Metastatic Renal Cell Carcinoma Clinical Trial
Official title:
Everolimus (Afinitor) in Patients With Metastatic Renal Cell Carcinoma Following Progression on Prior Bevacizumab Treatment
An estimated 10,000 metastatic renal cell carcinoma (RCC) patients receive first-line
therapy in the Russian Federation. Bevacizumab (Avastin) in combination with
interferon-alpha (IFN) is a recommended first-line treatment for metastatic RCC according to
clinical recommendations of Russian Ministry of Health from 15.07.2010. Two randomized phase
III trials (AVOREN, CALGB) showed that 50% of patients will progress on bevacizumab plus IFN
within 8.5 - 10.2 months and will need sequential therapy.
Everolimus (Afinitor) is a single agent which was evaluated and demonstrated efficacy in
randomized phase III study (RECORD-1) in metastatic RCC patients after failure of targeted
therapy. However, in this trial everolimus was compared with placebo for the treatment of
patients whose disease had progressed on treatment with sunitinib or sorafenib (n=227). Only
9% (n=24) of patients received bevacizumab. Thus, efficacy data of everolimus in patients
with disease progression on first-line bevacizumab is limited.
Evaluating the effectiveness of everolimus in metastatic RCC patients with failure on
bevacizumab with/without interferon alpha has a scientific and practical sense, and it is
important for Russian Federation.
17563 new cases of renal cancer and 83790 associated deaths have recorded in the Russian
Federation in 2008. Renal cell carcinoma (RCC) is responsible for 4,3% of all malignancies,
with increased risk of disease after the age of 60 years. Renal cell carcinoma accounts for
90% renal neoplasms, and in 85% of renal cell carcinoma cases light-cell morphology is
diagnosed. Papillary, chromophobic cancer and cancer of the kidney collecting tubules.
30% patients with localized renal cell carcinoma are found to progress after surgical
treatment. In the other 30% renal cell carcinoma is established at the dissemination stage.
Therefore approximately 60% of renal cell carcinoma patients are estimated to have
metastases.
According to estimations by Kidney Cancer Research Bureau, currently first line treatment is
indicated to approximately 10,000 patients with metastatic renal cell carcinoma in Russia
annually.
Until recently opportunities for systemic treatment in metastatic renal cell carcinoma were
limited to administration of cytokines and clinical research investigating novel
medications. Various combinations and doses of interleukin-2 (IL-2) and interferon-alpha
(IFN) have been investigated in randomized studies in metastatic renal cell carcinoma.
Immunotherapy was found to have only limited efficacy (overall response rate 15-16%,
survival of 12 months). Therefore target medicines, specifically - tyrosine kinase
inhibitors and mTOR inhibitors, are under development as first and subsequent lines of
treatment.
According to standards of medical care established by the Ministry of Health and Social
Development of the Russian Federation as of July 15, 2010, combination of bevacizumab
(Avastin™) and interferon is recommended as first line treatment. According to two
randomized phase III trials (AVOREN, CALGB) more than half of patients are expected to
require further treatment for disease progression in 8,5-10,2 months. Everolimus (Afinitor)
is the only medicine that has been investigated in a phase III multicenter study (RECORD-1)
as second and subsequent lines of treatment for metastatic renal cell carcinoma resistant to
targeted agents. However, most patients (n=277) had received sunitinib or sorafenib prior to
enrolment; only some of them (24 patients (9%) had received bevacizumab. Therefore currently
convincing evidence of everolimus efficacy after progression on prior treatment with
bevacizumab or bevacizumab + IFN is lacking.
Hence it is deemed reasonable and practically relevant to investigate everolimus efficacy in
patients with metastatic renal cell carcinoma previously treated on bevacizumab-containing
regimens, in the Russian Federation.
Efficacy endpoints
Primary:
Primary endpoint is the proportion of progression-free patients for 2 months (based on
results of a phase III study)
Secondary:
Median progression-free survival and overall survival from the time of enrolment Response
rate, according to RECIST 1.1 Treatment safety and tolerability according to NCI-CTCAE v.4.0
Patients quality of life, according to EORTC QLQ-C30 questionnaire
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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