用利妥昔单抗、甲氨蝶呤、依托膦酸和长春新碱(R-MIV) 进行诱导免疫化疗是治疗原发性中枢神经系统淋巴瘤的一种安全有效方法,包括最近COVID-19疫情的经验。
Safety and efficacy of induction immunochemotherapy with rituximab, methotrexate, ifosfamide, and vincristine (R-MIV) in patients with primary CNS lymphoma including recent COVID-19 pandemic experience.
发表日期:2023 Feb 10
作者:
Beata Ostrowska, Katarzyna Domanska-Czyz, Joanna Romejko-Jarosinska, Michal Osowiecki, Lukasz Targonski, Lidia Poplawska, Robert Konecki, Martyna Kotarska, Marcin Szymanski, Anna Borawska, Monika Swierkowska, Anna Dabrowska-Iwanicka, Agnieszka Druzd-Sitek, Ewa Paszkiewicz-Kozik, Ewa Mroz-Zycinska, Joanna Tajer, Elzbieta Wojciechowska-Lampka, Wlodzimierz Osiadacz, Grzegorz Rymkiewicz, Grazyna Lapinska, Marta Wojewodzka-Mirocha, Wojciech Michalski, Jan Walewski
来源:
BRITISH JOURNAL OF HAEMATOLOGY
摘要:
原句:Clinical data on primary central nervous system (CNS) lymphoma (PCNSL) patients is mostly generated from prospective studies, and many frail real-world patients are not included. Recently, the diagnosis and treatment of PCNSL patients was confounded by the COVID-19 pandemic. In particular, treatment with high-dose cytarabine was linked to increased risk of pneumonia and virus persistence. We report on outcome of the induction regimen R-MIV (rituximab, methotrexate, ifosfamide, and vincristine) involving intensive administration of high-dose methotrexate (3.5 g/m2 ) with ifosfamide, every 2 weeks and rituximab once per week for six doses. The median age and performance status (PS) for 64 patients was 58 years and 2 (PS 3; 22%) respectively. The overall response rate by magnetic resonance imaging/computed tomography (MRI/CT) was 73% (n = 46/63), with an additional 17.5% (n = 11/63) patients without measurable disease at baseline. Grade 3-4 haematological toxicity was low for R-MIV (neutropenia: 25% and thrombocytopenia: 1%). Three patients (4.7%) died from treatment-related toxicity. Co-existence of SARS-CoV-2 infection with cytomegalovirus reactivation and the varicella-zoster virus in two patients was fatal. Fifty patients (78%) were eligible for consolidation. Median progression-free and overall survival were not reached (median follow-up: 44 months). In conclusion, the R-MIV regimen is feasible in routine practice, effective and safe, even during the COVID-19 pandemic.© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
原译:临床数据大多数来自前瞻性研究,而许多脆弱的现实患者并未被纳入。最近,COVID-19大流行对PCNSL患者的诊断和治疗造成了混乱。特别是,高剂量的阿糖胞苷治疗被认为增加了肺炎和病毒持续性的风险。我们报告了使用高剂量甲氨蝶呤(3.5 g/m2),伊福司胺和长春新碱每2周一次,以及利妥昔单抗每周一次6次的诱导方案R-MIV的疗效。64名患者的中位年龄和表现状态(PS) 分别为58岁和2(PS3;22%)。利用磁共振成像/计算机断层扫描(MRI/CT)的总体反应率为73%(n=46/63),还有17.5%的患者(n=11/63)在基线时没有可测量的疾病。R-MIV的3-4级血液毒性很低(中性粒细胞减少症:25%和血小板减少症:1%)。三名患者(4.7%)因治疗相关毒性死亡。两名患者同时感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)、巨细胞病毒复活和水痘带状疱疹病毒会导致死亡。50名患者(78%)符合巩固治疗条件。中位进展生存期和总生存期均未达到(中位随访期:44个月)。总之,R-MIV方案在常规实践中使用可行、有效且安全,即使在COVID-19大流行期间也是如此。© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
Clinical data on primary central nervous system (CNS) lymphoma (PCNSL) patients is mostly generated from prospective studies, and many frail real-world patients are not included. Recently,the diagnosis and treatment of PCNSL patients was confounded by the COVID-19 pandemic. In particular, treatment with high-dose cytarabine was linked to increased risk of pneumonia and virus persistence. We report on outcome of the induction regimen R-MIV (rituximab, methotrexate, ifosfamide, and vincristine) involving intensive administration of high-dose methotrexate (3.5 g/m2 ) with ifosfamide, every 2 weeks and rituximab once per week for six doses. The median age and performance status (PS) for 64 patients was 58 years and 2 (PS 3; 22%) respectively. The overall response rate by magnetic resonance imaging/computed tomography (MRI/CT) was 73% (n = 46/63), with an additional 17.5% (n = 11/63) patients without measurable disease at baseline. Grade 3-4 haematological toxicity was low for R-MIV (neutropenia: 25% and thrombocytopenia: 1%). Three patients (4.7%) died from treatment-related toxicity. Co-existence of SARS-CoV-2 infection with cytomegalovirus reactivation and the varicella-zoster virus in two patients was fatal. Fifty patients (78%) were eligible for consolidation. Median progression-free and overall survival were not reached (median follow-up: 44 months). In conclusion, the R-MIV regimen is feasible in routine practice, effective and safe, even during the COVID-19 pandemic.© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.