Malik Mateusz, Radecka Barbara, Gełej Marek, Jackowska Aleksandra, Filipczyk-Cisarż Emilia, Żurowska Michalina, Hetman Katarzyna, Foszczyńska-Kłoda Małgorzata, Kania-Zembaczyńska Beata, Mańka Danuta, Orlikowska Marlena, Bodnar Lubomir
Clinical Oncology Department, Lower Silesian Oncology, Pulmonology and Hematology Center, 53-413 Wroclaw, Poland.
Department of Oncology, Institute of Medical Sciences, University of Opole, 45-040 Opole, Poland.
Biomedicines. 2024 Sep 11;12(9):2076. doi: 10.3390/biomedicines12092076.
In advanced-stage colorectal cancer (CRC), a strategy based on a sequence of systemic therapies brings survival benefits in most patients. Trifluridine and tipiracil hydrochloride (TT) is a chemotherapy drug effective in patients in the third- or later line setting. No highly specific biomarkers have been established for TT therapy so far. However, a systemic immune-inflammation index (SII), which is based on platelet, neutrophil and lymphocyte counts is applied to predict prognosis. In this retrospective, multicenter study, clinical data on 179 metastatic CRC patients treated with TT were collected. To evaluate factors predicting TT therapy response and overall survival, univariate logistic regression analysis was conducted. Subsequently, factors with < 0.05 in univariate analysis were included in multivariate analysis. In the multivariate analysis of progression-free survival (PFS), three favorable parameters were significant: good to moderate histological differentiation ( = 0.0038), carcinoembryonic antigen (CEA) < 5 ng/L ( = 0.0316) and SII ≤ 550 ( = 0.007). Favorable prognostic factors revealed in the multivariate analysis of overall survival (OS) were: <3 prior lines of treatment ( = 0.02), good to moderate histological differentiation ( = 0.0003), CEA < 5 ng/L ( = 0.0227) and SII ≤ 550 ( = 0.0001). Our study indicated that pre-treatment SII may be clinically useful for selecting likely responder patients and assessing the prognosis for mCRC patients treated with TT.
在晚期结直肠癌(CRC)中,基于一系列全身治疗的策略能使大多数患者获得生存益处。曲氟尿苷和盐酸替匹嘧啶(TT)是一种对三线及后续治疗线的患者有效的化疗药物。目前尚未建立用于TT治疗的高度特异性生物标志物。然而,一种基于血小板、中性粒细胞和淋巴细胞计数的全身免疫炎症指数(SII)被用于预测预后。在这项回顾性多中心研究中,收集了179例接受TT治疗的转移性CRC患者的临床数据。为了评估预测TT治疗反应和总生存的因素,进行了单因素逻辑回归分析。随后,将单因素分析中P<0.05的因素纳入多因素分析。在无进展生存期(PFS)的多因素分析中,三个有利参数具有显著性:良好至中等组织学分化(P = 0.0038)、癌胚抗原(CEA)<5 ng/L(P = 0.0316)和SII≤550(P = 0.007)。总生存期(OS)多因素分析中显示的有利预后因素为:先前治疗线数<3(P = 0.02)、良好至中等组织学分化(P = 0.0003)、CEA<5 ng/L(P = 0.0227)和SII≤550(P = 0.0001)。我们的研究表明,治疗前SII可能在临床上有助于选择可能有反应的患者,并评估接受TT治疗的mCRC患者的预后。