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dc.contributor.author Abdel-Fatah, TMA
dc.contributor.author Ball, GR
dc.contributor.author Thangavelu, PU
dc.contributor.author Reid, .LE
dc.contributor.author McCart, Reed AE
dc.contributor.author Saunus, JM
dc.contributor.author Duijf, PHG
dc.contributor.author Simpson, PT
dc.contributor.author Lakhani, SR
dc.contributor.author Pongor, Lőrinc
dc.contributor.author Győrffy, Balázs
dc.contributor.author Moseley, PM
dc.contributor.author Green, AR
dc.contributor.author Pockley, AG
dc.contributor.author Caldas, C
dc.contributor.author Ellis, IO
dc.contributor.author Chan, SYT
dc.date.accessioned 2020-09-28T09:12:38Z
dc.date.available 2020-09-28T09:12:38Z
dc.date.issued 2020
dc.identifier 85088210743
dc.identifier.citation journalVolume=3;journalIssueNumber=7;journalTitle=JAMA NETWORK OPEN;pagination= e209486, pages: 14;journalAbbreviatedTitle=JAMA NETW OPEN;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8414
dc.identifier.uri doi:10.1001/jamanetworkopen.2020.9486
dc.description.abstract Importance: There is no proven test that can guide the optimal treatment, either endocrine therapy or chemotherapy, for estrogen receptor-positive breast cancer. Objective: To investigate the associations of sperm-associated antigen 5 (SPAG5) transcript and SPAG5 protein expressions with treatment response in systemic therapy for estrogen receptor-positive breast cancer. Design, Settings, and Participants: This retrospective cohort study included patients with estrogen receptor-positive breast cancer who received 5 years of adjuvant endocrine therapy with or without neoadjuvant anthracycline-based combination chemotherapy (NACT) derived from 11 cohorts from December 1, 1986, to November 28, 2019. The associations of SPAG5 transcript and SPAG5 protein expression with pathological complete response to NACT were evaluated, as was the association of SPAG5 mRNA expression with response to neoadjuvant endocrine therapy. The associations of distal relapse-free survival with SPAG5 transcript or SPAG5 protein expressions were analyzed. Data were analyzed from September 9, 2015, to November 28, 2019. Main Outcomes and Measures: The primary outcomes were breast cancer-specific survival, distal relapse-free survival, pathological complete response, and clinical response. Outcomes were examined using Kaplan-Meier, multivariable logistic, and Cox regression models. Results: This study included 12 720 women aged 24 to 78 years (mean [SD] age, 58.46 [12.45] years) with estrogen receptor-positive breast cancer, including 1073 women with SPAG5 transcript expression and 361 women with SPAG5 protein expression of locally advanced disease stage IIA through IIIC. Women with SPAG5 transcript and SPAG5 protein expressions achieved higher pathological complete response compared with those without SPAG5 transcript or SPAG5 protein expressions (transcript: odds ratio, 2.45 [95% CI, 1.71-3.51]; P < .001; protein: odds ratio, 7.32 [95% CI, 3.33-16.22]; P < .001). Adding adjuvant anthracycline chemotherapy to adjuvant endocrine therapy for SPAG5 mRNA expression in estrogen receptor-positive breast cancer was associated with prolonged 5-year distal relapse-free survival in patients without lymph node involvement (hazard ratio, 0.34 [95% CI, 0.14-0.87]; P = .03) and patients with lymph node involvement (hazard ratio, 0.35 [95% CI, 0.18-0.68]; P = .002) compared with receiving 5-year endocrine therapy alone. Mean (SD) SPAG5 transcript was found to be downregulated after 2 weeks of neoadjuvant endocrine therapy compared with pretreatment levels in 68 of 92 patients (74%) (0.23 [0.18] vs 0.34 [0.24]; P < .001). Conclusions and Relevance: These findings suggest that SPAG5 transcript and SPAG5 protein expressions could be used to guide the optimal therapies for estrogen receptor-positive breast cancer. Retrospective and prospective clinical trials are warranted.
dc.relation.ispartof urn:issn:2574-3805
dc.title Association of Sperm-Associated Antigen 5 and Treatment Response in Patients With Estrogen Receptor-Positive Breast Cancer
dc.type Journal Article
dc.date.updated 2020-08-07T10:02:44Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 31397298
dc.identifier.wos 000552096400004
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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