Phase I Study of DSTP3086S, an Antibody-Drug Conjugate Targeting Six-Transmembrane Epithelial Antigen of Prostate 1, in Metastatic Castration-Resistant Prostate Cancer

被引:60
作者
Danila, Daniel C. [1 ,2 ]
Szmulewitz, Russell Z. [3 ]
Vaishampayan, Ulka [4 ]
Higano, Celestia S. [5 ,6 ]
Baron, Ari D. [7 ]
Gilbert, Houston N. [8 ]
Brunstein, Flavia [8 ]
Milojic-Blair, Marija [8 ]
Wang, Bei [8 ]
Kabbarah, Omar [8 ]
Mamounas, Michael [8 ]
Fine, Bernard M. [8 ]
Maslyar, Daniel J. [8 ]
Ungewickell, Alexander [8 ]
Scher, Howard I. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[2] Weill Cornell Med Coll, New York, NY USA
[3] Univ Chicago, Chicago, IL 60637 USA
[4] Karmanos Canc Inst, Detroit, MI USA
[5] Univ Washington, Seattle, WA 98195 USA
[6] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[7] Calif Pacific Med Ctr, San Francisco, CA USA
[8] Genentech Inc, San Francisco, CA USA
关键词
CIRCULATING TUMOR-CELLS; INCREASED SURVIVAL; ABIRATERONE; ENZALUTAMIDE; PREDNISONE; VEDOTIN; MARKERS; SAFETY; STEAP;
D O I
10.1200/JCO.19.00646
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Six-transmembrane epithelial antigen of the prostate 1 (STEAP1) is highly expressed in prostate cancers. DSTP3086S is a humanized immunoglobulin G1 anti-STEAP1 monoclonal antibody linked to the potent antimitotic agent monomethyl auristatin E. This study evaluated the safety and activity of DSTP3086S in patients with metastatic castration-resistant prostate cancer. METHODS Patients were enrolled in a 3 + 3 dose escalation study to evaluate DSTP3086S (0.3 to 2.8 mg/kg intravenously) given once every 3 weeks followed by cohort expansion at the recommended phase II dose or weekly (0.8 to 1.0 mg/kg). RESULTS Seventy-seven patients were given DSTP3086S once every 3 weeks, and seven were treated weekly. Two patients in the once-every-3-weeks dose escalation had dose-limiting grade 3 transaminitis. Grade 3 hyperglycemia and grade 4 hypophosphatemia were dose-limiting toxicities in one patient treated at 1.0 mg/kg weekly. Initial cohort expansion evaluated dosing at 2.8 mg/kg once every 3 weeks (n = 10), but frequent dose reductions led to testing of 2.4 mg/kg (n = 39) in the expansion phase. Common related adverse events (> 20%) across doses (once every 3 weeks) were fatigue, peripheral neuropathy, nausea, constipation, anorexia, diarrhea, and vomiting. DSTP3086S pharmacokinetics were linear. Among 62 patients who received > 2 mg/kg DSTP3086S once every 3 weeks, 11 (18%) demonstrated a >= 50% decline in prostate-specific antigen; two (6%) of 36 with measurable disease at baseline achieved a radiographic partial response; and of 27 patients with informative unfavorable baseline circulating tumor cells >= 5/7.5 mL of blood, 16 (59%) showed conversions to favorable circulating tumor cells < 5. No prostate-specific antigen or RECIST responses were seen with weekly dosing. CONCLUSION DSTP3086S has acceptable safety at the recommended phase II dose level of 2.4 mg/kg once every 3 weeks. Antitumor activity at doses between 2.25 and 2.8 mg/kg once every 3 weeks supports the potential benefit of treating STEAP1-expressing metastatic castration-resistant prostate cancer with an STEAP1-targeting antibody-drug conjugate.
引用
收藏
页码:3518 / +
页数:11
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