Skip to main content

PRRT (Peptide Receptor Radionuclide Therapy)

Are you looking for an experienced specialist in the medical field PRRT (peptide receptor radionuclide therapy)? You will exclusively find specialists, clinics, and centers in their area of expertise in Germany, Austria, and Switzerland on the PRIMO MEDICO website.

FIND A SPECIALIST

Specialists in PRRT (Peptide Receptor Radionuclide Therapy)

Information About the Field of PRRT (Peptide Receptor Radionuclide Therapy)

What is PRRT?

PRRT is a nuclear medicine treatment for patients with neuroendocrine tumors that have formed metastases. The treatment is carried out during an inpatient stay in a hospital with a nuclear medicine department. The therapy is carried out in several cycles. Usually, four cycles take place at intervals of eight to twelve weeks.

For Which Patients Is PRRT Therapy Suitable?

A specific type of neuroendocrine tumor has many receptors on its surface to which the hormone somatostatin can bind. This characteristic can be exploited for these tumors' diagnosis and therapy by using receptors as target structures for antibodies and radioactive molecules. In PRRT, a radioactive molecule is coupled to a peptide molecule that is very similar to somatostatin and can therefore link to the somatostatin receptors on the neuroendocrine tumor. After linking, the coupled radioactive molecule's released radiation destroys all cells in the immediate surroundings and destroys the tumor cells. At the same time, healthy tissue is spared, since the radiation has a short range of only a few millimeters. Besides, the radioactive molecules emit gamma radiation that is intercepted outside the body; with this information, conclusions about the tumor's location and size can be drawn.

PRRT Procedure

The patient is admitted to the hospital for treatment. Usually, a hospital stay of two to five days can be expected. A doctor's consultation takes place on the first day, and blood will be drawn for laboratory values. The PRRT mainly affects the kidneys and bone marrow. It is, therefore, essential to determine their function before treatment. Shortly before the actual therapy, an infusion is administered to protect the kidneys. The peptide receptor, coupled with the radioactive molecule, is infused into the bloodstream via a venous cannula. The infusion runs for about half an hour. Afterward, the patient's radiation is monitored regularly, and full-body images confirm the therapy's success. If there are no complications and the patient is in good health considering the circumstances, the hospital can be left after the radiation drops below a specific limit.

Who covers the costs?

Health insurance companies do not automatically cover the costs of a PRRT. Before the therapy, an individual application for cost absorption must be submitted, explaining why the patient needs this therapy.

PRRT Experience

The success of the PRRT is very variable. It can lead to a total regression or a reduction in the volume of the tumors and metastases. PRRT can also prevent further growth so that the volume of the tumors remains the same. Unfortunately, it is also possible that patients may experience disease progression despite PRRT.

Which Doctors and Clinics Are Specialists in Peptide Receptor Radionuclide Therapy?

Every patient who needs a doctor wants the best medical care. Therefore, the patient is wondering where to find the best clinic. As this question cannot be answered objectively, and a reliable doctor would never claim to be the best one, we can only rely on a doctor's experience.

We help you to find an expert for your disease. All listed physicians and clinics have been reviewed by us for their outstanding specialization in PRRT (peptide receptor radionuclide therapy) and expect your inquiry or treatment request.

Sources:

  • Klöppel: Neuroendokrine Neoplasien. In: Der Pathologe. Band: 40, Nummer: 3, 2019, doi: 10.1007/s00292-019-0594-3, p. 211-219.
  • Chai et al.: Gastroenteropancreatic neuroendocrine neoplasms: selected pathology review and molecular updates. In: Histopathology. Band: 72, Nummer: 1, 2017, doi: 10.1111/his.13367, p. 153-167.
  • Holzer: Gastroenteropankreatische neuroendokrine Tumoren. In: Der Chirurg. Band: 85, Nummer: 8, 2014, doi: 10.1007/s00104-013-2679-5, p. 731-744.
  • Begum et al.: Neuroendokrine Tumoren des Verdauungstrakts – Daten des deutschen NET-Registers. In: Zentralblatt für Chirurgie - Zeitschrift für Allgemeine, Viszeral-, Thorax- und Gefäßchirurgie. 2020, doi: 10.1055/s-00000104, p. .
  • Rinke, Wiedenmann et al.: S2k-Leitlinie Neuroendokrine Tumore. In: Zeitschrift für Gastroenterologie. Band: 56, Nummer: 06, 2018, doi: 10.1055/a-0604-2924, p. 583-681.
  • Siebenhner et al.: Neuroendokrine Tumoren. In: Swiss Medical Forum ‒ Schweizerisches Medizin-Forum. 2019, doi: 10.4414/smf.2019.08257, p. .
  • Perren et al.: ENETS Consensus Guidelines for the Standards of Care in Neuroendocrine Tumors: Pathology - Diagnosis and Prognostic Stratification. In: Neuroendocrinology. Band: 105, Nummer: 3, 2017, doi: 10.1159/000457956, p. 196-200.
  • Perren et al.: Klassifikation und Pathologie gastroenteropankreatischer neuroendokriner Tumoren. In: Viszeralmedizin. Band: 26, Nummer: 4, 2010, doi: 10.1159/000322316, p. 234-240.
  • Choe et al.: What Is New in the 2017 World Health Organization Classification and 8th American Joint Committee on Cancer Staging System for Pancreatic Neuroendocrine Neoplasms?. In: Korean Journal of Radiology. Band: 20, Nummer: 1, 2018, doi: 10.3348/kjr.2018.0040, p. 5.
  • Böcker et al.: Lehrbuch Pathologie. 6. Auflage Elsevier 2019, ISBN: 978-3-437-17143-7.
  • Kumar et al.: Robbins and Cotran Pathologic Basis of Disease. Elsevier 2014, ISBN: 978-1-455-72613-4.
  • Sun, Kaufman: Ki-67: more than a proliferation marker. In: Chromosoma. Band: 127, Nummer: 2, 2018, doi: 10.1007/s00412-018-0659-8, p. 175-186.
  • Herold: Innere Medizin 2019. Herold 2018, ISBN: 978-3-981-46608-9.
  • Pavel et al.: Systemic Therapeutic Options for Carcinoid. In: Seminars in Oncology. Band: 40, Nummer: 1, 2013, doi: 10.1053/j.seminoncol.2012.11.003, p. 84-99.
  • Kasper et al.: Harrison's Principles of Internal Medicine 19/E (Vol.1 & Vol.2). 19. Auflage McGraw Hill Professional 2015, ISBN: 978-0-071-80216-1.
  • Phan et al.: Effect of lanreotide depot (LAN) on 5-hydroxyindoleacetic acid (5HIAA) and chromogranin A (CgA) in gastroenteropancreatic neuroendocrine (GEP NET) tumors: Correlation with tumor response and progression-free survival (PFS) from the phase III CLARINET study.. In: Journal of Clinical Oncology. Band: 35, Nummer: 15_suppl, 2017, doi: 10.1200/jco.2017.35.15_suppl.4095, p. 4095-4095.
  • Rinke et al.: Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: a report from the PROMID Study Group.. In: Journal of clinical oncology : official journal of the American Society of Clinical Oncology. Band: 27, Nummer: 28, 2009, doi: 10.1200/JCO.2009.22.8510, p. 4656-63.
  • Rinke et al.: Placebo-Controlled, Double-Blind, Prospective, Randomized Study on the Effect of Octreotide LAR in the Control of Tumor Growth in Patients with Metastatic Neuroendocrine Midgut Tumors (PROMID): Results of Long-Term Survival.. In: Neuroendocrinology. Band: 104, Nummer: 1, 2017, doi: 10.1159/000443612, p. 26-32.
  • Caplin et al.: Anti-tumour effects of lanreotide for pancreatic and intestinal neuroendocrine tumours: the CLARINET open-label extension study.. In: Endocrine-related cancer. Band: 23, Nummer: 3, 2016, doi: 10.1530/ERC-15-0490, p. 191-9.