SII、PNI与晚期胃癌患者免疫检查点抑制剂治疗疗效及预后的关系
Association of SII and PNI with Efficacy and Prognosis of Immune Checkpoint Inhibitors in Patients with Advanced Gastric Cancer
DOI: 10.12677/ACM.2022.125622, PDF,  被引量    科研立项经费支持
作者: 李 玲, 陶风英, 徐 菲, 袁胜利*:青岛大学附属青岛市市立医院本部肿瘤二科,山东 青岛;马春芬:青岛大学附属青岛市市立医院本部放射科,山东 青岛
关键词: SIIPNI晚期胃癌免疫检查点抑制剂Systemic Immune-Inflammation Index Prognostic Nutritional Index Advanced Gastric Cancer Immune Checkpoint Inhibitors
摘要: 目的:研究SII、PNI与晚期胃癌患者免疫检查点抑制剂(Immune checkpoint inhibitors, ICIs)治疗疗效及预后的关系。方法:选取2018年1月~2021年5月在青岛大学附属青岛市市立医院接受ICIs (主要为PD-1/PD-L1抑制剂)治疗的晚期胃癌患者65例。以各组中位数为SII、PNI截断值,根据是否大于截断值将患者分为低SII、PNI组及高SII、PNI组。比较两组患者免疫治疗后的疾病控制率(DCR)及无进展生存时间(PFS)。结果:65例入组患者的中位年龄为64岁,其中男性45例,女性20例。SII、PNI的截断值分别为563.3、43.2 ng/mL,其中低SII组32例,高SII组33例,低PNI组32例,高PNI组33例。高、低值组SII的DCR分别为51.5%、71.9%,治疗前SII水平与DCR之间不具有相关性(P > 0.05)。高、低值组PNI的DCR分别为75.8%、46.9%,PNI水平与DCR之间具有相关性(P < 0.05)。低SII、高PNI预示ICIs治疗的晚期胃癌患者较长的PFS (SII的HR = 0.407,95% CI:0.179~0.925,P = 0.032;PNI的HR = 3.438,95% CI:1.466~8.062,P = 0.005)。多因素分析结果显示,SII、PNI是PFS的独立风险因素(P < 0.05)。结论:SII、PNI可以预测晚期胃癌患者免疫治疗的疗效及预后,未来有望成为新的预测指标。
Abstract: Objective: To investigate whether SII, PNI are associated with Immune checkpoint inhibitors (ICIs) efficacy in patients with advanced gastric cancer. Methods: 65 patients with advanced gastric cancer who were treated with Immune checkpoint inhibitors (ICIs) at Qingdao Municipal Hospital affiliated to Qingdao University from January 2018 to May 2021 were enrolled in this retrospective study. The optimal cut-off values of SII, PNI for predicting efficacy and prognosis were determined accord-ing to the median of each group. Disease Control Rate (DCR) and Progression Free Survival (PFS) were calculated and compared using Kaplan-Meier method and log-rank test. Results: The median age of the 65 patients was 64 years old, including 45 males and 20 females. The optimal cut-off val-ues of SII/PNI were 563.3 and 43.2 ng/mL, respectively. 32 patients were in the low SII group, and 33 patients were in the high SII group, 32 patients were in the low PNI group, and 33 patients were in the high PNI group. The DCR of SII in high and low value groups was 51.5% and 71.9% respec-tively, and there was no correlation between SII level and DCR (P > 0.05). The DCR of PNI in high and low value groups was 75.8% and 46.9%, and there was a correlation between PNI level and DCR (P < 0.05). Low SII and high PNI were associated with longer PFS (HR for SII = 0.407, 95% CI: 0.179~0.925, P= 0.032; HR for PNI = 3.438, 95% CI: 1.466~8.062, P = 0.005). The results of multi-variate analysis showed that SII and PNI were independent risk factors for PFS (P < 0.05). Conclu-sion: SII and PNI can predict the efficacy and prognosis of immunotherapy in patients with ad-vanced gastric cancer, and are expected to be new predictors in the future.
文章引用:李玲, 陶风英, 马春芬, 徐菲, 袁胜利. SII、PNI与晚期胃癌患者免疫检查点抑制剂治疗疗效及预后的关系[J]. 临床医学进展, 2022, 12(5): 4295-4302. https://doi.org/10.12677/ACM.2022.125622

参考文献

[1] Bray, F., Ferlay, J., Soerjomataram, I., et al. (2018) Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA: A Cancer Journal for Clinicians, 68, 394-424. [Google Scholar] [CrossRef] [PubMed]
[2] Havel, J.J., Chowell, D. and Chan, T.A. (2019) The Evolving Landscape of Biomarkers for Checkpoint Inhibitor Immunotherapy. Nature Reviews Cancer, 19, 133-150. [Google Scholar] [CrossRef] [PubMed]
[3] Mantovani, A., Allavena, P., Sica, A., et al. (2008) Can-cer-Related Inflammation. Nature, 454, 436-444. [Google Scholar] [CrossRef] [PubMed]
[4] Zhang, Y., Chen, B., Wang, L., et al. (2019) Systemic Im-mune-Inflammation Index Is a Promising Noninvasive Marker to Predict Survival of Lung Cancer: A Meta-Analysis. Medicine (Baltimore), 98, e13788. [Google Scholar] [CrossRef
[5] Zhang, Y., Xiao, G. and Wang, R. (2019) Clinical Signifi-cance of Systemic Immune Inflammation Index (SII) and C-Reactive Protein-to-Albumin Ratio (CAR) in Patients with Esophageal Cancer: A Meta-Analysis. Cancer Management and Research, 11, 4185-4200. [Google Scholar] [CrossRef
[6] Chen, J.H., Zhai, E.T., Yuan, Y.J., et al. (2017) Systemic Immune Inflammation Index for Predicting Prognosis of Colorectal Cancer. World Journal of Gastroenterology, 23, 6261-6272. [Google Scholar] [CrossRef] [PubMed]
[7] Okada, S., Shimada, J., Kato, D., et al. (2017) Clinical Significance of Prognostic Nutritional Index after Surgical Treatment in Lung Cancer. The Annals of Thoracic Surgery, 104, 296-302. [Google Scholar] [CrossRef] [PubMed]
[8] Eo, W.K., Chang, H.J., Suh, J., et al. (2015) The Prognostic Nutritional Index Predicts Survival and Identifies Aggressiveness of Gastric Cancer. Nutrition and Cancer, 67, 1260-1267. [Google Scholar] [CrossRef] [PubMed]
[9] Tokunaga, R., Sakamoto, Y., Nakagawa, S., et al. (2015) Prognostic Nutritional Index Predicts Severe Complications, Recurrence, and Poor Prognosis in Patients with Colorectal Cancer Undergoing Primary Tumor Resection. Diseases of the Colon & Rectum, 58, 1048-1057. [Google Scholar] [CrossRef
[10] Chovanec, M., Cierna, Z., Miskovska, V., et al. (2018) Systemic Immune-Inflammation Index in Germ-Cell Tumours. British Journal of Cancer, 118, 831-838. [Google Scholar] [CrossRef] [PubMed]
[11] De Giorgi, U., Procopio, G., Giannarelli, D., et al. (2019) Association of Systemic Inflammation Index and Body Mass Index with Survival in Patients with Renal Cell Cancer Treated with Nivolumab. Clinical Cancer Research, 25, 3839-3846. [Google Scholar] [CrossRef
[12] Liu, J., Li, S., Zhang, S., et al. (2019) Systemic Immune-Inflammation Index, Neutrophil-to-Lymphocyte Ratio, Plate-let-to-Lymphocyte Ratio Can Predict Clinical Outcomes in Patients with Metastatic Non-Small-Cell Lung Cancer Treated with Nivolumab. Journal of Clinical Laboratory Analysis, 33, e22964. [Google Scholar] [CrossRef] [PubMed]
[13] 彭丽红. 外周血液学指标PD-1单抗治疗晚期非小细胞肺癌患者的疗效相关性分析[D]: [硕士学位论文]. 南昌: 南昌大学, 2020: 1-23.
[14] 罗文明, 刘利民, 王继, 等. PNI在评估免疫检查点抑制剂治疗晚期NSCLC患者的疗效与预后的作用[J]. 湖南师范大学学报(医学版), 2021, 18(2): 68-72.
[15] 王俊, 冉凤鸣, 钱羽. PD-L1表达检测的研究进展[J]. 实用肿瘤杂志, 2020, 35(1): 89-93.
[16] Fuchs, C.S., Doi, T., Jang, R.W., et al. (2018) Safety and Effi-cacy of Pembrolizumab Monotherapy in Patients with Previously Treated Advanced Gastric and Gastroesophageal Junc-tion Cancer: Phase 2 Clinical KEYNOTE-059 Trial. JAMA Oncology, 4, e180013.
[17] Kang, Y.K., Chen, L.T., Ryu, M.H., et al. (2022) Nivolumab plus Chemotherapy versus Placebo plus Chemotherapy in Patients with HER2-Negative, Untreated, Unresectable Advanced or Recurrent Gastric or Gastro-Oesophageal Junction Cancer (ATTRACTION-4): A Randomised, Multicentre, Double-Blind, Placebo-Controlled, Phase 3 Trial. The Lancet Oncology, 23, 234-247. [Google Scholar] [CrossRef
[18] Koizumi, K., Hjoo, S., Akashi, T., et al. (2007) Chemokine Receptors in Cancer Metastasis and Cancer Cell-Derived Chemokines in Host Immune Response. Cancer Science, 98, 1652-1658. [Google Scholar] [CrossRef] [PubMed]
[19] Labelle, M., Begum, S. and Hynes, R.O. (2011) Direct Signaling between Platelets and Cancer Cells Induces an Epithelial-Mesenchymal-Like Transition and Promotes Metasta-sis. Cancer Cell, 20, 576-590. [Google Scholar] [CrossRef] [PubMed]
[20] Rodio-Janeiro, B.K., Paradela-Dobarro, B., Raposeiras-Roubin, S., et al. (2015) Glycated Human Serum Albumin Induces NF-κB Activation and Endothelial Nitric Oxide Synthase Uncou-pling in Human Umbilical Vein Endothelial Cells. Journal of Diabetic Complications, 29, 984-992. [Google Scholar] [CrossRef] [PubMed]