ABVD and BEACOPP regimens' effects on fertility in young males with Hodgkin lymphoma.
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Bleomycin
/ adverse effects
Cyclophosphamide
/ adverse effects
Dacarbazine
/ adverse effects
Doxorubicin
/ adverse effects
Etoposide
/ adverse effects
Fertility
/ drug effects
Hodgkin Disease
/ drug therapy
Humans
Infertility, Male
/ chemically induced
Male
Prednisone
/ adverse effects
Procarbazine
/ adverse effects
Vinblastine
/ adverse effects
Vincristine
/ adverse effects
ABVD
BEACOPP
Fertility
Hodgkin lymphoma
Young males
Journal
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
ISSN: 1699-3055
Titre abrégé: Clin Transl Oncol
Pays: Italy
ID NLM: 101247119
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
21
07
2020
accepted:
31
08
2020
pubmed:
19
9
2020
medline:
15
12
2021
entrez:
18
9
2020
Statut:
ppublish
Résumé
Considering the increased cancer patient survivorship, the focus is now on addressing the impacts of treatment on quality of life. In young people, altered reproductive function is a major issue and its effects in young males are largely neglected by novel research. To improve clinician awareness, we systematically reviewed side effects of chemotherapy for Hodgkin lymphoma (HL) in young males. The review was prospectively registered (PROSPERO N. CRD42019122868). Three databases (Medline via PUBMED, SCOPUS, and Cochrane Library) were searched for studies featuring males aged 13-51-years who underwent chemotherapy for HL using ABVD (Adriamycin® (doxorubicin), bleomycin, vinblastine, and dacarbazine) or BEACOPP (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisolone) regimens. These chemotherapy regimens were compared against each other using sperm characteristics, FSH, and inhibin B levels to measure fertility levels. Data were extracted from five studies featuring 1344 patients. 6 months post-ABVD saw marked deterioration in sperm count, further reduced by more cycles (P = 0.05). Patients treated with BEACOPP rather than ABVD were more prone to oligospermia. Receiving fewer cycles of both regimens increased the likelihood of sperm production recovering. Patients treated with 6-8 cycles of BEACOPP did not recover spermiogenesis. ABVD and BEACOPP regimens significantly reduce fertility function to varying effects depending on treatment duration. ABVD temporarily causes significant reductions in male fertility, whereas BEACOPP's effects are more permanent. Therefore, clinicians should discuss fertility preservation with male patients receiving infertility-inducing gonadotoxic therapy. Further high-quality studies are required to more adequality describe the risk to fertility by chemotherapy.
Identifiants
pubmed: 32944834
doi: 10.1007/s12094-020-02483-8
pii: 10.1007/s12094-020-02483-8
pmc: PMC8084804
doi:
Substances chimiques
Bleomycin
11056-06-7
Procarbazine
35S93Y190K
Vincristine
5J49Q6B70F
Vinblastine
5V9KLZ54CY
Etoposide
6PLQ3CP4P3
Dacarbazine
7GR28W0FJI
Doxorubicin
80168379AG
Cyclophosphamide
8N3DW7272P
Prednisone
VB0R961HZT
Types de publication
Journal Article
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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