Efficacy and Safety of Bevacizumab/Temsirolimus Combination to Treat Advanced Renal Cell Carcinoma
Phase II Study of Efficacy and Safety of Bevacizumab in Combination With Temsirolimus, After 1st Line Anti-VEGF Treatment in Patients With Advanced Renal Cancer
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Studietype
Studietype
Registrering (Faktiske)
Registrering
Fase
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
-
-
-
Athens, Hellas, 11528
- General Peripheral Hospital of Athens "Alexandra"
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Athens, Hellas, 18547
- Metropolitan Hospital, 1st Dept of Medical Oncology
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Athens, Hellas, 18547
- Metropolitan Hospital, 2nd Dept of Medical Oncology
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Athens, Hellas, 14564
- Agii Anargiri Cancer Hospital, 3rd Dept of Medical Oncology
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Athens, Hellas, 11527
- General Hospital of Athens "Hippokratio"
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Athens, Hellas, 14564
- Agii Anargiri Cancer Hospital, 2nd Dept of Medical Oncology
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Rio, Patras, Hellas, 26500
- University Hospital of Patras
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Thessaloniki, Hellas, 56429
- Papageorgiou General Hospital
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Adult patients (18th year of age completed)
- Signed and dated written informed consent form prior to any procedures related to this protocol.
- Histologically confirmed advanced clear cell renal cancer.
- Measurable disease.
- Failure of first line anti-VEGF treatment.
- Performance status 0-2, according to Eastern Cooperative Oncology Group (ECOG) .
Satisfactory hematological parameters:
- White blood cell count > 4000 mm3.
- Platelet count 100000/mm3.
- Neutrophil blood cell count > 1200/ mm3 .
- Hemoglobin > 9,0 g/dL (can be achieved with red blood cell transfusion).
Satisfactory biochemical parameters:
- Serum creatinine < 2 x Upper Limit of Normal(ULN)
- Aspartate Aminotransferase (AST)<2,5 x ULN
- Alanine Transaminase (ALT)< 2,5 x ULN.
- Bilirubin <2 x ULN
- (For female patients) Absence of pregnancy (negative pregnancy test for women of reproductive age before enrollment).
- (For female patients) Non-lactating women.
- Use of efficient contraceptive measures (women and men) to prevent possible pregnancy of female patient or female partner of a male patient during treatment and until 6 months after the end of treatment.
Exclusion Criteria:
- Prior treatment with mTOR inhibitor.
- Major surgery (including open biopsy) or insufficient recovery or existence of major trauma within 4 weeks before enrollment.
- Uncontrolled hypertension.
- Active infection requiring systemic treatment within 4 weeks prior to enrollment.
- Minor surgery (for instance, catheter placement) within 2 days before enrollment.
- Scheduled major surgery within the treatment period.
- Medical history in the last 6 months prior to enrollment of significant cardiovascular disease, diabetes, cardiac infarction, unstable angina, uncontrolled arrhythmia or significant heart failure.
- Indications of uncontrolled metastases or disease progression in CNS lesions (the suspicion of uncontrolled metastases or disease progression should be eliminated by imaging techniques within 14 days prior to enrollment).
- Medical history in the last 5 years prior to enrollment of any other malignancies (excluding the basal or squamous skin cell carcinoma or in situ carcinoma of the cervix).
- History of non-healing wound including active gastric ulcer.
- History of fistula in the last 6 months prior to enrollment.
- History of gastrointestinal perforations.
- Patient incapacity (for psychiatric or social reasons) to conform with the protocol.
- History of hemorrhagic predisposition.
- History of hypersensitivity to the medications under investigation.
- Significant proteinurea.
- Prior immunotherapy within 4 weeks prior to enrollment.
- Prior radiation treatment within 2 weeks prior to enrollment.
- Concomitant medication with inducers or strong inhibitors of the coenzyme CYP3A4 (see Appendix 5 for an indicative list of active compounds).
- Concurrent participation in other interventional clinical trials with investigational medicinal products.
- History of chronic interstitial lung disease.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
|---|---|
|
Eksperimentell: Bevacizumab combined with temsirolimus
Bevacizumab 10mg/kg intravenous every 2 weeks Temsirolimus 25mg intravenous once weekly
|
Bevacizumab 10mg/kg intravenous every 2 weeks until disease progression, unacceptable toxicity or consent withdrawal.
Temsirolimus 25mg intravenous once weekly until disease progression, unacceptable toxicity or consent withdrawal.
|
Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
6-month Progression Free Survival (PFS)
Tidsramme: 32 months
|
Proportion of patients who are progression-free at 6month evaluation from treatment initiation
|
32 months
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression Free Survival (PFS)
Tidsramme: Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
PFS will be calculated from date of treatment initiation until disease progression or death (whichever occurs first)
|
Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
|
Overall Survival (OS)
Tidsramme: 48 months
|
OS will be calculated from the date of treatment initiation to the date of death or last contact
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48 months
|
|
Response Rate (RR)
Tidsramme: Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
RR is defined as the overall percentage of patients with partial (PR) or complete response (CR).
The evaluation of responses will be performed according to RECIST criteria
|
Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
|
Tumor Shrinkage
Tidsramme: Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
Tumor shrinkage will be computed using waterfall plots
|
Tumor assessments will be performed every 8 weeks during treatment and at discontinuation, unless it was performed within the last 4 weeks
|
|
Adverse Events (AEs) of all participants will be recorded and assessed upon signature of the informed consent form, until 30 days after the last administration of study treatment.
Tidsramme: 3 years
|
Adverse Events will be graded according to the NCI CTCAE v3.0 criteria and will be reported in a frequency table according to the highest severity grade observed per patient
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3 years
|
|
Quality of Life (QoL) assessment
Tidsramme: At baseline and every 8 weeks during treatment
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QoL will be assessed using the EORTC QLQ C-30 questionnaire.
The change in the QoL during treatment will be estimated using the Wilcoxon paired t-test
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At baseline and every 8 weeks during treatment
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Investigation of antiangiogenic factors (FGF, VEGF, VEGFRR)
Tidsramme: 36 months
|
Changes in serum levels of antiangiogenic factors during treatment and correlation to the outcome of study treatment.
|
36 months
|
Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Etterforskere
Etterforskere
- Studiestol: Aristotelis Bamias, MD, PhD, General Peripheral Hospital of Athens "Alexandra", Medical School, University of Athens
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Studiestart
Primær fullføring (Faktiske)
Primær fullføring
Studiet fullført (Faktiske)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Neoplasmer
- Urologiske neoplasmer
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Nyresykdommer
- Urologiske sykdommer
- Nyre-neoplasmer
- Fysiologiske effekter av legemidler
- Anti-infeksjonsmidler
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Antineoplastiske midler, immunologiske
- Angiogenese-hemmere
- Angiogenesemodulerende midler
- Vekststoffer
- Veksthemmere
- Antibakterielle midler
- Antibiotika, antineoplastisk
- Antifungale midler
- Bevacizumab
- Sirolimus
Andre studie-ID-numre
Andre studie-ID-numre
- HE 21/10
- 2010-020664-38 (EudraCT-nummer)
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