Ann Pediatr Endocrinol Metab.  2013 Dec;18(4):173-178. 10.6065/apem.2013.18.4.173.

Multicenter clinical trial of leuprolide acetate depot (Luphere depot 3.75 mg) for efficacy and safety in girls with central precocious puberty

Affiliations
  • 1Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea. pedhwang@ajou.ac.kr
  • 2Department of Pediatrics, Korea University Ansan Hospital, Ansan, Korea.
  • 3Department of Pediatrics, Korea Cancer Center Hospital, Seoul, Korea.
  • 4Department of Pediatrics, Bundang Jesang Hospital, Seongnam, Korea.
  • 5Department of Pediatrics, Chosun University School of Medicine, Gwangju, Korea.
  • 6Department of Pediatrics, Samsung Medical Center, Seoul, Korea.
  • 7Department of Pediatrics, Hallym University Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.

Abstract

PURPOSE
We evaluated the efficacy, safety and psychological aspect of monthly administrations of the gonadotropin-releasing hormone agonists (GnRHa), leuprolide acetate depot (Luphere depot 3.75 mg), in patients with precocious puberty.
METHODS
A total of 54 girls with central precocious puberty were administered with leuprolide acetate (Luphere depot 3.75 mg) every four weeks over 24 weeks. We evaluated the percentage of children exhibiting a suppressed luteinizing hormone (LH) response to GnRH (LH peak< or =3 IU/L), peak LH/follicle stimulating hormone (FSH) ratio of GnRH stimulation test less than 1, change in bone age/chronologic age ratio, change in the Tanner stage and change in eating habit and psychological aspect.
RESULTS
(1) The percentage of children exhibiting a suppressed LH response to GnRH, defined as an LH peak< or =3 IU/L at 24 weeks was 96.3 % (52/54). (2) The percentage of children exhibiting peak LH/FSH ratio<1 at 24 weeks of the study was 94.4 % (51/54). (3) The ratio of bone age and chronological age significantly declined from 1.27+/-0.07 to 1.24+/-0.01 after the 6 months of the study. (4) The mean Tanner stage manifested a significant change 2.3+/-0.48 at baseline, down to 1.70+/-0.61 at 24 weeks. (5) Based on the questionnaires, the score for eating habits showed a significant change from the baseline 34.0+/-6.8 to 31.3+/-6.8. (6) The psychological assessment did not exhibit a significant difference except with scores for sociability, problem behavior total score and other problems.
CONCLUSION
The leuprolide 3.75 mg (Luphere depot) is useful and safety for treating children with central precocious puberty.

Keyword

Leuprolide acetate; Central precocious puberty; Treatment outcome

MeSH Terms

Child
Eating
Female*
Gonadotropin-Releasing Hormone
Humans
Leuprolide*
Luteinizing Hormone
Puberty, Precocious*
Treatment Outcome
Surveys and Questionnaires
Gonadotropin-Releasing Hormone
Leuprolide
Luteinizing Hormone

Figure

  • Fig. 1 Patient disposition. FAS, full analysis set; PPS, per-protocol set.


Cited by  2 articles

Efficacy of Triptorelin 3-Month Depot Compared to 1-Month Depot for the Treatment of Korean Girls with Central Precocious Puberty in Single Tertiary Center
Lindsey Yoojin Chung, Eungu Kang, Hyo-Kyoung Nam, Young-Jun Rhie, Kee-Hyoung Lee
J Korean Med Sci. 2021;36(34):e219.    doi: 10.3346/jkms.2021.36.e219.

Short-term efficacy of 1-month and 3-month gonadotropin-releasing hormone agonist depots in girls with central precocious puberty
Min Jin Jeon, Jae Won Choe, Hye Rim Chung, Jae Hyun Kim
Ann Pediatr Endocrinol Metab. 2021;26(3):171-177.    doi: 10.6065/apem.2040134.067.


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