Conti J A, Kemeny N E, Saltz L B, André A M, Grossano D D, Bertino J R
Department of Medicine, Memorial Sloan-Kettering Cancer Center, Cornell University Medical College, New York, New York 10021.
Cancer. 1995 Feb 1;75(3):769-74. doi: 10.1002/1097-0142(19950201)75:3<769::aid-cncr2820750304>3.0.co;2-5.
No effective systemic salvage therapy exists for patients with advanced colorectal cancer who progress after receiving bolus fluorouracil (FU) and leucovorin (LV) chemotherapy. In vitro data suggest that bolus FU resistance can be overcome by continuous infusion (CI) FU, and that the cytotoxic effects of Mitomycin-C (MMC) and FU are synergistic. Based on this data, a Phase II trial of CI FU and LV with bolus MMC in patients with advanced colorectal carcinoma who progressed on only one previous chemotherapy regimen was performed.
Twenty-eight patients with advanced colorectal carcinoma who had progressed after one previous chemotherapy regimen of bolus FU/LV were treated with bolus MMC 10 mg/m2 every 6 weeks and CI FU 200 mg/m2/day admixed with LV 10 mg/m2/day given 14 days on/7 days off.
The partial response rate in 24 evaluable patients was 17% (95% confidence interval, 2-32%) with a median response duration of 9.5 months (range, 4.2-12.0 months). Twelve (50%) additional patients achieved disease stabilization. Median survival was 9.9 months in the whole group (28 patients) and 11.5 months in the 24 evaluable patients. The major toxicities were grade 4 diarrhea occurring in two patients and grade 3 mucositis occurring in five patients. There was minimal myelosuppression (grade 3 thrombocytopenia in one patient) and no occurrences of hand-foot syndrome or cardiotoxicity.
This regimen demonstrates modest activity with acceptable toxicity in colorectal cancer patients who have failed a single-bolus FU/LV regimen. Modifications of this and other infusional FU-based chemotherapy regimens should be explored as potential salvage chemotherapy regimens in advanced colorectal cancer.
对于接受推注氟尿嘧啶(FU)和亚叶酸钙(LV)化疗后病情进展的晚期结直肠癌患者,不存在有效的全身挽救治疗方法。体外数据表明,持续输注(CI)FU可克服推注FU耐药性,且丝裂霉素-C(MMC)和FU的细胞毒性作用具有协同性。基于这些数据,对仅在之前一种化疗方案中病情进展的晚期结直肠癌患者进行了CI FU和LV联合推注MMC的II期试验。
28例在之前推注FU/LV化疗方案中病情进展的晚期结直肠癌患者,每6周接受10 mg/m²推注MMC治疗,并接受CI FU 200 mg/m²/天与LV 10 mg/m²/天混合给药,给药14天,休息7天。
24例可评估患者的部分缓解率为17%(95%置信区间,2%-32%),中位缓解持续时间为9.5个月(范围,4.2-12.0个月)。另外12例(50%)患者病情稳定。全组(28例患者)的中位生存期为9.9个月,24例可评估患者的中位生存期为11.5个月。主要毒性反应为2例患者出现4级腹泻,5例患者出现3级黏膜炎。骨髓抑制轻微(1例患者出现3级血小板减少),未出现手足综合征或心脏毒性。
该方案在单剂量推注FU/LV方案治疗失败的结直肠癌患者中显示出适度活性且毒性可接受。应探索对该方案及其他基于FU输注的化疗方案进行改良,作为晚期结直肠癌潜在的挽救化疗方案。