Skip to main content

Advertisement

Log in

Retrospective comparison of cabergoline and bromocriptine effects in hyperprolactinemia: a single center experience

  • Original Article
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

Abstract

Introduction

Patients with hyperprolactinemia who require medical therapy are typically treated with dopamine agonists (DAs). In most cases, DAs normalize prolactin levels, control symptoms, and substantially decrease tumor size. Here, we aimed to compare the efficacy of cabergoline (CAB) and bromocriptine (BRC) in patients with hyperprolactinemia at a single center.

Methods

Retrospective analysis of the clinical records of 498 patients with hyperprolactinemia [mean age 33.3 ± 10.8 years (range 16–66), 450 women, and 48 men] who had received either CAB (n = 450) or BRC (n = 48) was performed.

Results

The mean age, gender distribution, and treatment duration were similar between the CAB and BRC groups (33.2 ± 11 vs. 34.1 ± 9.6 years, male/female 44/406 vs. 4/44, 18.7 ± 12.1 vs. 17.8 ± 6.0 months, respectively; p > 0.05 for all). Mean dosage was 1.5 ± 1.6 mg/week for CAB and 3.8 ± 2.7 mg/day for BRC. Baseline prolactin levels, frequency of galactorrhea, amenorrhea, oligomenorrhea, erectile dysfunction, infertility, and visual impairment were similar between the two groups, whereas the baseline tumor volume was higher in the CAB group. The prolactin normalization rate (87.4 vs. 41.4 %, p = 0.029) and tumor volume shrinkage (79.8 ± 39.1 vs. 54.1 ± 55.3 %, p = 0.015) were significantly higher in the CAB-treated patients than in the BRC-treated patients, while the tumor cure rates were similar. Symptom relief was higher in the CAB group than in the BRC group. More side effects were recorded in patients who took BRC (29.1 vs. 5.3 %, p < 0.001).

Conclusion

Our data revealed that CAB was more effective than BRC in controlling symptoms associated with hormone excess, normalizing serum prolactin levels, and shrinking prolactinomas.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Schlechte JA (2003) Clinical practice: prolactinoma. N Engl J Med 349:2035–2041

    Article  CAS  PubMed  Google Scholar 

  2. Daly AF, Rixhon M, Adam C, Dempegioti A, Tichomirowa MA, Beckers A (2006) High prevalence of pituitary adenomas: a cross-sectional study in the province of Liege, Belgium. J Clin Endocrinol Metab 91:4769–4775

    Article  CAS  PubMed  Google Scholar 

  3. Fernandez A, Karavitaki N, Wass JA (2010) Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK). Clin Endocrinol Oxf 72:377–382

    Article  PubMed  Google Scholar 

  4. Gillam MP, Molitch ME, Lombardi G, Colao A (2006) Advances in the treatment of prolactinomas. Endocr Rev 27:485–534

    Article  CAS  PubMed  Google Scholar 

  5. Maurer RA (1980) Dopaminergic inhibition of prolactin synthesis and prolactin messenger RNA accumulation in cultured pituitary cells. J Biol Chem 255:8092–8097

    CAS  PubMed  Google Scholar 

  6. Molitch ME (1999) Medical treatment of prolactinomas. Endocrinol Metab Clin N Am 28:143–169

    Article  CAS  Google Scholar 

  7. Pellegrini I, Rasolonjanahary R, Gunz G, Bertrand P, Delivet S, Jedynak CP, Kordon C, Peillon F, Jaquet P, Enjalbert A (1989) Resistance to bromocriptine in prolactinomas. J Clin Endocrinol Metab 69:500–509

    Article  CAS  PubMed  Google Scholar 

  8. Colao A, Di Sarno A, Sarnacchiaro F, Ferone D, Di Renzo G, Merola B, Annunziato L, Lombardi G (1997) Prolactinomas resistant to standard dopamine agonists respond to chronic cabergoline treatment. J Clin Endocrinol Metab 82:876–883

    Article  CAS  PubMed  Google Scholar 

  9. Verhelst J, Abs R, Maiter D, van den Bruel A, Vandeweghe M, Velkeniers B, Mockel J, Lamberigts G, Petrossians P, Coremans P, Mahler C, Stevenaert A, Verlooy J, Raftopoulos C, Beckers A (1999) Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients. J Clin Endocrinol Metab 84:2518–2522

    Article  CAS  PubMed  Google Scholar 

  10. Webster J (1999) Dopamine agonist therapy in hyperprolactinemia. J Reprod Med 44:1105–1110

    CAS  PubMed  Google Scholar 

  11. Del Dotto P, Bonuccelli U (2003) Clinical pharmacokinetics of cabergoline. Clin Pharmacok 42:633–645

    Article  Google Scholar 

  12. Serri O, Chik CL, Ur Ehud, Ezzat S (2003) Diagnosis and management of hyperprolactinemia. Can Med Ass J 169:575–581

    Google Scholar 

  13. Liu JK, Coldwell WT (2004) Contemporary management of prolactinomas. Neurosurg Focus 16:E2

    PubMed  Google Scholar 

  14. Webster J, Piscitelli G, Polli A, Ferrari CI, Ismail I, Scanlon MF (1994) A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhoea. Cabergoline comparative study group. N Engl J Med 331:904–909

    Article  CAS  PubMed  Google Scholar 

  15. Pascal- Vigneron V, Weryha G, Bosc M, Lectere J (1995) Hyperprolactinemic amenorrhea: treatment with cabergoline vs bromocriptine. Results of a national multicenter randomized double blind study. Press Med 24:753–757

    CAS  Google Scholar 

  16. Sabuncu T, Arikan E, Tasan E, Hatemi H (2001) Comparison of the effects of cabergoline and bromocriptine on prolactin levels in hyperprolactinemic patients. Intern Med 40:857–861

    Article  CAS  PubMed  Google Scholar 

  17. Al-Huseynei A, Mahmood IH, Al-Jubori ZS (2008) Comparison of the effects of cabergoline and bromocriptine in women with hyperprolactinemic amenorrhea. Middle East Fertile Soc J 13:33–88

    Google Scholar 

  18. Ferrari C, Paracchi A, Mattei AM, de Vincentiis S, D’Alberton A, Crosignani P (1992) Cabergoline in the long term therapy of hyperprolactinemic disorders. Arch Endocrinol (Copenh) 126:489–494

    CAS  Google Scholar 

  19. Biller BM, Molitch ME, Vance ML, Cannistraro KB, Davis KR, Simons JA, Schoenfelder JR, Klibanski A (1996) Treatment of prolactin secreting macroadenomas with the once-weekly dopamine agonist cabergoline. J Clin Endocrinol Meta 81:2338–2343

    CAS  Google Scholar 

  20. Colao A, Di Sarno A, Landi ML, Scavuzzo F, Cappabianca P, Pivonello R, Volpe R, Di Salle F, Cirillo S, Annunziato L, Lombardi G (2000) Macroprolactinoma shrinkage during cabergoline treatment is greater in naïve patients than in patients pretreated with other dopamine agonists: a prospective study in 110 patients. J Clin Endocrin Metab 85:2247–2252

    CAS  Google Scholar 

  21. Tartagni M, Nicastri PL, Diaferia A, Di Gesù I, Loizzi P (1995) Long term follow-up of women with amenorrhea-galactorrhea treated with bromocriptine. Clin Exp Obstet Gynecol 22:301–306

    CAS  PubMed  Google Scholar 

  22. Van der Heijden PF, de Wit W, Brownell J, Rolland R (1991) CV 205-502, a new dopamine agonist, versus bromocriptine in the treatment of hyperprolactinaemia. Eur J Obstet Gynecol Reprod Biol 40:111–118

    Article  PubMed  Google Scholar 

  23. Al-Suleiman SA, Najashi S, Rahman J (1989) Outcome of treatment with bromocriptine in patients with hyperprolactinaemia. Aust NZ J Obstet Gynaecol 29:176–179

    Article  CAS  Google Scholar 

  24. Molitch ME, Elton RL, Blackwell RE, Caldwell B, Chang RJ, Jaffe R, Joplin G, Robbins RJ, Tyson J, Thorner MO (1985) Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study. J Clin Endocrinol Metab 60:698–705

    Article  CAS  PubMed  Google Scholar 

  25. Colao A, Vitale G, Cappabianca P, Briganti F, Ciccarelli A, De Rosa M, Zarrilli S, Lombardi G (2004) Outcome of cabergoline treatment in men with prolactinoma: effects of a 24 months treatment on prolactin levels, tumor mass, recovery of pituitary function and semen analysis. J Clin Endocrinol Metab 89:1704–1711

    Article  CAS  PubMed  Google Scholar 

  26. Di Sarno A, Landi ML, Cappabianca P, Di Salle F, Rossi FW, Pivonello R, Di Somma C, Faggiano A, Lombardi G, Colao A (2001) Resistance to cabergoline as compared with bromocriptine in hyperprolactinemia: prevalence, clinical definition, and therapeutic strategy. J Clin Endocrinol Metab 86:5256–5261

    Article  PubMed  Google Scholar 

  27. Bahceci M, Sismanoglu A, Ulug U (2010) Comparison of cabergoline and bromocriptine in patients with asymptomatic incidental hyperprolactinemia undergoing ICSI-ET. Gynecol Endocrinol 26:505–508

    Article  CAS  PubMed  Google Scholar 

Download references

Conflict of interest

The authors declare no conflicting interests.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. Arduc.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Arduc, A., Gokay, F., Isik, S. et al. Retrospective comparison of cabergoline and bromocriptine effects in hyperprolactinemia: a single center experience. J Endocrinol Invest 38, 447–453 (2015). https://doi.org/10.1007/s40618-014-0212-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40618-014-0212-4

Keywords

Navigation