Haller D G
Hematology-Oncology Division, Hospital of the University of Pennsylvania, University of Pennsylvania Medical Center 19104, USA.
Eur J Cancer. 1995 Jul-Aug;31A(7-8):1255-63. doi: 10.1016/0959-8049(95)00258-k.
Adjuvant therapy of colorectal cancer is one of the most active areas of clinical oncology research. Although the data for the benefits from early trials of adjuvant therapy were inconclusive, these trials suffered from inadequate sample sizes, poor staging, potentially suboptimal treatment regimens and ill-defined prognostic subgroups. More recently, larger trials of higher scientific quality have demonstrated that regimens of fluorouracil plus levamisole in stage III colon cancer and fluorouracil with postoperative radiation in stages II and III rectal cancer can reduce mortality. Such regimens have now become standard practice in settings in which treatment is believed to be both efficacious and tolerable, and when the overall impact of therapy is considered to be clinically relevant. More recent advances in adjuvant treatment of colorectal cancer further support the role of fluorouracil-based regimens. Peri-operative portal vein infusions of fluorouracil demonstrate improved relapse-free and overall survival, and infusional fluorouracil administered with radiation for rectal primaries appears superior to less intensive bolus fluorouracil regimens. Completed trials of fluorouracil plus leucovorin combinations are awaiting maturation, with expectations for superior adjuvant activity based on demonstrated improved response rates for biochemically modulated fluorouracil in advanced metastatic colorectal cancer. New systemic agents are also entering large-scale adjuvant trials, including monoclonal antibody 17-1a, given alone and in conjunction with standard fluorouracil regimens. Additional cytotoxic drugs, including CPT-11 and Tomudex, offer new opportunities for alternative adjuvant regimens for the large, heterogeneous population of patients with resected colorectal cancer.
结直肠癌的辅助治疗是临床肿瘤学研究中最活跃的领域之一。尽管早期辅助治疗试验所获益处的数据尚无定论,但这些试验存在样本量不足、分期不佳、治疗方案可能不够优化以及预后亚组定义不明确等问题。最近,科学性更强的大型试验表明,III期结肠癌采用氟尿嘧啶加左旋咪唑方案,II期和III期直肠癌采用氟尿嘧啶加术后放疗,可降低死亡率。在认为治疗有效且可耐受,且治疗的总体影响具有临床相关性的情况下,此类方案现已成为标准治疗方法。结直肠癌辅助治疗的最新进展进一步支持了以氟尿嘧啶为基础的治疗方案的作用。围手术期门静脉输注氟尿嘧啶可改善无复发生存率和总生存率,直肠原发性肿瘤采用氟尿嘧啶联合放疗似乎优于强度较低的氟尿嘧啶推注方案。氟尿嘧啶加亚叶酸钙联合方案的已完成试验正在等待结果成熟,基于晚期转移性结直肠癌中生物化学调节氟尿嘧啶的反应率提高,预计其辅助活性更佳。新型全身治疗药物也正在进入大规模辅助治疗试验,包括单独使用及与标准氟尿嘧啶方案联合使用的单克隆抗体17-1a。其他细胞毒性药物,包括伊立替康和拓扑替康,为大量异质性的已切除结直肠癌患者提供了替代辅助治疗方案的新机会。