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血清胆固醇和长链脂肪酸水平的升高与非小细胞肺癌患者使用纳武利尤单抗的疗效相关。

Increased serum cholesterol and long-chain fatty acid levels are associated with the efficacy of nivolumab in patients with non-small cell lung cancer.

机构信息

Department of Chemotherapy, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, 431-3192, Japan.

Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, 431-3192, Japan.

出版信息

Cancer Immunol Immunother. 2022 Jan;71(1):203-217. doi: 10.1007/s00262-021-02979-4. Epub 2021 Jun 5.


DOI:10.1007/s00262-021-02979-4
PMID:34091744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8738455/
Abstract

BACKGROUND: Lipids have immunomodulatory functions and the potential to affect cancer immunity. METHODS: The associations of pretreatment serum cholesterol and long-chain fatty acids with the objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) were evaluated in 148 patients with non-small cell lung cancer who received nivolumab. RESULTS: When each lipid was separately evaluated, increased low-density lipoprotein (LDL)-cholesterol (P < 0.001), high-density lipoprotein (HDL)-cholesterol (P = 0.014), total cholesterol (P = 0.007), lauric acid (P = 0.015), myristic acid (P = 0.022), myristoleic acid (P = 0.035), stearic acid (P = 0.028), linoleic acid (P = 0.005), arachidic acid (P = 0.027), eicosadienoic acid (P = 0.017), dihomo-γ-linolenic acid (P = 0.036), and behenic acid levels (P = 0.032) were associated with longer PFS independent of programmed death ligand 1 (PD-L1) expression. Meanwhile, increased LDL-cholesterol (P < 0.001), HDL-cholesterol (P = 0.009), total cholesterol (P = 0.036), linoleic acid (P = 0.014), and lignoceric acid levels (P = 0.028) were associated with longer OS independent of PD-L1 expression. When multiple lipids were evaluated simultaneously, LDL-cholesterol (P = 0.003), HDL-cholesterol (P = 0.036), and lauric acid (P = 0.036) were independently predictive of PFS, and LDL-cholesterol (P = 0.008) and HDL-cholesterol (P = 0.031) were predictive of OS. ORR was not associated with any serum lipid. CONCLUSIONS: Based on the association of prolonged survival in patients with increased serum cholesterol and long-chain fatty acid levels, serum lipid levels may be useful for predicting the efficacy of immune checkpoint inhibitor therapy.

摘要

背景:脂质具有免疫调节功能,并有可能影响癌症的免疫。

方法:评估了 148 例接受纳武单抗治疗的非小细胞肺癌患者的预处理血清胆固醇和长链脂肪酸与客观缓解率(ORR)、无进展生存期(PFS)和总生存期(OS)之间的关系。

结果:当单独评估每种脂质时,发现低密度脂蛋白(LDL)-胆固醇(P < 0.001)、高密度脂蛋白(HDL)-胆固醇(P = 0.014)、总胆固醇(P = 0.007)、月桂酸(P = 0.015)、肉豆蔻酸(P = 0.022)、肉豆蔻油酸(P = 0.035)、硬脂酸(P = 0.028)、亚油酸(P = 0.005)、花生酸(P = 0.027)、二十碳二烯酸(P = 0.017)、二高-γ-亚麻酸(P = 0.036)和山嵛酸(P = 0.032)水平与独立于程序性死亡配体 1(PD-L1)表达的更长的 PFS 相关。同时,发现 LDL-胆固醇(P < 0.001)、HDL-胆固醇(P = 0.009)、总胆固醇(P = 0.036)、亚油酸(P = 0.014)和二十四烷酸(P = 0.028)水平与独立于 PD-L1 表达的更长的 OS 相关。当同时评估多种脂质时,LDL-胆固醇(P = 0.003)、HDL-胆固醇(P = 0.036)和月桂酸(P = 0.036)是 PFS 的独立预测因子,而 LDL-胆固醇(P = 0.008)和 HDL-胆固醇(P = 0.031)是 OS 的预测因子。ORR 与任何血清脂质均无关。

结论:基于患者血清胆固醇和长链脂肪酸水平升高与生存时间延长的相关性,血清脂质水平可能有助于预测免疫检查点抑制剂治疗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/ba855c131da6/262_2021_2979_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/c86a10209851/262_2021_2979_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/10861c645ff8/262_2021_2979_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/6b20c01b7fa1/262_2021_2979_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/cb7d583cfb47/262_2021_2979_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/9891cb8c0385/262_2021_2979_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/d171dd961fe5/262_2021_2979_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/261d9777152b/262_2021_2979_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/ba855c131da6/262_2021_2979_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/c86a10209851/262_2021_2979_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/10861c645ff8/262_2021_2979_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/6b20c01b7fa1/262_2021_2979_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/cb7d583cfb47/262_2021_2979_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/9891cb8c0385/262_2021_2979_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/d171dd961fe5/262_2021_2979_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/261d9777152b/262_2021_2979_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd8/10992766/ba855c131da6/262_2021_2979_Fig8_HTML.jpg

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本文引用的文献

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Evaluation of Programmed Death Ligand 1 (PD-L1) Gene Amplification and Response to Nivolumab Monotherapy in Non-small Cell Lung Cancer.

JAMA Netw Open. 2020-9-1

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Comprehensive assessment of multiple tryptophan metabolites as potential biomarkers for immune checkpoint inhibitors in patients with non-small cell lung cancer.

Clin Transl Oncol. 2021-2

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Cell Metab. 2019-4-25

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Cancer Immunol Res. 2018-8-24

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Association of body-mass index and outcomes in patients with metastatic melanoma treated with targeted therapy, immunotherapy, or chemotherapy: a retrospective, multicohort analysis.

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