Adjuvant androgen deprivation therapy for poor-risk, androgen receptor–positive salivary duct carcinoma

医学 涎腺导管癌 危险系数 内科学 佐剂 比例危险模型 雄激素剥夺疗法 辅助治疗 雄激素 比卡鲁胺 肿瘤科 泌尿科 胃肠病学 雄激素受体 癌症 置信区间 激素 前列腺癌
作者
Wim van Boxtel,Laura D. Locati,Adriana C. H. van Engen‐van Grunsven,Cristiana Bergamini,Marianne A. Jonker,E. Fiets,Stefano Cavalieri,S. Tooten,Ewout J. van den Bos,Pasquale Quattrone,Gerald W. Verhaegh,Jack A. Schalken,Lisa Licitra,Carla M.L. van Herpen
出处
期刊:European Journal of Cancer [Elsevier BV]
卷期号:110: 62-70 被引量:69
标识
DOI:10.1016/j.ejca.2018.12.035
摘要

Aim Salivary duct carcinoma (SDC), an aggressive subtype of salivary gland cancer, is androgen receptor (AR)–positive in 67–96% of cases. In patients with locally recurrent and metastatic (R/M) AR-positive SDC, androgen deprivation therapy (ADT) has an overall response rate of 18–64.7%. In this study, we describe the efficacy of adjuvant ADT in patients with poor-risk (stage 4a) AR-positive SDC. Methods This is a retrospective cohort study in which patients with stage 4a AR-positive SDC were offered adjuvant ADT, i.e. bicalutamide, luteinizing hormone-releasing hormone (LHRH) analogue or a combination of these after tumour resection. In the control group, data were collected on patients with stage 4a SDC who underwent a tumour resection but did not receive adjuvant ADT. Results Twenty-two AR-positive SDC patients were treated with adjuvant ADT for a median duration of 12 months. The control group consisted of 111 SDC patients. After a median follow-up of 20 months in the ADT-treated patients and 26 months in the control group, the 3-year disease-free survival (DFS) was estimated as 48.2% (95% confidence interval [CI] 14.0–82.4%) and 27.7% (95% CI 18.5–36.9%) (P = 0.037). Multivariable Cox regression analysis showed a hazard ratio of 0.138 (95% CI 0.025–0.751, P = 0.022) for DFS and 0.064 (95% CI 0.005–0.764, P = 0.030) for overall survival (OS) in favour of the ADT-treated patients. Conclusion Poor-risk, AR-positive SDC patients who received adjuvant ADT have a significantly longer DFS compared with patients in the control group, who did not receive adjuvant ADT. For OS, this was just below and above the significance level, in case there was or was no correction for confounders.
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