Towards an optimal treatment algorithm for metastatic pancreatic ductal adenocarcinoma (PDA)

被引:10
作者
Uccello, M. [1 ]
Moschetta, M. [1 ]
Mak, G. [1 ]
Alam, T. [1 ]
Henriquez, C. Murias [1 ]
Arkenau, H. -T. [1 ,2 ]
机构
[1] Sarah Cannon Res Inst UK, Drug Dev, London, England
[2] UCL, UCL Canc Inst, London, England
关键词
Pancreatic ductal adenocarcinoma; pancreatic cancer; second-line; chemotherapy; algorithm; 2ND-LINE COMBINATION THERAPIES; PHASE-III TRIAL; PLUS GEMCITABINE; FOLINIC ACID; CANCER; OXALIPLATIN; FOLFIRINOX; FLUOROURACIL; MULTICENTER; SURVIVAL;
D O I
10.3747/co.25.3708
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy remains the mainstay of treatment for advanced pancreatic ductal adenocarcinoma (PDA). Two randomized trials have demonstrated superiority of the combination regimens FOLFIRINOX (5-fluorouracil, leucovorin, oxaliplatin, and irinotecan) and gemcitabine plus nab-paclitaxel over gemcitabine monotherapy as a first-line treatment in adequately fit subjects. Selected PDA patients progressing to first-line therapy can receive second-line treatment with moderate clinical benefit. Nevertheless, the optimal algorithm and the role of combination therapy in second-line are still unclear. Published second-line PDA clinical trials enrolled patients progressing to gemcitabine-based therapies in use before the approval of nab-paclitaxel and FOLFIRINOX. The evolving scenario in second-line may affect the choice of the first-line treatment. For example, nanoliposomal irinotecan plus 5-fluouracil and leucovorin is a novel second-line option which will be suitable only for patients progressing to gemcitabine-based therapy. Therefore, clinical judgement and appropriate patient selection remain key elements in treatment decision. In this review, we aim to illustrate currently available options and define a possible algorithm to guide treatment choice. Future clinical trials taking into account sequential treatment as a new paradigm in PDA will help define a standard algorithm.
引用
收藏
页码:E90 / E94
页数:5
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