Recent Progress in the Medical Therapy of Pituitary Tumors
Overview
Affiliations
Management of pituitary tumors is multidisciplinary, with medical therapy playing an increasingly important role. With the exception of prolactin-secreting tumors, surgery is still considered the first-line treatment for the majority of pituitary adenomas. However, medical/pharmacological therapy plays an important role in controlling hormone-producing pituitary adenomas, especially for patients with acromegaly and Cushing disease (CD). In the case of non-functioning pituitary adenomas (NFAs), pharmacological therapy plays a minor role, the main objective of which is to reduce tumor growth, but this role requires further studies. For pituitary carcinomas and atypical adenomas, medical therapy, including chemotherapy, acts as an adjuvant to surgery and radiation therapy, which is often required to control these aggressive tumors. In the last decade, knowledge about the pathophysiological mechanisms of various pituitary adenomas has increased, thus novel medical therapies that target specific pathways implicated in tumor synthesis and hormonal over secretion are now available. Advancement in patient selection and determination of prognostic factors has also helped to individualize therapy for patients with pituitary tumors. Improvements in biochemical and "tumor mass" disease control can positively affect patient quality of life, comorbidities and overall survival. In this review, the medical armamentarium for treating CD, acromegaly, prolactinomas, NFA, and carcinomas/aggressive atypical adenomas will be presented. Pharmacological therapies, including doses, mode of administration, efficacy, adverse effects, and use in special circumstances are provided. Medical therapies currently under clinical investigation are also briefly discussed.
Multiomics Approach to Acromegaly: Unveiling Translational Insights for Precision Medicine.
Kim K, Ku C, Lee E Endocrinol Metab (Seoul). 2023; 38(5):463-471.
PMID: 37828709 PMC: 10613768. DOI: 10.3803/EnM.2023.1820.
Liu J, Wang J, Tian W, Xu Y, Li R, Zhao K Aging (Albany NY). 2022; 14(15):6066-6080.
PMID: 35963638 PMC: 9417224. DOI: 10.18632/aging.204206.
Aggressive prolactinoma (Review).
Valea A, Sandru F, Petca A, Dumitrascu M, Carsote M, Petca R Exp Ther Med. 2021; 23(1):74.
PMID: 34934445 PMC: 8652381. DOI: 10.3892/etm.2021.10997.
Recent Understanding and Future Directions of Recurrent Corticotroph Tumors.
Hinojosa-Amaya J, Lam-Chung C, Cuevas-Ramos D Front Endocrinol (Lausanne). 2021; 12:657382.
PMID: 33986726 PMC: 8111286. DOI: 10.3389/fendo.2021.657382.
Comparative Proteomic Study Shows the Expression of Hint-1 in Pituitary Adenomas.
Carrillo-Najar C, Rembao-Bojorquez D, Tena-Suck M, Zavala-Vega S, Gelista-Herrera N, Ramos-Peek M Diagnostics (Basel). 2021; 11(2).
PMID: 33671384 PMC: 7922225. DOI: 10.3390/diagnostics11020330.