
pmid: 23582925
Peptide receptor radionuclide therapy (PRRT) with radiolabelled somatostatin analogues plays an increasing role in the treatment of patients with inoperable or metastasised gatroenteropancreatic neuroendocrine tumours (GEP-NETs). (90)Y-DOTATOC and (177)Lu-DOTATATE are the most used radiopeptides for PRRT with comparable tumour response rates (about 15-35%). The side effects of this therapy are few and mild. However, amino acids should be used for kidney protection, especially during infusion of (90)Y-DOTATOC. Options to improve PRRT may include combinations of radioactive labelled somatostatin analogues and the use of radiosensitising drugs combined with PRRT. Other therapeutic applications of PRRT may include intra-arterial administration, neo-adjuvant treatment and additional PRRT cycles in patients with progressive disease, who have benefited from initial therapy. Considering the mild side-effects, PRRT may well become the first-line therapy in patients with metastasised or inoperable GEP-NETs if more widespread use of PRRT can be accomplished.
Octreotide, Peptides, Cyclic, Heterocyclic Compounds, 1-Ring, Neuroendocrine Tumors, EMC MM-01-39-03, Heterocyclic Compounds, Stomach Neoplasms, EMC MM-01-39-01, Intestinal Neoplasms, Retreatment, Organometallic Compounds, Humans, Yttrium Radioisotopes, Receptors, Somatostatin, Radiopharmaceuticals, Somatostatin, EMC MM-01-40-01
Octreotide, Peptides, Cyclic, Heterocyclic Compounds, 1-Ring, Neuroendocrine Tumors, EMC MM-01-39-03, Heterocyclic Compounds, Stomach Neoplasms, EMC MM-01-39-01, Intestinal Neoplasms, Retreatment, Organometallic Compounds, Humans, Yttrium Radioisotopes, Receptors, Somatostatin, Radiopharmaceuticals, Somatostatin, EMC MM-01-40-01
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