Comparison of Adjuvant Treatment With 177Lu-DOTATATE to Best Supportive Care in Patients After Resection of Neuroendocrine Liver Metastases

Trial Title: Comparison of Adjuvant Treatment With 177Lu-DOTATATE to Best Supportive Care in Patients After Resection of Neuroendocrine Liver Metastases

NCT ID: NCT05987176

Condition: Neuroendocrine Tumor G1 (NET G1)/Carcinoid
Neuroendocrine Tumor Grade 2
Neuroendocrine Tumors
Liver Metastases
Gastroenteropancreatic Neuroendocrine Tumor
Gastroenteropancreatic Neuroendocrine Neoplasm

Conditions: Official terms:
Neoplasm Metastasis
Liver Neoplasms
Neuroendocrine Tumors
Lutetium Lu 177 dotatate

Conditions: Keywords:
NETs
NECs
GEP-NETs
NELMAS
adjuvant
liver metastases

Study type: Interventional

Study phase: Phase 2

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Lutathera
Description: Dosage: In total 14.8 GBq (400 mCi) 177Lu-DOTATATE administered in two equally divided doses. Each dose to be infused over 30 minutes. Duration of treatment: Two administrations of 177Lu-DOTATATE (each treatment 7.4 GBQ (200 mCi) at 8±1-week intervals, which can be extended to 16 weeks for resolving acute toxicity.
Arm group label: Treatment - Arm B

Summary: An international multi-centre, open, randomised, parallel-group phase II study comparing adjuvant treatment with 177Lu-DOTATATE to best supportive care in patients after complete surgical removal of neuroendocrine liver metastases. In this study, adjuvant treatment with 177Lu-DOTATATE will be compared with best supportive care in patients with well differentiated grade 1 or 2 neuroendocrine tumours in the stomach, pancreas or gut (gastro-entero-pancreatic NETs) who had their primary tumour already removed or in whom both primary and liver tumour metastases removal will take place simultaneously, including removal of perihilar lymph nodes will be eligible. The primary objective is to compare overall disease-free survival at 3 years after treatment with 177Lu-DOTATATE to best supportive care between both treatment arms, with equal chances of entering either arm (1:1) Secondary objectives are to describe and compare the difference in disease-free survival in the liver, overall survival, time to the next anticancer treatment, the cost effectiveness and health-related quality of life. The safety and toxicity of 177Lu-DOTATATE as adjuvant therapy will also be described. Additionally, the clinical use of blood and urine analysis test (NETest) will be evaluated to identify microscopic remaining disease and detect early the return of the tumour.

Detailed description: There will be 2 arms: arm A consisting of best supportive care and arm B, the experimental treatment. Randomisation will be 1:1 as soon as possible after the liver surgery. The control arm will consist of standard of care. The study will be embedded within the regular clinical pathway for treatment and follow-up of patients with resectable NE LM. The follow-up will be according to current guidelines (e.g., Guidelines of the European Neuroendocrine Tumor Society for the management of advanced intestinal NET and pancreatic NET with locoregional and/or distant metastases). Patients will be followed up in the study for 3 years according to standard post-surgical follow-up protocol and thereafter in their local institution life-long according to follow-up after liver resection for NE LM. In the treatment arm 177Lu-DOTATATE will be applied. The first cycle will be applied 6±2 weeks after liver resection. The frequency of administration will be 2 cycles (8±1weeks between each cycle). The rationale for 2 cycles in the adjuvant setting instead of 4 (as per standard protocol in palliative setting), assumes that after the removal of the primary tumour and the liver metastases, there will be no macroscopic residual tumour. Thus, the treatment dose should be sufficient to target microscopic disease and have the smallest possible effect on healthy tissue. In the treatment arm, the patients will have 10 study visits for post -PRRT monitoring (blood tests and clinical assessments). Patients in the standard of care arm will have visits every 3 months. In both arms, patients will have one screening visit and one end of study visit. They will complete QoL questionnaires at baseline and at follow-up visits at 12, 24, and 36 months and bloods/urine will be collected for translational research prior to surgery (while in hospital) and at 6, 12, and 36 months. Signature of informed consent precedes all study-specific assessments. All patients will have a fresh tumour sample collected during the liver surgery. Disease recurrence will be measured in all patients using liver MRIs every 3 months for the first year and every 6 months for the second to third year and 68Ga DOTA-TATE PET CT every 12 months for 3 years. Any patient with disease recurrence ceases treatment and assessments and will proceed to standard of care treatment for recurrent liver metastases. Follow-up data will be collected for 5 years overall from the date of randomisation of the last patient.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Written informed consent prior to any study related procedures 2. Patients aged 18 years or older 3. ECOG / WHO performance status 0 or 1 4. Patients with well differentiated grade 1 or grade 2 (Ki67<20%) GEP NET confirmed by histological criteria with the primary localisation in stomach, pancreas, or gut 5. Patients after R0 (complete macroscopic and microscopic resection) or R1 (complete macroscopic resection, microscopically positive resection margins) resection of neuroendocrine liver metastases confirmed by histological criteria 6. Patients with a primary tumour already resected or in whom the primary tumour has been resected synchronously with liver metastases 7. MRI scan prior to surgery (within 4 -6 weeks) confirming liver metastases and no extrahepatic disease (except resectable perihilar lymph node involvement and/or primary tumour, if still in place) 8. Somatostatin receptor-based imaging (68Ga DOTA-TATE PET/CT prior to surgery (within 12 weeks) confirming liver metastases and no extrahepatic disease (except resectable perihilar lymph node involvement and/or primary tumour, if still in place) Exclusion Criteria: 1. Less than 4 weeks post-surgery, or any other medical treatment, including chemotherapy, radiotherapy, and intrahepatic therapy 2. High grade neuroendocrine tumours (G3 NET, or neuroendocrine carcinoma [NEC]) 3. After R2 (tumour debulking, macroscopically incomplete resection) resection of neuroendocrine liver metastases 4. Patients with non-resectable neuroendocrine liver metastases and/or non-resectable primary tumour and /or non-resectable perihilar lymph node metastases 5. Pregnancy 6. Subjects of childbearing potential (both male and female participants) not willing to use a combination of adequate contraceptive measures, e.g., oral contraceptives, IUD, barrier methods of contraception (condom or occlusive cap with spermicide) 7. Patients who have received prior systemic and/or liver-directed treatment for their metastatic NET other than somatostatin analogues 8. Hb concentration <5.0 mmol/L (<8.0 g/dL) 9. WBC <2x109/L (2000/mm3) 10. Platelets <75x109/L (75x103/mm3). 11. Total bilirubin >3 x ULN. 12. Serum albumin <3.0 g/dL unless prothrombin time is within the normal range. 13. Uncontrolled congestive heart failure (NYHA II, III, IV). 14. Uncontrolled diabetes mellitus as defined by a fasting blood glucose >2 ULN. 15. Prior external beam radiation therapy to more than 25% of the bone marrow. 16. Kidney failure with serum creatinine >150 µmol/L (>1.7 mg/dL) 17. Known hypersensitivity to somatostatin analogues

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Imperial College Healthcare NHS Trust

Address:
City: London
Zip: W12 0HS
Country: United Kingdom

Status: Recruiting

Contact:
Last name: Andrea Frilling, Prof

Phone: 02033138542
Email: a.frilling@imperial.ac.uk

Investigator:
Last name: Andrea Frilling, Prof
Email: Principal Investigator

Start date: August 2, 2024

Completion date: March 30, 2029

Lead sponsor:
Agency: Imperial College London
Agency class: Other

Collaborator:
Agency: The Taylor Family 2010 Charitable Trust
Agency class: Other

Collaborator:
Agency: Novartis/AAA
Agency class: Other

Source: Imperial College London

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05987176