临床治疗不治之症胰腺癌的适宜一线化疗方案:对患者总体生存和生活质量的考虑

Journal of Pancreatic Cancer Pub Date : 2021-08-06 eCollection Date: 2021-01-01 DOI:10.1089/pancan.2021.0005
Yasuko Murakawa, Kazunori Ootsuka, Makoto Abue
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引用次数: 2

摘要

目的:对于无法治愈的胰腺癌,其治疗目标是延长生存期和维持生活质量(QOL)。意外门诊会诊和急诊住院导致患者生活质量恶化。国家综合癌症网络(NCCN)指南推荐5-氟尿嘧啶/亚叶酸钙、奥沙利铂和伊立替康(FOLFIRINOX)以及吉西他滨加白蛋白结合紫杉醇(nabPTX+GEM)作为首选一线方案。日本临床实践指南进一步推荐GEM和替加富/吉美拉西/奥他拉西钾(S-1)。目前,没有任何治疗策略在患者临床过程的任何阶段考虑生活质量。方法:在本研究中,引入无住院生存期(HFS)作为总生存期(OS)定性方面的新指标。我们比较了四个一线化疗组的OS、住院时间(LOH)、OCT和HFS。结果:4个一线化疗组中位OS和HFS无显著差异,OS与LOH无强相关性。相比之下,在所有一线化疗组中,OS与OCT以及OS与HFS之间存在很强的相关性。mFOLFIRINOX和nabPTX+GEM的OCT与OS的比值相似。S-1的oct - os比最低。HFS与OS的比值从高到低依次为S-1、nabPTX+GEM、mFOLFIRINOX、GEM。结论:我们的研究结果表明一线mFOLFIRINOX和一线nabPTX+GEM的OS和HFS存在相关性差异。此外,在某些情况下,单独使用S-1可以获得良好的HFS。今后的化疗临床试验应在整个临床过程中考察患者的生活质量。
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The Appropriate First-Line Chemotherapy Regimen for Incurable Pancreatic Cancer in Clinical Practice: A Consideration of Patients' Overall Survival and Quality of Life.

Purpose: For incurable pancreatic cancer, the therapeutic goal is to prolong survival and maintain the quality of life (QOL). Unexpected outpatient consultation (OCT) and emergency hospitalization lead to QOL deterioration. The National Comprehensive Cancer Network (NCCN) guidelines recommend 5-fluorouracil/leucovorin, oxaliplatin, and irinotecan (FOLFIRINOX) and gemcitabine plus albumin-bound paclitaxel (nabPTX+GEM) as the preferred first-line regimens. Japanese clinical practice guidelines further recommend GEM and tegafur/gimeracil/oteracil potassium (S-1). Currently, no treatment strategy considers QOL at any stage during a patient's clinical course. Methods: In this study, hospital-free survival (HFS), defined as the period without hospitalization and OCT, was introduced as a new indicator of the qualitative aspect of overall survival (OS). We compared OS, length of hospitalization (LOH), OCT, and HFS for the four first-line chemotherapy groups. Results: No significant difference was observed in the median OS and HFS, nor was there a strong correlation between OS and LOH, based on the four first-line chemotherapy groups. In contrast, there were strong correlations between OS and OCT and between OS and HFS in all first-line chemotherapy groups. The ratio of OCT to OS was similar for mFOLFIRINOX and nabPTX+GEM. S-1 had the lowest OCT-to-OS ratio. The ratio of HFS to OS declined from highest to lowest in the order S-1, nabPTX+GEM, mFOLFIRINOX, and GEM. Conclusion: Our findings suggested existence of correlation differences between OS and HFS between first-line mFOLFIRINOX and first-line nabPTX+GEM. In addition, a good HFS was obtained with S-1 alone in some cases. In the future, clinical trials for chemotherapy should examine QOL during the entire clinical course.

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