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吉西他滨联合奥沙利铂治疗不可切除胆囊癌的多中心 II 期临床试验。

A Multicenter Phase II Trial of Gemcitabine Plus Oxaliplatin in Unresectable Gallbladder Cancer.

机构信息

Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea. ; Center for Liver Cancer, National Cancer Center, Goyang, Korea.

出版信息

Gut Liver. 2013 Sep;7(5):594-8. doi: 10.5009/gnl.2013.7.5.594. Epub 2013 Jun 11.

Abstract

BACKGROUND/AIMS: No standard chemotherapy has been established for advanced gallbladder cancer. The authors studied the activity and tolerability of a gemcitabine and oxaliplatin (GEMOX) combination in unresectable gallbladder cancer (GBC).

METHODS

Adult patients with pathologically confirmed unresectable GBC were prospectively recruited at three centers. No patient had received prior chemotherapy or radiotherapy. Patients received cycles of gemcitabine at 1,000 mg/m(2) on day 1, followed by oxaliplatin at 100 mg/m(2) on day 2, every 2 weeks. The primary study endpoint was time to progression.

RESULTS

Forty patients with unresectable GBC were enrolled. The median age was 60 years (range, 38 to 79 years). All patients showed good performance status. Of the 33 analyzable patients, 12 achieved partial response (36%), 17 stable disease (52%), and four progressive disease (12%). No patient achieved a complete response. The tumor control rate was 88%. At a median follow-up of 6.8 months, the median time to progression was 5.3 months (95% confidence interval [CI], 3.7 to 6.9), and median overall survival was 6.8 months (95% CI, 6.1 to 7.5). Nine of the 40 patients (23%) experienced at least a grade-3 adverse event, but no patient experienced a grade-4 adverse event.

CONCLUSIONS

GEMOX combination therapy is a feasible option and is well tolerated in unresectable GBC.

摘要

背景/目的:对于晚期胆囊癌,尚无标准的化疗方案。作者研究了吉西他滨联合奥沙利铂(GEMOX)联合方案在不可切除的胆囊癌(GBC)中的活性和耐受性。

方法

在三个中心前瞻性招募经病理证实为不可切除的 GBC 成年患者。所有患者均未接受过化疗或放疗。患者接受吉西他滨 1000mg/m2,第 1 天;奥沙利铂 100mg/m2,第 2 天,每 2 周 1 次。主要研究终点为无进展生存期。

结果

共纳入 40 例不可切除的 GBC 患者。中位年龄为 60 岁(范围,38 岁至 79 岁)。所有患者的表现状态良好。在 33 例可分析患者中,12 例部分缓解(36%),17 例稳定疾病(52%),4 例进展疾病(12%)。无完全缓解患者。肿瘤控制率为 88%。中位随访 6.8 个月时,中位无进展生存期为 5.3 个月(95%置信区间[CI],3.7 至 6.9),中位总生存期为 6.8 个月(95%CI,6.1 至 7.5)。40 例患者中有 9 例(23%)至少发生 1 级 3 级不良事件,但无 4 级不良事件。

结论

GEMOX 联合治疗方案在不可切除的 GBC 中是可行的选择,且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/3782675/73da47d9a494/gnl-7-594-g001.jpg

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