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脂质体伊立替康:转移性胰腺腺癌细胞癌的综述。

Liposomal Irinotecan: A Review in Metastatic Pancreatic Adenocarcinoma.

机构信息

Springer, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2017 May;77(7):785-792. doi: 10.1007/s40265-017-0741-1.

Abstract

Intravenous liposomal irinotecan injection (Onivyde) is approved for use in combination with 5-fluorouracil and leucovorin (5-FU/LV) in patients with metastatic pancreatic adenocarcinoma that has progressed following gemcitabine-based therapy. Liposomal irinotecan is a liposome-encapsulated formulation of the topoisomerase-1 inhibitor irinotecan, developed to overcome the pharmacological and clinical limitations of non-liposomal irinotecan. In the pivotal multinational, phase III NAPOLI-1 trial in patients with metastatic pancreatic adenocarcinoma that had progressed following gemcitabine-based therapy, liposomal irinotecan in combination with 5-FU/LV significantly prolonged median overall survival (OS; primary endpoint) and median progression-free survival (PFS) at the time of the primary analysis (after 313 events) and final analysis (after 382 events) compared with 5-FU/LV control therapy. The objective response rate was also significantly higher in the liposomal irinotecan plus 5-FU/LV group than in the control group. Liposomal irinotecan-based combination therapy had a manageable safety profile; the most common treatment-emergent adverse events (TEAEs) of grade ≥3 severity were haematological or gastrointestinal in nature. The incidence of neutropenic sepsis was low. In a setting where there is a paucity of second-line treatment options, liposomal irinotecan in combination with 5-FU/LV is an important emerging treatment option for metastatic adenocarcinoma of the pancreas that has progressed following gemcitabine-based therapy.

摘要

注射用脂质体伊立替康(Onivyde)与氟尿嘧啶和亚叶酸(5-FU/LV)联合用于吉西他滨治疗后进展的转移性胰腺腺癌患者。脂质体伊立替康是拓扑异构酶-1抑制剂伊立替康的脂质体包封制剂,旨在克服非脂质体伊立替康的药理学和临床局限性。在一项针对转移性胰腺腺癌患者的多中心、III 期 NAPOLI-1 试验中,这些患者在吉西他滨治疗后进展,脂质体伊立替康联合 5-FU/LV 与 5-FU/LV 对照治疗相比,显著延长了中位总生存期(OS;主要终点)和中位无进展生存期(PFS)在主要分析(在 313 例事件后)和最终分析(在 382 例事件后)。脂质体伊立替康联合 5-FU/LV 组的客观缓解率也显著高于对照组。脂质体伊立替康联合治疗具有可管理的安全性特征;最常见的 3 级及以上治疗相关不良事件(TEAE)为血液学或胃肠道性质。中性粒细胞减少性败血症的发生率较低。在二线治疗选择有限的情况下,脂质体伊立替康联合 5-FU/LV 是吉西他滨治疗后进展的转移性胰腺腺癌的一个重要新兴治疗选择。

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