Phase 4
Completed N=246
An Open-label, Multi-center, Expanded Access Study of Everolimus in Participants With Advanced Neuroendocrine Tumors (NETs) (Core Study) and an Extension Study to the Open-label, Multi-center, Expanded Access Study of Everolimus in Patients With Advanced NETs (E1)
Source: ClinicalTrials.gov NCT01595009 ↗Enrolled (actual)
246
Serious AEs
34.9%
Results posted
Nov 2018
Primary outcomePrimary: Number and Percentage of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and Deaths (Core) — 90; 109; 25; 59 Participants
◆ Published Evidence
No publication linked
No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.
Summary
This record combines the results of CRAD001K24133 and CRAD001K24133E1. The purpose of the CRAD001K24133 study was to evaluate the safety profile of everolimus in patients with advanced neuroendocrine tumors of pancreatic origin (pNETs) and to provide access of everolimus to this patient population. Everolimus was taken by participants until disease progression, unacceptable toxicity, death, discontinuation from the trial for any other reason, or when it became commercially available for this indication, or until May 30, 2012, whichever came first. Prior to amendment 1, the study enrolled participants with NET of the lung (L-NETs) and gastrointestinal (GI) (GI-NETs) origin. The core study was stopped (per protocol) because everolimus was approved for pNETs. All ongoing patients with pNETs were switched to commercially available everolimus. For GI and lung NETs, everolimus was not approved at the time the core study was stopped. Therefore, patients with GI or lung NETs were not able to switch to commercial drug. To provide study medication access to these patients beyond 30 May 2012, the open label extension study, CRAD001K24133E1, was conducted. In the extension study, RAD001K24133E1, participants with GI or lung NETs who had not progressed during therapy with everolimus in the core study and who had not suffered from intolerable toxicity, were enrolled and treated with everolimus in order to provide data on long-term safety and efficacy. Patients were treated until it became commercially available in the respective indication or until documented tumor progression, unacceptable toxicity, any other reason or until study end on 31 May 2017, whichever came first.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number and Percentage of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and Deaths (Core) |
90; 109; 25; 59; 5; 10 | — |
| PRIMARY Number and Percentage of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and Deaths During the Extension Phase (E1) |
4; 11; 1; 4; 0; 1 | — |
| SECONDARY Investigator-assessed Progression Free Survival (PFS) (Core) |
7.62; 10.78 | — |
| SECONDARY Mean European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 (EORTC QLQ-C30) Score (Core) |
64.93; 60.53; 63.15; 58.91; 59.72; 56.59 | — |
| SECONDARY Mean EORTC QLQ-G.I. NET21 Score (Core) |
12.99; 23.52; 13.21; 17.85; 13.47; 16.79 | — |
| SECONDARY Number and Percentage of Participants With Ratings of 'no Problem, 'Some Problem' and 'Extreme Problem' in the EuroQol Five Dimensions Questionnaire (EQ-5D) (Core) |
84; 76; 31; 35; 2; 1 | — |
| SECONDARY Mean EQ-5D Visual Analogue Scale (VAS) Score (Core) |
68.8; 63.9; 69.3; 63.8; 64.6; 61.2 | — |
| SECONDARY Investigator-assessed Best Overall Response (Core) |
2; 1; 74; 84; 9; 8 | — |
| SECONDARY Investigator-assessed Progression Free Survival (PFS) (E1) |
159; 655 | — |
| SECONDARY Change in European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 (EORTC QLQ-C30) Score at the End of Treatment From Baseline (Baseline = First Day of Treatment in the Extension) (E1) |
0.00; -0.00; 6.67; 0.00; -16.67; 5.56 | — |
| SECONDARY Change in EORTC QLQ-G.I. NET21 Score at the End of Treatment From Baseline (Baseline = First Day of Treatment in the Extension) (E1) |
11.11; 7.41; 44.44; -0.93; 50.00; 0.00 | — |
| SECONDARY Change in EuroQol Five Dimensions Questionnaire (EQ-5D) Score at the End of Treatment From Baseline (Baseline = First Day of Treatment in the Extension) (E1) |
7.26; -8.58; -10.00; -4.17 | — |
| SECONDARY Investigator-assessed Best Overall Response During the Extension Phase (E1) |
0; 0; 0; 1; 2; 7 | — |
Eligibility Criteria
Core Inclusion:
- Age ≥ 18 years old
- Advanced (unresectable or metastatic) biopsy-proven NETs of pancreatic origin
- World health organization (WHO) Performance status of 0-2
- Adequate bone marrow function as shown by:
- Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
- Platelets ≥ 100 x 109/L
- Hemoglobin >9 g/dL
- Adequate liver function as shown by:
- Serum bilirubin ≤ 1.5 x upper limit of normal (ULN)
- Alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 2.5 x ULN. Patients with known liver metastases with an AST and ALT ≤ 5 x ULN
- International normalized ratio (INR) 1.5 x ULN
- Patients who had any severe and/or uncontrolled medical conditions such as:
Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction
≤ 6 months prior to enrollment, serious uncontrolled cardiac arrhythmia
- Active or uncontrolled severe infection
- A history of invasive fungal infections
- Severe hepatic impairment (Child Pugh class C)
- Severely impaired lung function
- Active bleeding diathesis
- Patients with a known history of Human immunodeficiency virus (HIV) seropositivity
- No other prior or concurrent malignancy was allowed except for, adequately treated basal cell or squamous cell skin cancer, or other adequately treated in situ cancer, or any other cancer from which the patient had been disease free for ≥ 3 years
- Patients within four weeks post-major surgery, open-biopsy, or significant traumatic injury to avoid wound healing complications. Minor procedures and percutaneous biopsies or placement of vascular access device required seven days prior to study entry
- Female patients who were pregnant or nursing
- Adults who were of reproductive potential who were not using effective birth control methods. Adequate contraceptives were to be used throughout the trial and for eight weeks after last study drug administration in female patients. Women of child bearing potential must have had a negative serum pregnancy test within seven days prior to first administration of study drug
- Patients who were unwilling to or unable to comply with the protocol
Extension Inclusion and Exclusion Criteria:
- The patient must provide a signed Informed Consent Form (ICF) for the extension study prior to any study related procedures
- Age ≥18 years old
- Completion of the whole treatment period in the CRAD001K24133 study
- Neuroendocrine tumor of gastrointestinal or pulmonary origin (pancreatic neuroendocrine tumors are excluded)
- No tumor progression during therapy with everolimus during CRAD001K24133 study (checked via radiologically assessment)
- No intolerable toxicity during therapy everolimus, or during combination therapy of everolimus and somatostatin analogues
Data sourced from ClinicalTrials.gov (NCT01595009). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.