Effects of ABVD chemotherapy on ovarian function: epidemiology, hormonal dosages and ultrasound morphologic analyses in 270 patients with Hodgkin's disease.

Anti-Mullerian hormone Hodgkin’s lymphoma early menopause fertility preservation ovarian failure

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2023
Historique:
received: 01 10 2022
accepted: 27 03 2023
medline: 8 5 2023
pubmed: 8 5 2023
entrez: 8 5 2023
Statut: epublish

Résumé

Classical Hodgkin Lymphoma (HL) is a lymphoproliferative disease typically diagnosed in the young. The excellent results obtained with current treatment lead to long survival with age-related complications affecting patients' survival and quality of life. One issue affecting HL patients is infertility. This problem can be easily overcome in males with seminal liquid cryopreservation, however, in females it is more complex either in terms of the quality of the cryopreserved material or the patients' age at diagnosis. Moreover, not all chemo- or radio-therapies have the same negative impact on fertility.The main objectives of this study was to collect epidemiological information on HL patients involved in fertility preservation counseling and to analyze the impact of ABVD (adriamycin, bleomycin, vinblastine, and dacarbazine), the standard treatment for HL, on ovarian function, hormonal levels and ovarian and uterine tissue morphologies. Patterns of fertility preservation were also reported. Data were obtained from 270 female patients at HL onset who were interested in fertility counseling prior to therapy initiation. Each patient was assessed at HL diagnosis for levels of Anti-Mullerian Hormone (AMH), Follicle Stimulating Hormone (FSH), and 17β-oestradiol (17β-oe), with additional assessments at 6 and 12 months after chemotherapy. Patients were evaluated with ultrasound scans to study the number of ovarian follicles and the degree of uterine thickness at the same timepoints. The average patient AMH level showed a statistically significant reduction at 6 months after chemotherapy (p=0.05) and by the 12 month time point returned to near pre-chemotherapy values. FSH and 17β-oe levels did not significantly vary throughout the study period. ABVD chemotherapy was associated with a significant reduction of both ovarian follicles and endometrial thickness at the 6 month time point followed by a recovery at the 12 time point in both ovaries. Different results were observed when patients changed treatment to a more intensive one. Based on the results from the hormonal measurements and the follicle echography, it appears that the toxic effect of ABVD on fertility is transient, whereas, in contrast, more intensive therapies may potentially be more harmful and long-lasting.

Identifiants

pubmed: 37152067
doi: 10.3389/fonc.2023.1059393
pmc: PMC10160490
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1059393

Informations de copyright

Copyright © 2023 Ciccarone, Cavaceppi, Tesei, Brunetti, Pulsoni, Annibali, Gasparoli, Battistini, Hohaus, Pelliccia, Tafuri, Cox, Cantonetti, Rigacci and Abruzzese.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Mariavita Ciccarone (M)

Associazione Gemme Dormienti Organizzazione Non Lucrativa di Utilità Sociale (ONLUS), Rome, Italy.
Gynecologic Unit , San Carlo di Nancy Hospital, Rome, Italy.

Paola Cavaceppi (P)

Associazione Gemme Dormienti Organizzazione Non Lucrativa di Utilità Sociale (ONLUS), Rome, Italy.
LabAurelia, Rome, Italy.

Cristiano Tesei (C)

Associazione Gemme Dormienti Organizzazione Non Lucrativa di Utilità Sociale (ONLUS), Rome, Italy.

Stefania Brunetti (S)

Associazione Gemme Dormienti Organizzazione Non Lucrativa di Utilità Sociale (ONLUS), Rome, Italy.

Alessandro Pulsoni (A)

Department of Cellular Biotechnology and Haematology, Sapienza University, Rome, Italy.

Ombretta Annibali (O)

UOC Haematology Stem Cell Transplantation, University Campus Bio Medico, Rome, Italy.

Cristiano Gasparoli (C)

Laboratory Medicine, San Carlo di Nancy Hospital, Rome, Italy.

Roberta Battistini (R)

UOC Ematologia e Trapianti CSE, Azienda Ospedaliera (AO) San Camillo Forlanini, Rome, Italy.

Stefan Hohaus (S)

Policlinico Gemelli Foundation, Catholic University of the Sacred Heart, Rome, Italy.

Sabrina Pelliccia (S)

Haematology Unit, Azienda Ospedaliera- Universitaria Sant'Andrea, Rome, Italy.

Agostino Tafuri (A)

Haematology Unit, Azienda Ospedaliera- Universitaria Sant'Andrea, Rome, Italy.

Maria Christina Cox (MC)

Hematology, Tor Vergata University Hospital, Rome, Italy.

Maria Cantonetti (M)

Hematology, Tor Vergata University Hospital, Rome, Italy.

Luigi Rigacci (L)

UOC Ematologia e Trapianti CSE, Azienda Ospedaliera (AO) San Camillo Forlanini, Rome, Italy.

Elisabetta Abruzzese (E)

Hematology, S. Eugenio Hospital, Tor Vergata University, ASL Roma2, Rome, Italy.

Classifications MeSH