Tan Ya Hwee, Lim Ryan Mao Heng, Tan Jing Yuan, Lim Boon Yee, Binte Nur Ayuni, Taib Muhammad, Ong Choon Kiat, Cheng Chee Leong, Yeoh Kheng Wei, Lim Soon Thye, Chan Jason Yongsheng
Division of Medical Oncology, National Cancer Centre Singapore, 30 Hospital Boulevard, 168583, Singapore, Singapore.
SingHealth Duke-NUS Blood Cancer Centre, Singapore, Singapore.
Ann Hematol. 2025 Aug 25. doi: 10.1007/s00277-025-06561-1.
Given that most PCNSL cases are diagnosed at a late age, they may be unsuitable for consolidation therapy with autologous stem cell transplantation (HDC-ASCT). We thus examine the outcomes of PCNSL in a multiethnic Asian population treated with HD-MTX-based chemotherapy and consolidation WBRT, so as to benchmark current treatment outcomes.
We conducted a retrospective study involving patients (n = 129) diagnosed with PCNSL at the National Cancer Centre Singapore from 2000 to 2019. The median follow-up duration was 47.0 months. Survival analyses were performed using the Kaplan-Meier method and Cox proportional models.
The cohort consisted of 76 male and 53 female patients with a median age of 60 years. 85 patients received HD-MTX-based induction therapy as per DeAngelis, while 44 were treated with the Shah protocol. In univariate analyses, male sex, ECOG scores ≥ 1, non-germinal center subtype, use of DeAngelis protocol, and methotrexate dose < 3 g/m were significantly correlated with worse PFS and OS. In a multivariate model, the Shah protocol conferred significantly improved outcomes as compared with the DeAngelis protocol for PFS (HR 0.43, 95% CI 0.25-0.73, p = 0.0019) and OS (HR 0.31, 95% CI 0.16-0.59, p = 0.0004). Using gene expression profiling, poor risk PCNSL patients had a higher trend of CD8 T-cells, macrophages and Th-1 cells, upregulation of TIGIT and HAVCR2, and downregulation in WNT11 and CD44.
Our study demonstrates that contemporary HD-MTX-based chemoimmunotherapy induction regimens achieve good disease responses in PCNSL. We also highlight significant prognostic factors and a potential role for immunotherapy in PCNSL.
鉴于大多数原发性中枢神经系统淋巴瘤(PCNSL)病例在较晚年龄被诊断出来,它们可能不适合采用自体干细胞移植(大剂量化疗联合自体干细胞移植,HDC-ASCT)进行巩固治疗。因此,我们研究了在一个多民族亚洲人群中,接受基于大剂量甲氨蝶呤(HD-MTX)化疗和巩固性全脑放疗(WBRT)的PCNSL患者的治疗结果,以便为当前的治疗结果提供基准。
我们进行了一项回顾性研究,纳入了2000年至2019年在新加坡国立癌症中心被诊断为PCNSL的患者(n = 129)。中位随访时间为47.0个月。使用Kaplan-Meier方法和Cox比例模型进行生存分析。
该队列包括76名男性和53名女性患者,中位年龄为60岁。85名患者按照DeAngelis方案接受了基于HD-MTX的诱导治疗,而44名患者接受了Shah方案治疗。在单因素分析中,男性、东部肿瘤协作组(ECOG)评分≥1、非生发中心亚型、使用DeAngelis方案以及甲氨蝶呤剂量<3 g/m与较差的无进展生存期(PFS)和总生存期(OS)显著相关。在多变量模型中,与DeAngelis方案相比,Shah方案在PFS(风险比[HR] 0.43,95%置信区间[CI] 0.25 - 0.73,p = 0.0019)和OS(HR 0.31,95% CI 0.16 - 0.59,p = 0.0004)方面的治疗结果有显著改善。使用基因表达谱分析,高危PCNSL患者的CD8 T细胞、巨噬细胞和Th-1细胞有更高的趋势,TIGIT和HAVCR2上调,WNT11和CD44下调。
我们的研究表明,当代基于HD-MTX的化疗免疫治疗诱导方案在PCNSL中能取得良好的疾病反应。我们还强调了PCNSL中的重要预后因素以及免疫治疗的潜在作用。