Organ protection in PSMA-targeted radionuclide therapy of prostate cancer
View Patent ↗A method of reducing radiation exposure of a non-cancerous tissue of a patient diagnosed with a cancer includes administering to the patient an agent capable of competing for binding sites on a surface of the non-cancerous tissue, provided that the administration is carried out after a waiting period that follows administration of a compound including a radionuclide to the patient, the compound having affinity for both a cancerous tissue and the non-cancerous tissue, and, further provided that the binding sites have an affinity for both the agent and the compound.
1. A method of reducing radiation exposure of a non-cancerous tissue of a patient diagnosed with prostate cancer, the method comprising:
administering to the patient a compound comprising a radionuclide and a recognition moiety for Prostate Specific Membrane Antigen (“PSMA”), the compound binding to both cancerous prostate tissue and the non-cancerous tissue, and,
after a waiting period of 1 hour to 60 hours, administering an agent in an amount sufficient to cause a displacement of the bound compound from the binding sites in the non-cancerous tissue by binding of the agent thereto while retaining the radionuclide in the cancerous tissue thereby reducing the exposure of the non-cancerous tissue to the radionuclide;
wherein:
the binding sites are attached to both the agent and the compound, and
the agent has a different chemical structure from the compound, or
the agent has the same chemical structure as the compound absent the radionuclide, and
the agent comprises a recognition moiety for PSMA: the compound is a Glu-urea-based PSMA ligand; and the agent comprises a Glu-urea-based PSMA ligand, a phosphinyl containing moiety, 7-(L-2-amino-2-carboxyethylthio)-2-(2,2-dimethylcyclopropanecarboxamide)-2-heptenoic acid, 2-(phosphonomethyl)pentanedioic acid, or 2-(3-mercaptopropyl)pentanedioic acid (2-MPPA).
2. The method of claim 1 , wherein the non-cancerous tissue is kidney tissue, salivary gland tissue, lacrimal gland tissue, parotid gland tissue, or small intestine tissue.
3. The method of claim 1 , wherein the radionuclide is a radioactive isotope of Ga, I, Y, Lu, Bi, Ac, Re, In, Th, or Tc.
4. The method of claim 1 , wherein the compound is MIP-1555, MIP-1519, MIP-1545, MIP-1427, MIP-1428, MIP-1379, MIP-1072, MIP-1095, MIP-1558, MIP-1405, or MIP-1404; wherein:
and M is a radionuclide and x I is a radionuclide of iodine.
5. The method of claim 1 , wherein the agent comprises: 2-[[methylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[ethylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[propylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[butylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[cyclohexylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[phenylhydroxyphosphinyl]methyl]pentanedioic acid; 2-[[(phenylmethyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[((2-phenylethyl)methyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[((3-phenylpropyl)methyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[((3-phenylbutyl)methyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[((2-phenylbutyl)methyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[(4-phenylbutyl)hydroxyphosphinyl]methyl]pentanedioic acid; 2-[[(aminomethyl)hydroxyphosphinyl]methyl]pentanedioic acid; 7-(L-2-amino-2-carboxyethylthio)-2-(2,2-dimethylcyclopropanecarboxamide)-2-heptenoic acid; 2-(phosphonomethyl)pentanedioic acid; N-[methylhydroxyphosphinyl]glutamic acid; N-[ethylhydroxyphosphinyl]glutamic acid; N-[propylhydroxyphosphinyl]glutamic acid; N-[butylhydroxyphosphinyl]glutamic acid; N-[phenylhydroxyphosphinyl]glutamic acid; N-[(phenylmethyl)hydroxyphosphinyl]glutamic acid; N-[((2-phenylethyl)methyl)hydroxyphosphinyl]glutamic acid; N-methyl-N-[phenylhydroxyphosphinyl]glutamic acid; 2-(3-mercaptopropyl)pentanedioic acid (2-MPPA), a pharmaceutically acceptable salt thereof; or a mixture of any two or more thereof.
6. The method of claim 1 , wherein the agent is cold MIP-1555, cold MIP-1519, cold MIP-1545, cold MIP-1427, cold MIP-1428, cold MIP-1379, cold MIP-1072, cold MIP-1095, cold MIP-1558, cold MIP-1405, or cold MIP-1404; wherein:
and M is absent or is a non-radionuclide metal and x I is a non-radionuclide of iodine.
7. The method of claim 1 , wherein the compound is administered to the subject from about 0.2 mg/kg to about 100 mg/kg.
8. The method of claim 1 , wherein the agent is administered to the subject from about 0.2 mg/kg to about 100 mg/kg.
9. The method of claim 1 , wherein the compound is represented as:
wherein x is a radionuclide of iodine.
10. The method of claim 1 , wherein the agent is represented as
wherein x I is a non-radionuclide of iodine.