Liepe Knut, Brogsitter Claudia, Leonhard Johannes, Wunderlich Gerd, Hliscs Rainer, Pinkert Joerg, Folprecht Gunnar, Kotzerke Joerg
Department of Nuclear Medicine, Hospital Kassel, Mönchebergstr. 41-43, 34125 Kassel, Germany.
Jpn J Clin Oncol. 2007 Dec;37(12):942-50. doi: 10.1093/jjco/hym137. Epub 2007 Dec 19.
This paper describes the feasibility of intra-arterial high-activity administration of (188)Re-microspheres.
Patients with unresectable colorectal liver metastases or hepatocellular cancer (HCC) received single treatments with (188)Re-microspheres. The administered activity was calculated to give a liver dose of 100 Gy. From post-therapeutic scans and urine sampling, the dose to the liver, metastases and bladder was calculated. Toxicity was assessed up to 3 months after administration by means of the Common Terminology Criteria for Adverse Events v3.0 (Trotti et al. CTCAE v3.0: development of a comprehensive grading system for the adverse effects of cancer treatment. Semin Radiat Oncol 2003;13(3):176-81). Response was evaluated on CT.
13.6 +/- 4.7 GBq (188)Re-microspheres was administered selective in the feeding artery of the tumour to 10 patients (3 x HCC and 7 x colorectal liver metastases). There was a low urinary excretion rate of 8.9 +/- 3.8% of administered activity within 96 h. The absorbed dose to the tumour, normal liver (excluding the tumour) and bladder was 10.24 +/- 5.02 Gy/GBq (128 +/- 47 Gy), 3.94 +/- 2.52 Gy/GBq (50 +/- 33 Gy) and 0.27 +/- 0.20 Gy/GBq (2.4 +/- 1.9 Gy), respectively. There was an acceptable rate of toxicity in 30% of grades I and II, respectively, and 10% with grade III. There was reversible in the most patients within 14 days after treatment. The response was assessed on CT: two patients had a partial response (PR), five patients had stable disease and three patients had disease progression.
Treatment of colorectal liver metastases or HCC using high activities of (188)Re-microspheres was well tolerated and a PR was seen in 2 of 10 patients. The treatment represents a therapeutic option in these patients.
本文描述了动脉内高活度给予(188)Re微球的可行性。
不可切除的结直肠癌肝转移或肝细胞癌(HCC)患者接受(188)Re微球单次治疗。计算给药活度以使肝脏剂量达到100 Gy。根据治疗后扫描和尿液采样,计算肝脏、转移灶和膀胱的剂量。给药后长达3个月通过不良事件通用术语标准v3.0(Trotti等人,CTCAE v3.0:癌症治疗不良反应综合分级系统的开发。《放射肿瘤学杂志》2003年;13(3):176 - 81)评估毒性。通过CT评估反应。
向10例患者(3例HCC和7例结直肠癌肝转移)的肿瘤供血动脉选择性给予13.6±4.7 GBq(188)Re微球。96小时内给药活度的尿排泄率较低,为8.9±3.8%。肿瘤、正常肝脏(不包括肿瘤)和膀胱的吸收剂量分别为10.24±5.02 Gy/GBq(128±47 Gy)、3.94±2.52 Gy/GBq(50±33 Gy)和