Actively Recruiting
Study to Assess the Safety and Effectiveness of Novel Radiopharmaceutical Terbium-161 DOTATATE in Metastatic Neuroendocrine Tumors
Led by Tata Memorial Hospital · Updated on 2026-02-11
20
Participants Needed
2
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Gastro-enteropancreatic Neuro-endocrine tumors (GEP-NETs) are rare slow-growing cancers which commonly involve the abdominal organs like liver, stomach, intestines and pancreas. Their incidence has been documented to have increased over the last decade, thus resulting in treatment options being developed to treat these cancers. These cancers spread commonly to the liver, followed by lungs, bones and other sites. Depending on the extent of disease seen on scan, treatment is planned. Patients are advised Peptide Receptor Radionuclide Therapy (PRRT), which is the current standard of treatment for metastatic GEP-NETs. Radio-isotopes labeled to octreotide analogs bind to somatostatin receptors on surface of cancer cells and deliver radiation to the cancer cells when injected into the body. Lu-177 (Lutetium-177) is one such radioisotope which has been used for tagging to the octreotide and is known as Lu-177 DOTATATE PRRT, which is now routinely used in clinical practice. Terbium-161 is another radioisotope which can be labeled to octreotide and used for PRRT. It has advantages over Lu-177 such that it specifically reaches the tumor sites and does not affect the surrounding normal cells, due to its higher penetrating capacity and shorter range of travel. This will benefit patients as the effectiveness of PRRT will be higher with lesser side effects. However, the investigators can only do this by performing a study. Response to treatment can be evaluated by performing scans and side effects, if any can be studied by performing blood tests.
CONDITIONS
Official Title
Study to Assess the Safety and Effectiveness of Novel Radiopharmaceutical Terbium-161 DOTATATE in Metastatic Neuroendocrine Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female, age greater than 18 years
- Histopathological diagnosis of well-differentiated GEP-NET
- Positive Ga-68-DOTANOC PET/CT, Krennings score greater than or equal to 3
- Locally advanced/inoperable disease or metastatic disease
- Patients who have shown disease progression with Lu-177 DOTATATE PRRT
- Karnofsky performance-status score of at least 60 or ECOG performance status less than or equal to 2
- Life expectancy greater than 6 months
You will not qualify if you...
- Serum creatinine level of more than 1.6 mg/dl or a creatinine clearance of less than 50 ml/min
- Hemoglobin level of less than 8.0 g per deciliter
- Red blood cell count less than 300,000 per cubic millimeter
- White cell count of less than 2000 per cubic millimeter
- Platelet count of less than 75,000 per cubic millimeter
- Total bilirubin level of more than 3 times the upper limit of the normal range
- Serum albumin level greater than 3.0 g/dl
- Pregnancy and lactation
- Patients with concurrent malignancies
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Tata Memorial Hospital, Mumbai, India
Mumbai, Maharashtra, India, 400012
Actively Recruiting
2
Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)
Navi Mumbai, Maharashtra, India, 410210
Actively Recruiting
Research Team
A
Ameya Puranik, DNB
CONTACT
S
Sushil Yadav, MSc
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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