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RCOG World Congress 2023

June 12 - 14, 2023 | London, UK

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EP.0039

Impact of cancer on reproductive outcomes of women undergoing oocyte cryopreservation

Part of Topic

Reproductive Medicine/Assisted Reproduction

Video

Does cancer reduce a woman's chance of getting pregnant? A retrospective study

Background

Cancer survivorship is increasing worldwide and subsequently the demand for urgent fertility preservation (FP) is growing. There remains limited evidence on the optimal management for women seeking FP, particularly those with cancer.

Aims and Objectives

The aim of this study was to evaluate reproductive outcomes of women with breast cancer (BC), haematological cancer (HC) and healthy controls seeking oocyte cryopreservation, and the potential confounding factors. The purpose of this study is to develop more evidence towards the optimum protocol for COS.

Methods

Data was extracted on patient and treatment characteristics and reproductive outcomes. Data was electronically recorded, uniquely coded, checked, and pseudo-anonymised. Descriptive statistics, natural frequencies, Pearson correlation and linear regression models were employed to summarise the outcomes, with p<0.05 indicating a statistical significance. The primary outcome was the number of oocytes; mature (MII) and immature (GV). The study was a service evaluation of routine practice and therefore exempt from ethical approval.

Study Design: Cross-sectional cohort study, using retrospective data from 335 women who received oocyte cryopreservation at a tertiary fertility centre in London between 07/11/2019-09/11/2021.

Results

254 healthy controls, 33 BC and 24 HC patients were included after excluding post-chemotherapy FP patients and women with a previous cancer history. Women with cancer had a significantly lower response following COS compared to healthy controls with an adjusted mean difference (aMD) of 4.2 (95%CI -6.6 to -1.6, p=0.001). There was no statistically significant adjusted difference in the number of oocytes between the triggers; Buserelin, human chorionic gonadotropin (HCG) and dual trigger (Buserelin as reference: (aMD-0.44, 95%CI -3.64-2.76, p=0.785) (aMD-1.92, 95%CI -4.85-1.01, p=0.198) respectively). Those with BC had similar numbers of oocytes compared to controls (aMD-1.27, 95%CI -4.48-1.94, p=0.437), whereas women with HC had significantly fewer (aMD 8.4, 95% CI -13.2 to -3.8, p=0.001).

Conclusions

•FP has a vital role to play for women with cancer who have not started/completed their family.
•The Buserelin trigger yielded similar outcomes to an HCG or Dual trigger
•Women with cancer should not expect significantly poorer FP outcomes
•Women should utilise a Buserelin protocol to maximise outcomes and safety.
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