Nonhormonal therapy for endometriosis: a randomized, placebo-controlled, pilot study of cabergoline versus norethindrone acetate

Amy D DiVasta, Catherine Stamoulis, Jenny Sadler Gallagher, Marc R Laufer, Raymond Anchan, Mark D Hornstein, Amy D DiVasta, Catherine Stamoulis, Jenny Sadler Gallagher, Marc R Laufer, Raymond Anchan, Mark D Hornstein

Abstract

Objective: To estimate the efficacy and safety of a novel nonhormonal therapeutic agent, cabergoline, compared with that of the standard clinical therapy, norethindrone acetate (NETA), for the treatment of endometriosis-associated pain in young women with endometriosis.

Design: Randomized, double-blind, placebo-controlled pilot study.

Setting: Tertiary care center.

Patients: Women (n = 9) with surgically confirmed endometriosis.

Interventions: A random, double-blind assignment to either NETA (5 mg/day) + placebo twice weekly or cabergoline (0.5 mg) twice weekly + placebo daily for 6 months.

Main outcome measures: We collected the measures of pelvic pain and laboratory parameters every 3 months.

Results: We observed a decrease in pain scores and increase in pain relief in women randomized to receive cabergoline, who appeared to show similar or more improvements than women treated with NETA. The serum measures of vascular endothelial growth factor receptor 1 declined over 6 months in those who received cabergoline. Cabergoline was well tolerated, and no serious adverse events occurred.

Conclusions: Safe, effective adjunct treatments are lacking for patients with endometriosis who do not respond to standard care. Because the growth of endometriosis requires angiogenesis, blood vessel growth is an attractive therapeutic target. This pilot study suggests that cabergoline, a vascular endothelial growth factor pathway inhibitor, is an effective therapeutic option for women with chronic pain due to endometriosis. Building upon this investigation, we will conduct larger, randomized trials of cabergoline, advancing research on the best treatments for endometriosis-particularly disease resistant to hormonal therapies.

Clinical trial registration number: clinicaltrials.gov; registration number NCT02542410.

Keywords: Angiogenesis; cabergoline; endometriosis; nonhormonal therapy; norethindrone acetate.

© 2021 The Authors.

Figures

Figure 1
Figure 1
Changes in the measurement of pain over 6 months in 9 women randomized to receive either cabergoline or NETA. (A) Pain severity score today. (B) Worst pain severity score in the last 24 hours. (C) Average pain severity score. (D) Worst pain severity score in the last month. NETA = norethindrone acetate.
Figure 2
Figure 2
Changes in the measurement of VEGF-R1 over 6 months in 9 women randomized to receive either cabergoline or NETA. NETA = norethindrone acetate; VEGF-R1 = vascular endothelial growth factor receptor 1.
Supplemental Figure 1
Supplemental Figure 1
Patient recruitment, enrollment, and disposition.

References

    1. Zondervan K.T., Becker C.M., Missmer S.A. Endometriosis. N Engl J Med. 2020;382:1244–1256.
    1. Taylor H.S., Kotlyar A.M., Flores V.A. Endometriosis is a chronic systemic disease: clinical challenges and novel innovations. Lancet. 2021;397:839–852.
    1. ACOG Committee Opinion. Number 310, April 2005. Endometriosis in adolescents. Obstet Gynecol. 2005;105:921–927.
    1. Nothnick W., Alali Z. Recent advances in the understanding of endometriosis: the role of inflammatory mediators in disease pathogenesis and treatment. F1000Research. 2016;5
    1. Nnoaham K.E., Hummelshoj L., Webster P., d’Hooghe T., de Cicco Nardone F., de Cicco Nardone C., et al. Impact of endometriosis on quality of life and work productivity: a multicenter study across ten countries. Fertil Steril. 2011;96:366–373.
    1. Hoshiai H., Ishikawa M., Sawatari Y., Noda K., Fukaya T. Laparoscopic evaluation of the onset and progression of endometriosis. Am J Obstet Gynecol. 1993;169:714–719.
    1. Thomas E.J., Cooke I.D. Impact of gestrinone on the course of asymptomatic endometriosis. Br Med J (Clin Res Ed) 1987;294:272–274.
    1. Ozkan S., Arici A. Advances in treatment options of endometriosis. Gynecol Obstet Invest. 2009;67:81–91.
    1. Youngster M., Laufer M.R., Divasta A.D. Endometriosis for the primary care physician. Curr Opin Pediatr. 2013;25:454–462.
    1. Gallagher J.S., Missmer S.A., Hornstein M.D., Laufer M.R., Gordon C.M., DiVasta A.D. Long-term effects of gonadotropin-releasing hormone agonists and add-back in adolescent endometriosis. J Pediatr Adolesc Gynecol. 2018;31:376–381.
    1. Parazzini F., Fedele L., Busacca M., Falsetti L., Pellegrini S., Venturini P.L., et al. Postsurgical medical treatment of advanced endometriosis: results of a randomized clinical trial. Am J Obstet Gynecol. 1994;171:1205–1207.
    1. Hornstein M.D., Hemmings R., Yuzpe A.A., Heinrichs W.L. Use of nafarelin versus placebo after reductive laparoscopic surgery for endometriosis. Fertil Steril. 1997;68:860–864.
    1. Telimaa S., Puolakka J., Rönnberg L., Kauppila A. Placebo-controlled comparison of danazol and high-dose medroxyprogesterone acetate in the treatment of endometriosis. Gynecol Endocrinol. 1987;1:13–23.
    1. Becker C.M., Gattrell W.T., Gude K., Singh S.S. Reevaluating response and failure of medical treatment of endometriosis: a systematic review. Fertil Steril. 2017;108:125–136.
    1. Shifren J.L., Tseng J.F., Zaloudek C.J., Ryan I.P., Meng Y.G., Ferrara N., et al. Ovarian steroid regulation of vascular endothelial growth factor in the human endometrium: implications for angiogenesis during the menstrual cycle and in the pathogenesis of endometriosis. J Clin Endocrinol Metab. 1996;81:3112–3118.
    1. Asante A., Taylor R.N. Endometriosis: the role of neuroangiogenesis. Annu Rev Physiol. 2011;73:163–182.
    1. Taylor R.N., Hummelshoj L., Stratton P., Vercellini P. Pain and endometriosis: etiology, impact, and therapeutics. Middle East Fertil Soc J. 2012;17:221–225.
    1. Walsh D.A., Pearson C.I. Angiogenesis in pathogenesis of inflammatory joint and lung diseases. Arthritis Res. 2001;3:147–153.
    1. Nap A.W., Griffioen A.W., Dunselman G.A., Bouma-Ter Steege J.C., Thijssen V.L., Evers J.L., et al. Antiangiogenesis therapy for endometriosis. J Clin Endocrinol Metab. 2004;89:1089–1095.
    1. Eremina V., Jefferson J.A., Kowalewska J., Hochster H., Haas M., Weisstuch J., et al. VEGF inhibition and renal thrombotic microangiopathy. N Engl J Med. 2008;358:1129–1136.
    1. Elice F., Rodeghiero F. Side effects of anti-angiogenic drugs. Thromb Res. 2012;129:S50–S53.
    1. Basu S., Sarkar C., Chakroborty D., Nagy J., Mitra R.B., Dasgupta P.S., et al. Ablation of peripheral dopaminergic nerves stimulates malignant tumor growth by inducing vascular permeability factor/vascular endothelial growth factor-mediated angiogenesis. Cancer Res. 2004;64:5551–5555.
    1. Basu S., Nagy J.A., Pal S., Vasile E., Eckelhoefer I.A., Bliss V.S., et al. The neurotransmitter dopamine inhibits angiogenesis induced by vascular permeability factor/vascular endothelial growth factor. Nat Med. 2001;7:569–574.
    1. Robert E., Musatti L., Piscitelli G., Ferrari C.I. Pregnancy outcome after treatment with the ergot derivative, cabergoline. Reprod Toxicol. 1996;10:333–337.
    1. Ricci E., Parazzini F., Motta T., Ferrari C.I., Colao A., Clavenna A., et al. Pregnancy outcome after cabergoline treatment in early weeks of gestation. Reprod Toxicol. 2002;16:791–793.
    1. Colao A., Abs R., Bárcena D.G., Chanson P., Paulus W., Kleinberg D.L. Pregnancy outcomes following cabergoline treatment: extended results from a 12-year observational study. Clin Endocrinol (Oxf) 2008;68:66–71.
    1. Delgado-Rosas F., Gómez R., Ferrero H., Gaytan F., Garcia-Velasco J., Simón C., et al. The effects of ergot and non-ergot-derived dopamine agonists in an experimental mouse model of endometriosis. Reproduction. 2011;142:745–755.
    1. Gómez R., Abad A., Delgado F., Tamarit S., Simón C., Pellicer A., et al. Effects of hyperprolactinemia treatment with the dopamine agonist quinagolide on endometriotic lesions in patients with endometriosis-associated hyperprolactinemia. Fertil Steril. 2011;95:882–888.e1.
    1. Dworkin R.H., Turk D.C., Wyrwich K.W., Beaton D., Cleeland C.S., Farrar J.T., et al. Interpreting the clinical importance of treatment outcomes in chronic pain clinical trials: IMMPACT recommendations. J Pain. 2008;9:105–121.
    1. Howard F.M. Laparoscopic evaluation and treatment of women with chronic pelvic pain. J Am Assoc Gynecol Laparosc. 1994;1:325–331.
    1. Keller S., Bann C.M., Dodd S.L., Schein J., Mendoza T.R., Cleeland C.S. Validity of the brief pain inventory for use in documenting the outcomes of patients with noncancer pain. Clin J Pain. 2004;20:309–318.
    1. Cleeland C.S., Ryan K.M. Pain assessment: global use of the Brief Pain Inventory. Ann Acad Med Singapore. 1994;23:129–138.
    1. Beck A.T., Brown G., Steer R.A. The Psychological Corporation; San Antonio, TX: 1996. Beck depression inventory II manual.
    1. Dworkin R.H., Corbin A.E., Young J.P., Sharma U., LaMoreaux L., Bockbrader H., et al. Pregabalin for the treatment of postherpetic neuralgia: a randomized, placebo-controlled trial. Neurology. 2003;60:1274–1283.
    1. Wernicke J.F., Pritchett Y.L., D’Souza D.N., Waninger A., Tran P., Iyengar S., et al. A randomized controlled trial of duloxetine in diabetic peripheral neuropathic pain. Neurology. 2006;67:1411–1420.
    1. Kashikar-Zuck S., Flowers S.R., Claar R.L., Guite J.W., Logan D.E., Lynch-Jordan A.M., et al. Clinical utility and validity of the functional disability inventory among a multicenter sample of youth with chronic pain. Pain. 2011;152:1600–1607.
    1. Pupo-Nogueira A., de Oliveira R.M., Petta C.A., Podgaec S., Dias J.A., Abrao M.S. Vascular endothelial growth factor concentrations in the serum and peritoneal fluid of women with endometriosis. Int J Gynaecol Obstet. 2007;99:33–37.
    1. Gagne D., Gagné D., Pagé M., Robitaille G., Hugo P., Gosselin D. Levels of vascular endothelial growth factor (VEGF) in serum of patients with endometriosis. Hum Reprod. 2003;18:1674–1680.
    1. Othman E.E., Hornung D., Salem H.T., Khalifa E.A., El-Metwally T.H., Al-Hendy A. Serum cytokines as biomarkers for nonsurgical prediction of endometriosis. Eur J Obstet Gynecol Reprod Biol. 2008;137:240–246.
    1. Xavier P., Belo L., Beires J., Rebelo I., Martinez-de-Oliveira J., Lunet N., et al. Serum levels of VEGF and TNF-alpha and their association with C-reactive protein in patients with endometriosis. Arch Gynecol Obstet. 2006;273:227–231.
    1. Vodolazkaia A., El-Aalamat Y., Popovic D., Mihalyi A., Bossuyt X., Kyama C.M., et al. Evaluation of a panel of 28 biomarkers for the non-invasive diagnosis of endometriosis. Hum Reprod. 2012;27:2698–2711.
    1. Cho S.H., Oh Y.J., Nam A., Kim H.Y., Park J.H., Kim J.H., et al. Evaluation of serum and urinary angiogenic factors in patients with endometriosis. Am J Reprod Immunol. 2007;58:497–504.
    1. Ferrero S., Ragni N., Remorgida V. Antiangiogenic therapies in endometriosis. Br J Pharmacol. 2006;149:133–135.
    1. McLaren J., Prentice A., Charnock-Jones D.S., Smith S.K. Vascular endothelial growth factor (VEGF) concentrations are elevated in peritoneal fluid of women with endometriosis. Hum Reprod. 1996;11:220–223.
    1. Kalu E., Sumar N., Giannopoulos T., Patel P., Croucher C., Sherriff E., et al. Cytokine profiles in serum and peritoneal fluid from infertile women with and without endometriosis. J Obstet Gynaecol Res. 2007;33:490–495.
    1. Rathore N., Kriplani A., Yadav R.K., Jaiswal U., Netam R. Distinct peritoneal fluid ghrelin and leptin in infertile women with endometriosis and their correlation with interleukin-6 and vascular endothelial growth factor. Gynecol Endocrinol. 2014;30:671–675.
    1. Kianpour M., Nematbakhsh M., Ahmadi S.M., Jafarzadeh M., Hajjarian M., Pezeshki Z., et al. Serum and peritoneal fluid levels of vascular endothelial growth factor in women with endometriosis. Int J Fertil Steril. 2013;7:96–99.
    1. Wang H., Gorpudolo N., Li Y., Feng D., Wang Z., Zhang Y. Elevated vascular endothelia growth factor-A in the serum and peritoneal fluid of patients with endometriosis. J Huazhong Univ Sci Technolog Med Sci. 2009;29:637–641.
    1. Küpker W., Schultze-Mosgau A., Diedrich K. Paracrine changes in the peritoneal environment of women with endometriosis. Hum Reprod Update. 1998;4:719–723.
    1. Novella-Maestre E., Carda C., Ruiz-Sauri A., Garcia-Velasco J.A., Simon C., Pellicer A. Identification and quantification of dopamine receptor 2 in human eutopic and ectopic endometrium: a novel molecular target for endometriosis therapy. Biol Reprod. 2010;83:866–873.
    1. Santoro L., D’Onofrio F., Flore R., Gasbarrini A., Santoliquido A., D’Onofrio F., et al. Endometriosis and atherosclerosis: what we already know and what we have yet to discover. Am J Obstet Gynecol. 2015;213:326–331.
    1. Donnez J., Binda M.M., Donnez O., Dolmans M.M. Oxidative stress in the pelvic cavity and its role in the pathogenesis of endometriosis. Fertil Steril. 2016;106:1011–1017.
    1. Mu F., Harris H.R., Rich-Edwards J.W., Hankinson S.E., Rimm E.B., Spiegelman D., et al. A prospective study of inflammatory markers and risk of endometriosis. Am J Epidemiol. 2018;187:515–522.
    1. Mahnke J.L., Dawood M.Y., Huang J.C. Vascular endothelial growth factor and interleukin-6 in peritoneal fluid of women with endometriosis. Fertil Steril. 2000;73:166–170.
    1. Novella-Maestre E., Carda C., Noguera I., Ruiz-Saurí A., García-Velasco J.A., Simón C., et al. Dopamine agonist administration causes a reduction in endometrial implants through modulation of angiogenesis in experimentally induced endometriosis. Hum Reprod. 2009;24:1025–1035.
    1. As-Sanie S., Soliman A.M., Evans K., Erpelding N., Lanier R., Katz N.P. Healthcare utilization and cost burden among women with endometriosis by opioid prescription status in the first year after diagnosis: a retrospective claims database analysis. J Med Econ. 2020;23:371–377.
    1. Steele A. Opioid use and depression in chronic pelvic pain. Obstet Gynecol Clin North Am. 2014;41:491–501.

Source: PubMed

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