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A Phase 1/2 multicenter trial of DKN-01 as monotherapy or in combination with docetaxel for the treatment of metastatic castration-resistant prostate cancer (mCRPC)

医学 多西紫杉醇 前列腺癌 临床终点 肿瘤科 联合疗法 队列 内科学 恩扎鲁胺 丹麦克朗 临床试验 癌症 雄激素受体 Wnt信号通路 生物化学 化学 基因
作者
David R. Wise,Russell K. Pachynski,Samuel R. Denmeade,Rahul Aggarwal,Jiehui Deng,Victor Adorno Febles,Arjun Vasant Balar,Minas P. Economides,Cynthia A. Loomis,Shanmugapriya Selvaraj,Michael Haas,Michael H. Kagey,Walter Newman,Jason Baum,Andrea B. Troxel,Sarah Griglun,Dayna Leis,Ning Yang,Viktoriya Aranchiy,Sabrina Rocha Machado,Erika Waalkes,Gabrielle Gargano,Nadia Soamchand,Amrutesh S. Puranik,Pratip K. Chattopadhyay,Ezeddin Fedal,Fang‐Ming Deng,Qinghu Ren,Luis Chiriboga,Jonathan Melamed,Cynthia A. Sirard,Kwok-Kin Wong
出处
期刊:Prostate Cancer and Prostatic Diseases [Springer Nature]
标识
DOI:10.1038/s41391-024-00798-z
摘要

Dickkopf-related protein 1 (DKK1) is a Wingless-related integrate site (Wnt) signaling modulator that is upregulated in prostate cancers (PCa) with low androgen receptor expression. DKN-01, an IgG4 that neutralizes DKK1, delays PCa growth in pre-clinical DKK1-expressing models. These data provided the rationale for a clinical trial testing DKN-01 in patients with metastatic castration-resistant PCa (mCRPC).This was an investigator-initiated parallel-arm phase 1/2 clinical trial testing DKN-01 alone (monotherapy) or in combination with docetaxel 75 mg/m2 (combination) for men with mCRPC who progressed on ≥1 AR signaling inhibitors. DKK1 status was determined by RNA in-situ expression. The primary endpoint of the phase 1 dose escalation cohorts was the determination of the recommended phase 2 dose (RP2D). The primary endpoint of the phase 2 expansion cohorts was objective response rate by iRECIST criteria in patients treated with the combination.18 pts were enrolled into the study-10 patients in the monotherapy cohorts and 8 patients in the combination cohorts. No DLTs were observed and DKN-01 600 mg was determined as the RP2D. A best overall response of stable disease occurred in two out of seven (29%) evaluable patients in the monotherapy cohort. In the combination cohort, five out of seven (71%) evaluable patients had a partial response (PR). A median rPFS of 5.7 months was observed in the combination cohort. In the combination cohort, the median tumoral DKK1 expression H-score was 0.75 and the rPFS observed was similar between patients with DKK1 H-score ≥1 versus H-score = 0.DKN-01 600 mg was well tolerated. DKK1 blockade has modest anti-tumor activity as a monotherapy for mCRPC. Anti-tumor activity was observed in the combination cohorts, but the response duration was limited. DKK1 expression in the majority of mCRPC is low and did not clearly correlate with anti-tumor activity of DKN-01 plus docetaxel.
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