Evidence map›Paper›PMID 41060533›Full record

ArticleJournal of assisted reproduction and genetics2025

Single euploid embryo transfer outcomes following cancer and systemic chemotherapy.

Johanna Suskin, Keri Bergin, Morgan Baird, Joseph Lee, Alan B Copperman, Erkan Buyuk, Jovana Lekovich

Abstract read
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Article in Journal of assisted reproduction and genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Johanna Suskin *Icahn School of Medicine at Mount Sinai, 1 Gustave Levy Place, New York, NY, 10029, USA.
Keri Bergin *Icahn School of Medicine at Mount Sinai, 1 Gustave Levy Place, New York, NY, 10029, USA. bergin.keri@gmail.com.ORCID http://orcid.org/0000-0001-6438-8591
Morgan BairdReproductive Medicine Associates of New York, 635 Madison Ave 10th floor, New York, NY, 10022, USA.
Joseph LeeReproductive Medicine Associates of New York, 635 Madison Ave 10th floor, New York, NY, 10022, USA.
Alan B CoppermanReproductive Medicine Associates of New York, 635 Madison Ave 10th floor, New York, NY, 10022, USA.
Erkan BuyukIcahn School of Medicine at Mount Sinai, 1 Gustave Levy Place, New York, NY, 10029, USA.
Jovana LekovichIcahn School of Medicine at Mount Sinai, 1 Gustave Levy Place, New York, NY, 10029, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSystemic chemotherapy may impair future reproduction due to its gonadotoxic effects. There are limited data on pregnancy outcomes in patients with a history of chemotherapy who undergo single euploid embryo transfer (SEET). MATERIALS AND

methodsThis retrospective cohort study included patients with prior chemotherapy who underwent SEET from 2011 to 2023. Cycles were matched 1:3 with controls by oocyte age, age at SEET, BMI, and year. Wilcoxon rank, chi-square, and adjusted logistic regression were used for analysis. A sub-analysis was performed to compare patients who had SEET using oocytes retrieved pre- and post-chemotherapy.

resultsFifty-five cycles from 32 patients with prior chemotherapy were matched to 165 control cycles. In the chemotherapy group, 23 cycles (41.8%) used embryos derived from oocytes pre-chemotherapy, while 32 cycles (58.2%) used embryos derived from oocytes post-chemotherapy. Endometrial thickness was significantly lower with prior chemotherapy vs. controls (8 mm vs 9 mm, respectively; p = 0.02). Ongoing pregnancy/live birth rate was similar in patients with prior chemotherapy and controls (56.4% vs. 57.0%, p = 0.94). Adjusted analysis confirmed the findings (aOR 1.5, CI 0.79-2.8, p = 0.21). Pregnancy, clinical pregnancy, and loss rates were similar. The subgroup analysis showed no statistical difference in outcomes in patients who used pre-chemotherapy vs. post-chemotherapy oocytes. However, a trend towards poorer outcomes in patients who used post-chemotherapy oocytes was observed.

conclusionsOutcomes after SEET in patients with prior chemotherapy are comparable to controls. A possible trend toward reduced success using post-chemotherapy oocytes warrants further investigation. Understanding the potential mechanisms by which chemotherapy may affect future fertility is important for survivorship care.

Indexed as

Antineoplastic AgentsNeoplasmsOocytesSingle Embryo TransferAdultCase-Control StudiesChi-Square DistributionFemaleFertility PreservationFertilization in VitroHumansLive BirthLogistic ModelsOocyte RetrievalPregnancyPregnancy OutcomeAntineoplastic AgentsARTCancerChemotherapySingle euploid embryo transfer

Identifiers

PMID41060533
PMCPMC12705475

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.