| Eligibility |
Inclusion Criteria:
1. Written informed consent obtained from the subject prior to performing any
protocol-related procedures.
2. Age >18 years at time of study entry.
3. Subjects must have histologically confirmed diagnosis of one of the following
advanced/metastatic neuroendocrine tumor types:
1. Cohort 1: Well-moderately differentiated neuroendocrine tumors of the lung (
mitotic count =10 mitoses x 10 HPF), also known as typical and atypical lung
carcinoids, that have progressed to prior somatostatin analog therapy and/or one
prior targeted therapy or chemotherapy (only one prior systemic therapy, with the
exception of patients that have been treated with somatostatin analogues and
other systemic treatment, when two prior treatments are allowed).
2. Cohort 2: Well-moderately differentiated G1/G2 (WHO grade 1 and 2)
gastrointestinal neuroendocrine tumors after progression to somatostatin analogs
and one targeted therapy (prior targeted therapy could be everolimus or a
multikinase inhibitor). Prior therapies with interferon alpha-2b or
radionucleotide therapy are allowed.
3. Cohort 3: Well-moderately differentiated neuroendocrine tumors G1/G2 (WHO grade 1
and 2) from pancreatic origin after progression to standard therapies
(chemotherapy, somatostatin analogs and target therapy); patients must be treated
with at least two prior systemic treatment lines and a maximum of four previous
treatment lines.
4. Cohort 4: Neuroendocrine neoplasms (WHO grade 3) of gastroenteropancreatic origin
of unknown primary site (excluding lung primary tumors) after progression to
first-line chemotherapy with a platinum based regimen.
4. For patients included in cohorts 1, 2 and 3: WHO Classification G1/G2 (mitotic count
=10 mitoses x 10 HPF) lung typical and atypical carcinoids for cohort 1, G1/G2
(Ki67=20% and mitotic count =20 mitoses x 10 HPF) gastrointestinal for cohort 2
(including stomach, small intestine and colorectal origins), G1/G2 (Ki67=20% and
mitotic count =20 mitoses x 10 HPF) pancreatic for cohort 3.
5. For patients included in cohort 4: WHO classification G3 (Ki67>20% or mitotic count
>20 mitoses x 10 HPF) gastroenteropancreatic neuroendocrine carcinomas (NEC) or liver
metastases of G3 NEC of unknown primary site.
6. Subjects must have evidence of measurable disease meeting the following criteria:
1. In case of more than one target lesion, it should be identified at least 1 lesion
of = 1.0 cm in the longest diameter for a non lymph node, or = 1.5 cm in the
short-axis diameter for a lymph node, which is serially measurable according to
RECIST 1.1 using computerized tomography/magnetic resonance imaging (CT/MRI). If
there is only one target lesion and it is a non-lymph node, it should have a
longest diameter of = 1.5 cm.
2. Lesions that have had external beam radiotherapy (EBRT) or loco-regional
therapies such as radiofrequency (RF) ablation or liver embolization must show
evidence of progressive disease based on RECIST 1.1 to be deemed a target lesion.
3. Subjects must show evidence of disease progression by radiologic image techniques
within 12 months (an additional month will be allowed to accommodate actual dates
of performance of scans, i.e., within = 13 months) prior to signing informed
consent, according to RECIST 1.1 .
7. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
8. Life expectancy of at least 12 weeks.
9. Adequate normal organ and marrow function as defined below: Haemoglobin = 9.0 g/dL;
Absolute neutrophil count (ANC) = 1.5 x 109/L (> 1500 per mm3); Platelet count = 100 x
109/L (>100,000 per mm3).
10. Serum bilirubin = 1.5 x institutional upper limit of normal (ULN). This will not apply
to subjects with confirmed Gilbert's syndrome (persistent or recurrent
hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or
hepatic pathology), who will be allowed only in consultation with their physician.
11. AST (SGOT)/ALT (SGPT) = 2.5 x institutional upper limit of normal unless liver
metastases are present, in which case it must be = 5x ULN.
12. Serum creatinine CL>40 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault
1976) or by 24-hour urine collection for determination of creatinine clearance.
13. Female subjects must either be of non-reproductive potential (ie, 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.
14. Subject 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.
Exclusion Criteria:
1. Involvement in the planning and/or conduct of the study.
2. Participation in another clinical study with an investigational product during the
last 4 weeks.
3. WHO Classification G3 neuroendocrine neoplasms of lung origin (oat cell/large cell
lung cancer).
4. Prior treatment with anti-PDL-1/anti-PD-1 or anti-CTL-4 therapy.
5. Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable
angina pectoris, cardiac arrhythmia, active peptic ulcer disease or gastritis, active
bleeding diatheses including any subject known to have evidence of acute or chronic
hepatitis B (e.g., HBsAg reactive), hepatitis C (e.g., HCV RNA [qualitative] is
detected) or known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies),
or psychiatric illness/social situations that would limit compliance with study
requirements or compromise the ability of the subject to give written informed
consent.
6. Known history of previous clinical diagnosis of tuberculosis.
7. Current or prior use of immunosuppressive medication within 28 days before the first
dose of durvalumab or tremelimumab, with the exceptions of intranasal and inhaled
corticosteroids or systemic corticosteroids at physiological doses, which are not to
exceed 10 mg/day of prednisone, or an equivalent corticosteroid.
8. Active or prior documented autoimmune disease within the past 2 years NOTE: Subjects
with vitiligo, Grave's disease, or psoriasis not requiring systemic treatment (within
the past 2 years) are not excluded.
9. Active or prior documented inflammatory bowel disease (e.g., Crohn's disease,
ulcerative colitis).
10. History of allogeneic organ transplant.
11. History of hypersensitivity to durvalumab, tremelimumab or any excipient.
12. Subjects having a diagnosis of immunodeficiency or are receiving systemic steroid
therapy or any other form of immunosuppressive therapy within 28 days prior to the
first dose of trial treatment.
13. Knowledge of active central nervous system (CNS) metastases and/or carcinomatous
meningitis. Subjects with previously treated brain metastases may participate provided
they have stable brain metastases [without evidence of progression by imaging
confirmed [by magnetic resonance imaging (MRI) if MRI was used at prior imaging, or
confirmed by computed tomography (CT) imaging if CT used at prior imaging] for at
least four weeks prior to the first dose of trial treatment; also, any neurologic
symptoms must have returned to baseline], have no evidence of new or enlarging brain
metastases,and have not used steroids for brain metastases for at least 7 days prior
to trial treatment. This exception does not include carcinomatous meningitis, as
subjects with carcinomatous meningitis are excluded regardless of clinical stability.
14. Receipt of live attenuated vaccination within 30 days prior to study entry or within
30 days of receiving durvalumab or tremelimumab. Note: The killed virus vaccines used
for seasonal influenza vaccines for injection are allowed; however intranasal
influenza vaccines (e.g., FluMist®) are live attenuated vaccines, and are not allowed.
15. Subjects having known history of, or any evidence of interstitial lung disease or
active, noninfectious pneumonitis.
16. Any prior Grade =3 immune-related adverse event (irAE) while receiving any previous
immunotherapy agent, or any unresolved irAE >Grade 1.
17. Subjects who have received any anti-cancer treatment within 21 days or any
investigational agent within 30 days prior to the first dose of study drug and should
have recovered from any toxicity related to previous anti-cancer treatment. This does
not apply to the use of somatostatin analogues for symptomatic therapy.
18. Major surgery within 3 weeks prior to the first dose of study drug.
19. Subjects having > 1+ proteinuria on urine dipstick testing will undergo 24h urine
collection for quantitative assessment of proteinuria. Subjects with urine protein = 1
g/24h will be ineligible.
20. Significant cardiovascular impairment: history of congestive heart failure greater
than New York Heart Association (NYHA) Class II, unstable angina; myocardial
infarction or stroke within 6 months of the first dose of study drug, or cardiac
arrhythmia requiring medical treatment.
21. Mean QT interval corrected for heart rate (QTc) =470 ms calculated from 3
electrocardiograms (ECGs) using Fredericia's Correction.
22. Bleeding or thrombotic disorders or use of anticoagulants, such as warfarin, or
similar agents requiring therapeutic international normalized ration (INR)monitoring.
Treatment with low molecular weight heparin (LMWH) is allowed.
23. Active hemoptysis (bright red blood of at least 0.5 teaspoon) within 3 weeks prior to
the first dose of study drug.
24. Patients with tumoral disease in the head and neck region, such as paratracheal or
periesophageal lymph node involvement, or with infiltration of structures in the
digestive tract, or vascular pathways that represent a risk of increased bleeding.
25. Patients of cohort 1 with neuroendocrine tumors of pulmonary origin or pulmonary
metastases with evidence of active bleeding.
26. Patients with evidence of digestive bleeding.
27. Active infection (any infection requiring treatment).
28. Active malignancy (except for differentiated thyroid carcinoma, or definitively
treated melanoma in-situ, basal or squamous cell carcinoma of the skin, or carcinoma
in-situ of the cervix) within the past 24 months.
29. Female patients who are pregnant or breastfeeding or male or female patients of
reproductive potential who are not willing to employ highly effective birth control
from screening to 180 days after the last dose of durvalumab + tremelimumab
combination therapy or 90 days after the last dose of durvalumab monotherapy,
whichever is the longer time period.
30. Documented active alcohol or drug abuse.
31. Patients with a prior history of non-compliance with medical regimens.
32. Any condition that, in the opinion of the investigator, would interfere with
evaluation of study treatment or interpretation of patient safety or study results.
|
