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November 7, 2025
Brand Name :
Netspot
Synonyms :
gallium ga-68 dotatate
Class :
Diagnostic Imaging Agents
Dosage forms and strengths Â
single-dose kitÂ
lyophilized powder+ Buffer solutionÂ
40mcg (dotatate)+1mLÂ
Dosage forms and strengthsÂ
single-dose kitÂ
lyophilized powder+ Buffer solutionÂ
40mcg(dotatate)+1mLÂ
Refer adult dosingÂ
may decrease the diagnostic effect of Androgen Deprivation Therapy Agents
lanreotide exerts its influence on gallium ga 68 dotatate by engaging in receptor binding competition, thereby diminishing its effects
octreotide exerts its influence on gallium ga 68 dotatate by engaging in receptor binding competition, thereby diminishing its effects
pasireotide exerts its influence on gallium ga 68 dotatate by engaging in receptor binding competition, thereby diminishing its effects
Actions and Spectrum:Â
Action: gallium ga-68 dotatate is a radiopharmaceutical used in a medical imaging technique known as positron emission tomography (PET). It is specifically designed to target and visualize neuroendocrine tumors in the body. The action of gallium ga-68 dotatate is based on its ability to bind to somatostatin receptors that are overexpressed on the surface of neuroendocrine tumor cells.Â
Spectrum:Â Â
Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs): These tumors arise from neuroendocrine cells in the gastrointestinal tract and pancreas. They can be in the stomach, small intestine, colon, rectum, and pancreas.Â
Pulmonary Neuroendocrine Tumors: These tumors develop in the lungs and are categorized into subtypes, including typical and atypical carcinoids, large cell neuroendocrine carcinoma (LCNEC), and small cell lung cancer (SCLC).Â
Frequency not defined Â
Gastrointestinal disorders: Nausea and vomitingÂ
Injection site pain and burning sensationÂ
General disorders and administration site conditions Â
Black Box Warning:Â Â
None
Contraindication/Caution:Â Â
Hypersensitivity: Patients with a known hypersensitivity or severe allergic reaction to gallium ga-68 dotatate or any of its components should not receive this radiopharmaceutical.Â
Pregnancy and Breastfeeding: gallium ga-68 dotatate may pose risks to the developing fetus, and its use is generally not recommended during pregnancy. Similarly, breastfeeding women should avoid this radiopharmaceutical due to the potential risk of radiation exposure to the infant.Â
Children: The safety and efficacy of gallium ga-68 dotatate have not been well-established in pediatric populations. Its use in children should be carefully considered, and alternative imaging modalities may be preferred.Â
Impaired Renal Function: Since gallium ga-68 dotatate is eliminated mainly through the kidneys, patients with severe renal impairment may experience increased radiation exposure or delayed clearance. Physicians should assess kidney function before administering the radiopharmaceutical and consider the risk-benefit ratio.Â
Drug Interactions: gallium ga-68 dotatate may interact with certain medications or treatments, affecting the accuracy of the PET scan or causing adverse effects. Â
Pre-existing Medical Conditions: Patients with certain medical conditions, such as severe cardiovascular disease or other serious illnesses, may require special precautions or alternative imaging options. Physicians should carefully evaluate the patient’s overall health status before proceeding with the procedure.Â
Previous Radiopharmaceutical Exposure: Patients who have recently received other radiopharmaceuticals may need to wait for a specified period before undergoing a gallium ga-68 dotatate PET scan to avoid potential interference or overlapping radiation effects.Â
Pregnancy warnings:    Â
Pregnancy category: N/AÂ
Lactation: Excreted into human milk is unknownÂ
Pregnancy Categories:        Â
Category A: Studies that were well-controlled and met expectations revealed no risk to the fetus in either the first or second trimester.Â
Category B: There were a lack of studies on pregnant women and no evidence of risk to the fetus in animal experiments.  Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.  Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this category
Pharmacology:Â Â
gallium ga-68 dotatate is a radiopharmaceutical used in nuclear medicine for diagnostic imaging purposesÂ
Pharmacodynamics:Â Â
gallium ga-68 dotatate is a radiolabeled derivative of octreotide, a synthetic peptide analogue of somatostatin. Somatostatin receptors are expressed on the surface of certain neuroendocrine tumor cells. gallium ga-68 dotatate binds selectively to somatostatin receptor subtypes, predominantly subtype 2 (SSTR2), which are highly expressed on neuroendocrine tumor cells.  Â
Pharmacokinetics:Â
AbsorptionÂ
gallium ga-68 dotatate is administered intravenously, typically as an injection. Upon administration, it rapidly enters the bloodstream and circulates throughout the body.Â
DistributionÂ
gallium ga-68 dotatate is designed to target somatostatin receptors, which are overexpressed in certain neuroendocrine tumors. After injection, it distributes in the body and accumulates in tissues expressing these receptors, particularly in neuroendocrine tumor cells.Â
MetabolismÂ
gallium ga-68 dotatate is not significantly metabolized in the body. It remains in its unchanged form during its circulation.Â
Excretion and EliminationÂ
gallium ga-68 dotatate is primarily excreted through the kidneys. It is filtered by the glomeruli in the kidneys and then eliminated in the urine. A small portion may be excreted through the hepatobiliary system and eliminated in the feces.Â
Administration: Â
Radiotracer Injection:Â
gallium ga-68 dotatate is administered intravenously (IV) into the patient’s vein. The dose is calculated based on the patient’s weight and other factors.Â
Uptake Time:Â
The patient will wait for a specific amount of time after the injection to allow the radiotracer to circulate and accumulate in the target tissues. This uptake time is typically around 45 to 60 minutes, but it may vary based on the imaging center’s protocols.Â
Imaging Procedure:Â
The patient will be positioned on the PET scanner bed, and the imaging procedure will begin. The PET scanner detects the gamma rays emitted by the decaying ga-68 radioisotope to create images of the distribution of dotatate in the body.Â
Patient information leafletÂ
Generic Name: gallium ga-68 dotatateÂ
Why do we use gallium ga-68 dotatate?Â
Neuroendocrine Tumor Imaging: gallium ga-68 dotatate is highly sensitive in detecting and localizing neuroendocrine tumors (NETs). These tumors often express somatostatin receptors, and is gallium ga-68 dotatate a radiolabeled molecule that binds to these receptors, allowing for precise imaging of the tumor and its extent.Â
Differentiation from Other Lesions: In cases where a patient has multiple lesions, gallium ga-68 dotatate can help differentiate between neuroendocrine tumors and other types of tumors or lesions, aiding in accurate diagnosis and treatment planning.Â
Neuroblastoma Imaging: gallium ga-68 dotatate PET is also used in the evaluation of neuroblastoma, a type of cancer that commonly affects children. It helps in identifying primary tumors and metastatic sites, guiding treatment decisions.Â
Improved Detection of Metastases: gallium ga-68 dotatate can detect small metastases and occult tumors that may be missed by other imaging modalities, leading to a more comprehensive assessment of disease spread.Â