Khazaeli M B, Saleh M N, Wheeler R H, Huster W J, Holden H, Carrano R, LoBuglio A F
Comprehensive Cancer Center, University of Alabama, Birmingham 35294.
J Natl Cancer Inst. 1988 Aug 17;80(12):937-42. doi: 10.1093/jnci/80.12.937.
Twenty-five patients with metastatic gastrointestinal adenocarcinoma received one to four infusions of large doses (400 mg) of murine monoclonal antibody CO17-1A (17-1A). The pharmacokinetics of 17-1A at the time of first, second, third, or fourth infusion were not statistically different; plasma half-lives were 15.0 +/- 1.7 hours (n = 5), 15.1 +/- 1.8 (n = 10), 25.3 +/- 6.2 (n = 3), and 14.4 +/- 1.8 (n = 5), respectively. Most patients had an antibody response to 17-1A, with peak levels occurring 15-22 days after infusion. The presence of serum antibody to 17-1A at the time of the second or third infusion did not significantly alter the pharmacokinetics of this large dose of antibody. Four of 25 patients failed to develop an antibody response, but this did not correlate with the amount of 17-1A administered. The administration of four doses of 400 mg over 1 week provided continuously circulating 17-1A for 10 days.
25例转移性胃肠道腺癌患者接受了1至4次大剂量(400毫克)鼠单克隆抗体CO17 - 1A(17 - 1A)输注。首次、第二次、第三次或第四次输注时17 - 1A的药代动力学无统计学差异;血浆半衰期分别为15.0±1.7小时(n = 5)、15.1±1.8(n = 10)、25.3±6.2(n = 3)和14.4±1.8(n = 5)。大多数患者对17 - 1A有抗体反应,峰值水平出现在输注后15 - 22天。第二次或第三次输注时血清中17 - 1A抗体的存在并未显著改变该大剂量抗体的药代动力学。25例患者中有4例未产生抗体反应,但这与所给予的17 - 1A量无关。在1周内给予4剂400毫克可使17 - 1A持续循环10天。