Systemic immunoinflammatory index and prognostic nutrition index for predicting pathologic responses of patients with advanced gastric cancer after neoadjuvant therapy for advanced gastric cancer.

IF 3.6 3区 医学 Q2 ONCOLOGY American journal of cancer research Pub Date : 2024-08-25 eCollection Date: 2024-01-01 DOI:10.62347/PAYM2267
Meng Fan, Jin Tang, Wei Du, Yang-Feng Du, Hai-Jun Liu
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Abstract

To investigate the value of prognostic nutrition index (PNI) and systemic immunoinflammatory index (SII) for predicting pathological responses of patients with advanced gastric cancer (GC) after neo-adjuvant chemotherapy (NACT). The clinicopathological data of 326 patients with advanced GC who received NACT in Xiangya School of Medicine, Central South University (The First People's Hospital of Changde City) from January 2017 to December 2021 were retrospectively collected. The SII and PNI of patients were calculated. The receiver operating characteristics (ROC) curve was leveraged for getting the optimal cutoff values of SII and PNI. The pathological response of patients after NACT, as obtained from their postoperative pathological examinations, was evaluated based on the tumor regression grade (TRG) criteria. Multivariate regression analysis was employed for identifying factors that led to various pathological responses after NACT in advanced GC patients. The log-rank test was utilized for between-group comparison of patients' survival curves. The SII and PNI were 507.45 and 48.48 respectively, and their levels were divided into high and low groups. Pathological response (TRG 0-1) was observed in 66 cases (20.25%), while non-pathological response (TRG 2-3) was observed in 260 cases (79.75%). The results of multivariate logistic regression analysis showed that tumor diameter < 5 cm, ypT T0-T2, ypN N0, chemotherapy regimen XELOX (capecitabine combined with oxaliplatin), SII < 507.45 (P=0.002), PNI > 48.48 were all independent factors affecting the pathological responses of advanced GC patients after NACT (all P < 0.05). With SII and PNI being included, the AUC was 0.821 (95% CI: 0.765-0.876), and the specificity was 87.90% and the sensitivity was 64.20%. The Kaplan-Meier survival curve analysis showed that NACT patients with tumor diameter < 5 cm, ypT T0-T2, ypN N0, XELOX chemotherapy regimen, SII < 507.45 and SII ≥ 507.45 had a higher survival rate. (P < 0.001). Before treatment, tumor diameter < 5 cm, ypT T0-T2, ypN N0, chemotherapy regimen XELOX, SII < 507.45, PNI > 48.48 were all independent factors affecting the pathological response of advanced GC patients after NACT. Moreover, the inclusion of SII and PNI increased the accuracy of predicting the pathological response of patients after NACT.

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预测晚期胃癌新辅助治疗后病理反应的全身免疫炎症指数和预后营养指数
目的 探讨预后营养指数(PNI)和全身免疫炎症指数(SII)对晚期胃癌(GC)患者新辅助化疗(NACT)后病理反应的预测价值。该研究回顾性收集了2017年1月至2021年12月在中南大学湘雅医学院(常德市第一人民医院)接受NACT治疗的326例晚期胃癌患者的临床病理资料。计算患者的SII和PNI。利用接收者操作特征曲线(ROC)获得 SII 和 PNI 的最佳临界值。根据肿瘤回归分级(TRG)标准,对患者术后病理检查获得的 NACT 病理反应进行评估。多变量回归分析用于确定导致晚期 GC 患者 NACT 术后不同病理反应的因素。采用对数秩检验比较患者的组间生存曲线。SII和PNI分别为507.45和48.48,分为高、低两组。病理反应(TRG 0-1)66 例(20.25%),非病理反应(TRG 2-3)260 例(79.75%)。多变量逻辑回归分析结果显示,肿瘤直径小于5厘米、ypT T0-T2、ypN N0、化疗方案XELOX(卡培他滨联合奥沙利铂)、SII小于507.45(P=0.002)、PNI大于48.48均是影响晚期GC患者NACT后病理反应的独立因素(P均小于0.05)。包括 SII 和 PNI 在内,AUC 为 0.821(95% CI:0.765-0.876),特异性为 87.90%,敏感性为 64.20%。Kaplan-Meier生存曲线分析显示,肿瘤直径小于5厘米、ypT T0-T2、ypN N0、XELOX化疗方案、SII小于507.45和SII≥507.45的NACT患者生存率更高。(P < 0.001).治疗前,肿瘤直径小于 5 cm、ypT T0-T2、ypN N0、化疗方案 XELOX、SII < 507.45、PNI > 48.48 都是影响晚期 GC 患者 NACT 后病理反应的独立因素。此外,SII和PNI的加入提高了预测NACT后患者病理反应的准确性。
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263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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