Primary Medical Therapy of Micro- and Macroprolactinomas in Men1
Joseph J. Pinzone,
Laurence Katznelson,
Daniel C. Danila,
Donna K. Pauler,
Caleb S. Miller and
Anne Klibanski
Neuroendocrine Unit and the General Clinical Research Center,
Massachusetts General Hospital and Harvard Medical School, Boston,
Massachusetts 02114
Address all correspondence and requests for reprints to: Anne Klibanski, M.D., Neuroendocrine Unit, Massachusetts General Hospital, 55 Fruit Street, Bulfinch 457, Boston, Massachusetts 02114. E-mail:
aklibanski{at}partners.org
The presentation and long-term therapeutic responses of PRL-secreting
pituitarytumors in men have been only partially studied.
Gender-specificdifferences in tumor size at clinical presentation and
possibledifferences in tumor biology in men compared to women make it
importantto determine treatment outcomes of male patients with
prolactinomas.
We performed a retrospective review of men with prolactinomasmedically
managed at Massachusetts General Hospital between1980 and 1997. We
identified 46 male patients with prolactinomasmanaged with medical
therapy alone. Twelve patients had microadenomas,defined as a serum
PRL level greater than 15 ng/mL and a normalpituitary scan or a tumor
smaller than 1 cm. Thirty-four patientshad macroprolactinomas, defined
by a serum PRL greater than200 ng/mL and pituitary adenoma larger than
1 cm. Bromocriptine,quinagolide, and/or
cabergoline were administered as medicaltherapy. All
patients had at least one follow-up visit, andthe most recent serum
PRL measurement after initiating dopamineagonist therapy was
reported.
Baseline clinical characteristics for patients with macroprolactinomas
andmicroprolactinomas showed a larger proportion of patients with
macroprolactinomasreporting a history of headache (74%
vs. 0%), whereas the prevalenceof sexual dysfunction
and testosterone deficiency was similarbetween the two groups. Median
serum PRL at presentation was99 ng/mL (range, 16385 ng/mL)
vs. 1415 ng/mL (range,38767,900 ng/mL), in the
microprolactinoma and macroprolactinomagroups, respectively.
A normal PRL level was achieved in a similar percentage of menwith
microprolactinomas vs. macroprolactinomas (83%
vs. 79%,respectively). Although the majority of
patients in both groupswere treated with bromocriptine, a
comparable number of patientswith microprolactinomas
vs. macroprolactinomas achieved a normalPRL level with
cabergoline therapy. The response rates for
bromocriptineand cabergoline were similar in
both groups. No patient witha microprolactinoma required hormone
replacement therapy, incontrast to patients with macroprolactinomas,
who required thyroid,testosterone, and/or glucocorticoid replacement
therapy. Nopatient had evidence of an increase in tumor size during
therapy.
In summary, we investigated the clinical presentation and treatment
outcomein men with prolactinomas. We found that normalization of serum
PRLlevels occurs in approximately 80% of men with prolactinomas.Of
importance, dopamine agonist administration yielded similarbiochemical
remission rates in men with microprolactinomas andmacroprolactinomas.
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