Rosenthal D I, Carbone D P
Department of Radiation Oncology, Harold C. Simmons Comprehensive Cancer Center, University of Texas, Southwestern Medical Center at Dallas, USA.
J Infus Chemother. 1995 Spring;5(2):46-54.
Taxol (paclitaxel) is the prototype of a new class of cancer drugs, the taxanes. This group of anticancer agents have a novel mechanism of action, broad clinical activity, and potential as clinical radiosensitizers. Paclitaxel may be the most efficacious single chemotherapy agent for head and neck cancer with a 40% response rate for patients with recurrent disease. As it is possible to achieve durable control with radiotherapy of locally advanced head and neck cancer in only a minority of cases, chemotherapy drugs such as paclitaxel are being used with radiotherapy in an attempt to improve tumor control. Paclitaxel stabilizes microtubules and leads to accumulation of cells at the G2/mitosis phase of the cell cycle, which is a necessary condition for its antitumor effect, and also the phase with the greatest relative radiosensitivity. Paclitaxel has been shown to be a radiosensitizer in vitro for some but not all cell lines studied. In vitro dose-response data for paclitaxel paradoxically suggest that prolonged exposure to relatively low concentrations--those easily achievable clinically--may be more effective than higher doses both for direct cytotoxicity and radiosensitization. These data suggest that paclitaxel has potential as a clinical radiosensitizer for head and neck cancer, and phase I trials are in progress. We review the laboratory and clinical studies supplying the rationale, risks, and potential benefits for the concurrent use of paclitaxel and radiotherapy, the current investigational clinical trials, including our NCI-sponsored phase I trials with continuous infusion paclitaxel as a potential radiosensitizer for head and neck cancer.(ABSTRACT TRUNCATED AT 250 WORDS)
紫杉醇是一类新型抗癌药物紫杉烷类的原型。这类抗癌药物具有独特的作用机制、广泛的临床活性以及作为临床放射增敏剂的潜力。紫杉醇可能是治疗头颈癌最有效的单一化疗药物,对复发性疾病患者的缓解率为40%。由于仅在少数情况下局部晚期头颈癌的放射治疗能够实现持久控制,因此正在将紫杉醇等化疗药物与放射治疗联合使用,以试图提高肿瘤控制效果。紫杉醇可使微管稳定,并导致细胞在细胞周期的G2/有丝分裂期积聚,这是其抗肿瘤作用的必要条件,也是相对放射敏感性最高的阶段。已证明紫杉醇对部分但并非所有研究的细胞系在体外具有放射增敏作用。紫杉醇的体外剂量反应数据自相矛盾地表明,对于直接细胞毒性和放射增敏作用而言,长时间暴露于相对较低浓度(临床上易于达到的浓度)可能比高剂量更有效。这些数据表明紫杉醇有潜力作为头颈癌的临床放射增敏剂,目前I期试验正在进行中。我们回顾了为紫杉醇与放射治疗联合使用提供理论依据、风险和潜在益处的实验室及临床研究,以及当前的临床研究试验,包括我们由美国国立癌症研究所赞助的以持续输注紫杉醇作为头颈癌潜在放射增敏剂的I期试验。(摘要截选于250词)