Wikipedia

Radionuclide therapy

(Redirected from Molecular radiotherapy)

Radionuclide therapy (RNT, also known as unsealed source radiotherapy or molecular radiotherapy) uses radioactive substances called radiopharmaceuticals to treat medical conditions, particularly cancer. These are introduced into the body by various means (injection or ingestion 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]

Radionuclide therapy
ICD-9-CM92.28

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]

Clinical use

edit

Thyroid conditions

edit
See also: Iodine-131 § Medical use

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]

Bone metastasis

edit
See also: Targeted alpha-particle therapy

Radium-223 chloride, strontium-89 chloride and samarium-153 EDTMP are used to treat secondary cancer in the bones.[9][10] Radium and strontium mimic calcium in the body.[11] Samarium is bound to tetraphosphate EDTMP, phosphates are taken up by osteoblastic (bone forming) repairs that occur adjacent to some metastatic lesions.[12]

Bone marrow conditions

edit

Beta emitting phosphorus-32 (32P), as sodium phosphate, is used to treat overactive bone marrow, in which it is otherwise naturally metabolised.[13][14][15]

Joint inflammation

edit

Yttrium-90 colloid

edit

An yttrium-90 (90Y) colloidal suspension is used for radiosynovectomy in the knee joint.[16]

Liver tumours

edit

Yttrium-90 spheres

edit
Main article: Selective internal radiation therapy

90Y in the form of a resin or glass spheres can be used to treat primary and metastatic liver cancers.[17]

Neuroendocrine tumours

edit

Iodine-131 mIBG

edit

131I-mIBG (metaiodobenzylguanidine) is used for the treatment of phaeochromocytoma and neuroblastoma.[18]

Lutetium-177

edit
See also: Peptide receptor radionuclide therapy

177Lu is bound with a DOTA chelator to target neuroendocrine tumours.[19]

Experimental antibody based methods

edit

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]

References

edit
  1. ^ Buscombe, J.; Navalkissoor, S. (1 August 2012). "Molecular radiotherapy". Clinical Medicine. 12 (4): 381–386. doi:10.7861/clinmedicine.12-4-381. PMC 4952132. PMID 22930888.
  2. ^ Volkert, Wynn A.; Hoffman, Timothy J. (1999). "Therapeutic Radiopharmaceuticals". Chemical Reviews. 99 (9): 2269–2292. doi:10.1021/cr9804386. PMID 11749482.
  3. ^ Nicol, Alice; Waddington, Wendy (2011). Dosimetry for radionuclide therapy. York: Institute of Physics and Engineering in Medicine. ISBN 9781903613467.
  4. ^ Martin, Elizabeth A; McFerran, Tanya A, eds. (2014). A dictionary of nursing (6th ed.). Oxford: Oxford University Press. doi:10.1093/acref/9780199666379.001.0001. ISBN 9780199666379.
  5. ^ Radioligand therapy, a ‘game-changer’ for cancer treatment, forces manufacturers to race against a ticking clock
  6. ^ Silberstein, E. B.; Alavi, A.; Balon, H. R.; Clarke, S. E. M.; Divgi, C.; Gelfand, M. J.; Goldsmith, S. J.; Jadvar, H.; Marcus, C. S.; Martin, W. H.; Parker, J. A.; Royal, H. D.; Sarkar, S. D.; Stabin, M.; Waxman, A. D. (11 July 2012). "The SNMMI Practice Guideline for Therapy of Thyroid Disease with 131I 3.0". Journal of Nuclear Medicine. 53 (10): 1633–1651. doi:10.2967/jnumed.112.105148. PMID 22787108.
  7. ^ IAEA (1996). Manual on therapeutic uses of iodine-131 (PDF). Vienna: International Atomic Energy Agency. p. 7.
  8. ^ IAEA; ICRP (2009). Release of patients after radionuclide therapy. Vienna, Austria: International Atomic Energy Agency. ISBN 978-92-0-108909-0.
  9. ^ 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. PMID 24775727.
  10. ^ Lutz, Stephen; Berk, Lawrence; Chang, Eric; Chow, Edward; Hahn, Carol; Hoskin, Peter; Howell, David; Konski, Andre; Kachnic, Lisa; Lo, Simon; Sahgal, Arjun; Silverman, Larry; von Gunten, Charles; Mendel, Ehud; Vassil, Andrew; Bruner, Deborah Watkins; Hartsell, William (March 2011). "Palliative Radiotherapy for Bone Metastases: An ASTRO Evidence-Based Guideline". International Journal of Radiation Oncology, Biology, Physics. 79 (4): 965–976. doi:10.1016/j.ijrobp.2010.11.026. PMID 21277118.
  11. ^ Goyal, Jatinder; Antonarakis, Emmanuel S. (October 2012). "Bone-targeting radiopharmaceuticals for the treatment of prostate cancer with bone metastases". Cancer Letters. 323 (2): 135–146. doi:10.1016/j.canlet.2012.04.001. PMC 4124611. PMID 22521546.
  12. ^ Serafini, AN (15 June 2000). "Samarium Sm-153 lexidronam for the palliation of bone pain associated with metastases". Cancer. 88 (12 Suppl): 2934–9. doi:10.1002/1097-0142(20000615)88:12+<2934::AID-CNCR9>3.0.CO;2-S. PMID 10898337. S2CID 45863868.
  13. ^ 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. PMID 17396258. S2CID 21759615.
  14. ^ Raj, Gurdeep. Advanced Inorganic Chemistry Vol 1. Krishna Prakashan Media. p. 497. ISBN 9788187224037.
  15. ^ Gropper, Sareen S.; Smith, Jack L. (2012-06-01). Advanced Nutrition and Human Metabolism. Cengage Learning. p. 432. ISBN 978-1133104056.
  16. ^ 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. PMID 9364646.
  17. ^ Allen, Theresa M. (October 2002). "Ligand-targeted therapeutics in anticancer therapy". Nature Reviews Cancer. 2 (10): 750–763. doi:10.1038/nrc903. PMID 12360278. S2CID 21014917.
  18. ^ 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. PMID 26761540.
  19. ^ Maqsood, Muhammad Haisum; Tameez Ud Din, Asim; Khan, Ameer H (30 January 2019). "Neuroendocrine Tumor Therapy with Lutetium-177: A Literature Review". Cureus. 11 (1): e3986. doi:10.7759/cureus.3986. PMC 6443107. PMID 30972265.
  20. ^ Morgenstern, Alfred; Bruchertseifer, Frank; Apostolidis, Christos (1 June 2012). "Bismuth-213 and Actinium-225 – Generator Performance and Evolving Therapeutic Applications of Two Generator-Derived Alpha-Emitting Radioisotopes". Current Radiopharmaceuticals. 5 (3): 221–227. doi:10.2174/1874471011205030221. PMID 22642390.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Radionuclide_therapy&oldid=1244485663"