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

机译:伊立替康脂质体治疗转移性胰腺癌的研究:患者选择和观点

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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.
机译:胰腺癌是一种高度致死性疾病,其死亡率与不断增加的发病率紧密匹配。胰腺导管腺癌(PDAC)是最常见的组织学类型,倾向于在肿瘤进展的早期转移。对于转移性PDAC,吉西他滨一直是过去三十年的主要治疗手段。自2010年以来,治疗方式发生了变化,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nab-紫杉醇和吉西他滨。纳米脂质体包封的伊立替康(nal-IRI)被开发为一种新型制剂,可改善药物的输送,有效性和限制毒性。 Nal-IRI与亚叶酸调节的氟尿嘧啶(5-FU / LV)结合使用,在一项大型的随机III期临床试验(NAPOLI-1)中被发现,可以显着提高吉西他滨类药物治疗患者的总体生存率。本文将重点探讨使用nal-IRI的价值,毒性,最新的临床经验以及在这种情况下改善患者预后的工具。

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