Department of Hematology and Oncology, University of Texas Southwestern at Dallas and Dallas VA Medical Center, Dallas, Texas 75201, USA. Henrikb.illum@ va.gov
Anticancer Drugs. 2011 Apr;22(4):324-9. doi: 10.1097/CAD.0b013e3283425c14.
Neoadjuvant radiation therapy with concurrent 5-fluorouracil-based chemotherapy is currently considered the standard of care for locally advanced rectal cancer. Pathologically complete response is a desirable outcome and has been associated with increased disease-free survival. There is a need to improve on this approach given that only approximately 10% achieve a pathologically complete response. Irinotecan has an established role in the treatment of metastatic rectal cancer. Both in-vitro and in-vivo data have shown promising radiosensitization properties. This study provides an overview of the published clinical trials evaluating the role of irinotecan as a radiosensitizer in the management of locally advanced rectal cancer. Although early-phase clinical trials initially showed promising results, this did not translate into improved outcome in a larger randomized phase II trial. Increased topoisomerase I expression has recently been identified as a possible predictive marker for improved response to irinotecan-based radiosensitization. This finding could help identify a subset of patients more likely to benefit from the addition of irinotecan in future trials.
新辅助放化疗联合氟尿嘧啶类化疗目前被认为是局部晚期直肠癌的标准治疗方法。病理完全缓解是一种理想的治疗效果,与无病生存期的延长相关。但目前仅有约 10%的患者能够达到病理完全缓解,因此需要改进这种治疗方法。伊立替康在转移性直肠癌的治疗中具有明确的作用。体外和体内数据均显示出有希望的放射增敏特性。本研究综述了已发表的临床试验,评估了伊立替康作为放射增敏剂在局部晚期直肠癌治疗中的作用。尽管早期临床试验最初显示出了有前景的结果,但这并没有转化为更大规模的随机二期临床试验中治疗效果的改善。最近发现拓扑异构酶 I 表达增加可能是对伊立替康放射增敏反应改善的一个潜在预测标志物。这一发现有助于确定在未来试验中更有可能从伊立替康加入中获益的患者亚组。