Cargando…

Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial

BACKGROUND: Chemotherapy-induced premature menopause leads to some consequences, including infertility. We initiated this randomized phase III trial to determine whether a cyclophosphamide-free adjuvant chemotherapy regimen would increase the likelihood of menses resumption and improve survival outc...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Ke-Da, Ge, Jing-Yu, Liu, Xi-Yu, Mo, Miao, He, Min, Shao, Zhi-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486325/
https://www.ncbi.nlm.nih.gov/pubmed/33822134
http://dx.doi.org/10.1093/jnci/djab065
_version_ 1784577720285396992
author Yu, Ke-Da
Ge, Jing-Yu
Liu, Xi-Yu
Mo, Miao
He, Min
Shao, Zhi-Ming
author_facet Yu, Ke-Da
Ge, Jing-Yu
Liu, Xi-Yu
Mo, Miao
He, Min
Shao, Zhi-Ming
author_sort Yu, Ke-Da
collection PubMed
description BACKGROUND: Chemotherapy-induced premature menopause leads to some consequences, including infertility. We initiated this randomized phase III trial to determine whether a cyclophosphamide-free adjuvant chemotherapy regimen would increase the likelihood of menses resumption and improve survival outcomes. METHODS: Young women with operable estrogen receptor-positive HER2-negative breast cancer after definitive surgery were randomly assigned to receive adjuvant epirubicin and cyclophosphamidefollowed by weekly paclitaxel (EC-wP) or epirubicin and paclitaxel followed by weekly paclitaxel (EP-wP). All patients received at least 5-year adjuvant endocrine therapy after chemotherapy. Two coprimary endpoints were the rate of menstrual resumption at 12 months after chemotherapy and 5-year disease-free survival in the intention-to-treat population. This study is registered at ClinicalTrials.gov (NCT01026116). All statistical tests were 2-sided. RESULTS: Between January 2011 and December 2016, 521 patients (median age = 34 years; interquartile range = 31-38 years) were enrolled, with 261 in the EC-wP group and 260 in the EP-wP group. The rate of menstrual resumption at 12 months after chemotherapy was 48.3% in EC-wP (95% confidence interval [CI] = 42.2% to 54.3%) and 63.1% in EP-wP (95% CI = 57.2% to 68.9%), with an absolute difference of 14.8% (95% CI = 6.37% to 23.2%, P < .001). The posthoc exploratory analysis by patient-reported outcome questionnaires indicated that pregnancy might occur in fewer women in the EC-wP group than in the EP-wP group. At a median follow-up of 62 months, the 5-year disease-free survival was 78.3% (95% CI = 72.2% to 83.3%) in EC-wP and 84.7% (95% CI = 79.3% to 88.8%) in EP-wP (stratified log-rank P = .07). The safety data were consistent with the known safety profiles of relevant drugs. CONCLUSIONS: The cyclophosphamide-free chemotherapy regimen might be associated with a higher probability of menses resumption.
format Online
Article
Text
id pubmed-8486325
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-84863252021-10-04 Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial Yu, Ke-Da Ge, Jing-Yu Liu, Xi-Yu Mo, Miao He, Min Shao, Zhi-Ming J Natl Cancer Inst Articles BACKGROUND: Chemotherapy-induced premature menopause leads to some consequences, including infertility. We initiated this randomized phase III trial to determine whether a cyclophosphamide-free adjuvant chemotherapy regimen would increase the likelihood of menses resumption and improve survival outcomes. METHODS: Young women with operable estrogen receptor-positive HER2-negative breast cancer after definitive surgery were randomly assigned to receive adjuvant epirubicin and cyclophosphamidefollowed by weekly paclitaxel (EC-wP) or epirubicin and paclitaxel followed by weekly paclitaxel (EP-wP). All patients received at least 5-year adjuvant endocrine therapy after chemotherapy. Two coprimary endpoints were the rate of menstrual resumption at 12 months after chemotherapy and 5-year disease-free survival in the intention-to-treat population. This study is registered at ClinicalTrials.gov (NCT01026116). All statistical tests were 2-sided. RESULTS: Between January 2011 and December 2016, 521 patients (median age = 34 years; interquartile range = 31-38 years) were enrolled, with 261 in the EC-wP group and 260 in the EP-wP group. The rate of menstrual resumption at 12 months after chemotherapy was 48.3% in EC-wP (95% confidence interval [CI] = 42.2% to 54.3%) and 63.1% in EP-wP (95% CI = 57.2% to 68.9%), with an absolute difference of 14.8% (95% CI = 6.37% to 23.2%, P < .001). The posthoc exploratory analysis by patient-reported outcome questionnaires indicated that pregnancy might occur in fewer women in the EC-wP group than in the EP-wP group. At a median follow-up of 62 months, the 5-year disease-free survival was 78.3% (95% CI = 72.2% to 83.3%) in EC-wP and 84.7% (95% CI = 79.3% to 88.8%) in EP-wP (stratified log-rank P = .07). The safety data were consistent with the known safety profiles of relevant drugs. CONCLUSIONS: The cyclophosphamide-free chemotherapy regimen might be associated with a higher probability of menses resumption. Oxford University Press 2021-04-02 /pmc/articles/PMC8486325/ /pubmed/33822134 http://dx.doi.org/10.1093/jnci/djab065 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Articles
Yu, Ke-Da
Ge, Jing-Yu
Liu, Xi-Yu
Mo, Miao
He, Min
Shao, Zhi-Ming
Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title_full Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title_fullStr Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title_full_unstemmed Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title_short Cyclophosphamide-Free Adjuvant Chemotherapy for Ovarian Protection in Young Women With Breast Cancer: A Randomized Phase 3 Trial
title_sort cyclophosphamide-free adjuvant chemotherapy for ovarian protection in young women with breast cancer: a randomized phase 3 trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486325/
https://www.ncbi.nlm.nih.gov/pubmed/33822134
http://dx.doi.org/10.1093/jnci/djab065
work_keys_str_mv AT yukeda cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT gejingyu cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT liuxiyu cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT momiao cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT hemin cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT shaozhiming cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial
AT cyclophosphamidefreeadjuvantchemotherapyforovarianprotectioninyoungwomenwithbreastcancerarandomizedphase3trial