The evaluation of efficacy and tolerability of gemcitabine vs. capecitabine therapy in the second-line setting for metastatic pancreatic cancer patients with poor performance status

Abdullah Sakin , Suleyman Sahin , Muhammed Mustafa atci , Cumhur Demir , Nurgul Yasar , Caglayan Geredeli , Sener Cihan
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Abstract

Aim

The aim of this study was to evaluate the efficacy and tolerability of single-agent gemcitabine vs. capecitabine therapy in the second-line setting for metastatic Pancreatic Cancer (mPC) patients with poor performance status.

Material and methods

A total of 48 patients with mPC, who were followed and treated in oncology center between 2012 and 2017, were included. After a failure of first-line therapy, patients with an ECOG-PS 2 treated with capecitabine or gemcitabine monotherapy in the secondline setting were retrospectively analyzed.

Results

Of the 48 patients, 26(54.2%) were males and 22(45.8%) were females. The median age of the patients was 62 years(range, 31-82). Treatment regimens in the first-line setting were as follows; gemcitabine+cisplatin in 24(50%) patients, gemcitabine+nub-paclitaxel in 4(8.3%) patients, FOLFIRINOX in 8(16.7%) patients, FOLFOX in 8(16.7%) patients, and gemcitabine+oxaliplatine in 4(8.3%) patients. After progression on first-line therapy, 29(60.5%) patients were treated with capecitabine in the second-line setting, while 19(39.5%) patients were given gemcitabine. Median progression-free survival was found to be 4 months(95% CI,1.9-6.0) in patients receiving capecitabine compared to 2 months(95% CI, 0.5-3.4) in those treated with gemcitabine (p=0.271). Median overall survival was 6.0 months(95% CI, 2.0-9.9) in patients receiving capecitabine therapy versus 5.0 months (95% CI, 1.0-8.9) in those treated with gemcitabine monotherapy (p=0.353).

Conclusions

Optimal second-line treatment for mPC has not yet been established. In the present study, capecitabine monotherapy was compared to gemcitabine and it was found that they both had similar efficacy in the second-line treatment for mPC patients who were not eligible for combination chemotherapy regimen.

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吉西他滨与卡培他滨在二线治疗转移性胰腺癌患者的疗效和耐受性评估
目的本研究的目的是评估单药吉西他滨与卡培他滨治疗在转移性胰腺癌(mPC)患者的二线治疗中的疗效和耐受性。材料与方法纳入2012 - 2017年在肿瘤中心随访治疗的48例mPC患者。在一线治疗失败后,在二线环境中接受卡培他滨或吉西他滨单药治疗的ECOG-PS 2患者进行回顾性分析。结果48例患者中,男性26例(54.2%),女性22例(45.8%)。患者中位年龄为62岁(范围31-82岁)。一线治疗方案如下:吉西他滨+顺铂24例(50%),吉西他滨+nub-紫杉醇4例(8.3%),FOLFIRINOX 8例(16.7%),FOLFOX 8例(16.7%),吉西他滨+奥沙利铂4例(8.3%)。在一线治疗进展后,29例(60.5%)患者在二线环境中接受卡培他滨治疗,19例(39.5%)患者接受吉西他滨治疗。卡培他滨组患者的中位无进展生存期为4个月(95% CI,1.9-6.0),而吉西他滨组患者的中位无进展生存期为2个月(95% CI, 0.5-3.4) (p=0.271)。接受卡培他滨治疗的患者中位总生存期为6.0个月(95% CI, 2.0-9.9),而接受吉西他滨单药治疗的患者中位总生存期为5.0个月(95% CI, 1.0-8.9) (p=0.353)。结论mPC的最佳二线治疗方案尚未确定。本研究将卡培他滨单药治疗与吉西他滨进行了比较,发现对于不符合联合化疗方案的mPC患者,两者在二线治疗中的疗效相似。
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来源期刊
CiteScore
0.10
自引率
0.00%
发文量
16
审稿时长
29 weeks
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