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Study of TAE added on chemotherapy in patients with metastatic neuroendocrine tumors

Efficacy and safety of Combination therapy of Hepatic Arterial Embolization and chemotherapy for the treatment of patients with metastatic neuroendocrine tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1061210015
Enrollment
18
Registered
2021-06-21
Start date
2021-07-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastroenteropancreatic neuroendocrine neoplasms

Interventions

Induction of everolimus at a dose of 10 mg once daily after TAE using with embosphere which contain embolic beads

Sponsors

Takeuchi Yasuto
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Patients who diagnosed with non-functionnal GEP-NEN of which grade was G1 confirmed pathologically 2 Patients with liver metastatic tumors who have no treatment history of TAE and chemotherapy 3 20 age old over 4 Patienst who have been fully informed consent 5 Regardless of gender 6 Less than 1 of performance status 7 Adequate hematologic and end-organ function

Exclusion criteria

Exclusion criteria: 1 Tumor thrombus or thrombus in the main and/or first portal vein 2 Moderate or severe ascites 3 Severe arteriovenous shunt in the liver 4 Allergy for contrast media 5 Less than 30 mL/min of eGFR 6 Allergy for Everolimus, Sirolimus and Sirolimus derivatives 7 Allergy for gelatin 8 Prior treatment with mTOR inhibitor 9 Long treatment with corticosteroids or other immunostimulatory agents 10 Significant cardiovascular, infectious, diabate or plumonary disease 11 The participant has a fasting glycemic level of 1.5 ULN or higher at the start of the screening period 12 Patients who diagnosed as Interstitial pneumonia by CT 13 Being pregnant or possibly pregnant 14 Patients who judged as not suitable for chemotherapy 15 Patients who judged as inappropriate candidate by the chief medical examine

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival

Secondary

MeasureTime frame
1 Overall Survival 2 Response Rate 3 Disease Control Rate 4 Adverse Event

Contacts

Public ContactNozomu Wada

Okayama University Hospital

nonsan0808@yahoo.co.jp+81-86-235-7219

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026