Leung W T, Lau W Y, Ho S, Chan M, Leung N, Lin J, Ho K C, Metreweli C, Johnson P J, Li A K
Joint Hepatoma Clinic, Prince of Wales Hospital, Chinese University of Hong Kong.
J Nucl Med. 1994 Aug;35(8):1313-8.
From August 1990 to June 1993, 26 patients with inoperable hepatocellular carcinoma were treated with intra-arterial iodine-131-Lipiodol (131I-L).
Iodine-131-Lipiodol was given through either an implantable arterial port (9 patients) or during hepatic angiography (17 patients). All 26 patients had multiple lesions, 3 had involved resection margin after surgical resection and 1 had diffuse infiltrative lesions. The median size of the largest tumor among 22 patients with a measurable lesion was 4.5 cm (2-9.5 cm). The end points are tumor response in terms of tumor size, change in serum alpha-fetoprotein level, toxicity of treatment and overall survival.
Twenty-three patients received a single treatment of 1.11-2.22 GBq (30-60 mCi)131I-L. Three patients received 2.22-4.44 GBq (60-120 mCi)131I-L in three fractions. Considering both radiological regression and reduction in serum alpha-fetoprotein level as objective response criteria, the overall response rate was 52% (13 out of 25 patients with evaluable disease). Ten out of 15 patients who had raised alpha-fetoprotein levels had more than 50% reduction and 8 patients had more than 90% reduction in alpha-fetoprotein level. Since analysis, 19 patients have died and 7 remain alive, giving a minimum median survival of 6 mo (range 1.2-16.6 mo), with 4 surviving more than 1 yr calculated from the day of treatment. There was only one patient who had late deterioration of liver function compatible with radiation hepatitis. There was no bone marrow toxicity documented in any patients.
Treatment with intra-arterial 131I-L was well tolerated in patients with inoperable hepatocellular carcinoma and produced an objective response of 52% with median survival of 6 mo. A fractionated dose of 131I-L was feasible and the radiation dose could be escalated safely.
1990年8月至1993年6月,26例无法手术的肝细胞癌患者接受了动脉内碘-131-碘化油(131I-L)治疗。
碘-131-碘化油通过植入式动脉端口(9例患者)或在肝血管造影期间给予(17例患者)。所有26例患者均有多个病灶,3例患者在手术切除后切缘受累,1例患者有弥漫性浸润性病灶。22例有可测量病灶的患者中,最大肿瘤的中位大小为4.5厘米(2 - 9.5厘米)。终点指标为根据肿瘤大小、血清甲胎蛋白水平变化、治疗毒性和总生存期评估的肿瘤反应。
23例患者接受了1.11 - 2.22GBq(30 - 60mCi)131I-L的单次治疗。3例患者分三次接受了2.22 - 4.44GBq(60 - 120mCi)131I-L的治疗。将放射学退缩和血清甲胎蛋白水平降低均视为客观反应标准,总体反应率为52%(25例可评估疾病患者中的13例)。15例甲胎蛋白水平升高的患者中,10例患者的甲胎蛋白水平降低超过50%,8例患者的甲胎蛋白水平降低超过90%。自分析以来,19例患者死亡,7例患者存活,最短中位生存期为6个月(范围1.2 - 16.6个月),从治疗之日起计算,4例患者存活超过1年。仅有1例患者出现与放射性肝炎相符的肝功能晚期恶化。未记录到任何患者有骨髓毒性。
动脉内131I-L治疗在无法手术的肝细胞癌患者中耐受性良好,客观反应率为52%,中位生存期为6个月。分次给予131I-L剂量是可行的,且放射剂量可安全增加。