nab-Paclitaxel for the treatment of pancreatic cancer

被引:28
作者
Kim, George [1 ]
机构
[1] Univ Florida Hlth Oncol, 21st Century Oncol, 7751 Baymeadows Rd E,Ste 205, Jacksonville, FL 32256 USA
来源
CANCER MANAGEMENT AND RESEARCH | 2017年 / 9卷
关键词
pancreatic cancer; nab-paclitaxel; metastatic; neoadjuvant; systematic review; PLUS GEMCITABINE; PHASE I/II; COMBINATION; THERAPY; REGIMEN; TRIAL;
D O I
10.2147/CMAR.S127840
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Nanoparticle albumin-bound paclitaxel (nab-P) plus gemcitabine (Gem) became a standard treatment option for metastatic pancreatic cancer (MPC) following positive results from a global phase III trial (MPACT). A large number of studies have now published results on the use of nab-P/Gem to treat advanced and early-stage disease, warranting a comprehensive review. The main goal of this systematic review is to summarize the efficacy and safety data of nab-P/Gem for the treatment of pancreatic cancer (PC). Methods: This systematic review includes results from studies that either published results in a peer-reviewed journal or presented the results at a major oncology conference. Results: Sixty-two studies were included (50 in the advanced/metastatic setting and 12 in the locally advanced setting). Most studies on the treatment of MPC were exclusively first line (33/50). Nevertheless, the studies in this review comprised a broad spectrum of patients, including those < 65 and = 65 years of age and those with a Karnofsky performance status of 70-100. Median overall survival (OS) in studies of nab-P/Gem in the advanced/metastatic setting ranged from 8.7 to 13.5 months. In addition, 15 studies of patients with advanced/metastatic PC examined nab-P/Gem as a backbone on which to add a variety of agents, including cancer stem cell inhibitors, stromal disrupting agents, and immune-modulating agents (median OS, 6.9-17 months). Ongoing trials are investigating nab-P/Gem with or without other agents across disease settings. Discussion: Studies conducted after MPACT have demonstrated that nab-P/Gem is an effective regimen for the first-line treatment of MPC for a wide range of patients. Regimens using nab-P/Gem as a backbone on which to combine additional agents are being studied actively, particularly in the advanced disease setting. Ongoing studies will yield valuable insights on the utility of nab-P-containing regimens to improve patient outcomes in PC in both earlier-stage and advanced disease.
引用
收藏
页码:85 / 96
页数:12
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