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J Gynecol Obstet Hum Reprod ; 50(5): 102035, 2021 May.
Article in English | MEDLINE | ID: mdl-33307239

ABSTRACT

BACKGROUND: Progress in oncology has improved patient survival. However, cancer chemotherapy can be gonadotoxic and affect their fertility. Recourse to fertility preservation before starting these treatments is therefore necessary in order to allow a better life quality after survival. The aim of this work was to study the impact of chemotherapy on ovarian reserve by AMH measurement. METHODS: This is a descriptive and longitudinal study from 2015 to 2018 carried out at Aziza Othmana hospital ART center in Tunis on patient aged less than 41 years who were candidates for fertility preservation. Patients included had AMH measurement prior to cancer treatment. We called them back to follow up the AMH level after chemotherapy. The AMH assay was performed by electrochemilumiescence technique. At the end, only 66 patients met the inclusion criteria. RESULTS: The most frequent pathologies were Hodgkin's lymphoma and breast cancer. The mean age of patients was 26.7 ± 6.8. The most used chemotherapy protocols were BEACOPP, ABVD or the combination of both in lymphoma and FEC + TXT for breast cancer treatment. A significant difference between AMH before and after chemotherapy was found for BEACOPP and FEC + TXT protocols (p < 10 3). The patient's age was correlated with the AMH decrease after chemotherapy (r = 0.577, p < 10 3). CONCLUSION: Our results showed that the high risk gonadotoxicity protocols were BEACOPP for lymphoma treatment and FEC + TXT for breast cancer treatment. However, studies with a larger sample and more time extended monitoring are necessary for a better gonadotoxicity understanding of the cancer treatments available today.


Subject(s)
Anti-Mullerian Hormone/analysis , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Breast Neoplasms/drug therapy , Fertility Preservation , Hodgkin Disease/drug therapy , Ovarian Reserve/drug effects , Adolescent , Adult , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bleomycin/adverse effects , Bleomycin/therapeutic use , Cyclophosphamide/adverse effects , Cyclophosphamide/therapeutic use , Dacarbazine/adverse effects , Dacarbazine/therapeutic use , Docetaxel/adverse effects , Docetaxel/therapeutic use , Doxorubicin/adverse effects , Doxorubicin/therapeutic use , Epirubicin/adverse effects , Epirubicin/therapeutic use , Etoposide/adverse effects , Etoposide/therapeutic use , Female , Fluorouracil/adverse effects , Fluorouracil/therapeutic use , Humans , Longitudinal Studies , Luminescent Measurements/methods , Ovarian Reserve/physiology , Prednisone/adverse effects , Prednisone/therapeutic use , Procarbazine/adverse effects , Procarbazine/therapeutic use , Vinblastine/adverse effects , Vinblastine/therapeutic use , Vincristine/adverse effects , Vincristine/therapeutic use , Young Adult
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