Phase II Study of Everolimus Combined With Octreotide LAR to Treat Advanced GI NET (EVERLAR)
|ClinicalTrials.gov Identifier: NCT01567488|
Recruitment Status : Completed
First Posted : March 30, 2012
Last Update Posted : January 3, 2018
The underlying hypothesis of the synergistic activity of octreotide and everolimus is based on the combination of a) a direct action of everolimus over mTOR (mammalian target of rapamycin), and b) the inhibitory effect of octreotide on the IGF-I (insulin like growth factor 1) system preventing the activation of the mTOR system by this factor. Both types of inhibition would completely cancel this signal transduction pathway, which is so important in neuroendocrine tumours.
Furthermore, the biological study proposed in this protocol will allow for better establishing the relationship between the activation of the IGFR-PI3K-mTOR signal transduction pathway (i.e., the mTOR pathway stimulated by IGFR) and treatment response; this information is relevant since the IGFR-PI3K-mTOR activation status could be a response prediction factor.
This study will provide significant additional information about the efficacy of the combination treatment of everolimus with octreotide LAR® in non-functioning GI NET.
|Condition or disease||Intervention/treatment||Phase|
|Gastrointestinal Neoplasms||Drug: Everolimus Drug: octreotide LAR||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||43 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase II Study on Everolimus, an mTOR Inhibitor (Oral Formulation), With Octreotide LAR® in Adult Patients With Advanced, Non-functioning, Well-differentiated Gastrointestinal Neuroendocrine Tumours (GI NET)|
|Actual Study Start Date :||June 8, 2011|
|Primary Completion Date :||September 1, 2014|
|Study Completion Date :||June 7, 2017|
|Experimental: Everolimus + Octreotide LAR treatment||
Other Name: AfinitorDrug: octreotide LAR
30 mg each 28 days
Other Name: Sandostatin LAR
- Percentage of patients with progression-free survival (PFS) [ Time Frame: After 12 month of study treatment ]Rate of patients
- Number of patients positive for insulin like growth factor 1 receptor (IGF1R) and ribosomal kinase S6 (S6K) phosphorylation. [ Time Frame: At baseline ]Activation status of mTOR pathway.
- Rate of patients with objective responses [ Time Frame: Each three cycles ]Includes duration of response
- Median and average of time for Overall survival [ Time Frame: At the end of the study ]Time from inclusion date up to date of death for any reason.
- Rate of patients with an early decrease of chromogranin A (CgA) levels [ Time Frame: Each cycle ]CgA levels will be measured when increased at baseline and up to its normalization.
- Percentage of patients with Adverse Events [ Time Frame: Each cycle ]Ocurred during the trial and up to 30 days after the last dose.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01567488
|Instituto Catalán de Oncologia|
|Hospitalet de Llobregat, Barcelona, Spain, 08907|
|Study Chair:||Ramón Salazar, MD, PhD||Grupo Espanol de Tumores Neuroendocrinos|