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17 January 2022 Preserving Oocytes in Oncofertility
Maria McClam, Shuo Xiao
Author Affiliations +
Abstract

The prodigious rise of cancer survival rates enables many cancer survivors to live long lives. Therefore, the side effects of cancer treatments as well as the long-term quality of life after cancer have become more relevant. Ovarian toxicity is a major off-target effect of anticancer agents for childhood and young adult female cancer patients. Both chemotherapy and irradiation have been demonstrated to damage the ovary and increase the risks of premature ovarian failure (POF), early menopause, ovarian endocrine disorders, and sub- or infertility. Oncofertility is an emerging and multidisciplinary research and medical field that focuses on providing cancer patients with fertility preservation options. Oocyte quality and quantity are one of the most important factors to determine women's fertility success; therefore, preserving oocytes is paramount for maintaining the ability of young female cancer patients' reproduction after their recovery. This review summarizes peer-reviewed literature on current oocyte preservation options in oncofertility. We describe in-depth oocyte and embryo cryopreservation, ovarian suppression, ovarian tissue cryopreservation, in vitro maturation, ovarian transposition, and adjuvant therapy. Further, we discuss current guidelines and practices of female fertility preservation that cover preserving oocytes.

Summary sentence Preserving oocytes is fundamental for maintaining the ability of young female cancer patients' reproduction.

Graphical Abstract

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© The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
Maria McClam and Shuo Xiao "Preserving Oocytes in Oncofertility," Biology of Reproduction 106(2), 328-337, (17 January 2022). https://doi.org/10.1093/biolre/ioac008
Received: 27 September 2021; Accepted: 13 January 2022; Published: 17 January 2022
KEYWORDS
cancer
fertility preservation
follicle
oncofertility
oocyte
ovary
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