Dirix L Y, Tonnesen F, Cassidy J, Epelbaum R, ten Bokkel Huinink W W, Pavlidis N, Sorio R, Gamucci T, Wolff I, Te Velde A, Lan J, Verweij J
University Hospital of Antwerp, Belgium.
Eur J Cancer. 1996 Oct;32A(11):2019-22. doi: 10.1016/0959-8049(96)00226-2.
In a phase II trial, the activity of EO9, a new bioreductive alkylating agent, was assessed. EO9 was used as second-line chemotherapy in breast cancer patients and as first-line chemotherapy for patients with gastric, pancreatic and colorectal cancer. EO9 was given as a 5 min i.v. infusion at a weekly dose of 12 mg/m2. 92 patients were entered; 22 with breast cancer, 26 with colon cancer, 24 with pancreatic cancer and 20 with gastric cancer. In general, the drug was well tolerated with nausea and vomiting occurring in 26.42 and 13.3% of courses, respectively. Reversible proteinuria was the main toxicity occurring in 45% of courses. Antitumour activity was not observed. At this dose and schedule, EO9 is not an active drug in the type of tumour studied.
在一项II期试验中,评估了一种新型生物还原烷基化剂EO9的活性。EO9用作乳腺癌患者的二线化疗药物,以及胃癌、胰腺癌和结直肠癌患者的一线化疗药物。EO9通过静脉输注5分钟给药,每周剂量为12mg/m²。共纳入92例患者,其中乳腺癌22例,结肠癌26例,胰腺癌24例,胃癌20例。总体而言,该药物耐受性良好,恶心和呕吐发生率分别为26.42%和13.3%。可逆性蛋白尿是主要毒性反应,发生率为45%。未观察到抗肿瘤活性。在此剂量和给药方案下,EO9在所研究的肿瘤类型中不是一种活性药物。