Guerra Geno, Nakase Taishi, Kachuri Linda, McCoy Lucie, Hansen Helen M, Rice Terri, Wiemels Joseph L, Wiencke John K, Molinaro Annette M, Wrensch Margaret, Francis Stephen S
Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, United States.
Department of Epidemiology & Population Health, Stanford University School of Medicine, Stanford, CA, United States.
J Natl Cancer Inst. 2025 Mar 1;117(3):545-553. doi: 10.1093/jnci/djae265.
Previous epidemiological studies have reported an association of serum immunoglobulin E (IgE) levels with reduced glioma risk, but the association between IgE and glioma prognosis has not been characterized. This study aimed to examine how sex, tumor subtype, and IgE class modulate the association of serum IgE levels with glioma risk and survival.
We conducted a case-control study using participants from the University of California San Francisco Adult Glioma Study (1997-2010). Serum IgE levels for total, respiratory, and food allergy were measured in adults diagnosed with glioma (n = 1319) and cancer-free control individuals (n = 1139) matched based on age, sex, and race and ethnicity. Logistic regression was adjusted for patient demographics to assess the association between IgE levels and glioma risk. Multivariable Cox regression adjusted for patient-specific and tumor-specific factors compared survival between the elevated and normal IgE groups. All statistical tests were 2-sided.
Elevated total IgE was associated with reduced risk of IDH wild-type glioma (risk ratio [RR] = 0.78, 95% CI = 0.71 to 0.86) and IDH-mutant glioma (RR = 0.73, 95% CI = 0.63 to 0.85). In multivariable Cox regression, positive respiratory IgE was associated with improved survival for IDH wild-type glioma (RR = 0.79, 95% CI = 0.67 to 0.93). The reduction in mortality risk was statistically significant in female individuals only (RR = 0.75, 95% CI = 0.57 to 0.98), with an improvement in median survival of 6.9 months (P < .001).
Elevated serum IgE was associated with improved prognosis for IDH wild-type glioma, with a more pronounced protective effect in female than male individuals, which has implications for the future study of IgE-based immunotherapies for glioma.
既往流行病学研究报告血清免疫球蛋白E(IgE)水平与胶质瘤风险降低有关,但IgE与胶质瘤预后之间的关联尚未明确。本研究旨在探讨性别、肿瘤亚型和IgE类别如何调节血清IgE水平与胶质瘤风险及生存之间的关联。
我们利用来自加利福尼亚大学旧金山分校成人胶质瘤研究(1997 - 2010年)的参与者进行了一项病例对照研究。对诊断为胶质瘤的成人(n = 1319)和无癌对照个体(n = 1139)测量了总IgE、呼吸道IgE和食物过敏IgE水平,这些对照个体根据年龄、性别、种族和民族进行匹配。采用逻辑回归并对患者人口统计学特征进行校正,以评估IgE水平与胶质瘤风险之间的关联。多变量Cox回归对患者特异性和肿瘤特异性因素进行校正,比较IgE水平升高组和正常组之间的生存情况。所有统计检验均为双侧检验。
总IgE升高与异柠檬酸脱氢酶(IDH)野生型胶质瘤风险降低相关(风险比[RR] = 0.78,95%置信区间[CI] = 0.71至0.86)以及IDH突变型胶质瘤风险降低相关(RR = 0.73,95% CI = 0.63至0.85)。在多变量Cox回归中,呼吸道IgE阳性与IDH野生型胶质瘤患者生存改善相关(RR = 0.79,95% CI = 0.67至0.93)。仅在女性个体中,死亡风险降低具有统计学意义(RR = 0.75,95% CI = 0.57至0.98),中位生存期改善6.9个月(P <.001)。
血清IgE升高与IDH野生型胶质瘤预后改善相关,在女性个体中的保护作用比男性更明显,这对未来基于IgE的胶质瘤免疫治疗研究具有启示意义。