Radioembolization of liver metastases from colorectal cancer using yttrium-90 microspheres with concomitant systemic oxaliplatin, fluorouracil, and leucovorin chemotherapy

被引:228
|
作者
Sharma, Ricky A.
Van Hazel, Guy A.
Morgan, Bruno
Berry, David P.
Blanshard, Keith
Price, David
Bower, Geoffrey
Shannon, Jennifer A.
Gibbs, Peter
Steward, William P.
机构
[1] Univ Oxford, Churchill Hosp, Dept Radiat Oncol & Biol, Oxford OX3 7LJ, England
[2] Univ Hosp Leicester, Dept Oncol, Leicester, Leics, England
[3] Univ Hosp Leicester, Dept Radiol, Leicester, Leics, England
[4] Univ Hosp Leicester, Dept Surg, Leicester, Leics, England
[5] Mt Med Ctr, Perth, WA, Australia
[6] Nepean Hosp, Sydney, NSW, Australia
[7] Royal Melbourne Hosp, Dept Med Oncol, Melbourne, Vic, Australia
关键词
D O I
10.1200/JCO.2006.08.7916
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Liver metastases represent the principal cause of death in patients with advanced colorectal cancer (CRC). Injection of resin microspheres (SIR Spheres) - containing the beta-emitter, yttrium-90 - into the arterial supply of the liver can cause radioembolization of metastases. This treatment has not been tested with the radiosensitizing chemotherapy, oxaliplatin, which appears synergistic in the treatment of CRC when combined with fluorouracil and leucovorin (FOLFOX). Patients and Methods A phase I study of SIR-Spheres therapy with modified FOLFOX4 systemic chemotherapy was conducted in patients with inoperable liver metastases from CRC who had not previously received chemotherapy for metastatic disease. Oxaliplatin (30 to 85 mg/m(2)) was administered for the first three cycles with full FOLFOX4 doses from cycle 4 until cycle 12. The primary end point was toxicity. Results Twenty patients were enrolled onto the study. Five patients experienced National Cancer Institute (NCI; Bethesda, MD) grade 3 abdominal pain, two of whom had microsphere-induced gastric ulcers. The dose-limiting toxicity was grade 3 or 4 neutropenia, which was recorded in 12 patients. One episode of transient grade 3 hepatotoxicity was recorded. Mean splenic volume increased by 92% following 6 months of protocol therapy. Partial responses were demonstrated in 18 patients and stable disease in two patients. Two patients underwent partial hepatic resection following protocol therapy. Median progression-free survival was 9.3 months, and median time to progression in the liver was 12.3 months. Conclusion The maximum-tolerated dose was 60 mg/m(2) of oxaliplatin for the first three cycles, with full FOLFOX4 doses thereafter. This chemoradiation regime merits evaluation in phase II-III trials.
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收藏
页码:1099 / 1106
页数:8
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