Radionuclide therapy

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As radionuclide therapy (also Endoradiotherapie ) are therapies refer to operations where radionuclides are used in non-enclosed form. The most frequently used radionuclide therapies are radioiodine therapy and - by a large margin - radiosynoviorthesis . Radionuclide therapy is counted among the nuclear medicine therapies.

Principles of enrichment

The highest possible activity of the radionuclide used in the target tissue is desired in order to achieve a high and therapeutically effective focus dose there. At the same time, the radiation exposure for the tissue that has not been pathologically changed should be as low as possible. For this purpose, suitable enrichment mechanisms must be selected.

The radiopharmaceutical can - if it is not very diffusible - be introduced locally into a pre-existing cavity ( e.g. joints , pleura (pleura), peritoneum (peritoneum) or cysts ) (intracavitary therapy). In other therapies, the radiopharmaceutical enters the target tissue via metabolic processes, via coupling to receptors or specific binding of antibodies .

Nuclides used

In the early days, only natural radionuclides such as radium or thorium were available, the decay radiation of which had a proportion of high-energy beta and gamma rays that was unfavorable for near-field therapy. They were also used in ignorance or in disregard of the associated risks (see Peteosthor ). Today only or predominantly beta emitters are used, only in exceptional cases alpha emitters ( 224 Ra ). If the nuclide used also emits gamma radiation , this radiation does not contribute to the therapeutic effect, but can be used to create a scintigram to monitor the therapy . The bremsstrahlung of certain beta emitters can also be used for a scintigram.

The colloidal 198 Au used from 1945 for injection into cavities (intracavitary therapy) was initially replaced by the pure beta emitter 32 P due to its unfavorable radiation properties . Other beta emitters such as 90 Y , 89 Sr , 186 Re or 169 Er were added later . For the radioiodine therapy , which has the highest specificity of the metabolic accumulation rates, only the beta emitter 131 I is predominantly used. For the other methods, either 131 I or 90 Y is usually used.

List of radionuclide therapies

This alphabetical list is not exhaustive. The therapies that are frequently performed are highlighted in bold. The other therapies are partly out of date, experimental or reserved for a few centers. The colored highlighting is used to assign neighboring lines to one another.

Surname indication Enrichment Mechanism Radiopharmaceutical nuclide Type of radiation HWZ annotation
MIBG therapy Neuroendocrine tumors , especially pheochromocytoma active uptake in neuroendocrine cells , storage in neurosecretory granules Metaiodbenzylguanidine 131 I. predominantly β emitter 8.02 days see also MIBG scintigraphy
palliative therapy of skeletal metastases Bone metastases Incorporation in calcium phosphate Strontium chloride 89 Sr pure β radiator 50.6 days  
Yttrium citrate 90 Y pure β radiator 2.67 days
palliative therapy of skeletal metastases Bone metastases Attachment to the bone surface Bisphosphonates
e.g. B. HEDP or EDTMP
186 Re pure β radiator 3.72 days  
153 Sm pure β radiator 1.93 days
peritoneal therapy recurrent malignant ascites ( ascites ) Puncture of the abdominal cavity Protein colloid 90 Y pure β radiator 2.67 days  
32 P pure β radiator 14.3 days
pleural therapy recurrent malignant pleural effusion Puncture of the pleural space Protein colloid 90 Y pure β radiator 2.67 days Alternative: pleurodesis
32 P pure β radiator 14.3 days
Radioimmunotherapy various cancers specific antibody binding Immunoconjugates div.      
Example:
Ibritumomab-Tiuxetan
malignant lymphoma of B cells specific antibody binding to CD20 Immunoconjugate of ibritumomab and tiuxetan 90 Y pure β radiator 2.67 days  
Radioiodine therapy Thyroid autonomy , Graves' disease , goiter , thyroid cancer active uptake in thyroid cells ( sodium iodide symporter ), incorporation into thyroid hormones (including thyroid peroxidase ) Sodium iodide 131 I. predominantly β emitter 8.02 days in many countries only possible as a stationary
Radiopeptide therapy neuroendocrine tumors specific binding to the somatostatin receptor Edotreotide (DOTATOC) 90 Y pure β radiator 2.67 days  
Radiophosphorus therapy Polycythemia vera , essential thrombocythemia Incorporation into nucleic acids , incorporation into calcium phosphate Dihydrogen phosphate or sodium phosphate 32 P pure β radiator 14.3 days  
Radiosynoviorthesis Rheumatoid arthritis , activated osteoarthritis Injection into the affected joint Protein colloid 90 Y pure β radiator 2.67 days Nuclide depending on the size of the joint being treated; mostly possible on an outpatient basis
186 Re predominantly β emitter 3.72 days
169 he pure β radiator 9.40 days
224 Ra Radium Chloride Therapy Ankylosing spondylitis (Bechterew's disease)   Radium chloride 224 ra α emitters 3.66 days  
Selective internal radiotherapy Liver cell carcinoma , cholangiocellular carcinoma , liver metastases selective angiography of the hepatic artery Microspheres 90 Y pure β radiator 2.67 days see also transarterial chemoembolization
Lipiodol 131 I. predominantly β emitter 8.02 days

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  • H. Schicha, M. Dietlein, K. Scheidhauer. Therapy with unsealed radioactive substances. In: U. Büll, H. Schicha, H.-J. Biersack, WH Knapp, Chr. Reiners, O. Schober . Nuclear medicine. Stuttgart, New York 2001. ISBN 3-13-128123-5