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中性粒细胞与淋巴细胞比值及血小板与淋巴细胞比值作为阿替利珠单抗联合贝伐单抗治疗不可切除肝细胞癌的预后生物标志物

Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Prognostic Biomarkers in Unresectable Hepatocellular Carcinoma Treated with Atezolizumab plus Bevacizumab.

作者信息

Wu Yue Linda, Fulgenzi Claudia Angela Maria, D'Alessio Antonio, Cheon Jaekyung, Nishida Naoshi, Saeed Anwaar, Wietharn Brooke, Cammarota Antonella, Pressiani Tiziana, Personeni Nicola, Pinter Matthias, Scheiner Bernhard, Balcar Lorenz, Huang Yi-Hsiang, Phen Samuel, Naqash Abdul Rafeh, Vivaldi Caterina, Salani Francesca, Masi Gianluca, Bettinger Dominik, Vogel Arndt, Schönlein Martin, von Felden Johann, Schulze Kornelius, Wege Henning, Galle Peter R, Kudo Masatoshi, Rimassa Lorenza, Singal Amit G, Sharma Rohini, Cortellini Alessio, Gaillard Vincent E, Chon Hong Jae, Pinato David J, Ang Celina

机构信息

Department of Medicine, Division of Hematology/Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, Du Cane Road, London W12 0HS, UK.

出版信息

Cancers (Basel). 2022 Nov 26;14(23):5834. doi: 10.3390/cancers14235834.

Abstract

Systemic inflammation is a key risk factor for hepatocellular carcinoma (HCC) progression and poor outcomes. Inflammatory markers such as the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) may have prognostic value in HCC treated with standard of care atezolizumab plus bevacizumab (Atezo-Bev). We conducted a multicenter, international retrospective cohort study of patients with unresectable HCC treated with Atezo-Bev to assess the association of NLR and PLR with overall survival (OS), progression-free survival (PFS), and objective response rates. Patients with NLR ≥ 5 had a significantly shorter OS (9.38 vs. 16.79 months, p < 0.001) and PFS (4.90 vs. 7.58 months, p = 0.03) compared to patients with NLR < 5. NLR ≥ 5 was an independent prognosticator of worse OS (HR 2.01, 95% CI 1.22−3.56, p = 0.007) but not PFS. PLR ≥ 300 was also significantly associated with decreased OS (9.38 vs. 15.72 months, p = 0.007) and PFS (3.45 vs. 7.11 months, p = 0.04) compared to PLR < 300, but it was not an independent prognosticator of OS or PFS. NLR and PLR were not associated with objective response or disease control rates. NLR ≥ 5 independently prognosticated worse survival outcomes and is worthy of further study and validation.

摘要

全身炎症是肝细胞癌(HCC)进展和预后不良的关键危险因素。中性粒细胞与淋巴细胞比值(NLR)和血小板与淋巴细胞比值(PLR)等炎症标志物可能对接受标准治疗阿替利珠单抗联合贝伐单抗(阿替利珠单抗-贝伐单抗)治疗的HCC患者具有预后价值。我们对接受阿替利珠单抗-贝伐单抗治疗的不可切除HCC患者进行了一项多中心、国际回顾性队列研究,以评估NLR和PLR与总生存期(OS)、无进展生存期(PFS)和客观缓解率之间的关联。与NLR<5的患者相比,NLR≥5的患者OS(9.38个月对16.79个月,p<0.001)和PFS(4.90个月对7.58个月,p = 0.03)显著缩短。NLR≥5是OS较差的独立预后因素(HR 2.01,95%CI 1.22−3.56,p = 0.007),但不是PFS的独立预后因素。与PLR<300相比,PLR≥300也与OS降低(9.38个月对15.72个月,p = 0.007)和PFS降低(3.45个月对7.11个月,p = 0.04)显著相关,但它不是OS或PFS的独立预后因素。NLR和PLR与客观缓解率或疾病控制率无关。NLR≥5独立预测生存结果较差,值得进一步研究和验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a0/9737420/99cb699aa4f7/cancers-14-05834-g001a.jpg

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