Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Department of Gastroenterology, Gifu Prefectural Tajimi Hospital, Gifu, Japan.
J Gastroenterol Hepatol. 2024 Oct;39(10):2158-2168. doi: 10.1111/jgh.16672. Epub 2024 Jun 28.
Serum interleukin-6 (IL-6) before the administration of atezolizumab plus bevacizumab (Atez + Bev) is a prognostic biomarker in patients with hepatocellular carcinoma (HCC) treated with Atez + Bev. We previously revealed that the neutrophil-to-lymphocyte ratio and serum chemokine levels during treatment with Atez + Bev were more useful as prognostic biomarkers. Therefore, we examined the predictive ability of serum IL-6 for the efficacy of Atez + Bev in patients with HCC.
We enrolled 94 patients with HCC who received treatment with Atez + Bev. Initial responses were assessed through dynamic computed tomography or magnetic resonance imaging. The levels of IL-6 in serum were measured before and at the initiation of the second course of Atez + Bev. Subsequently, the relationship of IL-6 levels with treatment efficacy was evaluated.
IL-6 levels at the initiation of the second course tended to be higher in patients with progressive disease versus those with non-progressive disease in the initial evaluation (P = 0.054). Moreover, the cutoff value (7.4 pg/mL) was useful in stratifying patients by overall survival (i.e. low vs high: not reached vs 21.4 months, respectively, P = 0.001) and progression-free survival (low vs high: 11.9 vs 5.2 months, respectively, P = 0.004). This result was reproduced in patients with HCC who received Atez + Bev as first-line therapy. In the multivariate analyses, IL-6 levels at the initiation of the second course were independent predictive factors for progression-free and overall survival.
Serum levels of IL-6 at the initiation of the second course of treatment may predict Atez + Bev efficacy and prognosis in HCC.
在接受阿替利珠单抗联合贝伐珠单抗(Atez+Bev)治疗的肝细胞癌(HCC)患者中,治疗前的血清白细胞介素-6(IL-6)是一种预后生物标志物。我们之前发现,在接受 Atez+Bev 治疗期间,中性粒细胞与淋巴细胞比值和血清趋化因子水平作为预后生物标志物更为有用。因此,我们研究了血清 IL-6 对 HCC 患者 Atez+Bev 疗效的预测能力。
我们纳入了 94 例接受 Atez+Bev 治疗的 HCC 患者。通过动态计算机断层扫描或磁共振成像评估初始反应。在开始第二疗程的 Atez+Bev 之前和同时测量血清 IL-6 水平。随后,评估了 IL-6 水平与治疗效果的关系。
在初始评估中,疾病进展患者的第二疗程开始时的 IL-6 水平趋于高于非进展患者(P=0.054)。此外,该截断值(7.4 pg/mL)在总生存期(即低 vs 高:未达到 vs 21.4 个月,分别,P=0.001)和无进展生存期(低 vs 高:11.9 vs 5.2 个月,分别,P=0.004)方面也可用于分层患者。该结果在接受 Atez+Bev 作为一线治疗的 HCC 患者中得到了重现。在多变量分析中,第二疗程开始时的 IL-6 水平是无进展生存期和总生存期的独立预测因素。
治疗第二疗程开始时的血清 IL-6 水平可能预测 HCC 患者 Atez+Bev 的疗效和预后。