Phase I and pharmacokinetic study of PKC412, an inhibitor of protein kinase C

被引:192
|
作者
Propper, DJ
McDonald, AC
Man, A
Thavasu, P
Balkwill, F
Braybrooke, JP
Caponigro, F
Graf, P
Dutreix, C
Blackie, R
Kaye, SB
Ganesan, TS
Talbot, DC
Harris, AL
Twelves, C
机构
[1] Western Infirm & Associated Hosp, Beatson Oncol Ctr, Canc Res Campaign, Dept Med Oncol, Glasgow G11 6NT, Lanark, Scotland
[2] Imperial Canc Res Fund Labs, London, England
[3] Novartis Pharma AG, Basel, Switzerland
关键词
D O I
10.1200/JCO.2001.19.5.1485
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: N-Benzoyl staurosporine (PKC412) is a protein kinase C inhibitor with antitumor activity in laboratory models. We determined the toxicity of oral PKC412 administered daily for repeat cycles of 28 days. Patients and Methods: Thirty-two patients with advanced solid cancers were treated at seven dose levels (12.5 to 300 mg daily) for a total of 68 cycles. Results: The most frequent treatment-related toxicities were nausea, vomiting, fatigue, and diarrhea. At the two top dose levels (225 and 300 mg/d), 15 of 16 patients experienced nausea/vomiting (common toxicity criteria [CTC], version 1), grade 2 in nine of 16 and grade 3 in three of 16 patients; and six of 16 patients developed CTC grade 2 diarrhea. After 1 month of treatment, there were significant reductions in circulating lymphocyte (P <.02) and monocyte (P <.01) counts in patients receiving doses greater than or equal to 100 mg/d. Nevertheless, only two patients developed myelosuppression (both grade 2). Of two patients with progressive cholangiocarcinoma, one attained stable disease lasting 4.5 months and one a partial response lasting 4 months. There was a linear relationship between PKC412 dose and area under the curve(0-24 hours) and maximum plasma concentration with marked interpatient variability. The estimated median elimination half-life was 1.6 days (range, 0.9 to 4.0 days), and a metabolite with a median half-life of 36 days was detected. Steady-state PKC412 plasma levels at the top three dose cohorts (150 to 300 mg) were five to 10 times the cellular 50% inhibitory concentration for PKC412 of 0.2 to 0.7 mu mol/L. Conclusion: PKC412 can be safely administered by chronic oral therapy, and 150 mg/d is suitable for phase II studies. The pharmacokinetics and lack of conventional toxicity indicate that pharmacodynamic measures may be additionally needed to optimize the drug dose and schedule. J Clin Oncol 19:1485-1492. (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:1485 / 1492
页数:8
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