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Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia
OBJECTIVE: This study aimed to explore the single-agent chemotherapy actinomycin D on ovarian reserve by measuring the anti-Mullerian hormone (AMH) levels before, during, and after chemotherapy. METHODS: This study recruited premenopausal women aged 15 to 45 with a newly diagnosed low-risk gestation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423527/ https://www.ncbi.nlm.nih.gov/pubmed/37290904 http://dx.doi.org/10.1136/ijgc-2023-004292 |
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author | Xue, Wei Cang, Wei Zhao, Jun Feng, Fengzhi Wan, Xirun Ren, Tong Qiu, Ling Yang, Junjun Xiang, Yang |
author_facet | Xue, Wei Cang, Wei Zhao, Jun Feng, Fengzhi Wan, Xirun Ren, Tong Qiu, Ling Yang, Junjun Xiang, Yang |
author_sort | Xue, Wei |
collection | PubMed |
description | OBJECTIVE: This study aimed to explore the single-agent chemotherapy actinomycin D on ovarian reserve by measuring the anti-Mullerian hormone (AMH) levels before, during, and after chemotherapy. METHODS: This study recruited premenopausal women aged 15 to 45 with a newly diagnosed low-risk gestational trophoblastic neoplasia needing actinomycin D. AMH was measured at baseline, during chemotherapy, and 1, 3, and 6 months after the last chemotherapy. The reproductive outcomes were also documented. RESULTS: Of the 42 women recruited, we analyzed 37 (median: 29 years; range 19–45) with a complete dataset. The follow-up was 36 months (range 34–39). Actinomycin D significantly decreased AMH concentrations during treatment, from 2.38±0.92 ng/mL to 1.02±0.96 ng/mL (p<0.05). Partial recovery was seen at 1 month and 3 months after treatment. Full recovery was reached 6 months after treatment among patients younger than 35 years. The only factor correlated with the extent of AMH reduction at 3 months was age (r=0.447, p<0.05). Notably, the number of courses of actinomycin D was not associated with the extent of AMH reduction. A total of 18 (90%) of 20 patients who had a desire to conceive had live births with no adverse pregnancy outcomes. CONCLUSION: Actinomycin D has a transient and minor effect on ovarian function. Age is the only factor that impacts the patient’s rate of recovery. Patients will achieve favorable reproductive outcomes after actinomycin D treatment. |
format | Online Article Text |
id | pubmed-10423527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-104235272023-08-14 Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia Xue, Wei Cang, Wei Zhao, Jun Feng, Fengzhi Wan, Xirun Ren, Tong Qiu, Ling Yang, Junjun Xiang, Yang Int J Gynecol Cancer Original Research OBJECTIVE: This study aimed to explore the single-agent chemotherapy actinomycin D on ovarian reserve by measuring the anti-Mullerian hormone (AMH) levels before, during, and after chemotherapy. METHODS: This study recruited premenopausal women aged 15 to 45 with a newly diagnosed low-risk gestational trophoblastic neoplasia needing actinomycin D. AMH was measured at baseline, during chemotherapy, and 1, 3, and 6 months after the last chemotherapy. The reproductive outcomes were also documented. RESULTS: Of the 42 women recruited, we analyzed 37 (median: 29 years; range 19–45) with a complete dataset. The follow-up was 36 months (range 34–39). Actinomycin D significantly decreased AMH concentrations during treatment, from 2.38±0.92 ng/mL to 1.02±0.96 ng/mL (p<0.05). Partial recovery was seen at 1 month and 3 months after treatment. Full recovery was reached 6 months after treatment among patients younger than 35 years. The only factor correlated with the extent of AMH reduction at 3 months was age (r=0.447, p<0.05). Notably, the number of courses of actinomycin D was not associated with the extent of AMH reduction. A total of 18 (90%) of 20 patients who had a desire to conceive had live births with no adverse pregnancy outcomes. CONCLUSION: Actinomycin D has a transient and minor effect on ovarian function. Age is the only factor that impacts the patient’s rate of recovery. Patients will achieve favorable reproductive outcomes after actinomycin D treatment. BMJ Publishing Group 2023-08 2023-06-08 /pmc/articles/PMC10423527/ /pubmed/37290904 http://dx.doi.org/10.1136/ijgc-2023-004292 Text en © IGCS and ESGO 2023. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, an indication of whether changes were made, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Xue, Wei Cang, Wei Zhao, Jun Feng, Fengzhi Wan, Xirun Ren, Tong Qiu, Ling Yang, Junjun Xiang, Yang Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title | Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title_full | Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title_fullStr | Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title_full_unstemmed | Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title_short | Effect of actinomycin D on ovarian reserve in low-risk gestational trophoblastic neoplasia |
title_sort | effect of actinomycin d on ovarian reserve in low-risk gestational trophoblastic neoplasia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423527/ https://www.ncbi.nlm.nih.gov/pubmed/37290904 http://dx.doi.org/10.1136/ijgc-2023-004292 |
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