一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:KDM5D expression in lung carcinoma and its association with clinicopathologic parameters and survival.
KDM5D expression in lung carcinoma and its association with clinicopathologic parameters and survival.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
KDM5D 表达在单因素 Cox 回归中显示与死亡率存在未调整的关联。然而,在调整临床病理变量或校正多重比较后,该关联不显著。鉴于文献中相互矛盾的发现,有必要进一步开展研究、进行方法学标准化,并深入探索 KDM5D 及 KDM5 家族。
在全球范围内,肺癌是男性中最常见的恶性肿瘤,其发病率和死亡率均高于女性。性染色体分析可能为这些差异提供见解。位于Y染色体上的KDM5D被认为是一种肿瘤抑制因子。正在进行的研究探索KDM5D在恶性肿瘤中的作用及治疗途径。我们评估了免疫组化表达与临床病理参数及生存之间的关联。
共分析了102例男性肺癌患者,这些患者在2014年6月1日至2023年10月31日期间在一家三级医疗中心接受了trucut或切除术。评估的参数包括年龄、肿瘤类型、TNM分期、TIL(肿瘤浸润淋巴细胞)和KDM5D表达。还对切除术评估了其他参数。将JAD1D(KDM5D)抗体应用于未染色玻片,使用Q评分法量化表达水平,并通过ROC曲线确定截断值。
死亡风险的截断值计算为8,但未发现对复发或进展有显著意义的值。高表达(>8)的患者总生存期显著较低。较高水平与最大肿瘤直径增大、pN1、M1及以上受累、IVA-IVB期疾病以及轻至中度TIL(肿瘤浸润淋巴细胞)相关。这些特征及KDM5D升高在死亡组中显著更高。
Globally, lung cancer is the most common malignancy among males, with higher incidence and mortality rates than in females. Sex chromosome analyses may provide insights into these disparities. KDM5D, located on the Y chromosome, is recognized as a tumor suppressor. Ongoing studies explore KDM5D's role in malignancies and therapeutic pathways. We evaluated the association of immunohistochemical expression with clinicopathologic parameters and survival.
A total of 102 male lung carcinoma patients who underwent trucut or resection procedures between June 1, 2014, and October 31, 2023, at a tertiary care center were analyzed. Evaluated parameters included age, tumor type, TNM stage, tumor-infiltrating lymphocytes, and KDM5D expression. Additional parameters were also assessed for resections. The JAD1D (KDM5D) antibody was applied to unstained slides, expression levels were quantified using the Q score method, and a cut-off was determined by the ROC curve.
A cut-off value of 8 was calculated for mortality, but no significant value was found for recurrence or progression. Patients with high expression (>8) had significantly lower overall survival. Higher levels were associated with increased maximum tumor diameter, involvement of pN1, M1 and above, stage IVA-IVB disease, and mild to moderate tumor-infiltrating lymphocytes. These features and elevated KDM5D were significantly higher in the exitus group.
KDM5D expression showed an unadjusted association with mortality in univariate Cox regression. However, this association was not significant after adjusting for clinicopathological variables or correcting for multiple comparisons. Given conflicting findings in the literature, further studies, methodological standardization, and deeper exploration of KDM5D and the KDM5 family are warranted.
MEMBER ACCOUNT
登录成功会直接打开下一页。