Abstract
Background
Prolactinomas are the commonest functional tumors of the pituitary gland. There are still controversies regarding medical therapy in specific clinical situations. Patients may be managed by different specialists in the Middle East and North Africa (MENA) region and no data exist on patterns of clinical management.
Objectives
To ascertain the diagnostic and therapeutic approaches to prolactinomas among relevant professionals from the MENA region.
Methods
An online survey of a large sample of physicians was conducted. The questionnaire covered various aspects of diagnosis and treatment of prolactinomas. 468 respondents were included; 36 % were endocrinologists; 49 % worked in public facilities and 81 % graduated more than 10 years. 40 and 30 % would have seen 1–5 and more than 5 suspected or confirmed prolactinomas over a 6 months period, respectively.
Results
Regarding the diagnosis, 30 % of the respondents considered that prolactin levels <100 ng/ml exclude the presence of a prolactinoma. 21 % of respondents considered prolactin levels >250 ng/ml compatible with macroprolactinomas only, whereas others accepted this to be compatible also with microprolactinomas, macroprolactinaemia and drug-induced hyperprolactinemia (50, 42 and 36 % respectively). 71 % of respondents favored the screening for macroprolactin in asymptomatic individuals with hyperprolactinemia. Regarding the treatment, 84 % of respondents would treat microprolactinomas even in the absence of symptoms whereas 72 % of the respondents would treat microprolactinomas only if symptoms exist. 60 and 49 % of the respondents chose cabergoline as the drug of choice to treat macroprolactinomas and microprolactinomas respectively. Similar proportions had no preference of either cabergoline or bromocriptine as the best treatment for macroprolactinoma (27 %) and microprolactinomas (32 %). 46 and 75 % of respondents favored treatment withdrawal 2–3 years after prolactin normalization in patients with macroprolactinomas and microprolactinomas, respectively whereas 10 % of respondents withdraw treatment after menopause in either case. 94 % of respondents considered medical therapy as the primary treatment for microprolactinomas. In case of pregnancy, 49 % considered bromocriptine as the drug of choice for women who wish to become pregnant. 65 and 38 % of respondents advocated discontinuation of treatment with dopamine agonists in patients with microprolactinomas and macroprolactinomas, respectively. Finally, 48 % would allow breast-feeding without restriction, 28 % would restrict it to patients with microprolactinomas and 25 % would not recommend it for women with prolactinomas.
Conclusions
This is the first study of the clinical management of prolactinomas in the MENA region. Some of the practices are not in line with the latest Endocrine and Pituitary Societies guidelines. These warrant further discussions of contemporary guidelines in regional forums.
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References
Glezer A, Bronstein MD (2015) Prolactinomas. Endocrinol Metab Clin North Am 44(1):71–78
Klibanski A (2010) Prolactinomas. N Engl J Med 362:1219–1226
Rogers A, Karavitaki N, Wass JA (2014) Diagnosis and management of prolactinomas and non-functioning pituitary adenomas. BMJ 10(349):g5390
Casanueva FF, Molitch ME, Schlechte JA, Abs R, Bonert V, Bronstein MD et al (2006) Guidelines of the pituitary society for the diagnosis and management of prolactinomas. Clin Endocrinol (Oxf) 65:265–273
Melmed S, Casanueva FF, Hoffman AR, Kleinberg DL, Montori VM, Schlechte JA et al (2011) Diagnosis and treatment of hyperprolactinemia: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 96(2):273–288
Maiter D, Delgrange E (2014) Therapy of endocrine disease: the challenges in managing giant prolactinomas. Eur J Endocrinol 170(6):R213–R227
Tirosh A, Shimon I (2016) Current approach to treatments for prolactinomas. Minerva Endocrinol 41(3):316–323
Vilar L, Naves LA, Casulari LA, Azevedo MF, Albuquerque JL, Serfaty FM et al (2010) Management of prolactinomas in Brazil: an electronic survey. Pituitary 13:199–206
Samson SL, Hamrahian AH, Ezzat S, AACE Neuroendocrine and Pituitary Scientific Committee (2015) American College of Endocrinology (ACE). American Association of Clinical Endocrinologists, American College of Endocrinology disease state clinical review: Clinical relevance of macroprolactin in the absence of or presence of true hyperprolactinaemia. Endocr Pract 21(12):1427–1435
Cuny T, Barlier A, Feelders R, Weryha G, Hofland LJ, Ferone D, Gatto F (2015) Medical therapies in pituitary adenomas: current rationale for the use and future perspectives. Ann Endocrinol (Paris) 76(1):43–58
Hu J, Zheng X, Zhang W, Yang H (2015) Current drug withdrawal strategy in prolactinoma patients treated with cabergoline: a systematic review and meta-analysis. Pituitary 18(5):745–751
Verhelst J, Abs R, Maiter D, Vandeweghe M, Velkeniers B, Mockel J et al (1999) Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients. J Clin Endocrinol Metab 84:2518–2522
Webster J, Piscitelli G, Polli A, Ferrari CI, Ismail I, Scanlon MF (1994) A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. N Engl J Med 331:904–909
Auriemma RS, Pivonello R, Ferreri L, Priscitelli P, Colao A (2015) Cabergoline use for pituitary tumors and valvular disorders. Endocrinol Metab Clin North Am 44(1):89–97
Kreutzer J, Buslei R, Wallaschofski H, Hofmann B, Nimsky C, Fahlbusch R et al (2008) Operative treatment of prolactinomas: indications and results in a current consecutive series of 212 patients. Eur J Endocrinol 158(1):11–18
Babey M, Sahli R, Vajtai I, Andres RH, Seiler RW (2011) Pituitary surgery for small prolactinomas as an alternative to treatment with dopamine agonists. Pituitary 14(3):222–230
Schlechte J, Dolan K, Sherman B, Chapler F, Luciano A (1989) The natural history of untreated hyperprolactinemia: a prospective analysis. J Clin Endocrinol Metab 68:412–418
Biswas M, Smith J, Jadon D, McEwan P, Rees DA, Evans LM et al (2005) Long-term remission following withdrawal of dopamine agonist therapy in subjects with microprolactinomas. Clin Endocrinol (Oxf) 63:26–31
Kharlip J, Salvatori R, Yenokyan G, Wand GS (2009) Recurrence of hyperprolactinemia after withdrawal of long-term cabergoline therapy. J Clin Endocrinol Metab 94:2428–2436
Iacovazzo D, De Marinis L (2015) Treatment of hyperprolactinemia in post-menopausal women: pros. Endocrine 48(1):76–78
Faje AT, Klibanski A (2015) The treatment of hyperprolactinemia in postmenopausal women with prolactin-secreting microadenomas: cons. Endocrine 48(1):79–82
Maiter D (2016) Prolactinoma and pregnancy: from the wish of conception to lactation. Ann Endocrinol 77(2):128–134
Acknowledgments
The authors would like to express their gratitude for all respondents who shared their expertise and opinions by participating in the survey.
Authors’ contribution
SAB adapted and conducted the electronic aspects of the survey. All others contributed to the manuscript and approved its final version.
Funding
This study received no funding whatsoever.
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Conflict of interest
Salem A. Beshyah has received research grants from Novo Nordisk, Eli Lilly, Sanofi and Merck (MSD) and has received speaker’s honoraria from Novartis, Servier, Abbotts, Merck Serono and Boehringer Ingelheim for subjects unrelated to this research. Ibrahim H. Sherif , Farida Chentli, Amir Hamrahian, Aly B. Khalil, Hussein Raef, Mohamed El-Fikki and Selim Jambart declare that they have no conflict of interest.
Ethical approval
This article does not contain any studies with human participants or animals performed by any of the authors. All participants provided an informed explicit consent to participate electronically before they proceed to participation in the survey. All data are collected anonymously.
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Beshyah, S.A., Sherif, I.H., Chentli, F. et al. Management of prolactinomas: a survey of physicians from the Middle East and North Africa. Pituitary 20, 231–240 (2017). https://doi.org/10.1007/s11102-016-0767-5
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DOI: https://doi.org/10.1007/s11102-016-0767-5