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Article: Androgen Receptor Splice Variant 7 Predicts Shorter Response in Patients with Metastatic Hormone-sensitive Prostate Cancer Receiving Androgen Deprivation Therapy

TitleAndrogen Receptor Splice Variant 7 Predicts Shorter Response in Patients with Metastatic Hormone-sensitive Prostate Cancer Receiving Androgen Deprivation Therapy
Authors
KeywordsAndrogen deprivation therapy
Androgen receptor splice variant 7
Immunohistochemical staining
Metastatic hormone-sensitive prostate cancer
Prospective cohort study
Issue Date2021
Citation
European Urology, 2021, v. 79, n. 6, p. 879-886 How to Cite?
AbstractBackground: Whether AR-V7 expression can predict the response in patients with metastatic hormone-sensitive prostate cancer (mHSPC) who receive androgen deprivation therapy (ADT) remains to be explored. Objective: To evaluate the predictive value of AR-V7 expression in the prognosis of mHSPC patients receiving ADT. Design, setting, and participants: In this multicenter prospective cohort study, 310 mHSPC patients commencing ADT were enrolled. Standard immunohistochemical staining was used to assess AR-V7 protein expression in biopsy tissues collected before initiation of ADT. Outcome measurements and statistical analysis: Kaplan-Meier survival estimates and Cox regression analyses were used to evaluate associations of AR-V7 status (positive vs negative) with progression-free survival (PFS) and overall survival (OS). Results and limitations: Sixty-four (21%) patients were AR-V7–positive and 246 (79%) patients were AR-V7–negative. The median follow-up for patients not confirmed dead was 25 mo (interquartile range 10–30). Compared to AR-V7-negative patients, AR-V7-positive patients had significantly shorter PFS (hazard ratio [HR] 47.39, 95% confidence interval [CI] 25.83–86.94) and OS (HR 3.57, 95% CI 1.46–8.72). In multivariable analysis, AR-V7 was an independent predictive factor (HR 7.61, 95% CI 5.24–11.06) for shorter PFS. Limitations include the sample size and follow-up period. Conclusions: AR-V7 expression in primary cancer tissue is correlated with poor prognosis for mHSPC patients receiving ADT. Patient summary: In this study of men with metastatic hormone-sensitive prostate cancer, AR-V7 protein expression in primary cancer tissue was associated with poor outcomes on androgen deprivation therapy.
Persistent Identifierhttp://hdl.handle.net/10722/369548
ISSN
2023 Impact Factor: 25.3
2023 SCImago Journal Rankings: 6.928

 

DC FieldValueLanguage
dc.contributor.authorLi, Heng-
dc.contributor.authorZhang, Yucong-
dc.contributor.authorLi, Dong-
dc.contributor.authorMa, Xin-
dc.contributor.authorXu, Kai-
dc.contributor.authorDing, Beichen-
dc.contributor.authorLi, Hongzhao-
dc.contributor.authorWang, Zhize-
dc.contributor.authorOuyang, Wei-
dc.contributor.authorLong, Gongwei-
dc.contributor.authorZeng, Jin-
dc.contributor.authorLiu, Haoran-
dc.contributor.authorYan, Libin-
dc.contributor.authorZhang, Yangjun-
dc.contributor.authorLiu, Zheng-
dc.contributor.authorGuan, Wei-
dc.contributor.authorHu, Zhiquan-
dc.contributor.authorLiu, Cong-
dc.contributor.authorWan, Jie-
dc.contributor.authorWang, Guoping-
dc.contributor.authorPu, Xiaoyong-
dc.contributor.authorZhang, Minghui-
dc.contributor.authorGuo, Linlang-
dc.contributor.authorAn, Ruihua-
dc.contributor.authorQi, Jiping-
dc.contributor.authorGuo, Aitao-
dc.contributor.authorYe, Zhangqun-
dc.contributor.authorLiu, Jiumin-
dc.contributor.authorZhang, Xu-
dc.contributor.authorXu, Hua-
dc.date.accessioned2026-01-27T09:16:18Z-
dc.date.available2026-01-27T09:16:18Z-
dc.date.issued2021-
dc.identifier.citationEuropean Urology, 2021, v. 79, n. 6, p. 879-886-
dc.identifier.issn0302-2838-
dc.identifier.urihttp://hdl.handle.net/10722/369548-
dc.description.abstractBackground: Whether AR-V7 expression can predict the response in patients with metastatic hormone-sensitive prostate cancer (mHSPC) who receive androgen deprivation therapy (ADT) remains to be explored. Objective: To evaluate the predictive value of AR-V7 expression in the prognosis of mHSPC patients receiving ADT. Design, setting, and participants: In this multicenter prospective cohort study, 310 mHSPC patients commencing ADT were enrolled. Standard immunohistochemical staining was used to assess AR-V7 protein expression in biopsy tissues collected before initiation of ADT. Outcome measurements and statistical analysis: Kaplan-Meier survival estimates and Cox regression analyses were used to evaluate associations of AR-V7 status (positive vs negative) with progression-free survival (PFS) and overall survival (OS). Results and limitations: Sixty-four (21%) patients were AR-V7–positive and 246 (79%) patients were AR-V7–negative. The median follow-up for patients not confirmed dead was 25 mo (interquartile range 10–30). Compared to AR-V7-negative patients, AR-V7-positive patients had significantly shorter PFS (hazard ratio [HR] 47.39, 95% confidence interval [CI] 25.83–86.94) and OS (HR 3.57, 95% CI 1.46–8.72). In multivariable analysis, AR-V7 was an independent predictive factor (HR 7.61, 95% CI 5.24–11.06) for shorter PFS. Limitations include the sample size and follow-up period. Conclusions: AR-V7 expression in primary cancer tissue is correlated with poor prognosis for mHSPC patients receiving ADT. Patient summary: In this study of men with metastatic hormone-sensitive prostate cancer, AR-V7 protein expression in primary cancer tissue was associated with poor outcomes on androgen deprivation therapy.-
dc.languageeng-
dc.relation.ispartofEuropean Urology-
dc.subjectAndrogen deprivation therapy-
dc.subjectAndrogen receptor splice variant 7-
dc.subjectImmunohistochemical staining-
dc.subjectMetastatic hormone-sensitive prostate cancer-
dc.subjectProspective cohort study-
dc.titleAndrogen Receptor Splice Variant 7 Predicts Shorter Response in Patients with Metastatic Hormone-sensitive Prostate Cancer Receiving Androgen Deprivation Therapy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.eururo.2021.01.037-
dc.identifier.pmid33579577-
dc.identifier.scopuseid_2-s2.0-85100807979-
dc.identifier.volume79-
dc.identifier.issue6-
dc.identifier.spage879-
dc.identifier.epage886-
dc.identifier.eissn1873-7560-

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