Inclusion Criteria:
1. Patients having voluntarily signed and dated IRB/IEC-approved written informed consent
form in accordance with regulatory and institutional guidelines before the performance
of any protocol-related procedures.
2. Patients with advanced/metastatic, histologically confirmed, well-differentiated Grade
3 NET or poorly-differentiated NEC of the pancreas, gastrointestinal tract, lung and
unknown primary site at diagnosis or after progression to one systemic treatment.
Patients will be enrolled in two cohorts based on the therapy of their aforementioned
cancer: Cohort 1: Patients with no previous chemotherapy. Cohort 2: Patients who have
received one line of chemotherapy.
3. Age ≥18 years.
4. Patients must have measurable disease based on RECIST v.1.1 meeting the following
criteria:
1. Lesions that have had external beam radiotherapy or loco-regional therapies such
as radiofrequency ablation or liver embolization must show evidence of
progressive disease based on RECIST v.1.1 to be deemed a target lesion.
2. Patients in cohort 2 must show evidence of disease progression by radiologic
image techniques according to RECIST v.1.1 within 3 months prior to signing
informed consent.
5. Confirmed presence of somatostatin receptors on tumour lesions based on positive
PET-Gallium (SomaKit) imaging within 8 weeks prior to enrolment in the study. At least
one lesion should have an uptake of 64-Gallium higher than the normal liver according
to investigator judgement.
6. Karnofsky Performance Score ≥ 60 and Eastern Cooperative Oncology Group (ECOG)
performance status (PS) ≤ 2.
7. Life expectancy of ≥ 6 months.
8. Adequate normal organ and marrow function as defined below:
1. Haemoglobin concentration ≥ 8.0 g/dL (5.0 mmol/L).
2. WBC ≥ 2x10 9/L (2000/mm3).
3. Platelets ≥75x10 9/L (75x103/mm3).
9. Adequate renal function defined as serum creatinine ≤150 μmol/L or 1.7 mg/dL, or a
creatinine clearance or measured glomerular filtration rate (using plasma clearance
methods) of ≥ 50 mL/min.
10. Adequate hepatic function defined as total bilirubin ≤3 x ULN and aspartate
aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN (≤ 5 x ULN if
liver metastases are present).
11. Serum albumin ≥ 3.0 g/dL (or serum albumin < 3.0 g/dL if prothrombin time is within
the normal range).
12. Female patients must either be of non-reproductive potential (i.e., post-menopausal by
history: ≥60 years old and no menses for ≥1 year without an alternative medical cause;
OR history of hysterectomy, OR history of bilateral tubal ligation, OR history of
bilateral oophorectomy) or must have a negative serum pregnancy test upon study entry.
Both women and men must agree to use a medically acceptable method of contraception
throughout the treatment period and for six months after discontinuation of treatment.
Acceptable methods of contraception include intrauterine device, oral contraceptive,
subdermal implant and/or double barrier.
13. Patient is willing and able to comply with the protocol for the duration of the study
including undergoing treatment and scheduled visits and examinations including
follow-up.
14. Recovery to Grade ≤ 1 from any adverse event (AE) derived from previous treatment
(excluding alopecia and/or cutaneous toxicity and/or asthenia).
Exclusion Criteria:
1. Treatment with >30 mg Octreotide LAR at 3-4 weeks intervals within 12 weeks prior to
enrolment in the study.
2. Peptide receptor radionuclide therapy (PRRT) at any time prior to enrolment in the
study.
3. Targeted surgery, radiotherapy (external beam), chemotherapy, embolization,
interferons, mTOR-inhibitors or other investigational therapy within 12 weeks prior to
enrolment in the study. In Cohort 2, chemotherapy should be administered at least 4
weeks prior to first dose of the treatment.
4. Prior treatment with anti-PDL-1/anti-PD-1 or anti-CTL-4 therapy.
5. Known brain metastases, unless these metastases have been treated and stabilized for
at least 24 weeks prior to enrolment in the study. Patients with a history of brain
metastases must have a head CT with contrast to document stable disease prior to
enrolment in the study.
6. Uncontrolled congestive heart failure (NYHA II-IV).
7. Uncontrolled diabetes mellitus as defined by a fasting blood glucose >2 ULN.
8. Any patient receiving treatment with short-acting Octreotide, which cannot be
interrupted for 24 h before and 24 h after the administration of 177Lu-DOTATATE , or
any patient receiving treatment with Octreotide LAR, which cannot be interrupted for
at least 6 weeks before the administration of 177Lu-DOTATATE, unless the tumour uptake
observed by Somakit imaging during continued Octreotide treatment is at least as high
as normal liver uptake observed by planar imaging.
9. Acute or chronic hepatitis B (e.g., Hepatitis B surface antigen reactive), hepatitis C
(e.g., HCV RNA [qualitative] is detected) or known history of Human Immunodeficiency
Virus (HIV) (HIV 1/2 antibodies).
10. Active, known, or suspected autoimmune disease within the past 2 years. NOTE: Patients
with Type I diabetes mellitus, residual hypothyroidism due to autoimmune thyroiditis
only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or
alopecia) and Grave's disease not requiring systemic treatment within the past 2 years
are not excluded.
11. Patients with a condition requiring systemic treatment with either corticosteroids (>
10 mg daily prednisone equivalent) or other immunosuppressive medications within 14
days of start of study treatment. NOTE: Inhaled or topical steroids, and systemic
steroid doses > 10 mg daily prednisone equivalent for adrenal replacement are
permitted in the absence of active autoimmune disease.
12. Active or prior documented inflammatory bowel disease (e.g., Crohn's disease,
ulcerative colitis).
13. History of allogeneic organ transplant.
14. Known hypersensitivity to nivolumab, 177Lu-DOTATATE or its excipients.
15. Patients with any other significant medical, psychiatric, or surgical condition,
currently uncontrolled by treatment, which may interfere with completion of the study.
Patients must have recovered from the effects of major surgery or significant
traumatic injury at least 14 days before starting treatment.
16. Prior external beam radiation therapy to more than 25% of the bone marrow.
17. Urinary incontinence.
18. Subjects with previous malignancies (except non-melanoma skin cancers, and the
following in situ cancers: bladder, gastric, esophageal, colon, endometrial,
cervical/dysplasia, melanoma, or breast) unless a complete remission was achieved at
least 5 years prior to study entry AND no additional therapy is required during the
study period. 19. Prisoners or patients who are compulsory detained.
20. Established or suspected pregnancy or when pregnancy has not been excluded. 21. Kidney failure with creatinine clearance < 30 mL/min
