Real-world evidence on first- and second-line palliative chemotherapy in advanced pancreatic cancer

被引:13
作者
Blomstrand, Hakon [1 ]
Batra, Atul [2 ]
Cheung, Winson Y. [3 ]
Elander, Nils Oskar [1 ]
机构
[1] Linkoping Univ, Dept Biomed & Clin Sci, S-58185 Linkoping, Sweden
[2] All India Inst Med Sci, Dept Med Oncol, New Delhi 110029, India
[3] Univ Calgary, Dept Oncol, Calgary, AB T2N 4N1, Canada
关键词
Pancreatic cancer; Palliative therapy; Cancer chemotherapy; Gemcitabine; Paclitaxel; nano albumin-bound; Folfirinox; PACLITAXEL PLUS GEMCITABINE; PHASE-III TRIAL; NAB-PACLITAXEL; FOLFIRINOX FAILURE; OXALIPLATIN COMBINATION; CAPECITABINE; MULTICENTER; SURVIVAL; THERAPY; ADENOCARCINOMA;
D O I
10.5306/wjco.v12.i9.787
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In spite of recent diagnostic and therapeutic advances, the prognosis of pancreatic ductal adenocarcinoma (PDAC) remains very poor. As most patients are not amenable to curative intent treatments, optimized palliative management is highly needed. One key question is to what extent promising results produced by randomized controlled trials (RCTs) correspond to clinically meaningful outcomes in patients treated outside the strict frames of a clinical trial. To answer such questions, real-world evidence is necessary. The present paper reviews and discusses the current literature on first- and second-line palliative chemotherapy in PDAC. Notably, a growing number of studies report that the outcomes of the two predominant first-line multidrug regimens, i.e. gemcitabine plus nab-paclitaxel (GnP) and folfirinox (FFX), is similar in RCTs and real-life populations. Outcomes of second-line therapy following failure of first-line regimens are still dismal, and considerable uncertainty of the optimal management remains. Additional RCTs and real-world evidence studies focusing on the optimal treatment sequence, such as FFX followed by GnP or vice versa, are urgently needed. Finally, the review highlights the need for prognostic and predictive biomarkers to inform clinical decision making and enable personalized management in advanced PDAC.
引用
收藏
页码:787 / 799
页数:13
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