Actively Recruiting
Metronomic Temozolomide in Unfit NENs Patients Metronomic Temozolomide in Unfit Patients With Advanced Neuroendocrine Neoplasms (NENs): MeTe Study
Led by European Institute of Oncology · Updated on 2024-11-18
46
Participants Needed
1
Research Sites
154 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Study design and rationale: Neuroendocrine neoplasms (NENs ) represent a heterogeneous group of malignancies, which differ in terms of behavio r and prognosis. Most of t hem are advanced at diagnosis t herefore systemic treatment is proposed. While over the last years many advanced have been made especially in terms of molecular targeted therapies (MTA) like everolimus and sunitinib, chemotherapy i n NENs still represents a controversial question. Temozolomide has been reported to be active alone or in combination with other drugs in neuroendocrine neoplasms (NENs) from different origin. So far there is not universal agreement on the right setting an d way of administration of this therapy. Objective: This is a multicentric phase II prospective interventional study to evaluate the clinical features of patients, who are judged unfit for systemic treatments, consecutively treated with a metronomic Temozolomide chemotherapy schedule in Italian centers with expertise in NEN and to explore also the methylation status of O6-methylguanine-DNA-methyltransferase (MGMT) and the polymorphism of thymidylate synthase (TS) by pyrosequencing in those patients of which tissues were available. This study will allow a better understanding of the role of metronomic temozolomide chemotherapy in NENs patients and help clinicians in answering some of the outstanding questions on their management. Method: Prospective analysis of clinical data of patients unfit for chemotherapy consecutively treated with metronomic temozolomide regimen in Italian centers with expertise in clinical and research NEN activity, for one year from the start of the accrual. Planning of study: Data from NENs patients of any age treated at these centers will be retrieved by searching the hospital information system and analysed. Eligible study population: Patients with histological diagnosis of low grade advanced NEN treated unfit for systemic treatments, for one year from the start of the accrual. Endpoints and evaluation parameters: Description of efficacy and toxicity of Temozolomide regimen in patients with advanced NENs with different primary sites unfit for systemic treatment and explored the pote ntial correlation with clinical/biological factors.
CONDITIONS
Official Title
Metronomic Temozolomide in Unfit NENs Patients Metronomic Temozolomide in Unfit Patients With Advanced Neuroendocrine Neoplasms (NENs): MeTe Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age greater than 18 years
- Histologically confirmed low grade gastroenteropancreatic NENs, bronchial carcinoids, or low grade NENs of unknown primary site
- Advanced disease that is unresectable locally or metastatic
- ECOG performance status 2 and/or moderate medullary impairment or severe comorbidities or more than 3 prior systemic antitumor therapies (excluding somatostatin analogues)
- Functioning or non-functioning tumors
- Evidence of progressive disease by CT scan or MRI
- Recovery from toxicities related to prior treatments with adequate wash-out period
- Ability to swallow pills
- Fertile men agree to use effective contraception during and for 6 months after treatment and are informed about possible infertility risks
You will not qualify if you...
- Prior treatment with temozolomide
- Women of child-bearing potential and men able to father a child who do not agree to use adequate contraception during and after the trial
- Pregnancy, nursing, or refusal to undergo required pregnancy testing
- Patients who have not signed informed consent
- Known active hepatitis B or C infection or HIV carrier
- Treatment with systemic therapies within 1 month prior to screening
- Hypersensitivity to temozolomide, dacarbazine, or excipients
- Known brain metastases or cranial epidural disease unless stable and treated for at least 3 months
- Pregnant or lactating females
- Chronic treatment with valproic acid
AI-Screening
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Trial Site Locations
Total: 1 location
1
European Institute of Oncology, IEO, IRCCS
Milan, Italy, 20141
Actively Recruiting
Research Team
F
Francesca Spada, MD, PhD
CONTACT
D
Darina Tamayo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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