A phase II experience with neoadjuvant irinotecan (CPT-II), 5-fluorouracil (5-FU) and leucovorin (LV) for colorectal liver metastases

被引:34
作者
Bathe, Oliver F. [1 ,2 ]
Ernst, Scott [3 ]
Sutherland, Francis R. [1 ]
Dixon, Elijah [1 ]
Butts, Charles [4 ]
Bigam, David [5 ]
Holland, David [6 ]
Porter, Geoffrey A. [7 ]
Koppel, Jennifer [1 ]
Dowden, Scot [2 ]
机构
[1] Univ Calgary, Dept Surg, Calgary, AB, Canada
[2] Univ Calgary, Dept Oncol, Calgary, AB, Canada
[3] London Reg Canc Ctr, Dept Oncol, London, ON N6A 4L6, Canada
[4] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
[5] Univ Alberta, Dept Surg, Edmonton, AB, Canada
[6] Lethbridge Canc Ctr, Dept Oncol, Lethbridge, AB, Canada
[7] Dalhousie Univ, Dept Surg, Halifax, NS B3H 4H2, Canada
来源
BMC CANCER | 2009年 / 9卷
关键词
MULTICENTER RANDOMIZED-TRIAL; PLUS FOLINIC ACID; HEPATIC RESECTION; CANCER PATIENTS; CHEMOTHERAPY; SURGERY; FLUOROURACIL; SURVIVAL; OXALIPLATIN; RECURRENCE;
D O I
10.1186/1471-2407-9-156
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chemotherapy may improve survival in patients undergoing resection of colorectal liver metastases (CLM). Neoadjuvant chemotherapy may help identify patients with occult extrahepatic disease (averting unnecessary metastasectomy), and it provides in vivo chemosensitivity data. Methods: A phase II trial was initiated in which patients with resectable CLM received CPT-11, 5-FU and LV for 12 weeks. Metastasectomy was performed unless extrahepatic disease appeared. Postoperatively, patients with stable or responsive disease received the same regimen for 12 weeks. Patients with progressive disease received either second-line chemotherapy or best supportive care. The primary endpoint was disease-free survival (DFS); secondary endpoints included overall survival (OS) and safety. Results: 35 patients were accrued. During preoperative chemotherapy, 16 patients (46%) had grade 3/4 toxicities. Resection was not possible in 5 patients. One patient died of arrhythmia following surgery, and 1 patient had transient liver failure. During the postoperative treatment phase, 12 patients (55%) had grade 3/4 toxicities. Deep venous thrombosis (DVT) occurred in II patients (34%) at various times during treatment. Of those who underwent resection, median DFS was 23.0 mo. and median OS has not been reached. The overall survival from time of diagnosis of liver metastases was 51.6 mo for the entire cohort. Conclusion: A short course of chemotherapy prior to hepatic metastasectomy may serve to select candidates best suited for resection and it may also direct postoperative systemic treatment. Given the significant incidence of DVT, alternative systemic neoadjuvant regimens should be investigated, particularly those that avoid the use of a central venous line.
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页数:10
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