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Randomized Controlled Trial
. 2013 Mar 1;31(7):903-9.
doi: 10.1200/JCO.2012.42.8185. Epub 2012 Nov 5.

Gonadotropin-releasing hormone agonist for the prevention of chemotherapy-induced ovarian failure in patients with lymphoma: 1-year follow-up of a prospective randomized trial

Affiliations
Randomized Controlled Trial

Gonadotropin-releasing hormone agonist for the prevention of chemotherapy-induced ovarian failure in patients with lymphoma: 1-year follow-up of a prospective randomized trial

Isabelle Demeestere et al. J Clin Oncol. .

Abstract

Purpose: To assess the efficacy of gonadotropin-releasing hormone agonist (GnRHa) in preventing chemotherapy-induced ovarian failure in patients treated for Hodgkin or non-Hodgkin lymphoma within the setting of a multicenter, randomized, prospective trial.

Patients and methods: Patients age 18 to 45 years were randomly assigned to receive either the GnRHa triptorelin plus norethisterone (GnRHa group) or norethisterone alone (control group) concomitantly with alkylating agents containing chemotherapy. The primary end point was the premature ovarian failure (POF) rate (follicle-stimulating hormone [FSH] ≥ 40 IU/L) after 1 year of follow-up.

Results: Eighty-four of 129 randomly assigned patients completed the 1-year follow-up. The mean FSH values were higher in the control group than in the GnRHa group during chemotherapy; however, this difference was no longer observed after 6 months of follow-up. After 1 year, 20% and 19% of patients in the GnRHa and control groups, respectively, exhibited POF (P = 1.00). More than half of patients in each group completely restored their ovarian function (FSH < 10 IU/L), but the anti-Müllerian hormone values were higher in the GnRHa group than in the control group (1.4 ± 0.35 v 0.5 ± 0.15 ng/mL, respectively; P = .040). The occurrence of adverse events was similar in both groups with the exception of metrorrhagia, which was more frequently observed in the control group than the GnRHa group (38.4% v 15.6%, respectively; P = .024).

Conclusion: Approximately 20% of patients in both groups exhibited POF after 1 year of follow-up. Triptorelin was not associated with a significant decreased risk of POF in young patients treated for lymphoma but may provide protection of the ovarian reserve.

Trial registration: ClinicalTrials.gov NCT01160315.

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Comment in

  • GnRH agonist for the prevention of chemotherapy-induced ovarian failure in lymphoma.
    Blumenfeld Z, Dann E. Blumenfeld Z, et al. J Clin Oncol. 2013 Oct 10;31(29):3721. doi: 10.1200/JCO.2012.47.8222. Epub 2013 Sep 3. J Clin Oncol. 2013. PMID: 24002509 No abstract available.
  • Reply to Z. Blumenfeld et al.
    Demeestere I, Brice P, Peccatori FA, Kentos A, Gaillard I, Zachee P, Casasnovas O, Van Den Neste E, Dechene J, De Maertelaer V, Bron D, Englert Y. Demeestere I, et al. J Clin Oncol. 2013 Oct 10;31(29):3722-3. doi: 10.1200/JCO.2013.50.7129. Epub 2013 Sep 3. J Clin Oncol. 2013. PMID: 24002513 No abstract available.

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