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脾脏体积对接受纳米脂质体伊立替康治疗的转移性胰腺腺癌患者生存的影响。

The impact of spleen volume on the survival of metastatic pancreatic adenocarcinoma patients receiving nanoliposomal irinotecan.

作者信息

Yang Shih-Hung, Chiang Nai-Jung, Chiu Sz-Chi, Chou Wen-Chi, Bai Li-Yuan, Li Chung-Pin, Su Yung-Yeh, Chiu Tai-Jan, Chuang Shih-Chang, Peng Cheng-Ming, Chan De-Chuan, Chen Jen-Shi, Yen Chia-Jui, Chen Yen-Yang, Chiu Chang-Fang, Chen Li-Tzong, Shan Yan-Shen

机构信息

Department of Oncology, National Taiwan University Hospital Taipei, Taiwan.

Graduate Institute of Oncology, National Taiwan University College of Medicine Taipei, Taiwan.

出版信息

Am J Cancer Res. 2022 Apr 15;12(4):1884-1898. eCollection 2022.

Abstract

Nanoliposomal irinotecan (nal-IRI) plus 5-fluorouracil and leucovorin (NalFL) comprises the current standard for gemcitabine-failed metastatic pancreatic ductal adenocarcinoma (PDAC). As liposomes generally accumulate in the spleen, we evaluated the impact of spleen volume on prognosis. We enrolled patients with metastatic PDAC who failed gemcitabine-based therapy and were initiated on NalFL between August 2018 and November 2020. The spleen volume before NalFL administration was evaluated. They were stratified into dose subgroups (i.e. low, < 48 mg/m; intermediate, 48 - < 64 mg/m; high, ≥ 64 mg/m) by the average nal-IRI dose during the entire treatment, and multivariate analysis of overall survival (OS) was performed. We included 547 patients with a median age of 63 years (range, 27-89 years) and a median of 1 (range, 0-7) palliative chemotherapy regimen. The median spleen volume was 245 mL (range, 82-817 mL). Among patients with splenomegaly (≥ 245 mL), the low-dose subgroup had the worst median time to treatment failure (TTF, 1.8 months vs. 2.5 months vs. 2.5 months, P = 0.020) and OS (3.3 months vs. 5.9 months vs. 6.6 months, P = 0.018) as against no prognostic impact in patients without splenomegaly. In the multivariate analysis of patients with splenomegaly, performance status (PS) ≥ 2, body surface area (BSA) < 1.6 m, prior fluoropyrimidine use, liver metastasis, and low-dose subgroup were independent poor prognostic factors. A low average nal-IRI dose was significantly associated with poor prognosis, especially among patients with splenomegaly. Further pharmacological studies should validate the relevance of spleen volume on the treatment outcomes of nal-IRI.

摘要

纳米脂质体伊立替康(nal-IRI)联合5-氟尿嘧啶和亚叶酸钙(NalFL)是目前吉西他滨治疗失败的转移性胰腺导管腺癌(PDAC)的标准治疗方案。由于脂质体通常在脾脏中蓄积,我们评估了脾脏体积对预后的影响。我们纳入了在2018年8月至2020年11月期间接受基于吉西他滨的治疗失败并开始接受NalFL治疗的转移性PDAC患者。评估了NalFL给药前的脾脏体积。根据整个治疗期间的平均nal-IRI剂量将患者分为剂量亚组(即低剂量组,<48mg/m;中剂量组,48 - <64mg/m;高剂量组,≥64mg/m),并对总生存期(OS)进行多因素分析。我们纳入了547例患者,中位年龄为63岁(范围27 - 89岁),中位接受1次(范围0 - 7次)姑息化疗方案。中位脾脏体积为245mL(范围82 - 817mL)。在脾肿大(≥245mL)的患者中,低剂量亚组的中位治疗失败时间(TTF,1.8个月对2.5个月对2.5个月,P = 0.020)和OS(3.3个月对5.9个月对6.6个月,P = 0.018)最差,而在无脾肿大的患者中无预后影响。在脾肿大患者的多因素分析中,体能状态(PS)≥2、体表面积(BSA)<1.6m²、既往使用氟嘧啶、肝转移和低剂量亚组是独立的不良预后因素。低平均nal-IRI剂量与不良预后显著相关,尤其是在脾肿大的患者中。进一步的药理学研究应验证脾脏体积与nal-IRI治疗结果的相关性。

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