Lawrence W, Terz J J, Horsley S, Donaldson M, Lovett W L, Brown P W, Ruffner B W, Regelson W
Ann Surg. 1975 May;181(5):616-23. doi: 10.1097/00000658-197505000-00016.
A combined intraoperative and postoperative adjuvant program of 5 minus Fluorouracil (5 FU) for patients undergoing "curative" resection for adenocarcinoma of the colon and rectum was initiated as a randomized clinical trial in January 1968. Patients at the Medical College of Virginia and the University of Virginia were randomly assigned to an intraluminal 5 FU or intraluminal control (Saline) group and were so treated at the time of surgical resection if findings at operation indicated that all gross neoplastic disease could be resected. Patients with operative findings denoting incurability were eliminated from the study after surgical exploration. Those patients receiving intraluminal 5 FU (30mg/kg) received intravenous 5 FU (10mg/kg) on each of the two first postoperative days and 5 subsequent postoperative courses of oral 5FU (90 mg/kg in each 18 day course) over a one year period. By December 31, 1973 (6 years) 156 patients undergoing "curative" resection were entered into the study. SU therapy with the control or "No Treat" group reveal no significant benefit from this intensive adjuvant course of 5 FU thus far. Continued assessment of these patient groups and their subgroups will be required to develop confidence in these findings but the data thus far suggest no potential benefit from this particular adjuvant program.
1968年1月,一项针对接受结肠癌和直肠癌“根治性”切除术患者的术中及术后联合辅助治疗方案启动,该方案采用5-氟尿嘧啶(5-FU),作为一项随机临床试验。弗吉尼亚医学院和弗吉尼亚大学的患者被随机分配至腔内5-FU组或腔内对照组(生理盐水组),如果手术结果表明所有肉眼可见的肿瘤性疾病均可切除,则在手术切除时接受相应治疗。手术探查后,手术结果显示无法治愈的患者被排除在研究之外。接受腔内5-FU治疗的患者(30mg/kg)在术后头两天每天接受静脉注射5-FU(10mg/kg),并在术后一年的时间里随后接受5个疗程的口服5-FU(每18天疗程90mg/kg)。到1973年12月31日(6年),共有156例接受“根治性”切除术的患者进入该研究。到目前为止,对照组或“不治疗”组的5-FU辅助强化疗程未显示出显著益处。需要对这些患者组及其亚组进行持续评估,以便对这些结果有信心,但目前的数据表明,该特定辅助治疗方案没有潜在益处。