ISSN 1518 0557
Ovarian response after random-start controlled ovarian stimulation to cryopreserve oocytes in cancer patients

2018; 22
Ana Paula CB Campos, Guilherme Geber, Rodrigo Hurtado, Marcos Sampaio, Selmo Geber
JBRA Assist. Reprod. 2018; 22 (4):352-354

Received January 26, 2018
Accepted August 05, 2018
Abstract

Objective: To evaluate COS and oocyte retrieval results in ART treatment cycles initiated at any stage of the menstrual cycle (random start) in cancer patients, who could not postpone the onset of cancer treatment. Methods: Prospective observational study of 26 women with cancer, with an indication to start cancer treatment within the next 20 days and wishing to preserve their fertility. Ovarian stimulation started immediately with FSH followed by GnRH antagonist for pituitary suppression and GnRH agonist for oocyte maturation. Treatment started from day 1 to day 14 of the menstrual cycle was considered to be in the follicular phase, and that started from day 15 to day 28 was considered to be in the luteal phase. Oocyte retrieval was performed 34h after GnRH agonist administration. After identi cation and maturity classification, metaphase II oocytes were cryopreserved using vitrification. Results: A total of 13 women had breast cancer, 4 ovarian cancer, 3 Central Nervous System cancer, 3 endometrial cancer, 2 cervical cancer and one bowel cancer. Thirteen patients started treatment during follicular phase and 13 during luteal phase. We found similar results for the duration of treatment, total dose of follicle stimulating hormone, number of ampoules of gonadotropin releasing hormone antagonist, mean number of follicles identified at ultrasound on the day of trigger and retrieval, number of aspirated oocytes and Metaphase II oocytes. Conclusion: Random-start controlled ovarian stimulation for emergency fertility preservation for minimizing delay in oncologic treatment for cancer patients does not interfere with the number of metaphase II oocytes, and therefore can be routinely used for stimulation followed by cryopreservation.


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doi: 10.5935/1518-0557.20180065

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