Desai Sethi Urology Institute and Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Cell Rep Med. 2024 Aug 20;5(8):101644. doi: 10.1016/j.xcrm.2024.101644.
HSD3B1 encodes 3β-hydroxysteroid dehydrogenase-1, which converts adrenal dehydroepiandrosterone to 5α-dihydrotestosterone and is inherited in adrenal-permissive (AP) or adrenal-restrictive forms. The AP allele is linked to castration resistance, mainly in low-volume tumors. Here, we investigate the association of HSD3B1 alleles with outcomes in ARCHES, a multinational, double-blind, randomized, placebo-controlled phase 3 trial that demonstrated clinical benefit with enzalutamide plus androgen deprivation therapy (ADT) in men with metastatic hormone-sensitive prostate cancer (mHSPC) compared to those treated with placebo plus ADT. There are no significant differences between genotypes for clinical efficacy endpoints. Enzalutamide significantly improves radiographic progression-free survival and overall survival vs. placebo irrespective of HSD3B1 status. Men with the AP genotype have higher post-progression mortality and treatment-emergent adverse events, including hypertension, cardiovascular events, and gynecomastia, but a lower fracture rate. Overall, enzalutamide is beneficial in men with mHSPC independent of the HSD3B1 genotype. Inherited polymorphisms of HSD3B1 may account for differential toxicities.
HSD3B1 编码 3β-羟甾脱氢酶-1,它将肾上腺脱氢表雄酮转化为 5α-二氢睾酮,并以肾上腺允许(AP)或肾上腺限制形式遗传。AP 等位基因与去势抵抗有关,主要存在于小体积肿瘤中。在这里,我们研究了 HSD3B1 等位基因与 ARCHES 结果的关联,ARCHES 是一项多中心、双盲、随机、安慰剂对照的 3 期临床试验,与安慰剂加雄激素剥夺治疗(ADT)相比,enzalutamide 加 ADT 治疗转移性激素敏感前列腺癌(mHSPC)的男性具有临床获益。基因型与临床疗效终点无显著差异。与安慰剂相比,无论 HSD3B1 状态如何,enzalutamide 均显著改善放射学无进展生存期和总生存期。AP 基因型的男性在疾病进展后死亡率和治疗相关不良事件(包括高血压、心血管事件和男性乳房发育)更高,但骨折率较低。总体而言,enzalutamide 对 mHSPC 男性有益,与 HSD3B1 基因型无关。HSD3B1 的遗传多态性可能导致不同的毒性。