Wen Pengfei, Li Fan, Xie Yao, Chen Wei, Wang Tingting, Zhuo Xiaoxue, Wang Lin
Department of Dermatology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Cancer Med. 2025 Sep;14(17):e71151. doi: 10.1002/cam4.71151.
Classical mycosis fungoides (CMF), the most common form of primary cutaneous T-cell lymphoma, shows marked heterogeneity in disease progression and prognosis, while reliable molecular prognostic markers remain scarce. This study aimed to evaluate the prognostic significance of GATA-binding protein 3 (GATA3) expression in early-stage CMF.
We retrospectively analyzed 106 patients with early-stage CMF diagnosed at West China Hospital, Sichuan University, between 2009 and 2021. Immunohistochemistry (IHC) was performed to assess GATA3 expression in dermal tumor cells. Associations with progression-free survival (PFS) and overall survival (OS) were examined using Cox regression models adjusted by inverse probability of treatment weighting (IPTW). Receiver operating characteristic (ROC) curve analysis was conducted to evaluate predictive performance.
High GATA3 expression (≥ 60%) was detected in 92.5% of cases. Elevated GATA3 levels were significantly associated with reduced PFS and OS. IPTW-adjusted Cox regression confirmed high GATA3 expression as an independent adverse prognostic factor. ROC curve analysis demonstrated strong predictive performance for CMF progression (AUC = 0.867), with an optimal cutoff of 57.5% (sensitivity 73.7%, specificity 94.3%). For clinical applicability, a 60% threshold was adopted.
High GATA3 expression is an independent adverse prognostic biomarker in early-stage CMF. Incorporating GATA3 into risk stratification models may improve prognostic accuracy and guide personalized treatment strategies.
经典蕈样肉芽肿(CMF)是原发性皮肤T细胞淋巴瘤最常见的形式,其疾病进展和预后存在显著异质性,而可靠的分子预后标志物仍然匮乏。本研究旨在评估GATA结合蛋白3(GATA3)表达在早期CMF中的预后意义。
我们回顾性分析了2009年至2021年间在四川大学华西医院确诊的106例早期CMF患者。采用免疫组织化学(IHC)方法评估真皮肿瘤细胞中GATA3的表达。使用经治疗权重逆概率(IPTW)调整的Cox回归模型检验其与无进展生存期(PFS)和总生存期(OS)的相关性。进行受试者工作特征(ROC)曲线分析以评估预测性能。
92.5%的病例检测到高GATA3表达(≥60%)。GATA3水平升高与PFS和OS降低显著相关。IPTW调整后的Cox回归证实高GATA3表达是一个独立的不良预后因素。ROC曲线分析显示对CMF进展具有较强的预测性能(AUC = 0.867),最佳截断值为57.5%(敏感性73.7%,特异性94.3%)。为了临床应用,采用了60%的阈值。
高GATA3表达是早期CMF的一个独立不良预后生物标志物。将GATA3纳入风险分层模型可能会提高预后准确性并指导个性化治疗策略。