5-Fluorouracil/Leucovorin Combined with Irinotecan and Oxaliplatin (FOLFIRINOX) as Second-Line Chemotherapy in Patients with Advanced Pancreatic Cancer Who Have Progressed on Gemcitabine-Based Therapy

被引:43
|
作者
Lee, Min Geun [1 ,2 ,5 ]
Lee, Sang Hyub [1 ,2 ,3 ]
Lee, Seung June [1 ,2 ,4 ]
Lee, Yoon Suk [1 ,2 ,4 ]
Hwang, Jin-Hyeok [1 ,2 ,4 ]
Ryu, Ji Kon [1 ,2 ,3 ]
Kim, Yong-Tae [1 ,2 ,3 ]
Kim, Dong Uk [6 ]
Woo, Sang Myung [7 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Liver Res Inst, Seoul 110744, South Korea
[3] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[4] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Songnam, South Korea
[5] Hanmaeum Hosp, Dept Internal Med, Cheju, South Korea
[6] Pusan Natl Univ, Sch Med, Dept Internal Med, Pusan, South Korea
[7] Natl Canc Ctr, Ctr Liver Canc, Goyang, South Korea
关键词
Metastatic pancreatic adenocarcinoma; Second-line chemotherapy; FOLFIRINOX; PROGNOSTIC-FACTOR; SOLID TUMORS; ADENOCARCINOMA; TRIAL; GUIDELINES; CA-19-9;
D O I
10.1159/000356158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aims: There is no standard consensus on a strategy in the second-line setting for gemcitabine-refractory advanced pancreatic cancer. This study evaluated the activity and tolerability of oxaliplatin, irinotecan, 5-fluorouracil and leucovorin (FOLFIRINOX) as a second-line therapy in advanced pancreatic adenocarcinoma pretreated with a gemcitabine-based regimen. Methods: A retrospective survey was carried out on 18 patients with advanced pancreatic cancer who had been on gemcitabine-based chemotherapy and were then treated with FOLFIRINOX as a second-line therapy. Results: One patient (5.6%) had a confirmed complete response, 4 (22.2%) had confirmed partial responses and 5 (27.8%) had stable disease, resulting in a rate of disease control of 55.6% (95% CI, 33.3-77.8%). The median progression-free survival and median survival were 2.8 months and 8.4 months, respectively. Seven patients (38.9%) experienced grade 3-4 neutropenia. Grade 3 or 4 nonhematologic adverse events included nausea (38.9%) and vomiting (16.7%). Conclusions: These results suggest the modest clinical activity regarding efficacy and the acceptable toxicity profile with the FOLFIRINOX regimen as a second-line treatment. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:273 / 279
页数:7
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