Response to Ovarian Stimulation for Urgent Fertility Preservation before Gonadotoxic Treatment in BRCA-Pathogenic-Variant-Positive Breast Cancer Patients

Author:

El Moujahed Lina1,Philis Robin2,Grynberg Michael12ORCID,Laot Lucie1,Mur Pauline1,Amsellem Noemi1,Mayeur Anne3,Benoit Alexandra1,Rakrouki Sophia2,Sifer Christophe4,Peigné Maeliss2ORCID,Sonigo Charlotte156

Affiliation:

1. Department of Reproductive Medicine and Fertility Preservation, Université Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Antoine Beclere Hospital, 92140 Clamart, France

2. Department of Reproductive Medicine and Fertility Preservation, Université Sorbonne Paris Nord, Assistance Publique-Hôpitaux de Paris, Jean Verdier Hospital, 93143 Bondy, France

3. Service de Biologie de la Reproduction—CECOS, Université Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Antoine Beclere Hospital, 92140 Clamart, France

4. Department of Biology of Reproduction and CECOS, Université Sorbonne Paris Nord, Assistance Publique-Hôpitaux de Paris, Jean Verdier Hospital, 93143 Bondy, France

5. Inserm, Physiologie et Physiopathologie Endocrinienne, Université Paris-Saclay, 94276 Le Kremlin-Bicêtre, France

6. Department of Reproductive Medicine, Hôpital Antoine Béclère, 157 Avenue de la Porte Trivaux, 92140 Clamart, France

Abstract

BRCA 1/2 pathogenic variants increase the risk of developing early and aggressive breast cancers (BC). For these patients, fertility potential can be directly affected by oncologic treatments. In addition, evidence indicates that BRCA-mutated women had a significant reduction in their ovarian reserve. In order to improve their chances of conception after the completion of cancer treatments, fertility preservation should be proposed before the administration of gonadotoxic drugs, ideally by oocyte vitrification after controlled ovarian hyperstimulation (COH). The present investigation aims to assess the ovarian response to COH in BRCA 1/2-pathogenic-variant carriers diagnosed with BC. Patient characteristics and COH outcomes were compared between BRCA-positive (n = 54) and BRCA-negative (n = 254) patients. The number of oocytes recovered did not differ between the two groups. However, the oocyte maturation rate and the number of mature oocytes obtained (7 (4.5–11.5) vs. 9 (5–14) oocytes, p = 0.05) were significantly lower in the BRCA-mutated patients. Although individualized COH protocols should be discussed, BRCA-mutated patients would benefit from FP before BC occurs, in order to cope with the potential accelerated decline of their ovarian reserve, optimize the success rate of FP by repeating COH cycles, and to preserve the feasibility of PGT-M by collecting a large amount of eggs.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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