Spotlight on liposomal irinotecan for metastatic pancreatic cancer: patient selection and perspectives

被引:18
|
作者
Woo, Wonhee [1 ]
Carey, Edward T. [1 ]
Choi, Minsig [1 ]
机构
[1] SUNY Stony Brook, Dept Med, Div Hematol Oncol, HSC 15-053E,101 Nicholls Rd, Stony Brook, NY 11794 USA
来源
ONCOTARGETS AND THERAPY | 2019年 / 12卷
关键词
liposomal irinotecan; nal-IRI; pancreatic cancer; pancreatic ductal adenocarcinoma; refractory cancer; NANOLIPOSOMAL IRINOTECAN; 2ND-LINE CHEMOTHERAPY; GEMCITABINE; THERAPY; TUMOR; ADENOCARCINOMA; OXALIPLATIN; FOLFIRINOX; SURVIVAL; COMBINATION;
D O I
10.2147/OTT.S167590
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pancreatic cancer is a highly lethal disease, where the mortality closely matches increasing incidence. Pancreatic ductal adenocarcinoma (PDAC) is the most common histologic type that tends to metastasize early in tumor progression. For metastatic PDAC, gemcitabine had been the mainstay treatment for the past three decades. The treatment landscape has changed since 2010, and current first-line chemotherapy includes triplet drugs like FOLFIRINOX (folinic acid, 5-fluorouracil, irinotecan, and oxaliplatin), and doublet agents like nab-paclitaxel and gemcitabine. Nanoliposomal encapsulated irinotecan (nal-IRI) was developed as a novel formulation to improve drug delivery, effectiveness, and limit toxicities. Nal-IRI, in combination with leucovorin-modulated fluorouracil (5-FU/LV), was found in a large randomized phase III clinical trial (NAPOLI-1) to significantly improve overall survival in patients who progressed on gemcitabine-based therapy. This review will focus on the value of using nal-IRI, toxicities, recent clinical experiences, and tools to improve patient outcomes in this setting.
引用
收藏
页码:1455 / 1463
页数:9
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