Fertility considerations in the management of gynecologic malignancies

Gynecol Oncol. 2011 Mar;120(3):326-33. doi: 10.1016/j.ygyno.2010.09.012. Epub 2010 Oct 13.

Abstract

Goals: Gynecologic cancers represent a significant proportion of malignancies affecting women. Historically, cancer treatment focused primarily on eradicating disease, irrespective of the impact on fertility. The implementation of early detection protocols and advanced treatment regimens has resulted in improved prognosis for gynecologic cancer patients. With this improvement, more attention is now paid to quality-of-life issues. Fertility preservation (FP) has become an integral component in the selection and execution of gynecological cancer management. In this report we address gynecologic malignancies as they relate to future fertility potential.

Methods: We review reproductive principles such as ovarian reserve, uterine function, cervical competence, and early obstetrical management, as well as available FP methods. In addition, we discuss the potential damage that cancer and cancer treatments can impart on the female reproductive system. We offer general recommendations regarding baseline screening tests useful in assessing the feasibility of FP. Lastly, cancer-specific FP methods are presented.

Results: Oocyte quantity and quality naturally decline with advancing age. In most patients, the slope of decline steepens significantly after the age of 35. Reliable ovarian reserve measures exist and should be utilized to assess and triage potential candidates for FP. Advancements in FP, particularly in oocyte cryopreservation (OC), have improved the success rates associated with the techniques available to cancer patients. Currently, where successfully available, OC appears to be the preferred method for single women diagnosed with a gynecologic malignancy as it affords reproductive autonomy, whereas embryo cryopreservation using a donor gamete remains an alternative.

Conclusions: In gynecologic oncology, effective treatments to achieve cancer survival can compromise the ability to subsequently conceive and/or carry a child. Therefore, as the field of oncofertility continues to expand, a discussion regarding FP should be initiated when tailoring a cancer treatment protocol.

Publication types

  • Review

MeSH terms

  • Cervix Uteri / physiology
  • Cryopreservation
  • Female
  • Fertility* / drug effects
  • Fertility* / radiation effects
  • Fertilization in Vitro
  • Genital Neoplasms, Female / physiopathology
  • Genital Neoplasms, Female / therapy*
  • Gonadotropin-Releasing Hormone / agonists
  • Humans
  • Oocytes / physiology
  • Ovulation
  • Reproduction / physiology
  • Uterus / physiology

Substances

  • Gonadotropin-Releasing Hormone