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单纯原发性玻璃体视网膜淋巴瘤中全身无化疗疗法联合玻璃体内甲氨蝶呤的复发情况及预后:基于两项前瞻性队列研究的分析

Relapses and outcomes of systemic chemo-free therapies combined with intravitreous methotrexate in isolated primary vitreoretinal lymphoma: an analysis based on two prospective cohort studies.

作者信息

Chen Hongyun, Zhuang Zhe, Zhang Xiao, Zhou Daobin, Zhang Meifen, Zhang Wei

机构信息

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.

Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.

出版信息

Ann Hematol. 2025 May 26. doi: 10.1007/s00277-025-06414-x.

Abstract

The definitive therapeutic paradigm for primary vitreoretinal lymphoma (PVRL) remains controversial, with ongoing debates surrounding the comparative efficacy of localized ocular therapy, high-dose systemic chemotherapy, and combined-modality approaches. The benefit of systemic administration of methotrexate is unambiguous and severe adverse events related to intense chemotherapy are reported. Immunomodulators such as lenalidomide and Bruton's tyrosine kinase (BTK) inhibitors, like zanubrutinib, have not been explored for their safety and efficacy as first-line treatments for PVRL. This study aimed to analyze the safety and efficacy of chemo-free combination regimens in newly diagnosed PVRL patients. In our study, systemic chemo-free regimens were administrated as induction therapy, including the ZR regimen (zanubrutinib and rituximab), and the R2 regimen (lenalidomide and rituximab). Of the 44 patients, 41 (93.2%) achieved complete remission following induction therapy. No severe systemic adverse events were observed. After a median follow-up of 25.1 months, 17 patients (38.6%) suffered relapses, including one intraocular relapse and 17 brain relapses. By the final follow-up, 5 patients (11.4%) had died from disease progression. The median PFS and OS were 22.1 and 71.5 months, respectively. The ZR regimen demonstrated a longer PFS compared to the R2 regimen (10.9 months vs. not reached; log-rank test, P = 0.00044), positioning it as a promising treatment option for PVRL patients.

摘要

原发性玻璃体视网膜淋巴瘤(PVRL)的确定性治疗模式仍存在争议,围绕局部眼部治疗、大剂量全身化疗和联合治疗方法的比较疗效展开了持续辩论。甲氨蝶呤全身给药的益处是明确的,并且有与强化化疗相关的严重不良事件的报道。来那度胺等免疫调节剂和布鲁顿酪氨酸激酶(BTK)抑制剂(如泽布替尼)作为PVRL一线治疗的安全性和有效性尚未得到探索。本研究旨在分析新诊断的PVRL患者中无化疗联合方案的安全性和有效性。在我们的研究中,无全身化疗方案作为诱导治疗,包括ZR方案(泽布替尼和利妥昔单抗)和R2方案(来那度胺和利妥昔单抗)。44例患者中,41例(93.2%)在诱导治疗后实现完全缓解。未观察到严重的全身不良事件。中位随访25.1个月后,17例患者(38.6%)复发,包括1例眼内复发和17例脑复发。到最后随访时,5例患者(11.4%)死于疾病进展。中位无进展生存期(PFS)和总生存期(OS)分别为22.1个月和71.5个月。与R2方案相比,ZR方案显示出更长的PFS(10.9个月对未达到;对数秩检验,P = 0.00044),使其成为PVRL患者有前景的治疗选择。

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