Anti-Müllerian hormone: a novel biomarker for aggressive prostate cancer? Emerging evidence from a prospective study of radical prostatectomies.

IF 2.4 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Stavros Kontogiannis, Georgios Markantes, Maria Stamou, Michail Tsagkarakis, Irini Mamali, Konstantinos Giannitsas, Petros Perimenis, Neoklis Georgopoulos, Anastasios Athanasopoulos
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引用次数: 0

Abstract

Purpose: Prostate cancer patients are a heterogeneous group as regards the aggressiveness of the disease. The relationship of steroid hormones with the aggressiveness of prostate cancer is unclear. It is known that the anti-Müllerian hormone (AMH) inhibits prostate cancer cell lines in vitro. The aim of this study is to investigate the relationship of AMH and steroid hormones with the aggressiveness of prostate cancer.

Methods: This was a prospective study of consecutive radical prostatectomy patients. We measured the following hormones: total testosterone, sex hormone-binding globulin, albumin, luteinizing hormone, follicle-stimulating hormone, estradiol, dehydroepiandrosterone sulfate, androstenedione, and AMH. The minimum follow-up after radical prostatectomy was 5 years. For the aggressiveness of prostate cancer, we considered the following three variables: post-operative Gleason score (GS) ≥ 8, TNM pΤ3 disease, and prostate-specific antigen (PSA) biochemical recurrence (BCR).

Results: In total, 91 patients were enrolled. The mean age and PSA were 64.8 years and 9.3 ng/dl, respectively. The median post-operative GS was 7. Low AMH blood levels were correlated with higher post-operative GS (p = 0.001), as well as with PSA BCR (p = 0.043). With pT3 disease, only albumin was (negatively) correlated (p = 0.008). ROC analysis showed that AMH is a good predictor of BCR (AUC 0.646, 95% CI 0.510-0.782, p = 0.043); a cutoff value of 3.06 ng/dl had a positive prognostic value of 71.4% and a negative prognostic value of 63.3% for BCR. Cox regression analysis showed that AMH is a statistically significant and independent prognostic marker for BCR (p = 0.013). More precisely, for every 1 ng/ml of AMH rise, the probability for PSA BCR decreases by 20.8% (HR = 0.792). Moreover, in Kaplan-Meier analysis, disease-free survival is more probable in patients with AMΗ ≥ 3.06 ng/ml (p = 0.004).

Conclusions: Low AMH blood levels were correlated with aggressive prostate cancer in this radical prostatectomy cohort of patients. Therefore, AMH could be a prognostic biomarker for the aggressiveness of the disease.

Abstract Image

抗缪勒氏管激素:侵袭性前列腺癌的新型生物标志物?前列腺癌根治术前瞻性研究的新证据。
目的:就疾病的侵袭性而言,前列腺癌患者是一个异质性群体。类固醇激素与前列腺癌侵袭性的关系尚不清楚。已知抗缪勒氏管激素(AMH)对体外前列腺癌细胞株有抑制作用。本研究旨在探讨 AMH 和类固醇激素与前列腺癌侵袭性的关系:方法:这是一项前瞻性研究,对象是连续接受根治性前列腺切除术的患者。我们测量了以下激素:总睾酮、性激素结合球蛋白、白蛋白、黄体生成素、卵泡刺激素、雌二醇、硫酸脱氢表雄酮、雄二酮和 AMH。前列腺癌根治术后的随访时间最短为 5 年。对于前列腺癌的侵袭性,我们考虑了以下三个变量:术后格里森评分(GS)≥ 8、TNM pΤ3 病变和前列腺特异性抗原(PSA)生化复发(BCR):共有 91 名患者入选。平均年龄和 PSA 分别为 64.8 岁和 9.3 ng/dl。低 AMH 血液水平与较高的术后 GS 相关(p = 0.001),也与 PSA BCR 相关(p = 0.043)。对于 pT3 疾病,只有白蛋白(负)相关(p = 0.008)。ROC 分析表明,AMH 是 BCR 的良好预测指标(AUC 0.646,95% CI 0.510-0.782,p = 0.043);3.06 ng/dl 的临界值对 BCR 的预后具有 71.4% 的阳性预测价值和 63.3% 的阴性预测价值。Cox 回归分析表明,AMH 是 BCR 有统计学意义的独立预后标志物(p = 0.013)。更确切地说,AMH每升高1纳克/毫升,PSA BCR的概率就会降低20.8%(HR = 0.792)。此外,在卡普兰-米尔分析中,AMΗ≥3.06纳克/毫升的患者无病生存的概率更高(P = 0.004):在这组前列腺癌根治术患者中,低AMH血药浓度与侵袭性前列腺癌相关。因此,AMH可作为疾病侵袭性的预后生物标志物。
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来源期刊
CiteScore
5.90
自引率
0.00%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Hormones-International Journal of Endocrinology and Metabolism is an international journal published quarterly with an international editorial board aiming at providing a forum covering all fields of endocrinology and metabolic disorders such as disruption of glucose homeostasis (diabetes mellitus), impaired homeostasis of plasma lipids (dyslipidemia), the disorder of bone metabolism (osteoporosis), disturbances of endocrine function and reproductive capacity of women and men. Hormones-International Journal of Endocrinology and Metabolism particularly encourages clinical, translational and basic science submissions in the areas of endocrine cancers, nutrition, obesity and metabolic disorders, quality of life of endocrine diseases, epidemiology of endocrine and metabolic disorders.
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