Koeller Jim, Surinach Andy, Arikian Steven R, Zivkovic Marko, Janeczko Patrick, Cockrum Paul, Kim George
University of Texas at Austin, Center for Pharmacoeconomic Studies, UTHSC, 7703 Floyd Curl Drive - MC 6220, San Antonio, TX 78229, USA.
Genesis Research, Hoboken, NJ, USA.
Ther Adv Med Oncol. 2020 Aug 17;12:1758835920944052. doi: 10.1177/1758835920944052. eCollection 2020.
There are questions surrounding the real-world effectiveness of chemotherapeutic treatments for pancreatic ductal adenocarcinoma. This literature review compared the clinical characteristics and outcomes of available real-world evidence (RWE) for liposomal irinotecan in combination with 5-fluorouracil (5-FU) and leucovorin (LV), a treatment regimen indicated for patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) who previously progressed on gemcitabine-based therapy. A targeted literature search was conducted in the PubMed Central® and Embase® databases to identify available RWE regarding patients with mPDAC receiving liposomal irinotecan published within the last 5 years (January 2014-September 2019). Data were extracted for prior lines of therapy, performance status, overall survival (OS), progression-free survival (PFS), duration of exposure, and adverse events. Six studies met inclusion criteria. A comparison of baseline patient characteristics and results with the included evidence reveals a clinically fragile, real-world patient population in terms of age (range: 61-68), prior lines of therapy with 34-61% of patients receiving ⩾2 lines of lines of prior therapy and performance status [49.8-100% of patients with Eastern Cooperative Oncology Group (ECOG) 0-1]. Studies observed wide OS (range: 5.3-9.4 months) and similar PFS (range: 2.3-4.1 months), with two studies measuring duration of exposure (7.3 weeks, 3.1 months). Patients analyzed by RWE studies tended to be older with significant disease progression, poor performance status, and more heavily pretreated compared with the phase III registrational trial (NAPOLI-1). Despite this, patients treated with liposomal irinotecan + 5-FU/LV therapy had similar outcomes as those in NAPOLI-1.
关于化疗治疗胰腺导管腺癌在现实世界中的有效性存在一些问题。本综述比较了脂质体伊立替康联合5-氟尿嘧啶(5-FU)和亚叶酸(LV)这一治疗方案的现有真实世界证据(RWE)的临床特征和结果,该方案适用于先前接受过吉西他滨为基础治疗的转移性胰腺导管腺癌(mPDAC)患者。在PubMed Central®和Embase®数据库中进行了有针对性的文献检索,以确定过去5年(2014年1月至2019年9月)内发表的关于接受脂质体伊立替康治疗的mPDAC患者的可用RWE。提取了先前治疗线数、体能状态、总生存期(OS)、无进展生存期(PFS)、暴露持续时间和不良事件的数据。六项研究符合纳入标准。将基线患者特征和结果与纳入的证据进行比较,发现在年龄(范围:61-68岁)、先前治疗线数(34-61%的患者接受≥2线先前治疗)和体能状态方面(东部肿瘤协作组(ECOG)0-1级的患者占49.8-100%),这是一个临床脆弱的真实世界患者群体。研究观察到广泛的OS(范围:5.3-9.4个月)和相似的PFS(范围:2.3-4.1个月),有两项研究测量了暴露持续时间(7.3周,3.1个月)。与III期注册试验(NAPOLI-1)相比,RWE研究分析的患者往往年龄更大,疾病进展显著,体能状态差,且预处理更重。尽管如此,接受脂质体伊立替康+5-FU/LV治疗的患者与NAPOLI-1中的患者有相似的结果。