Sultana Asma, Shore Susannah, Raraty Michael Gt, Vinjamuri Sobhan, Evans Jonathan E, Smith Catrin Tudur, Lane Steven, Chauhan Seema, Bosonnet Lorraine, Garvey Conall, Sutton Robert, Neoptolemos John P, Ghaneh Paula
Division of Surgery and Oncology, University of Liverpool, Liverpool, UK.
BMC Cancer. 2009 Feb 25;9:66. doi: 10.1186/1471-2407-9-66.
Advanced pancreatic cancer has a poor prognosis, and the current standard of care (gemcitabine based chemotherapy) provides a small survival advantage. However the drawback is the accompanying systemic toxicity, which targeted treatments may overcome. This study aimed to evaluate the safety and tolerability of KAb201, an anti-carcinoembryonic antigen monoclonal antibody, labelled with I(131) in pancreatic cancer (ISRCTN 16857581).
Patients with histological/cytological proven inoperable adenocarcinoma of the head of pancreas were randomised to receive KAb 201 via either the intra-arterial or intravenous delivery route. The dose limiting toxicities within each group were determined. Patients were assessed for safety and efficacy and followed up until death.
Between February 2003 and July 2005, 25 patients were enrolled. Nineteen patients were randomised, 9 to the intravenous and 10 to the intra-arterial arms. In the intra-arterial arm, dose limiting toxicity was seen in 2/6 (33%) patients at 50 mCi whereas in the intravenous arm, dose limiting toxicity was noted in 1/6 patients at 50 mCi, but did not occur at 75 mCi (0/3).The overall response rate was 6% (1/18). Median overall survival was 5.2 months (95% confidence interval = 3.3 to 9 months), with no significant difference between the intravenous and intra-arterial arms (log rank test p = 0.79). One patient was still alive at the time of this analysis.
Dose limiting toxicity for KAb201 with I(131) by the intra-arterial route was 50 mCi, while dose limiting toxicity was not reached in the intravenous arm.
晚期胰腺癌预后较差,当前的标准治疗方案(以吉西他滨为基础的化疗)仅能带来微小的生存获益。然而,其缺点是伴随的全身毒性,而靶向治疗可能会克服这一问题。本研究旨在评估131I标记的抗癌胚抗原单克隆抗体KAb201在胰腺癌中的安全性和耐受性(国际标准随机对照试验编号:ISRCTN 16857581)。
经组织学/细胞学证实为不可切除的胰头腺癌患者被随机分配,通过动脉内或静脉内给药途径接受KAb 201治疗。确定每组中的剂量限制毒性。对患者进行安全性和疗效评估,并随访至死亡。
2003年2月至2005年7月期间,共招募了25名患者。19名患者被随机分组,9名接受静脉给药,10名接受动脉内给药。在动脉内给药组中,50毫居里时2/6(33%)的患者出现剂量限制毒性,而在静脉给药组中,50毫居里时1/6的患者出现剂量限制毒性,但75毫居里时未出现(0/3)。总体缓解率为6%(1/18)。中位总生存期为5.2个月(95%置信区间 = 3.3至9个月),静脉给药组和动脉内给药组之间无显著差异(对数秩检验p = 0.79)。在本次分析时,有1名患者仍存活。
动脉内途径给予131I标记的KAb201的剂量限制毒性为50毫居里,而静脉给药组未达到剂量限制毒性。