Gallium ga 68 edotreotide

(Ga 68 DOTATOC®)

Gallium ga 68 edotreotide

Drug updated on 12/11/2024

Dosage FormInjection (intravenous; 18.5 MBq/mL to 148 MBq/mL [0.5 mCi/mL to 4 mCi/mL])
Drug ClassRadioactive diagnostic agents
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for use with positron emission tomography (PET) for localization of somatostatin receptor positive neuroendocrine tumors (NETs) in adult and pediatric patients.

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Summary
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  • This summary is based on the review of five systematic review(s)/meta-analysis(es). [1-5]
  • Neuroendocrine tumors (NETs) demonstrated higher true positivity rates with Fluorodopa F 18 positron emission tomography (PET), specifically (68)Ga-DOTA-TATE at 78.4% and (64)Cu-DOTATATE at 82.4%, compared to (111)In-DTPA-Octreotide at 63.7% and (99m)Tc-EDDA/HYNIC-TOC at 58.5%.
  • Meningiomas showed effective detection and radiation therapy planning using (68)Ga-DOTA-SSTR PET, significantly influencing treatment decisions, with stable disease achieved in 66.6% of patients undergoing peptide receptor radionuclide therapy (PRRT).
  • Pancreatic neuroendocrine tumors (pNETs) exhibited a pooled sensitivity of 79.6% (95% confidence interval (CI): 71-87%) and specificity of 95% (95% CI: 75-100%), indicating high accuracy for detection and staging of these tumors.
  • For meningiomas, grade 1-2 hematological toxicity was the most common side effect observed in PRRT studies.
  • In patients with gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs), both (225)Ac-DOTATATE and (213)Bi-DOTATOC (177) demonstrated partial responses without significant hematological, renal, or hepatotoxicity, indicating a favorable safety profile.
  • The studies encompassed various populations, including patients with NETs demonstrating higher true positivity rates with PET tracers; patients with meningiomas benefiting from (68)Ga-DOTA-SSTR PET for diagnosis and radiation therapy planning, achieving stable disease in a significant proportion; patients with GEP-NENs showing partial responses with targeted alpha-particle therapy without significant adverse effects; and patients with pNETs exhibiting high sensitivity (79.6%, 95% CI: 71-87%) and specificity (95%, 95% CI: 75-100%) for tumor detection.