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益气逐瘀汤联合 FOLFOX-4 一线治疗转移性结直肠癌。

Yiqi zhuyu decoction combined with FOLFOX-4 as first-line therapy in metastatic colorectal cancer.

机构信息

Department of Colorectal and Anal Surgery, First Affiliated Hospital of Guiyang College of Traditional Chinese Medicine, Guiyang, China.

出版信息

Chin J Integr Med. 2011 Aug;17(8):593-9. doi: 10.1007/s11655-011-0822-z. Epub 2011 Aug 9.

Abstract

OBJECTIVE

To evaluate the efficacy and safety of yiqi zhuyu decoction (YZD) combined with oxaliplatin plus 5-flurouracil/leucovorin (FOLFOX-4) in the patients with metastatic colorectal cancer (MCRC).

METHODS

A total of 120 patients with MCRC were randomly divided into the experimental group (FOLFOX-4 plus YZD, 60 cases) and the control group (FOLFOX-4 plus placebo, 60 cases), according to the sequence of hospitalization from January 2005 to December 2007. The treatment was supposed to be continued until disease progression (PD) or for 48 weeks (i.e., up to 24 cycles of FOLFOX-4). Response rate (RR), progression-free survival (PFS), overall survival (OS) and adverse events (AEs) were observed.

RESULTS

RR was 41.5% in the experimental group and 34.0% in the control group [odds ratio (OR): 1.18, 95% CI: 0.77 to 1.82, P=0.432]. Median PFS were 9.0 months and 8.0 months, respectively [hazard ratio (HR): 0.78, 95% CI: 0.53 to 1.15, P=0.215]. Median OS were 21.0 months and 18.0 months (HR: 0.65, 95% CI: 0.43 to 0.99, P=0.043) and grade 3/4 AEs were 56.6% and 76.7% (OR: 0.61, 95% CI: 0.18 to 0.87, P=0.020), respectively.

CONCLUSIONS

YZD combined with FOLFOX-4 chemotherapy significantly improved OS in this first-line trial in the patients with MCRC and significantly decreased grade 3/4 AEs. However, RR was not improved, and PFS did not reach statistical significance by the addition of YZD. The treatment of YZD combined with FOLFOX-4 may be necessary in order to optimize efficacy and safety.

摘要

目的

评价益气逐瘀汤(YZD)联合奥沙利铂加多柔比星/亚叶酸钙(FOLFOX-4)治疗转移性结直肠癌(MCRC)患者的疗效和安全性。

方法

将 2005 年 1 月至 2007 年 12 月收治的 120 例 MCRC 患者按住院顺序随机分为实验组(FOLFOX-4+YZD,60 例)和对照组(FOLFOX-4+安慰剂,60 例)。治疗应持续到疾病进展(PD)或 48 周(即最多 24 个周期的 FOLFOX-4)。观察两组的缓解率(RR)、无进展生存期(PFS)、总生存期(OS)和不良事件(AEs)。

结果

实验组的 RR 为 41.5%,对照组为 34.0%[比值比(OR):1.18,95%可信区间(CI):0.77 至 1.82,P=0.432]。中位 PFS 分别为 9.0 个月和 8.0 个月[风险比(HR):0.78,95%CI:0.53 至 1.15,P=0.215]。中位 OS 分别为 21.0 个月和 18.0 个月(HR:0.65,95%CI:0.43 至 0.99,P=0.043),3/4 级 AEs 发生率分别为 56.6%和 76.7%(OR:0.61,95%CI:0.18 至 0.87,P=0.020)。

结论

在一线治疗转移性结直肠癌患者中,YZD 联合 FOLFOX-4 化疗可显著提高 OS,并显著降低 3/4 级 AEs。然而,RR 并未得到改善,且加入 YZD 后 PFS 未达到统计学意义。为了优化疗效和安全性,可能需要 YZD 联合 FOLFOX-4 进行治疗。

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