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高剂量环磷酰胺和利妥昔单抗而不进行干细胞移植:用于低级别 B 细胞、转化型和套细胞淋巴瘤的可行性研究。

High-dose cyclophosphamide and rituximab without stem cell transplant: a feasibility study for low grade B-cell, transformed and mantle cell lymphomas.

机构信息

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21287, USA.

出版信息

Leuk Lymphoma. 2011 Nov;52(11):2076-81. doi: 10.3109/10428194.2011.594191. Epub 2011 Jul 14.

DOI:10.3109/10428194.2011.594191
PMID:21756035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3390263/
Abstract

Relapse after autologous stem cell transplant for low grade B-cell lymphoma is common secondary to ineffective conditioning and/or tumor autograft contamination. We investigated high-dose cyclophosphamide and rituximab without stem cell rescue as first-line or salvage therapy in lymphomas. After establishing safety, accrual was increased to evaluate event-free survival (EFS). Eighty-one adults received rituximab (375 mg/m(2) days 1, 4, 8, 11, 45, 52), cyclophosphamide (50 mg/kg days 15-18), and pegfilgrastim (day 20). Forty-two patients had low grade B-cell lymphoma [grade I/II follicular (69%), transformed lymphoma (17%), other (15%)]: 45% were treated without measurable disease. Thirty-nine patients had mantle cell lymphoma: 82% were treated without measurable disease. All achieved hematopoietic recovery; 46% required brief hospitalizations. The 5-year EFS and overall survival (OS) for patients with low grade B-cell and transformed lymphoma were 40% and 72%, respectively. The 5-year EFS and OS for patients with MCL were 39% and 62%, respectively. This low-toxicity therapeutic approach obviates the need for stem cell products and establishes a platform for future therapies.

摘要

自体干细胞移植治疗低级 B 细胞淋巴瘤后复发很常见,这主要是由于预处理无效和/或肿瘤自体移植物污染。我们研究了高剂量环磷酰胺和利妥昔单抗,无需干细胞挽救,作为淋巴瘤的一线或挽救治疗。在确定安全性后,增加入组人数以评估无事件生存(EFS)。81 名成年人接受利妥昔单抗(375mg/m2,第 1、4、8、11、45、52 天)、环磷酰胺(50mg/kg,第 15-18 天)和培非格司亭(第 20 天)。42 例患者患有低级 B 细胞淋巴瘤[I/II 级滤泡性(69%)、转化性淋巴瘤(17%)、其他(15%)]:45%的患者未经测量疾病治疗。39 例患有套细胞淋巴瘤:82%的患者未经测量疾病治疗。所有患者均实现造血恢复;46%的患者需要短暂住院。低级 B 细胞和转化性淋巴瘤患者的 5 年 EFS 和总生存率(OS)分别为 40%和 72%。MCL 患者的 5 年 EFS 和 OS 分别为 39%和 62%。这种低毒性治疗方法避免了对干细胞产品的需求,并为未来的治疗方法建立了平台。

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