| Literature DB >> 30371800 |
Halle C F Moore1, Joseph M Unger2, Kelly-Anne Phillips3,4,5, Frances Boyle6, Erika Hitre7, Anna Moseley2, David J Porter8, Prudence A Francis3,4,5, Lori J Goldstein9, Henry L Gomez10, Carlos S Vallejos11, Ann H Partridge12, Shaker R Dakhil13,14, Agustin A Garcia14, Julie R Gralow15, Janine M Lombard16, John F Forbes4,16, Silvana Martino17, William E Barlow2, Carol J Fabian18, Lori M Minasian19, Frank L Meyskens20, Richard D Gelber21, Gabriel N Hortobagyi22, Kathy S Albain23.
Abstract
Premature menopause is a serious long-term side effect of chemotherapy. We evaluated long-term pregnancy and disease-related outcomes for patients in S0230/POEMS, a study in premenopausal women with stage I-IIIA estrogen receptor-negative, progesterone receptor-negative breast cancer to be treated with cyclophosphamide-containing chemotherapy. Women were randomly assigned to standard chemotherapy with or without goserelin, a gonadotropin-releasing hormone agonist, and were stratified by age and chemotherapy regimen. All statistical tests were two-sided. Of 257 patients, 218 were eligible and evaluable (105 in the chemotherapy + goserelin arm and 113 in the chemotherapy arm). More patients in the chemotherapy + goserelin arm reported at least one pregnancy vs the chemotherapy arm (5-year cumulative incidence = 23.1%, 95% confidence interval [CI] = 15.3% to 31.9%; and 12.2%, 95% CI = 6.8% to 19.2%, respectively; odds ratio = 2.34; 95% CI = 1.07 to 5.11; P = .03). Randomization to goserelin + chemotherapy was associated with a nonstatistically significant improvement in disease-free survival (hazard ratio [HR] = 0.55; 95% CI = 0.27 to 1.10; P = .09) and overall survival (HR = 0.45; 95% CI = 0.19 to 1.04; P = .06). In this long-term analysis of POEMS/S0230, we found continued evidence that patients randomly assigned to receive goserelin + chemotherapy were not only more likely to avoid premature menopause, but were also more likely to become pregnant without adverse effect on disease-related outcomes.Entities:
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Year: 2019 PMID: 30371800 PMCID: PMC6657277 DOI: 10.1093/jnci/djy185
Source DB: PubMed Journal: J Natl Cancer Inst ISSN: 0027-8874 Impact factor: 13.506