Clinical Trial Finder

Inclusion Criteria:

• - Histological confirmation of well-differentiated Grade 1/Grade 2 NET from gastrointestinal, pancreatic, pulmonary or unknown primary sites.

• - Metastatic or locally advanced and unresectable disease, measurable by images.

• - Disease progression by RECIST 1.1 in the last 6 months assessed by local investigators.

• - At least one previous line of systemic treatment (suspended for more than 3 weeks).

• - Eastern Cooperative Oncology Group (ECOG) 0-2 o Good organ function: - Hemoglobin > 8 g/dL.

• - Neutrophils ≥ 1,500/mm³ - Platelets > 90,000/mm³ - Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 2.5 x ULN [upper limit of normal] or ≤ 5 x ULN for patients with liver metastases.

• - Bilirubin ≤ 1.5 x ULN, creatinine < 1.5 mg/dL.

Exclusion Criteria:

• - Aggressive disease requiring cytotoxic therapy.

• - Severe/uncontrolled comorbid conditions that deem participant unfit for everolimus therapy, as per investigators' judgement.

- MiNEN

Everolimus toxicity can also be serious, requiring hospital medical assistance. In a study with more than 100 Latin American patients led by our group, approximately 20% of patients with NET treated with everolimus 10mg/day had serious infections, such as pneumonia, abscesses, pyelonephritis, with 7% developing opportunistic infections, such as toxoplasmosis and pneumocystosis, requiring hospital admissions. The rationale for testing 5mg/day comes from the results of phase I trials of everolimus, where a dose of 5mg/day was sufficient to inhibit cell proliferation by blocking the mTOR pathway. Therefore, everolimus 5mg/day appears to have antitumor effects equivalent to 10mg/day, but it is less toxic than 10mg/day. Retrospective data from our center also suggest that 5mg is similar to 10mg/daily in terms of time to treatment failure in patients with advanced NETs (unpublished data). Objectives:

• - To evaluate whether everolimus at a dose of 5 mg/day may be as effective, but safer, as 10 mg/day in the treatment of patients with advanced NET.

• - To compare progression-free survival and time to treatment failure between study arms.

• - To compare radiological response using RECIST v.

1.1 criteria.

• - To compare the frequency of grade > 1 toxicities using CTCAE v.

5.0.

• - To assess tolerability by measuring the frequency and intensity of adverse events measured by the CTCAE version 5.0 criteria and the need for temporary or permanent interruption of everolimus.

Methods: Randomized, open-label, phase II near-equivalence clinical trial of oral everolimus 5 mg vs.#46;10 mg oral/daily and continuously in patients with Grade 1 or Grade 2 metastatic NET, with tumor progression or intolerance to at least one line of treatment and with radiological disease progression within 6 months. Eligibility criteria: Inclusion:

• - Histological confirmation of well-differentiated Grade 1/Grade 2 NET from gastrointestinal, pancreatic, pulmonary or unknown primary sites.

• - Metastatic or locally advanced and unresectable disease, measurable by images.

• - Disease progression by RECIST 1.1 in the last 6 months assessed by local investigators.

• - At least one previous line of systemic treatment (suspended for more than 3 weeks).

• - Eastern Cooperative Oncology Group (ECOG) 0-2.

• - Good organ function: - Hemoglobin > 8 g/dL.

• - Neutrophils ≥ 1,500/mm³ - Platelets > 90,000/mm³ - Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 2.5 x ULN [upper limit of normal] or ≤ 5 x ULN for patients with liver metastases.

• - Bilirubin ≤ 1.5 x ULN, creatinine < 1.5 mg/dL.

Concomitant use of somatostatin analogues is allowed for patients with functioning NET. Exclusion:

• - Aggressive disease requiring cytotoxic therapy.

• - Severe/uncontrolled comorbid conditions that deem participant unfit for everolimus therapy, as per investigators' judgement.

• - MiNEN.

Procedures: Randomization 1:1 will be performed centrally by RedCap software at AC Camargo Cancer Center, Sao Paulo, Brasil.

• - Group 5 mg: participants will receive everolimus at a dose of 5 mg, orally, per day, continuously.

• - Group 10 mg group: participants will receive everolimus at a dose of 10 mg, orally, per day, continuously.

The participant will receive everolimus 5mg or 10mg and must take 1 (one) tablet, orally, once a day, after breakfast, starting within 4 weeks from randomization. Every 4 weeks of treatment will correspond to 1 treatment cycle. Before starting each cycle, participants will undergo a medical visit to evaluate undesirable effects, medical history, physical examination and check the results of blood tests. CT scans (or MRI, if applicable) will be performed at every 3 cycles to assess treatment antitumor effect until progression. The treatment will last until tumor progression by RECIST 1.1, intolerance/ severe adverse effects or consent withdrawal. Participants will be evaluated clinically and with laboratory tests every 4 weeks until resolution of any adverse effects of the treatment. Patients who receive at least one dose of everolimus will be evaluated for the occurrence of toxicities.Sample size: N=100 patients (50 per arm) H0= 50% progression free at 12 months H1= 42% progression free at 12 months (inferior value of the 95% CI, based on RADIANT trials) Alpha error (one-sided) = 5% Beta error = 10% Attrition rate = 20%

Arms

Experimental: Everolimus 5

oral everolimus 5 mg/daily continuously until progression or intolerance or consent withdrawal. dose reduction for toxicity is allowed.

Active Comparator: Everolimus 10

oral everolimus 10 mg/daily continuously until progression or intolerance or consent withdrawal. dose reduction for toxicity is allowed.

Interventions

Drug: - Everolimus 5 MG

oral everolimus 5 mg/daily