Τόμος 32 (2018) – Τεύχος 3 –Άρθρο 6 – Review of Clinical Pharmacology and Pharmacokinetics – Διεθνής Έκδοση – Volume 32 (2018) – Issue 3 – Article 6 – Review of Clinical Pharmacology and Pharmacokinetics – International Edition

Τίτλος – Title

An Update on Medical Treatments for Neuroendocrine Tumors and their Rare Dermatologic Complications

Συγγραφέας – Author

Vasiliki-Sofia Grech MD

Physician. General Hospital Of Karpenisi, Karpenisi, Greece

Παραπομπή – Citation

V.-S. Grech. An Update on Medical Treatments for Neuroendocrine Tumors and their Rare Dermatologic Complications. Review Clin. Pharmacol. Pharmacokinet. 2018, 32, 3, 147-165

Ημερομηνία Δημοσιευσης – Publication Date
25-10-2018
Γλώσσα Πλήρους Κειμένου –
Full Text Language

Αγγλικά – English

Λέξεις κλειδιά – Keywords
Neuroendocrine tumors, dermatologic metastasis, medical therapy, therapeutic applications
Λοιποί Όροι – Other Terms

Μελέτη

Study

Περίληψη –Summary

Neuroendocrine tumours (NET’s), are a plethoric group of tumours with rare dermatologic complications by means of metastasis. These cases require prompt diagnosis as can modify chemotherapy protocols. Until recently, only a few therapeutic options for oncologic control of these tumors were available, mostly for highly graded NETs but with notable side effects. Since surgery is not a curative option for metastatic cases, other medical therapies have been developed. A number of pivot clinical trials have proven that low to intermediate NETs can be effectively controlled via targeted therapies. The PROMID study demonstrated that octreotide LAR can delay tumor growth in low grade midgut NETs, CLARINET study showed the benefits of lanreotide in grade 2 tumors in the gastrointestinal (GI) tract, RADIANT study established the immunosuppressant drug everolimus as an effective therapy for lung and GI NETs and SUN1111 trial recognized sunitinib as a therapy for the advanced pancreatic NETs. Furthermore, carcinoid syndrome therapy, arising from hormones and neuroamnies secreted NETs and prophylaxis from the carcinoid crisis are also discussed.

Ongoing and planned fundamental studies for targeted therapies in NETs may widen their therapeutic applications, while the development of rational combinations may further improve their therapeutic outcome. These successes and the improved understanding of the underlying genetic and immunologic background are likely to lead to further important advances on the horizon.

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