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History of malignant neoplasia lessens oocyte developmental competence: a case-control study
OBJECTIVE: We investigated how history of malignant neoplasia affected oocyte developmental competence. METHODS: Fifty-two cycles of assisted reproductive technology (ART) in women with a history of malignant disease (case group) were compared with fifty-two matched cycles of ART in women with no ca...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Brazilian Society of Assisted Reproduction
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065778/ https://www.ncbi.nlm.nih.gov/pubmed/35243856 http://dx.doi.org/10.5935/1518-0557.20210113 |
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author | Jinno, Yuichi Tobai, Hisako Imai, Shiori Omura, Miho Takeuchi, Makoto Yoshida, Mitsuyo Yano, Noriko Goto, Miki Arimoto, Takahide |
author_facet | Jinno, Yuichi Tobai, Hisako Imai, Shiori Omura, Miho Takeuchi, Makoto Yoshida, Mitsuyo Yano, Noriko Goto, Miki Arimoto, Takahide |
author_sort | Jinno, Yuichi |
collection | PubMed |
description | OBJECTIVE: We investigated how history of malignant neoplasia affected oocyte developmental competence. METHODS: Fifty-two cycles of assisted reproductive technology (ART) in women with a history of malignant disease (case group) were compared with fifty-two matched cycles of ART in women with no cancer history (control group). Propensity score matching involving age and body mass index was used to select controls. Oocyte developmental competence and rates of pregnancy and livebirth were compared as main outcomes. To investigate whether the cancer itself had affected oocyte developmental competence, this outcome variable was compared between case cycles with and without cancer surgical histories. RESULTS: Numbers of fertilized oocytes (FO), cleaving embryos (CE), and superior CE (SCE) were significantly lower in cases than controls. Rates of fertilization and of development to SCE from retrieved oocytes (RO), FO, or CE also were lower in cases than controls (63, 25, 39, and 43% vs. 72, 36, 50, and 55%, respectively). Cases had significantly lower rates of clinical pregnancy and livebirth per embryo transfer than controls (7.6 and 1.5% vs. 20.4 and 14.0%). Rates of development to SCE from RO, FO, and CE showed no significance for differences between cases with and without cancer operations (22, 37, and 40% vs. 31, 42, and 49%). CONCLUSIONS: A woman's history of malignant neoplasia was associated with decreased oocyte developmental competence, possibly related to patient's background factors predisposing to tumor. |
format | Online Article Text |
id | pubmed-10065778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Brazilian Society of Assisted Reproduction |
record_format | MEDLINE/PubMed |
spelling | pubmed-100657782023-04-01 History of malignant neoplasia lessens oocyte developmental competence: a case-control study Jinno, Yuichi Tobai, Hisako Imai, Shiori Omura, Miho Takeuchi, Makoto Yoshida, Mitsuyo Yano, Noriko Goto, Miki Arimoto, Takahide JBRA Assist Reprod Original Article OBJECTIVE: We investigated how history of malignant neoplasia affected oocyte developmental competence. METHODS: Fifty-two cycles of assisted reproductive technology (ART) in women with a history of malignant disease (case group) were compared with fifty-two matched cycles of ART in women with no cancer history (control group). Propensity score matching involving age and body mass index was used to select controls. Oocyte developmental competence and rates of pregnancy and livebirth were compared as main outcomes. To investigate whether the cancer itself had affected oocyte developmental competence, this outcome variable was compared between case cycles with and without cancer surgical histories. RESULTS: Numbers of fertilized oocytes (FO), cleaving embryos (CE), and superior CE (SCE) were significantly lower in cases than controls. Rates of fertilization and of development to SCE from retrieved oocytes (RO), FO, or CE also were lower in cases than controls (63, 25, 39, and 43% vs. 72, 36, 50, and 55%, respectively). Cases had significantly lower rates of clinical pregnancy and livebirth per embryo transfer than controls (7.6 and 1.5% vs. 20.4 and 14.0%). Rates of development to SCE from RO, FO, and CE showed no significance for differences between cases with and without cancer operations (22, 37, and 40% vs. 31, 42, and 49%). CONCLUSIONS: A woman's history of malignant neoplasia was associated with decreased oocyte developmental competence, possibly related to patient's background factors predisposing to tumor. Brazilian Society of Assisted Reproduction 2023 /pmc/articles/PMC10065778/ /pubmed/35243856 http://dx.doi.org/10.5935/1518-0557.20210113 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jinno, Yuichi Tobai, Hisako Imai, Shiori Omura, Miho Takeuchi, Makoto Yoshida, Mitsuyo Yano, Noriko Goto, Miki Arimoto, Takahide History of malignant neoplasia lessens oocyte developmental competence: a case-control study |
title | History of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
title_full | History of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
title_fullStr | History of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
title_full_unstemmed | History of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
title_short | History of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
title_sort | history of malignant neoplasia lessens oocyte developmental
competence: a case-control study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065778/ https://www.ncbi.nlm.nih.gov/pubmed/35243856 http://dx.doi.org/10.5935/1518-0557.20210113 |
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