Delord Jean-Pierre, Puozzo Christian, Lefresne Florence, Bugat Roland
Institut Claudius Regaud, Toulouse, France.
Anticancer Res. 2009 Feb;29(2):553-60.
Vinorelbine (VRL)-cisplatin (CDDP) is an active doublet for advanced non-small cell lung cancer. CDDP has a narrow therapeutic index and may produce a cumulative nephrotoxicity over the treatment period. This study was to assess the risks of drug-drug interaction (DDI) over 3 consecutive cycles of VRL-CDDP combined treatments.
An open-label, nonrandomised, phase I study was carried out. Patients with normal hepatic/renal functions. D1: CDDP 100 mg/m2--D1, D8: oral VRL 60 mg/m2 q3w. Pharmacokinetics (PK) over the first 3 cycles. PK comparison between cycles and between study vs. literature.
Thirteen patients were evaluable for safety and PK. Adverse events were those frequently observed with CDDP or VRL, and consisted of hematological toxicities, nausea, vomiting and constipation. Concerning VRL and CDDP PK, no difference was detected between the 3 administrations nor between the study and reference values.
The absence of DDI between CDDP and oral VRL was demonstrated over 3 consecutive cycles of therapy.
长春瑞滨(VRL)-顺铂(CDDP)是晚期非小细胞肺癌的一种有效的双联化疗方案。顺铂的治疗指数较窄,在治疗期间可能会产生累积性肾毒性。本研究旨在评估连续3个周期的VRL-CDDP联合治疗中药物相互作用(DDI)的风险。
开展了一项开放标签、非随机的I期研究。纳入肝/肾功能正常的患者。第1天:顺铂100mg/m²——第1天,第8天:口服长春瑞滨60mg/m²,每3周一次。观察前3个周期的药代动力学(PK)。比较各周期之间以及研究结果与文献之间的PK。
13例患者可进行安全性和PK评估。不良事件为顺铂或长春瑞滨常见的不良事件,包括血液学毒性、恶心、呕吐和便秘。关于长春瑞滨和顺铂的PK,3次给药之间以及研究结果与参考值之间均未检测到差异。
在连续3个周期的治疗中,证实顺铂与口服长春瑞滨之间不存在药物相互作用。