Radionuclide therapy (RNT, also known as unsealed source radiotherapyormolecular radiotherapy) uses radioactive substances called radiopharmaceuticals to treat medical conditions, particularly cancer. These are introduced into the body by various means (injectionoringestion are the two most commonplace) and localise to specific locations, organs or tissues depending on their properties and administration routes. This includes anything from a simple compound such as sodium iodide that locates to the thyroid via trapping the iodide ion, to complex biopharmaceuticals such as recombinant antibodies which are attached to radionuclides and seek out specific antigens on cell surfaces.[1][2]
This is a type of targeted therapy which uses the physical, chemical and biological properties of the radiopharmaceutical to target areas of the body for radiation treatment.[3] The related diagnostic modality of nuclear medicine employs the same principles but uses different types or quantities of radiopharmaceuticals in order to image or analyse functional systems within the patient.
RNT contrasts with sealed-source therapy (brachytherapy) where the radionuclide remains in a capsule or metal wire during treatment and needs to be physically placed precisely at the treatment position.[4]
When the radionuclides are ligands (such as with Lutathera and Pluvicto), the technique is also known as radioligand therapy.
[5]
Iodine-131 (131I) is the most common RNT worldwide and uses the simple compound sodium iodide with a radioactive isotope of iodine. The patient (human or animal) may ingest an oral solid or liquid amount or receive an intravenous injection of a solution of the compound. The iodide ion is selectively taken up by the thyroid gland. Both benign conditions like thyrotoxicosis and certain malignant conditions like papillary thyroid cancer can be treated with the radiation emitted by radioiodine.[6] Iodine-131 produces beta and gamma radiation. The beta radiation released damages both normal thyroid tissue and any thyroid cancer that behaves like normal thyroid in taking up iodine, so providing the therapeutic effect, whilst most of the gamma radiation escapes the patient's body.[7]
Most of the iodine not taken up by thyroid tissue is excreted through the kidneys into the urine. After radioiodine treatment the urine will be radioactive or 'hot', and the patients themselves will also emit gamma radiation. Depending on the amount of radioactivity administered, it can take several days for the radioactivity to reduce to the point where the patient does not pose a radiation hazard to bystanders. Patients are often treated as inpatients and there are international guidelines, as well as legislation in many countries, which govern the point at which they may return home.[8]
At the Institute for Transuranium Elements (ITU) work is being done on alpha-immunotherapy, this is an experimental method where antibodies bearing alpha isotopes are used. Bismuth-213 is one of the isotopes which has been used. This is made by the alpha decay of actinium-225. The generation of one short-lived isotope from longer lived isotope is a useful method of providing a portable supply of a short-lived isotope. This is similar to the generation of technetium-99m by a technetium generator. The actinium-225 is made by the irradiation of radium-226 with a cyclotron.[20]
^Volkert, Wynn A.; Hoffman, Timothy J. (1999). "Therapeutic Radiopharmaceuticals". Chemical Reviews. 99 (9): 2269–2292. doi:10.1021/cr9804386. PMID11749482.
^Nicol, Alice; Waddington, Wendy (2011). Dosimetry for radionuclide therapy. York: Institute of Physics and Engineering in Medicine. ISBN9781903613467.
^Den, RB; Doyle, LA; Knudsen, KE (April 2014). "Practical guide to the use of radium 223 dichloride". The Canadian Journal of Urology. 21 (2 Supp 1): 70–6. PMID24775727.
^Tennvall, Jan; Brans, Boudewijn (30 March 2007). "EANM procedure guideline for 32P phosphate treatment of myeloproliferative diseases". European Journal of Nuclear Medicine and Molecular Imaging. 34 (8): 1324–1327. doi:10.1007/s00259-007-0407-4. PMID17396258. S2CID21759615.
^Siegel, Michael E.; Siegel, Herrick J.; Luck, James V. (October 1997). "Radiosynovectomy's clinical applications and cost effectiveness: A review". Seminars in Nuclear Medicine. 27 (4): 364–371. doi:10.1016/S0001-2998(97)80009-8. PMID9364646.
^Allen, Theresa M. (October 2002). "Ligand-targeted therapeutics in anticancer therapy". Nature Reviews Cancer. 2 (10): 750–763. doi:10.1038/nrc903. PMID12360278. S2CID21014917.
^Sharp, Susan E.; Trout, Andrew T.; Weiss, Brian D.; Gelfand, Michael J. (January 2016). "MIBG in Neuroblastoma Diagnostic Imaging and Therapy". RadioGraphics. 36 (1): 258–278. doi:10.1148/rg.2016150099. PMID26761540.