Sobczuk Paweł, Teterycz Paweł, Lugowska Iwona, Klimczak Anna, Bylina Elżbieta, Czarnecka Anna M, Kosela-Paterczyk Hanna, Osuch Czesław, Streb Joanna, Rutkowski Piotr
Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie Institute-Oncology Center, 02-781 Warsaw, Poland.
Department of Experimental and Clinical Physiology, Laboratory of Centre for Preclinical Research, Medical University of Warsaw, 02-097 Warsaw, Poland.
Oncol Lett. 2019 Sep;18(3):3373-3380. doi: 10.3892/ol.2019.10622. Epub 2019 Jul 16.
The neutrophil-to lymphocyte ratio (NLR) has been proven to be correlated with outcomes in various cancer types, including gastrointestinal stromal tumors (GIST). There is limited data regarding the clinical value of NLR during second line therapy after failure of imatinib and there is an urgent need for more precise predictive factors for therapy. The aim of this study was to assess the association of the pretreatment NLR with progression free survival (PFS) and overall survival (OS) in patients with unresectable/metastatic GIST treated with sunitinib in a second line of treatment. In this analysis 146 out of 230 patients with unresectable/metastatic GIST were included, who were treated between 2005 and 2016 with sunitinib after failure of imatinib, with complete clinical data. In all patients, the NLR was assessed at baseline. The NLR cutoff of 2.4 was selected. The Kaplan-Meier method with the long-rank test and Cox proportional hazards model were applied for statistical analysis. Median PFS was 12.4 months with a 2-year rate of 27.1% and a 5-year rate of 4.8%. Median OS was 22.8 months, whereas 2- and 5-year rates were 47.8 and 13.8%, respectively. Patients with NLR>2.4 had significantly shorter OS: Median OS was 30 months for NLR≤2.4 vs. 16.4 months for NLR>2.4 (P=0.002); median PFS was 18.2 vs. 9.6 (P=0.075), respectively. In a multivariate model adjusted for mitotic index, primary location of tumor and driver mutation in exon 11, NLR was proven to be independently associated with OS (HR 1.92, 95% CI 1.27-2.9, P=0.002) but not PFS (HR 1.31, 95%CI 0.89-1.93, P=0.17). The present data demonstrate that NLR can serve as an independent prognostic factor for patients with advanced GIST treated with sunitinib.
中性粒细胞与淋巴细胞比值(NLR)已被证明与包括胃肠道间质瘤(GIST)在内的多种癌症类型的预后相关。关于伊马替尼治疗失败后二线治疗期间NLR的临床价值的数据有限,因此迫切需要更精确的治疗预测因素。本研究的目的是评估在二线治疗中接受舒尼替尼治疗的不可切除/转移性GIST患者治疗前NLR与无进展生存期(PFS)和总生存期(OS)之间的关联。在该分析中,纳入了230例不可切除/转移性GIST患者中的146例,这些患者在2005年至2016年间伊马替尼治疗失败后接受了舒尼替尼治疗,并拥有完整的临床数据。在所有患者中,在基线时评估NLR。选择NLR临界值为2.4。采用Kaplan-Meier法和长秩检验以及Cox比例风险模型进行统计分析。中位PFS为12.4个月,2年率为27.1%,5年率为4.8%。中位OS为22.8个月,而2年和5年率分别为47.8%和13.8%。NLR>2.4的患者OS明显较短:NLR≤2.4时中位OS为30个月,而NLR>2.4时为16.4个月(P=0.002);中位PFS分别为18.2和9.6(P=0.075)。在针对有丝分裂指数、肿瘤原发部位和第11外显子驱动突变进行调整的多变量模型中,NLR被证明与OS独立相关(HR 1.92,95%CI 1.27-2.9,P=0.002),但与PFS无关(HR 1.31,95%CI 0.89-1.93,P=0.17)。目前的数据表明,NLR可作为接受舒尼替尼治疗的晚期GIST患者的独立预后因素。