Relationship between energetic gap and sensitivity to anti-programmed cell death 1 immune checkpoint inhibitors in non-small cell lung cancer patients: The ELY-2 study

IF 2.9 Q3 NUTRITION & DIETETICS Clinical nutrition ESPEN Pub Date : 2024-09-06 DOI:10.1016/j.clnesp.2024.09.002
Manuela Tiako Meyo , Pascaline Boudou-Rouquette , Jennifer Arrondeau , Jeanne Qiong Yu Chen , Laure Hirsch , Nathalie Neveux , Elizabeth Fabre , Caroline Guidet , Diane Damotte , Marie Wislez , Jérôme Alexandre , Jean-Philippe Durand , Guillaume Ulmann , François Goldwasser
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Abstract

Background & aims

We previously reported in the ELY prospective study that increased resting energy expenditure (REE) – so-called hypermetabolism – worsened tumor response, 6-month progression-free (PFS) and overall survival (OS) in metastatic non-small cell lung cancer (mNSCLC) patients treated with immune checkpoint inhibitors (ICI). Here, we investigated the effect of caloric coverage on the sensitivity to ICI.

Methods

We retrospectively analysed a multicentric database of mNSCLC patients treated with ICI. All patients had a baseline nutritional assessment including REE measured with indirect calorimetry and a dietitian estimation of food intakes. Measured/theoretical REE ≥110% defined hypermetabolism. Intakes ≥90% of estimated needs defined caloric coverage. The primary endpoint was PFS. Secondary endpoints included response rate and OS.

Results

Among 162 patients, 84 (51.9%) were normometabolic, and 78 (48.1%) hypermetabolic. In hypermetabolic patients, 40 (51.3%) met their caloric needs (group A) while 38 (48.7%) did not (group B). Median PFS was 4.3 vs. 1.9 months in groups A and B, respectively (HR: 0.49, 95%CI [0.31–0.80], p = 0.004). The PFS achieved in the group A and in normometabolic patients were similar (HR: 0.99, 95%CI [0.65–1.51], p = 0.95). In multivariate analysis, caloric coverage was independently associated with improved PFS in hypermetabolic patients (HR: 0.56, 95%CI [0.31–0.99], p = 0.048). Among hypermetabolic patients, the median OS was higher in the group A (HR: 0.58, 95%CI [0.35–0.95], p = 0.03).

Conclusion

Energy supply is a critical determinant of the sensitivity to ICI in NSCLC patients. A randomized study to evaluate the benefit of early nutritional intervention is warranted.

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非小细胞肺癌患者的能量间隙与对抗程序性细胞死亡 1 免疫检查点抑制剂的敏感性之间的关系:ELY-2 研究
背景与目的:我们曾在ELY前瞻性研究中报道,静息能量消耗(REE)增加--即所谓的高代谢--会恶化接受免疫检查点抑制剂(ICI)治疗的转移性非小细胞肺癌(mNSCLC)患者的肿瘤反应、6个月无进展(PFS)和总生存期(OS)。在此,我们研究了热量覆盖对 ICI 敏感性的影响:我们对接受 ICI 治疗的 mNSCLC 患者的多中心数据库进行了回顾性分析。所有患者都进行了基线营养评估,包括用间接热量计测量的 REE 和营养师估算的食物摄入量。测量/理论 REE ≥ 110% 定义为代谢亢进。摄入量≥估计需求量的 90% 定义为热量覆盖。主要终点是 PFS。次要终点包括应答率和OS:在 162 名患者中,84 人(51.9%)代谢正常,78 人(48.1%)代谢过高。在高代谢患者中,40 人(51.3%)能满足热量需求(A 组),38 人(48.7%)不能满足热量需求(B 组)。A 组和 B 组的中位生存期分别为 4.3 个月和 1.9 个月(HR:0.49,95%CI [0.31-0.80],P = 0.004)。A 组和正常代谢组患者的 PFS 相似(HR:0.99,95%CI [0.65-1.51],p = 0.95)。在多变量分析中,热量覆盖与高代谢患者的 PFS 改善独立相关(HR:0.56,95%CI [0.31-0.99],p = 0.048)。在高代谢患者中,A 组的中位 OS 更高(HR:0.58,95%CI [0.35-0.95],p = 0.03):能量供应是决定 NSCLC 患者对 ICI 敏感性的关键因素。结论:能量供应是决定 NSCLC 患者对 ICI 敏感性的关键因素,有必要进行随机研究,以评估早期营养干预的益处。
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来源期刊
Clinical nutrition ESPEN
Clinical nutrition ESPEN NUTRITION & DIETETICS-
CiteScore
4.90
自引率
3.30%
发文量
512
期刊介绍: Clinical Nutrition ESPEN is an electronic-only journal and is an official publication of the European Society for Clinical Nutrition and Metabolism (ESPEN). Nutrition and nutritional care have gained wide clinical and scientific interest during the past decades. The increasing knowledge of metabolic disturbances and nutritional assessment in chronic and acute diseases has stimulated rapid advances in design, development and clinical application of nutritional support. The aims of ESPEN are to encourage the rapid diffusion of knowledge and its application in the field of clinical nutrition and metabolism. Published bimonthly, Clinical Nutrition ESPEN focuses on publishing articles on the relationship between nutrition and disease in the setting of basic science and clinical practice. Clinical Nutrition ESPEN is available to all members of ESPEN and to all subscribers of Clinical Nutrition.
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