Adana Research and Training State Hospital, Adana, Turkey.
Medical Oncology Department, Inonu University, Malatya, Turkey.
J Gastrointest Cancer. 2023 Mar;54(1):11-19. doi: 10.1007/s12029-021-00789-6. Epub 2022 Feb 4.
Hepatocellular cancer (HCC) is an aggressive tumor with an increasing incidence in recent years. Life expectancy is limited, especially due to limited effective treatments and tumor biology. In this study, we aimed to examine the effect of neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), prognostic nutritional index (PNI) parameters of treatment efficacy of patients using sorafenib in primary systemic therapy, progression-free survival (PFS), and overall survival (OS).
In this study, we retrospectively analyzed 78 patients who used sorafenib as a first-line systemic treatment. NLR, PLR, and PNI values were calculated with the existing formulas. Cut-off values for these markers were determined by performing ROC curve analysis. These values were determined respectively as 2.88, 111.05, and 38.25. Patients were divided into two groups according to this threshold value. OS and PFS values were calculated using a Cox proportional risk model. The effects of markers on OS and PFS were examined based on the cut-off value.
The mean PFS was 7.1 (range 1-46) months, and the mean OS was 14.1 (range 1.5-94) months. The pre-treatment decreased NLR (< 2.88) value was prognostic for higher PFS and OS rates. These values were determined respectively as 9.23 ± 1.79 and 3.45 ± 0.32 months for PFS and 21.17 ± 4.53 and 5.32 ± 0.53 months for OS. Pre-treatment decreased PLR (< 111.05) was found to be a positively significant prognostic value for both survival. These values were determined respectively as 7.37 ± 1.43 months and 3.16 ± 0.47 months for PFS and 21.12 ± 5.52 months and 6.16 ± 0.87 months for OS. And also, low PNI (< 38.25) value was prognostic for lower PFS and rates. These values were determined respectively as 7.47 ± 0.59 months and 3.25 ± 0.21 months for PFS and 16.36 ± 4.37 months and 5.15 ± 0.42 for OS. All three parameters were found to be statistically significant (p < 0.05) for both OS and PFS as independent prognostic markers.
Today, as the standard first-line treatment of HCC has shifted to combinations with immunotherapy (IO), IO transportation is not possible in most countries of the world. However, there are also patients who achieve great survival with only sorafenib. The important point is to identify the biomarkers that predict which patient will benefit better from which treatment. With the markers in our study and a scoring system that can be obtained with these markers, it can be evaluated which patient will be given IO combination and which patient will be given only TKI treatment. We think that such a scoring system can be used to identify suitable patients, especially in countries where, for financial reasons, not every patient can access Immunotherapy. The advantage of these tests is that they are inexpensive, easily calculable and standardized.
Number and date of registration: 2021/2088, 01-06-2021, retrospectively registered.
肝细胞癌(HCC)是一种侵袭性肿瘤,近年来发病率呈上升趋势。由于治疗方法有限和肿瘤生物学特性,患者的预期寿命有限。本研究旨在探讨中性粒细胞-淋巴细胞比值(NLR)、血小板-淋巴细胞比值(PLR)、预后营养指数(PNI)等参数对索拉非尼一线系统治疗患者的疗效、无进展生存期(PFS)和总生存期(OS)的影响。
本研究回顾性分析了 78 例使用索拉非尼作为一线系统治疗的患者。采用现有的公式计算 NLR、PLR 和 PNI 值。通过 ROC 曲线分析确定这些标志物的截断值。这些值分别确定为 2.88、111.05 和 38.25。根据该阈值将患者分为两组。使用 Cox 比例风险模型计算 OS 和 PFS 值。根据截断值检查标志物对 OS 和 PFS 的影响。
中位 PFS 为 7.1(范围 1-46)个月,中位 OS 为 14.1(范围 1.5-94)个月。治疗前降低的 NLR(<2.88)值预示着更高的 PFS 和 OS 率。这些值分别为 9.23±1.79 个月和 3.45±0.32 个月用于 PFS 和 21.17±4.53 个月和 5.32±0.53 个月用于 OS。治疗前降低的 PLR(<111.05)被发现对两种生存均有显著的预后价值。这些值分别为 7.37±1.43 个月和 3.16±0.47 个月用于 PFS 和 21.12±5.52 个月和 6.16±0.87 个月用于 OS。此外,低 PNI(<38.25)值预示着 PFS 和生存率较低。这些值分别为 7.47±0.59 个月和 3.25±0.21 个月用于 PFS 和 16.36±4.37 个月和 5.15±0.42 个月用于 OS。所有三个参数均被发现是 OS 和 PFS 的独立预后标志物,具有统计学意义(p<0.05)。
如今,HCC 的标准一线治疗已转向免疫疗法(IO)联合治疗,而在世界上大多数国家,IO 联合治疗并不可能。然而,也有一些患者仅使用索拉非尼就取得了很好的生存。重要的是要确定预测哪些患者将从哪种治疗中获益更好的生物标志物。有了我们研究中的标志物和可以通过这些标志物获得的评分系统,可以评估哪些患者将接受 IO 联合治疗,哪些患者将仅接受 TKI 治疗。我们认为,这样的评分系统可以用于识别合适的患者,特别是在那些由于财务原因,并非每个患者都能获得免疫治疗的国家。这些测试的优点是它们价格低廉、易于计算和标准化。
注册号和日期:2021/2088,2021 年 6 月 1 日,回顾性注册。