Department of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Cancer Res Treat. 2008 Mar;40(1):22-6. doi: 10.4143/crt.2008.40.1.22. Epub 2008 Mar 31.
Gemcitabine is the most active agent to treat unresectable pancreatic cancer. The superiority of combining other drugs with cisplatin is still controversial; therefore, we performed a retrospective analysis of gemcitabine versus gemcitabine combined with cisplatin to determine the treatment outcomes for patients with locally advanced or metastatic pancreatic cancer.
From 2001 to 2007, we enrolled 60 patients who were treated with gemcitabine or gemcitabine combined with cisplatin for locally advanced or metastatic pancreatic cancer. Gemcitabine 1, 000 mg/m(2) (G) was administrated at day 1 and day 8 every 3 weeks. Cisplatin 60 mg/m(2) was added at day 1 every 3 weeks to the gemcitabine schedule (GP).
NUMBER OF G: GP was 34: 26, locally advanced to metastatic ratio was 35% to 65% in group G and 46% to 54% in group GP. Median follow up duration was 29 months. The median number of chemotherapy cycles was 4 (range: 2 approximately 11) for the G group, and 4 (range: 1 approximately 11) for the GP group. The response rate of the G and GP groups was 17% and 11%, respectively. The progression free survival (PFS) was 4.5 months and 2.8 months, respectively, for the G and GP groups. The overall survival (OS) was 10.7 and 8.7 months respectively, for the G and GP groups, but there is no statistically significant difference of the PFS (p=0.2396) and OS (p=0.4643) between the 2 groups. The hematological toxicity profile was similar (the grade III neutropenia and thrombocytopenia was 4.4% and 3.1%, respectively, in G group, and 7.5% and 2.8%, respectively, in the GP group). But non-hematological toxicities such as skin rash, abnormal liver function and nausea/vomiting were observed in 3 patients of the GP group. On the prognostic factor analysis, no factors predicted a longer PFS and OS for both the G and GP groups.
Gemcitabine single treatment might be more tolerable and it had the same efficacy compared to cisplatin combination treatment in this retrospective study.
吉西他滨是治疗不可切除胰腺癌最有效的药物。联合其他药物与顺铂治疗的优势仍存在争议;因此,我们对吉西他滨与吉西他滨联合顺铂治疗局部晚期或转移性胰腺癌的疗效进行了回顾性分析。
2001 年至 2007 年,我们纳入了 60 例局部晚期或转移性胰腺癌患者,他们接受吉西他滨或吉西他滨联合顺铂治疗。吉西他滨 1000mg/m²(G)于每 3 周的第 1 天和第 8 天给药。顺铂 60mg/m²(GP)于每 3 周的第 1 天添加到吉西他滨方案中。
吉西他滨组(G):GP 组 34:26,局部晚期至转移性比例 G 组为 35%至 65%,GP 组为 46%至 54%。中位随访时间为 29 个月。吉西他滨组化疗周期中位数为 4(范围:2 至 11),GP 组为 4(范围:1 至 11)。G 组和 GP 组的缓解率分别为 17%和 11%。G 组和 GP 组的无进展生存期(PFS)分别为 4.5 个月和 2.8 个月,总生存期(OS)分别为 10.7 个月和 8.7 个月,但两组间 PFS(p=0.2396)和 OS(p=0.4643)无统计学差异。血液学毒性谱相似(G 组的 III 级中性粒细胞减少和血小板减少分别为 4.4%和 3.1%,GP 组分别为 7.5%和 2.8%)。但在 GP 组中有 3 例观察到皮疹、肝功能异常和恶心/呕吐等非血液学毒性。在预后因素分析中,G 组和 GP 组均无预测 PFS 和 OS 延长的因素。
在这项回顾性研究中,吉西他滨单药治疗可能更耐受,且与顺铂联合治疗疗效相当。