Smith D, Gallagher N
Clatterbridge Centre for Oncology, Clatterbridge Road, Bebington, Wirral, Cheshire CH63 4JY, UK.
Eur J Cancer. 2003 Jul;39(10):1377-83. doi: 10.1016/s0959-8049(03)00271-5.
ZD9331 is a novel antifolate inhibitor of thymidylate synthase (TS). This multicentre, randomised, phase II/III study compared the efficacy and safety of ZD9331 with gemcitabine in 55 patients with chemonai;ve, locally advanced or metastatic pancreatic cancer. Patients received intravenous (i.v.) ZD9331 (n=30), on days 1 and 8 of a 3-week cycle or i.v. gemcitabine (n=25), once a week for 7 weeks followed by a 1-week rest, then on days 1, 8 and 15 of a 4-week cycle. Objective tumour response and clinical benefit response (CBR) were similar for both groups. More ZD9331 patients were alive at the data cut-off point compared with gemcitabine patients (13 and 8%, respectively). Median survival (152 versus 109 days, respectively) and time to progression (70 versus 58 days, respectively) were longer in the ZD9331 group. Nausea and vomiting (grade 1/2) were the most common toxicities in both groups. These results suggest that, in pancreatic cancer, ZD9331 is equivalent to gemcitabine and may offer a promising alternative to current therapies.
ZD9331是一种新型的胸苷酸合成酶(TS)抗叶酸抑制剂。这项多中心、随机、II/III期研究比较了ZD9331与吉西他滨在55例初治、局部晚期或转移性胰腺癌患者中的疗效和安全性。患者接受静脉注射(i.v.)ZD9331(n = 30),在3周周期的第1天和第8天给药,或静脉注射吉西他滨(n = 25),每周一次,共7周,随后休息1周,然后在4周周期的第1天、第8天和第15天给药。两组的客观肿瘤反应和临床获益反应(CBR)相似。与吉西他滨组患者相比,在数据截止点时,ZD9331组存活的患者更多(分别为13%和8%)。ZD9331组的中位生存期(分别为152天和109天)和疾病进展时间(分别为70天和58天)更长。恶心和呕吐(1/2级)是两组中最常见的毒性反应。这些结果表明,在胰腺癌中,ZD9331与吉西他滨等效,可能为当前治疗提供一种有前景的替代方案。