Department of Internal Medicine, Erlangen University, Erlangen, Germany.
Med Sci Monit. 2010 Feb;16(2):CR49-55.
In 2003 Wein et al. published data after a short median follow up (23 months). Here we report on the long-term results.
MATERIAL/METHODS: The patients (n=20) received a neoadjuvant treatment regimen comprising biweekly 85 mg/m2 oxaliplatin (L-OHP) (2h-infusion, d 1, 15, 29 qd 57) and 500 mg/m2 calcium folinic acid (FA) (1-2h-infusion, d 1, 8, 15, 22, 29, 36 qd 57) followed by 2600 mg/m2 5-Fluorouracil (5-FU) (24h-infusion, d 1, 8, 15, 22, 29, 36 qd 57). Two cycles of chemotherapy were administered, with a third being added when the treatment was well tolerated. Thereafter, curative resection of the liver metastases was attempted.
After neoadjuvant therapy, imaging procedures revealed complete remission in 2 patients (10%) and partial remission in 18 patients (90%). Diarrhea (Common Toxicity Criteria toxicity grade 3) was observed in 6 patients (30%) as main symptom of toxicity, followed by vomiting in 3 patients (15%). Higher grade sensomotoric neuropathy did not present. The curative resectability rate (R0) was 80%. In 9 out of 18 patients (50%) undergoing surgical intervention minor postoperative complications occurred. No postoperative mortality was observed. Over a median follow up of 45,5 months the median survival of all patients is 3.0 years and the 5-year overall survival rate is 40%. The 5-year disease-free survival rate is 25%.
Neoadjuvant treatment with 5-FU combined with FA and L-OHP proved to be highly effective and well tolerated. Disease-free survival rates and median overall survival rates are promising.
2003 年,Wein 等人发表了短期随访(23 个月)的数据。在此,我们报告长期结果。
材料/方法:患者(n=20)接受了新辅助治疗方案,包括每周两次 85mg/m2 奥沙利铂(L-OHP)(2 小时输注,d1、15、29 qd57)和 500mg/m2 钙叶酸(FA)(1-2 小时输注,d1、8、15、22、29、36 qd57),随后给予 2600mg/m2 氟尿嘧啶(5-FU)(24 小时输注,d1、8、15、22、29、36 qd57)。共进行了两个周期的化疗,当治疗耐受良好时,再添加第三个周期。此后,尝试对肝转移灶进行治愈性切除。
新辅助治疗后,影像学检查显示 2 例患者(10%)完全缓解,18 例患者(90%)部分缓解。6 例患者(30%)主要表现为毒性的腹泻(常见毒性标准毒性等级 3),3 例患者(15%)出现呕吐。未出现更高等级的感觉运动性神经病。治愈性切除率(R0)为 80%。18 例接受手术干预的患者中,9 例(50%)发生轻微术后并发症。无术后死亡。在中位随访 45.5 个月时,所有患者的中位总生存时间为 3.0 年,5 年总生存率为 40%。5 年无疾病生存率为 25%。
5-FU 联合 FA 和 L-OHP 的新辅助治疗显示出高度有效性和良好的耐受性。无疾病生存率和中位总生存率令人鼓舞。