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聚焦脂质体伊立替康治疗转移性胰腺癌:患者选择与展望

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

作者信息

Woo Wonhee, Carey Edward T, Choi Minsig

机构信息

Division of Hematology/Oncology, Department of Medicine, Stony Brook University, Stony Brook, NY, USA,

出版信息

Onco Targets Ther. 2019 Feb 21;12:1455-1463. doi: 10.2147/OTT.S167590. eCollection 2019.

Abstract

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.

摘要

胰腺癌是一种致死率很高的疾病,其死亡率与发病率的上升密切相关。胰腺导管腺癌(PDAC)是最常见的组织学类型,在肿瘤进展早期往往会发生转移。对于转移性PDAC,在过去三十年中,吉西他滨一直是主要的治疗药物。自2010年以来,治疗格局发生了变化,目前的一线化疗包括三联药物,如FOLFIRINOX(亚叶酸、5-氟尿嘧啶、伊立替康和奥沙利铂),以及双联药物,如纳米白蛋白结合型紫杉醇和吉西他滨。纳米脂质体包裹的伊立替康(nal-IRI)作为一种新型制剂被开发出来,以改善药物递送、有效性并限制毒性。在一项大型随机III期临床试验(NAPOLI-1)中发现,nal-IRI与亚叶酸调节的氟尿嘧啶(5-FU/LV)联合使用,可显著提高在基于吉西他滨的治疗中病情进展的患者的总生存期。本综述将重点关注使用nal-IRI的价值、毒性、近期临床经验以及改善该情况下患者预后的工具。

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