Faculty of Medicine, Department of Medical Oncology, Gazi University, Ankara, Turkey.
Faculty of Medicine, Department of Pathology, Gazi University, Ankara, Turkey.
BMC Cancer. 2024 Aug 5;24(1):954. doi: 10.1186/s12885-024-12727-3.
Growth differentiation factor-15 (GDF-15), a member of the TGF-β superfamily, is overexpressed in various cancers and facilitates immune evasion by inhibiting T-cell activation. GDFATHER-TRIAL's phase 2a results demonstrated promising outcomes when combining the GDF-15 neutralizing antibody visugromab (CTL002) with nivolumab, enhancing the response to immunotherapy. This study evaluated the prognostic significance of GDF-15 expression in non-small cell lung cancer (NSCLC) tumor tissues in terms of immunotherapy response.
This retrospective study included 50 patients with metastatic NSCLC treated with nivolumab at Gazi University Hospital between January 2021 and July 2023. GDF-15 expression was evaluated using immunochemistry staining and categorized based on the intensity of cytoplasmic or membranous staining. Samples were divided into a low expression group (scores 0 and 1) and a high expression group (scores 2 and 3). The primary outcomes were progression-free survival (PFS) and overall survival (OS), which were analyzed using Kaplan‒Meier and Cox proportional hazards models. Objective response rates were assessed in secondary outcomes.
Of the 50 patients, 43 were men (86%), with a median age of 63.9 years. Half of the patients exhibited low GDF-15 expression. High GDF-15 expression correlated with shorter PFS and OS. The median PFS was 7.8 months for the low-expression group versus 4.4 months for the high-expression group (HR, 0.41; 95% CI, 0.20-0.83; p = 0.013). The median OS was 18.1 months for the low-expression group compared to 11.8 months for the high-expression group (HR, 0.36; 95% CI, 0.16-0.78; p = 0.007). The objective response rate was significantly greater in the low GDF-15 group (52%) than in the high GDF-15 group (24%) (p = 0.040).
Elevated GDF-15 expression in NSCLC tumor tissues is associated with poorer response to nivolumab, suggesting that GDF-15 is a potential prognostic biomarker for immunotherapy efficacy. These findings warrant further validation through prospective studies to optimize treatment strategies for NSCLC patients.
生长分化因子 15(GDF-15)是 TGF-β 超家族的成员,在各种癌症中过度表达,通过抑制 T 细胞激活来促进免疫逃逸。GDFATHER-TRIAL 的 2a 期结果表明,当将 GDF-15 中和抗体 visugromab(CTL002)与 nivolumab 联合使用时,对免疫疗法的反应有很好的效果,增强了对免疫疗法的反应。本研究评估了 GDF-15 在非小细胞肺癌(NSCLC)肿瘤组织中的表达在免疫治疗反应方面的预后意义。
本回顾性研究纳入了 2021 年 1 月至 2023 年 7 月期间在加济大学医院接受 nivolumab 治疗的 50 例转移性 NSCLC 患者。使用免疫化学染色评估 GDF-15 的表达,并根据细胞质或膜染色强度进行分类。样本分为低表达组(评分 0 和 1)和高表达组(评分 2 和 3)。主要结局是无进展生存期(PFS)和总生存期(OS),使用 Kaplan-Meier 和 Cox 比例风险模型进行分析。次要结局评估客观缓解率。
50 例患者中,43 例为男性(86%),中位年龄为 63.9 岁。一半的患者表现出低水平的 GDF-15 表达。高水平的 GDF-15 表达与较短的 PFS 和 OS 相关。低表达组的中位 PFS 为 7.8 个月,高表达组为 4.4 个月(HR,0.41;95%CI,0.20-0.83;p=0.013)。低表达组的中位 OS 为 18.1 个月,高表达组为 11.8 个月(HR,0.36;95%CI,0.16-0.78;p=0.007)。低 GDF-15 组的客观缓解率(52%)显著高于高 GDF-15 组(24%)(p=0.040)。
NSCLC 肿瘤组织中 GDF-15 表达升高与 nivolumab 反应较差相关,表明 GDF-15 是免疫治疗疗效的潜在预后生物标志物。这些发现需要通过前瞻性研究进一步验证,以优化 NSCLC 患者的治疗策略。