Sun Weijing, Haller Daniel
University of Pennsylvania Cancer Center, Philadelphia, Pennsylvania, USA.
Oncology (Williston Park). 2003 Sep;17(9 Suppl 8):16-9.
It is a continuing challenge for oncologists to effectively treat advanced/metastatic pancreatic and biliary cancer. Both irinotecan (CPT-11, Camptosar) and gemcitabine (Gemzar) have shown activity against these diseases with different mechanisms. Preclinical and clinical data also suggest additive or synergistic effects of the combination of these two agents with few or no overlapping toxicities. Phosphorylation of gemcitabine, a process of intracellular activation of the agent, is dose-rate dependent. It has been suggested that the fixed-dose-rate infusion of gemcitabine increases the concentration of intracellular triphosphate gemcitabine, which in turn may result in more objective responses and longer median survival compared to the standard infusion. This phase I study tests the toxicity of the combination of irinotecan with fixed-dose-rate infusion of gemcitabine, and determines the dose of the combination for phase II investigation.
对于肿瘤学家而言,有效治疗晚期/转移性胰腺癌和胆管癌一直是一项挑战。伊立替康(CPT-11,开普拓)和吉西他滨(健择)均已显示出针对这些疾病的活性,但其作用机制不同。临床前和临床数据还表明,这两种药物联合使用具有相加或协同效应,且毒性很少或没有重叠。吉西他滨的磷酸化是该药物细胞内激活的过程,它与剂量率相关。有人提出,与标准输注相比,吉西他滨的固定剂量率输注可提高细胞内三磷酸吉西他滨的浓度,这反过来可能会带来更多客观缓解并延长中位生存期。这项I期研究测试了伊立替康与吉西他滨固定剂量率输注联合使用的毒性,并确定用于II期研究的联合用药剂量。