Gonadal Function Recovery in Patients With Advanced Hodgkin Lymphoma Treated With a PET-Adapted Regimen: Prospective Analysis of a Randomized Phase III Trial (AHL2011)

Author:

Demeestere Isabelle1ORCID,Racape Judith2ORCID,Dechene Julie3,Dupuis Jehan4,Morschhauser Franck5ORCID,De Wilde Virginie6,Lazarovici Julien7,Ghesquieres Hervé8,Touati Mohamed9,Sibon David10ORCID,Alexis Magda11,Gac Anne-Claire12,Moatti Hannah13,Virelizier Emmanuelle14,Maisonneuve Hervé15,Pranger Delphine16,Houot Roch17ORCID,Fornecker Luc-Matthieu18ORCID,Tempescul Adrian19,André Marc20,Casasnovas René-Olivier21ORCID

Affiliation:

1. Research Laboratory on Human Reproduction and Fertility Clinic, CUB-Erasme, Université Libre de Bruxelles, Brussels, Belgium

2. Research Center in Epidemiology, Biostatistics and Clinical Research, School of Public Health, and Biomedical Research Department, CUB-Erasme, Université Libre de Bruxelles, Brussels, Belgium

3. Research Laboratory on Human Reproduction, Université Libre de Bruxelles, Brussels, Belgium

4. Department of Haematology, Hopital H. Mondor, Creteil, France

5. Department of Hematology, University of Lille, CHU Lille, EA 7365—GRITA—Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France

6. Department of Haematology, CUB-Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium

7. Department of Haematology Gustave Roussy, Université Paris-Saclay, Villejuif, France

8. Department of Haematology, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, et Université Claude Bernard Lyon-1, Pierre Bénite, France

9. Department of Haematology, CHU Limoges, Limoges, France

10. Department of Haematology, Hopital Necker, Paris, France

11. Department of Haematology, CH Orleans, Orleans, France

12. Department of Haematology, Institut d'hématologie de basse normandie, Caen, France

13. Department of Haematology, APHP, Hopital Saint Louis, Paris, France

14. Department of Haematology, Centre L. Bérard, Lyon, France

15. Department of Haematology, Hopital departemental de Vendée, La Roche sur Yon, France

16. Department of Haematology, Grand Hopital de Charleroi, Charleroi, Belgium

17. Department of Hematology, University Hospital of Rennes, Rennes, France

18. Department of Hematology, University Hospital of Strasbourg, Strasbourg, France

19. Department of Hematology, University Hospital of Brest, Brest, France

20. Department of Haematology, CHU UCL Namur, Université catholique de Louvain, Yvoir, Belgium

21. Department of Haematology, University Hospital F Mitterrand and Inserm UMR1231, Dijon, France

Abstract

PURPOSE The prospective, randomized AHL2011 trial demonstrated that the use of the doxorubicin, bleomycin, vinblastine, and dacarbazine regimen (ABVD) after two cycles of bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPescalated) in early responders on the basis of a positron emission tomography (PET)–driven strategy was safe and minimized toxicity compared with standard 6 BEACOPPescalated cycles. This substudy investigated the benefit of this strategy in gonadal function and fertility in patients under 45 years old. METHODS Ovarian function was assessed by serum measurement of follicle-stimulating hormone (FSH), estradiol, and anti-müllerian hormone in women, and semen analysis, FSH, and testosterone levels were used to evaluate testicular function in men at baseline, end of treatment, and during 5 years of follow-up. RESULTS A total of 145 women and 424 men, enrolled between May 19, 2011, and April 29, 2014, were included. The risk of premature ovarian insufficiency (FSH > 24 IU/L) and of having a low ovarian reserve (anti-müllerian hormone < 0.5 ng/mL) was reduced after treatment in the PET-driven group (odds ratio [OR], 0.20; 95% CI, 0.08 to 0.50; P = .001 and OR, 0.15; 95% CI, 0.04 to 0.56, P = .005, respectively). Both parameters were correlated with age and dose of alkylating agents. However, no significant differences were observed in terms of pregnancy rates. Men in the PET-driven group had a higher recovery rate of sperm parameters after treatment compared with the standard BEACOPPescalated group, as well as a lower risk of severe testicular damage (OR, 0.26; 95% CI, 0.13 to 0.5; P < .0001) and a higher likelihood of achieving pregnancy (OR, 3.7; 95% CI, 1.4 to 9.3; P = .004). CONCLUSION Although both treatments affected ovarian reserve and spermatogenesis, the PET-driven strategy decreased the risk of gonadal dysfunction and infertility in advanced Hodgkin lymphoma.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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