Feasibility of BU, CY and etoposide (BUCYE), and auto-SCT in patients with newly diagnosed primary CNS lymphoma: a single-center experience

被引:39
|
作者
Yoon, D. H. [1 ]
Lee, D. H. [1 ]
Choi, D. R. [1 ]
Sohn, B. S. [1 ]
Kim, S. [1 ]
Kim, S. W. [1 ]
Lee, J. S. [1 ]
Lee, S. W. [2 ]
Huh, J. [3 ]
Suh, C. [1 ]
机构
[1] Univ Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
[2] Univ Ulsan, Dept Radiat Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
[3] Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
关键词
primary CNS lymphoma; auto-SCT; BU; CY; etoposide; STEM-CELL TRANSPLANTATION; HIGH-DOSE CHEMOTHERAPY; CENTRAL-NERVOUS-SYSTEM; NON-HODGKINS-LYMPHOMA; RECURRENT PRIMARY CNS; LONG-TERM SURVIVAL; CONDITIONING REGIMEN; INTRAOCULAR LYMPHOMA; MALIGNANT-LYMPHOMA; 1ST-LINE TREATMENT;
D O I
10.1038/bmt.2010.71
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We investigated the feasibility of i.v. BU, CY and etoposide (BUCYE), followed by auto-SCT (ASCT) in patients with newly diagnosed primary central nervous system lymphoma (PCNSL). The planned treatment consisted of induction chemotherapy with five cycles of high-dose MTX and two cycles of high-dose cytarabine followed by conditioning with BUCYE (BU 3.2 mg/m(2), day -7 to day -5; CY 50 mg/kg, day -3 to day -2 and etoposide 200 mg/m(2), twice a day, days -5 and -4) and then ASCT. Between May 2005 and November 2008, 11 consecutive PCNSL patients were treated. All patients completed the treatment as planned, with no cases of treatment-related death or veno-occlusive disease. After BUCYE and ASCT, 10 patients achieved complete response (CR) or unconfirmed CR (CRu). Two patients, one partial response and one CRu, received further whole-brain radiotherapy, with all achieving CR. At a median follow-up of 25.0 months (8.8-50.7 months), six patients had relapsed, with a median event-free interval of 15.0 months (95% confidence interval, 4.5-25.6 months). Median survival time was not reached yet with a 2-year survival rate of 88.9%. The current treatment was feasible with a favorable tolerance profile. However, further regimen optimization is necessary because of high relapse rate. Bone Marrow Transplantation (2011) 46, 105-109; doi: 10.1038/bmt.2010.71; published online 12 April 2010
引用
收藏
页码:105 / 109
页数:5
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