Randomized Phase III of PRRT Versus Interferon

• Status: Withdrawn
• Trial end date: 2016-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to assess the benefit of 177Lu-DOTATATE versus interferon α-2b in patients with progressive, unresectable, non-pancreatic gastrointestinal neuroendocrine tumors resistant to therapy with somatostatin analogues, in terms of disease control.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Jules Bordet Institute
• Treatments: Interferon alpha-2; Interferon-alpha; Interferons; Lutetium Lu 177 dotatate; Octreotide

Criteria

Inclusion Criteria:

1. Adult patients (≥ 18 yrs).

2. Histology-proven non-pancreatic gastrointestinal NETs.

3. Disease progression under SSAs (SSAs-resistant disease). Disease progression must be documented with at least one of the following:

• Radiological disease progression (according to RECIST 1.1) on an MRI or CT over the last 12 months.

• Disease progression on a somatostatin receptor-imaging (PET/CT or SPECT/CT) over the last 12 months (apparition of new lesion(s) or increase in the transaxial plane diameter of more than 30% on the same imaging modality).

4. There should be at least one target lesion. A target lesion should fulfill all the following criteria:

• Uptake higher than the physiological liver uptake on the baseline 68Ga-DOTATATE PET/CT

• Longest transaxial plane diameter ≥ 20mm measured on the CT or MRI;

• Not previously irradiated.

5. Long-acting SSAs must be discontinued at least 4 weeks before the study treatment start date and, if needed, switched to short-acting analogues which must be stopped 48h before the treatment date.

6. Adequate renal function with GFR ≥ 50 mL/min/1.73m2 (evaluated by 51Cr-EDTA test).

7. Adequate bone marrow function with:

• Hemoglobin ≥ 9 g/dL;

• Neutrophil ≥ 1.5·109/L;

• Platelet count ≥ 100·109/L.

8. Adequate liver function with:

• Total Bilirubin ≤ 2xULN;

• Transaminases (AST and ALT) ≤ 5xULN;

• Serum albumin > 3.0 g/dL with normal prothrombin time (>70%) unless for patients under coumarin anticoagulation therapy.

9. ECOG Performance Status ≤ 1.

10. Women of childbearing potential and men with partners of childbearing potential must agree to use a highly effective form of contraception for the duration of study participation and up to six months after the end of the treatment. A pregnancy test (serum) must be performed within 2 weeks prior to inclusion for every female patient of childbearing potential and it must be negative.

11. Patient's written informed consent obtained prior to any study specific procedure.

12. All necessary baseline procedures should be performed within 2 weeks prior to randomization date.

Exclusion Criteria:

1. Resectable tumor with curative intent.

2. Any major surgery within the last 6 weeks prior to inclusion in the study.

3. Radiotherapy, chemotherapy, embolization, mammalian target of rapamycin (mTOR)-inhibitors, receptor tyrosine-kinase inhibitors or other investigational therapy within 12 weeks prior to inclusion in the study.

4. Previous PRRT or MIBG treatment.

5. Treatment with interferon 12 months prior to inclusion in the study.

6. Presence of non-benign 18FDG-positive lesions (higher than 2 x normal liver (or thoracic aorta uptake -SUVmax- in case of liver involvement)) without significant 68Ga-DOTATATE uptake.

7. Uncontrolled congestive heart failure (NYHA stade ≥ 2).

8. Diffuse bone marrow infiltration on the baseline 68Ga-DOTATATE PET/CT confirmed by MRI.

9. Prior external beam radiotherapy on kidneys or on more than 25% of bone marrow.

10. Patients with known uncontrolled brain metastases.

11. History of other active malignant disease or clinical remission less than 5 years (except in case of non melanoma skin cancer or in situ cervical carcinoma).

12. Known autoimmune hepatitis.

13. Patients after organ transplantation under immunosuppressive therapy.

14. Patients with a significant medical, neuro-psychiatric, or surgical condition, currently uncontrolled by treatment, which, in the investigator's opinion, may interfere with completion of the study.

15. Hypersensitivity to interferon α-2b or to any component of the product.

16. Pregnant or lactating patients.