Büchler M, Kübel R, Malfertheiner P, Friess H, Schulz G, Bosslet K, Beger H G
Abteilung für Allgemeine Chirurgie, Universität Ulm.
Dtsch Med Wochenschr. 1988 Mar 11;113(10):374-80. doi: 10.1055/s-2008-1067647.
In the course of a phase I study monoclonal antibody BW 494 was injected i.v. at a dose of 180-340 mg to 18 patients with advanced ductal pancreatic carcinoma. The murine IgG1-antibody is directed against a pancreatic carcinoma-associated glycoprotein. The antibody inhibits the functions of human pancreatic carcinoma cells. Diffuse muscle pain, which disappeared spontaneously, was noted by two patients 14 days after injection. Other side-effects were anaphylactoid reactions in two patients 12 and 19 days, respectively, on repeat antibody infusions. This event led to changes in the administration schema so that the total amount was given within ten days, after which there were no further allergic side-effects. Terminal antibody half-life was 47.8 h (initial half-life 0.2 h). Human anti-mouse antibodies in all eight patients tested for them developed within two to three weeks of the end of treatment. There were no tumour remissions. Progression of the tumour after treatment occurred in 12 patients (67%). In five patients the course was stable for at least three months after treatment, i.e. unchanged clinical status, unchanged tumour extent (CT), and stable tumour markers (CEA, CA 19-9) in serum. One female patient with a T3N1M0 carcinoma has so far lived for 16 months in full employment. The results justify the use of the monoclonal antibody in future controlled trials.
在一项I期研究过程中,向18例晚期胰腺导管癌患者静脉注射单克隆抗体BW 494,剂量为180 - 340mg。这种鼠源IgG1抗体针对一种胰腺癌相关糖蛋白。该抗体可抑制人胰腺癌细胞的功能。两名患者在注射后14天出现弥漫性肌肉疼痛,疼痛自行消失。其他副作用分别为两名患者在重复输注抗体后第12天和第19天出现类过敏反应。这一事件导致给药方案发生改变,使总量在十天内给予,此后未再出现过敏副作用。抗体终末半衰期为47.8小时(初始半衰期为0.2小时)。所有接受检测的8名患者在治疗结束后两到三周内均产生了人抗鼠抗体。没有出现肿瘤缓解情况。12例患者(67%)在治疗后肿瘤进展。5例患者在治疗后病情稳定至少三个月,即临床状态未改变、肿瘤范围(CT)未改变、血清肿瘤标志物(CEA、CA 19 - 9)稳定。一名患有T3N1M0癌的女性患者至今已正常工作生活了16个月。这些结果证明在未来的对照试验中使用该单克隆抗体是合理的。