Pharmacokinetics and Toxicity of Sodium Selenite in the Treatment of Patients with Carcinoma in a Phase I Clinical Trial: The SECAR Study

被引:91
作者
Brodin, Ola [1 ]
Eksborg, Staffan [2 ]
Wallenberg, Marita [3 ]
Asker-Hagelberg, Charlotte [4 ,5 ]
Larsen, Erik H. [6 ]
Mohlkert, Dag [7 ]
Lenneby-Helleday, Clara [1 ]
Jacobsson, Hans [8 ]
Linder, Stig [9 ,10 ]
Misra, Sougat [3 ]
Bjornstedt, Mikael [3 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp Sodersjukhuset, Dept Oncol, SE-11883 Stockholm, Sweden
[2] Karolinska Inst, Karolinska Univ Hosp Solna, Dept Womens & Childrens Hlth, SE-17176 Stockholm, Sweden
[3] Karolinska Inst, Karolinska Univ Hosp Huddinge, Div Pathol F46, Dept Lab Med, SE-14186 Stockholm, Sweden
[4] Med Prod Agcy, SE-75103 Uppsala, Sweden
[5] Karolinska Inst, Karolinska Univ Hosp, Dept Med, Clin Pharmacol Unit, SE-17176 Stockholm, Sweden
[6] Tech Univ Denmark, Natl Food Inst, DK-2860 Soborg, Denmark
[7] Karolinska Univ Hosp Sodersjukhuset, Dept Radiol, SE-17176 Stockholm, Sweden
[8] Karolinska Univ Hosp, Dept Radiol, SE-17176 Stockholm, Sweden
[9] Karolinska Inst, Dept Oncol Pathol, SE-17176 Stockholm, Sweden
[10] Linkoping Univ, Dept Med & Hlth, SE-58183 Linkoping, Sweden
关键词
sodium selenite; carcinoma; pharmacokinetics; maximum tolerated dose; CANCER-CELLS; TRANSPLANTABLE TUMOR; OXIDATIVE STRESS; DRUG-RESISTANT; CYTOTOXICITY; SENSITIVITY; INHIBITION; APOPTOSIS;
D O I
10.3390/nu7064978
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Sodium selenite at high dose exerts antitumor effects and increases efficacy of cytostatic drugs in multiple preclinical malignancy models. We assessed the safety and efficacy of intravenous administered sodium selenite in cancer patients' refractory to cytostatic drugs in a phase I trial. Patients received first line of chemotherapy following selenite treatment to investigate altered sensitivity to these drugs and preliminary assessment of any clinical benefits. Materials and Methods: Thirty-four patients with different therapy resistant tumors received iv sodium selenite daily for consecutive five days either for two weeks or four weeks. Each cohort consisted of at least three patients who received the same daily dose of selenite throughout the whole treatment. If 0/3 patients had dose-limiting toxicities (DLTs), the study proceeded to the next dose-level. If 2/3 had DLT, the dose was considered too high and if 1/3 had DLT, three more patients were included. Dose-escalation continued until the maximum tolerated dose (MTD) was reached. MTD was defined as the highest dose-level on which 0/3 or 1/6 patients experienced DLT. The primary endpoint was safety, dose-limiting toxic effects and the MTD of sodium selenite. The secondary endpoint was primary response evaluation. Results and Conclusion: MTD was defined as 10.2 mg/m(2), with a calculated median plasma half-life of 18.25 h. The maximum plasma concentration of selenium from a single dose of selenite increased in a nonlinear pattern. The most common adverse events were fatigue, nausea, and cramps in fingers and legs. DLTs were acute, of short duration and reversible. Biomarkers for organ functions indicated no major systemic toxicity. In conclusion, sodium selenite is safe and tolerable when administered up to 10.2 mg/m(2) under current protocol. Further development of the study is underway to determine if prolonged infusions might be a more effective treatment strategy.
引用
收藏
页码:4978 / 4994
页数:17
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