Abstract
Maintaining the ability to have biological children has been identified as an important component of quality of life in pediatric and adolescent cancer survivors, yet their fertility may be compromised by the interventions used to cure their cancer. Advances in reproductive technologies have increased the options for fertility preservation in this population. For postpubertal females, standard options for fertility preservation include oocyte and embryo cryopreservation. Ovarian tissue cryopreservation is an experimental methodology that may have efficacy when standard interventions are not possible due to time constraints. Ovarian tissue cryopreservation is the only option to cryopreserve ovarian follicles in prepubertal females diagnosed with cancer as they are not able to respond to ovarian stimulation. Type of cancer, age, pubertal development, the severity of illness at the time of diagnosis, and type of treatment all impact decision making related to these and other fertility preservation options. Discussions of fertility should occur at diagnosis and following treatment, as many survivors will have retained ovarian function post-treatment but may be at risk of premature menopause. This chapter summarizes the current options for fertility preservation for female pediatric and adolescent cancer patients.
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Review Questions and Answers
Review Questions and Answers
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Q1.
You have just diagnosed a 5-year-old girl with a rhabdomyosarcoma of the pelvis. Her treatment includes multiagent chemotherapy including cyclophosphamide and radiation to the tumor site. Which of the following would be an appropriate fertility preservation option for this patient?
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(a)
Embryo cryopreservation
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(b)
Ovarian tissue cryopreservation
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(c)
Use of GnRH agonist in conjunction with therapy
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(d)
Oocyte cryopreservation
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(a)
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A1.
(b). Ovarian tissue cryopreservation is the only option available to prepubertal females.
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Q2.
A 16-year-old female who has just been diagnosed with nonmetastatic Ewing’s sarcoma wishes to pursue oocyte cryopreservation. Her oncologist has agreed to a 3-week window to start therapy. Her last menstrual cycle started 10 days ago. Because the patient is mid-cycle, she cannot complete oocyte cryopreservation in the desired timeframe. True/False
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A2.
False. Ovarian hyperstimulation can utilize a random start protocol which, if the systems are in place to facilitate a rapid referral, should allow for stimulation and recovery of oocytes within the time frame outlined above.
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Q3.
An 18-year-old female survivor of Hodgkin lymphoma, off therapy for 5Â years, is being seen in long-term follow-up. She was treated with four cycles of BEACOPP and four cycles of COPP/ABV. Her menstrual cycle resumed 9Â months after the completion of therapy and has been regular since then. She did not undergo any fertility preservation procedures prior to the start of therapy. Appropriate interventions at the current clinic visit include:
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(a)
Check FSH, LH, and estradiol
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(b)
Discuss risk of premature menopause
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(c)
Discuss consideration of embryo or oocyte cryopreservation
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(d)
All of the above
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(a)
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A3.
(d) Female survivors who are treated with alkylating agents, particularly procarbazine, are at increased risk of developing premature menopause and should be monitored by checking reproductive hormones. They should also have a discussion about options for family building including consideration of embryo or oocyte cryopreservation.
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Kinnaman, M., Shea, K., Levine, J. (2019). Fertility Preservation Options for Female Pediatric and Adolescent Oncology Patients. In: Woodruff, T., Shah, D., Vitek, W. (eds) Textbook of Oncofertility Research and Practice. Springer, Cham. https://doi.org/10.1007/978-3-030-02868-8_9
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