Division of Medical Oncology, Weill Cornell Medicine, New York, NY 10065, USA.
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and NewYork Presbyterian, New York, NY 10021, USA.
Sci Transl Med. 2019 Mar 20;11(484). doi: 10.1126/scitranslmed.aav0891.
Histologic transformation to small cell neuroendocrine prostate cancer occurs in a subset of patients with advanced prostate cancer as a mechanism of treatment resistance. Rovalpituzumab tesirine (SC16LD6.5) is an antibody-drug conjugate that targets delta-like protein 3 (DLL3) and was initially developed for small cell lung cancer. We found that DLL3 is expressed in most of the castration-resistant neuroendocrine prostate cancer (CRPC-NE) (36 of 47, 76.6%) and in a subset of castration-resistant prostate adenocarcinomas (7 of 56, 12.5%). It shows minimal to no expression in localized prostate cancer (1 of 194) and benign prostate (0 of 103). DLL3 expression correlates with neuroendocrine marker expression, loss, and aggressive clinical features. DLL3 in circulating tumor cells was concordant with matched metastatic biopsy (87%). Treatment of DLL3-expressing prostate cancer xenografts with a single dose of SC16LD6.5 resulted in complete and durable responses, whereas DLL3-negative models were insensitive. We highlight a patient with neuroendocrine prostate cancer with a meaningful clinical and radiologic response to SC16LD6.5 when treated on a phase 1 trial. Overall, our findings indicate that DLL3 is preferentially expressed in CRPC-NE and provide rationale for targeting DLL3 in patients with DLL3-positive metastatic prostate cancer.
组织学转化为小细胞神经内分泌前列腺癌发生在一部分晚期前列腺癌患者中,是治疗耐药的一种机制。Rovalpituzumab tesirine(SC16LD6.5)是一种针对 Delta-like 蛋白 3(DLL3)的抗体药物偶联物,最初是为小细胞肺癌开发的。我们发现 DLL3 在大多数去势抵抗性神经内分泌前列腺癌(CRPC-NE)(47 例中的 36 例,76.6%)和一部分去势抵抗性前列腺腺癌(56 例中的 7 例,12.5%)中表达。它在局限性前列腺癌(194 例中的 1 例)和良性前列腺(103 例中的 0 例)中表达很少或没有。DLL3 的表达与神经内分泌标志物的表达、缺失和侵袭性临床特征相关。循环肿瘤细胞中的 DLL3 与匹配的转移性活检结果一致(87%)。用单剂量 SC16LD6.5 治疗表达 DLL3 的前列腺癌异种移植,导致完全和持久的反应,而 DLL3 阴性模型则不敏感。我们强调了一名神经内分泌前列腺癌患者,在接受 SC16LD6.5 的 1 期试验治疗时,表现出有意义的临床和影像学反应。总的来说,我们的发现表明 DLL3 在 CRPC-NE 中优先表达,并为在 DLL3 阳性转移性前列腺癌患者中靶向 DLL3 提供了依据。