Treatment of primary mediastinal large B cell lymphoma with an alternating chemotherapy regimen based on high-dose methotrexate

被引:13
作者
Fietz, T. [1 ]
Knauf, W. U. [1 ]
Hanel, M. [2 ]
Franke, A. [3 ]
Freund, M. [4 ]
Thiel, E. [1 ]
机构
[1] Charite Campus Benjamin Franklin, Dept Med Hematol Oncol & Transfus Med 3, D-12200 Berlin, Germany
[2] Klinikum Chemnitz, Chemnitz, Germany
[3] Univ Magdeburg, D-39106 Magdeburg, Germany
[4] Univ Rostock, Rostock, Germany
关键词
Primary mediastinal large B cell lymphoma; High-dose methotrexate; Long-term results; Prospective multicenter study; NON-HODGKINS-LYMPHOMA; MACOP-B; SINGLE-INSTITUTION; ELDERLY-PATIENTS; YOUNG-PATIENTS; RISK-FACTORS; SCLEROSIS; RITUXIMAB; THERAPY; CHOP;
D O I
10.1007/s00277-008-0625-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary mediastinal large B cell lymphomas (MLCL) differ from other diffuse large cell lymphomas, leading to a description as a separate entity in the current World Health Organization classification. Dose intensification improves long-term results, but no standard therapy has been established so far. We investigated the use of a high-dose methotrexate-based alternating chemotherapy regimen (B-ALL protocol of the German ALL study group) followed by consolidative mediastinal radiotherapy first as a single-center trial, then later as a prospective multicenter trial in 44 patients with a median age of 33 years. Response rates exceeded 90% with an overall survival rate of 80% in the single-center group (8.6 years median follow-up) and 82% in the multicenter group (2.5 years follow-up).Short-term toxicity was manageable, but required hospitalization: the rates of grade 3 or 4 toxicity were 20% (for mucositis), 42% (for neutropenia), 29% (for thrombocytopenia), and 9% (for neutropenic fever). No relapse occurred more than 2 years after diagnosis and initiation of treatment, but unfortunately, no patient with overt progression or relapse within these 2 years could be salvaged. Future directions in the treatment of MLCL will not focus on further dose intensification, but rather on the incorporation of (radio)immunotherapy as a therapeutic tool and gene expression profiling as well as positron emission tomography-computed tomography as stratifying tools.
引用
收藏
页码:433 / 439
页数:7
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