Bicalutamide and Third-Generation Aromatase Inhibitors in Testotoxicosis

Author:

Lenz Anne M.1,Shulman Dorothy1,Eugster Erica A.2,Rahhal Samar3,Fuqua John S.2,Pescovitz Ora H.4,Lewis Katherine A.2

Affiliation:

1. Department of Pediatric Endocrinology, Diabetes and Metabolism, All Children's Hospital and University of South Florida, St Petersburg, Florida;

2. Section of Pediatric Endocrinology, James Whitcomb Riley Hospital for Children, Indiana University, Indianapolis, Indiana;

3. Department of Pediatric Endocrinology, Peyton Manning Children's Hospital at St Vincent, Indianapolis, Indiana; and

4. Department of Pediatrics, University of Michigan, Ann Arbor, Michigan

Abstract

Testotoxicosis, a form of gonadotropin-independent precocious puberty, results from an activating mutation of the luteinizing hormone receptor expressed in testicular Leydig cells. Affected males experience early testosterone secretion, virilization, advancing bone age, and resultant short stature. Recently, the use of combination therapy with a potent antiandrogen agent (bicalutamide) and a third-generation aromatase inhibitor (anastrozole or letrozole) was reported to yield encouraging short-term results. We present here the results of longer-term treatment (4.5 and 5 years) with this combination therapy in 2 boys who demonstrated that it is well tolerated, slows bone-age advancement in the face of continued linear growth, and prevents progression of virilization.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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