Peptide receptor radionuclide therapy (PRRT) of neuroendocrine tumors with somatostatin analogues

Eur Rev Med Pharmacol Sci. 2010 Apr;14(4):347-51.

Abstract

Background: Clinical experience with the radiolabeled somatostatin analogues 90Y-DOTATOC and, more recently, 177Lu-DOTATATE, is ongoing since more than a decade in few centers. Dosimetric studies demonstrated that 90Y-DOTATOC and 177Lu-DOTATATE are able to deliver high doses to somatostatin receptor sst2-expressing tumors and low doses to normal organs.

Results and conclusions: Clinical studies demonstrated that partial and complete objective responses in up to 30% of patients can be obtained, with a great survival benefit in treated patients. Side effects may involve the kidney and the bone marrow and are usually mild. Renal protection is used to minimize the risk of a late decrease of renal function.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Humans
  • Lutetium / therapeutic use
  • Neuroendocrine Tumors / radiotherapy*
  • Octreotide / analogs & derivatives
  • Octreotide / therapeutic use
  • Radioisotopes / adverse effects
  • Radioisotopes / therapeutic use*
  • Radiopharmaceuticals / therapeutic use
  • Receptors, Peptide / drug effects*
  • Somatostatin / adverse effects
  • Somatostatin / analogs & derivatives*
  • Somatostatin / therapeutic use*
  • Yttrium Radioisotopes / therapeutic use

Substances

  • Antineoplastic Agents
  • Radioisotopes
  • Radiopharmaceuticals
  • Receptors, Peptide
  • Yttrium Radioisotopes
  • Somatostatin
  • Lutetium
  • Octreotide
  • Edotreotide