Franchi F, Barone C, Ricevuto E, Cassano A, Astone A, Pozzo C, Sofo L, Netri G, Ratto C, Coco C
Third Department of Internal Medicine, University La Sapienza, Roma, Italia.
Med Oncol Tumor Pharmacother. 1991;8(2):69-73. doi: 10.1007/BF02988856.
Ninety-six patients with colorectal cancer (stage B2-C) were randomized to the control arm or to receive adjuvant chemotherapy with folinic acid, FU and MMC. Ninety-three patients are evaluable. The median follow up is 12 months. The average time between surgery and the start of therapy is 28 days. Toxicity is evaluable in 36 of 41 treated patients. Four patients (10%) failed to complete the projected treatment due to toxicity. Toxicity observed in 208 courses of therapy was mostly gastrointestinal and hematological. No cases of treatment related death or cancer-associated hemolytic uremic syndrome (C-HUS) were reported. The average relative dose intensity (rDI) of the projected treatment was 82.6%. Our study is ongoing and further patients are required to achieve statistically significant results.
96例结直肠癌患者(B2 - C期)被随机分为对照组或接受亚叶酸、氟尿嘧啶和丝裂霉素的辅助化疗。93例患者可进行评估。中位随访时间为12个月。手术与治疗开始之间的平均时间为28天。41例接受治疗的患者中有36例可评估毒性。4例患者(10%)因毒性未能完成预计治疗。在208个疗程的治疗中观察到的毒性主要是胃肠道和血液学方面的。未报告与治疗相关的死亡病例或癌症相关性溶血尿毒综合征(C - HUS)。预计治疗的平均相对剂量强度(rDI)为82.6%。我们的研究正在进行中,需要更多患者才能取得具有统计学意义的结果。