Female cancer survivors are low responders and have reduced success compared with other patients undergoing assisted reproductive technologies
Related Experiment Video
Updated: May 26, 2026

Fertility Preservation Through Oocyte Vitrification: Clinical and Laboratory Perspectives
Published on: September 16, 2021
Sara E Barton1, Stacey A Missmer, Katharine F Berry
1Division of Reproductive Medicine, Department of Obstetrics, Gynecology, and Reproductive Biology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA. sbarton@partners.org
Objective:
To investigate the effect of prior chemotherapy and radiation on assisted reproductive technology (ART) outcomes.
Design:
Retrospective cohort study.
Setting:
University-based infertility clinic.
Patient(S):
Female cancer survivors who had received chemotherapy or radiation and all other women undergoing first-fresh IVF/intracytoplasmic sperm injection (ICSI) cycles.
Intervention(S):
Survivors' ART outcomes were compared with all women undergoing first-fresh IVF/ICSI cycles and those with male-factor infertility only. Multivariate logistic and Poisson regression analyses were used to estimate the effect of cancer therapy on ART outcomes.
Main Outcomes Measure(S):
Number of oocytes retrieved and embryos obtained; odds of cycle cancelation, clinical pregnancy, and live birth.
Result(S):
Compared with others undergoing IVF/ICSI, survivors had significantly fewer oocytes retrieved and embryos available for transfer. In addition, survivors were significantly more likely to be canceled (odds ratio [OR] 5.60, 95% CI 2.94-10.66) and had lower pregnancy and live birth rates (OR 0.30, 95% CI 0.13-0.68; and OR 0.27, 95% CI 0.10-0.69; respectively). Odds ratios were stronger when the comparison group was restricted to those with male-factor infertility only.
Conclusion(S):
Women who have received systemic therapy for malignancy should be considered to be low responders and counseled that their per-cycle live birth rate is lower than that of their peers. These data strongly support offering fertility preservation before cancer therapy when possible.
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