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口服递增剂量环孢素A联合4-表阿霉素治疗晚期结直肠癌的I期研究

Oral escalating dose of cyclosporine-a combined with 4-epidoxorubicin in advanced colorectal-cancer - a phase-I study.

作者信息

Cascinu S, Delferro E, Grianti C, Fedeli A, Catalano G

机构信息

OSPED RIUNITI PESARO,ANAL LAB,I-61100 PESARO,ITALY.

出版信息

Oncol Rep. 1995 Nov;2(6):1033-5. doi: 10.3892/or.2.6.1033.

Abstract

Multidrug resistance, a major factor in the resistance to drugs, can be reversed by cyclosporin A. It is generally given by intravenous route. The aim of the present study was to assess the possibility of achieving useful plasma levels, giving cyclosporin A orally in advanced colorectal cancer patients treated with 4-epidoxorubicin. Cyclosporin A was given orally twice a day, for four days. The starting study dose was 5 mg/kg. Dose in cohorts of 3 patients was escalated to 10, 15, 20, 30, 40 mg/kg if the previous dose was not able to determine the target blood level (2,000 ng/ml). Cyclosporin A blood levels were analyzed by a specific fluorescence polarization immunoassay method (TDx; Abbot Laboratoires, North Chigaco, IL). 4-epidoxorubicin was given at a fixed dose of 75 mg/m(2), every 3 weeks. None of the dose levels of cyclosporin A given orally produced the target blood level. Only two patients, receiving cyclosporin at a dose of 30 mg/kg, and two after a CsA dose of 40 mg/kg, presented blood levels higher than 1,000 ng/ml, but however, lower than 1,500 ng/ml. In conclusion, the oral route of administration of cyclosporin does not seem recommendable in order to reverse multidrug resistance because it is not able to produce sufficient plasma levels.

摘要

多药耐药是耐药的一个主要因素,环孢素A可逆转这种耐药性。环孢素A通常通过静脉途径给药。本研究的目的是评估在接受4-表阿霉素治疗的晚期结直肠癌患者中口服环孢素A达到有效血浆水平的可能性。环孢素A每天口服两次,共四天。研究起始剂量为5mg/kg。如果前一剂量未能达到目标血药浓度(2000ng/ml),则每组3例患者的剂量依次递增至10、15、20、30、40mg/kg。采用特异性荧光偏振免疫分析法(TDx;雅培实验室,伊利诺伊州北芝加哥)分析环孢素A的血药浓度。4-表阿霉素以固定剂量75mg/m²,每3周给药一次。口服的任何剂量水平的环孢素A均未达到目标血药浓度。只有两名接受30mg/kg剂量环孢素的患者以及两名接受40mg/kg剂量环孢素的患者血药浓度高于1000ng/ml,但低于1500ng/ml。总之,口服环孢素给药途径似乎不适合用于逆转多药耐药,因为它无法产生足够的血浆浓度。

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