Minsky B D, Cohen A M, Enker W E, Saltz L, Guillem J G, Paty P B, Kelsen D P, Kemeny N, Ilson D, Bass J, Conti J
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Int J Radiat Oncol Biol Phys. 1997 Jan 15;37(2):289-95. doi: 10.1016/s0360-3016(96)00487-7.
We report the local control and survival of two Phase I dose escalation trials of combined preoperative 5-fluorouracil (5-FU), low-dose leucovorin (LV), and radiation therapy followed by postoperative LV/5-FU for the treatment of patients with locally advanced and unresectable rectal cancer.
A total of 36 patients (30 primary and 6 recurrent) received two monthly cycles of LV/5-FU (bolus daily x 5). Radiation therapy (50.40 Gy) began on day 1 in the 25 patients who received concurrent treatment and on day 8 in the 11 patients who received sequential treatment. Postoperatively, patients received a median of four monthly cycles of LV/5-FU.
The resectability rate with negative margins was 97%. The complete response rate was 11% pathologic and 14% clinical for a total of 25%. The 4-year actuarial disease-free survival was 67% and the overall survival was 76%. The crude local failure rate was 14% and the 4-year actuarial local failure rate was 30%. Crude local failure was lower in the four patients who had a pathologic complete response (0%) compared with those who either did not have a pathologic complete response (16%) or who had a clinical complete response (20%).
Our preliminary data with the low-dose LV regimen reveal encouraging downstaging, local control, and survival rates. Additional follow-up is needed to determine the 5-year results. The benefit of downstaging on local control is greatest in patients who achieve a pathologic complete response.
我们报告两项I期剂量递增试验的局部控制情况和生存率,这两项试验采用术前联合5-氟尿嘧啶(5-FU)、低剂量亚叶酸(LV)和放疗,随后术后给予LV/5-FU,用于治疗局部晚期且不可切除的直肠癌患者。
共有36例患者(30例原发性和6例复发性)接受了两个周期的LV/5-FU(每日推注×5天)。25例接受同步治疗的患者于第1天开始放疗(50.40 Gy),11例接受序贯治疗的患者于第8天开始放疗。术后,患者接受中位四个周期的LV/5-FU治疗。
切缘阴性的可切除率为97%。病理完全缓解率为11%,临床完全缓解率为14%,总完全缓解率为25%。4年精算无病生存率为67%,总生存率为76%。粗局部失败率为14%,4年精算局部失败率为30%。与未达到病理完全缓解(16%)或达到临床完全缓解(20%)的患者相比,4例达到病理完全缓解的患者粗局部失败率较低(0%)。
我们使用低剂量LV方案的初步数据显示出令人鼓舞的降期、局部控制和生存率。需要进一步随访以确定5年结果。降期对局部控制的益处在达到病理完全缓解的患者中最为显著。