 years, bleeding diathesis or coagulopathy.

• Poorly controlled diabetes as defined by fasting serum glucose > 2.0 x ULN.

• Active (acute or chronic) or uncontrolled infection of bacterial, mycotic or viral genesis.

• Liver disease such as chronic active hepatitis or chronic persistent hepatitis.

• Patients with a known history of HIV seropositivity.

• QT prolongation (QTc > 450 msec).

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Renal Cell
• Metastatic Renal Cell Carcinoma

Intervention

Drug:
• Avastin in combination with Roferon-A

• Afinitor

• TKI: Sutent, Nexavar or Votrient
TKI

Locations

Country	Name	City	State
Germany	Charité Berlin	Berlin
Germany	University Hospital Bonn	Bonn
Germany	University Hospital Dresden	Dresden
Germany	University Hospital Düsseldorf	Düsseldorf
Germany	Waldkrankenhaus St. Marien	Erlangen
Germany	University Hospital Essen	Essen
Germany	University Hospital Frankfurt	Frankfurt
Germany	University Hospital Freiburg	Freiburg
Germany	University Hospital Göttingen	Göttingen
Germany	Oncological Practice Hannover	Hannover
Germany	University Hospital Hannover	Hannover
Germany	University Hospital Magdeburg	Magdeburg
Germany	University Hospital Tübingen	Tübingen

Sponsors (1)

Lead Sponsor	Collaborator
Central European Society for Anticancer Drug Research

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PFS rate of 2nd line treatment at 6 months after randomisation	PFS rate	6 months after randomisation
Secondary	PFS for 2nd line treatment	PFS	after completion of second-line treatment (expected median treatment 1st and 2nd line: 16 months)
Secondary	PFS for each treatment given	PFS	after completion of each treatment line (expected median treatment duration 1st line: 11 months, 2nd line: 5 months, 3rd line: 6 months)
Secondary	Overall Survival	OS	after death of patient
Secondary	number and severity (CTCAE 4.0) adverse events	AE	continuously throughout trial
Secondary	changes in quality of life throughout the Trial using FKSI questionnaires	quality of life	continuously throughout trial (baseline, week 5, week 11, every 12 weeks, end of treatment for all treatment lines via FKSI-10 questionnaire)
Secondary	ORR for each treatment given	ORR	after completion of each treatment line (expected median treatment duration 1st line: 11 months, 2nd line: 5 months, 3rd line: 6 months)