免疫检查点抑制剂治疗转移性食管鳞状细胞癌的预后营养指标

K. Yoshino, M. Tamba, H. Osumi, S. Fukuoka, M. Ogura, S. Udagawa, K. Shimozaki, T. Wakatsuki, E. Shinozaki, K. Yamaguchi, K. Chin, A. Ooki
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引用次数: 0

摘要

预后营养指数(PNI)是一种基于炎症和营养的指标,可作为各种癌症类型的预后因素。本研究旨在评估PNI与接受免疫检查点抑制剂(ICI)治疗的食管鳞状细胞癌(ESCC)患者生存率之间的关系。材料和方法这项单中心回顾性研究包括两个队列:109例患者接受纳武单抗单一治疗作为二线或后期治疗,92例患者接受一线ICI治疗(ICI加化疗或纳武单抗加伊匹单抗)。在纳武单抗单药治疗队列中,与PNI较低(16.2个月对5.5个月,P = 0.001)相比,PNI较高(PNI≥40.5)与更长的总生存期(OS)相关。在一线队列中,92例患者接受了ICI +化疗(n = 60)或nivolumab + ipilimumab (n = 32)。在ICI +化疗组(21.2个月vs 7.7个月,P = 0.0008)和nivolumab + ipilimumab组(未达到vs 10.2个月,P = 0.02)中,更高的PNI与更好的OS相关。多变量分析确定PNI状态是两个队列中独立的预后因素。治疗1个月后PNI的动态变化(δ PNI≥1.25)与接受纳武单抗单药或纳武单抗联合伊匹单抗的低PNI患者更好的无进展生存有关,但与接受一线ICI加化疗的患者无关。结论spni及其动态变化可作为ESCC患者接受ici治疗后预后的有效指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic nutritional index as a prognostic marker in metastatic esophageal squamous-cell carcinoma treated with immune checkpoint inhibitor

Background

The prognostic nutritional index (PNI) is an inflammation- and nutrition-based indicator that serves as a prognostic factor for various cancer types. This study aimed to evaluate the association between PNI and survival in patients with esophageal squamous-cell carcinoma (ESCC) receiving immune checkpoint inhibitor (ICI)-based therapies.

Materials and methods

This single-center retrospective study included two cohorts: 109 patients treated with nivolumab monotherapy as second-line or later therapy and 92 patients receiving first-line ICI-based treatments (ICI plus chemotherapy or nivolumab plus ipilimumab).

Results

In the nivolumab monotherapy cohort, higher PNI (PNI ≥ 40.5) was linked to longer overall survival (OS) compared with lower PNI (16.2 versus 5.5 months, P = 0.001). In the first-line cohort, 92 patients received ICI plus chemotherapy (n = 60) or nivolumab plus ipilimumab (n = 32). Higher PNI was linked to better OS in both the ICI plus chemotherapy (21.2 versus 7.7 months, P = 0.0008) and the nivolumab plus ipilimumab (not reached versus 10.2 months, P = 0.02) cohorts. Multivariate analysis identified PNI status as an independent prognostic factor in both cohorts. Dynamic changes in PNI (delta PNI ≥ 1.25) 1 month after treatment were linked to better progression-free survival in patients with lower PNI receiving nivolumab monotherapy or nivolumab plus ipilimumab but not in those receiving first-line ICI plus chemotherapy.

Conclusions

PNI and its dynamic changes may serve as useful indicators of prognosis in patients with ESCC receiving ICI-based therapies.
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