Phase II study of central nervous system (CNS)-directed chemotherapy including high-dose chemotherapy with autologous stem cell transplantation for CNS relapse of aggressive lymphomas

被引:100
作者
Korfel, Agnieszka [1 ]
Elter, Thomas [2 ]
Thiel, Eckhard [1 ]
Haenel, Matthias [3 ]
Moehle, Robert [4 ]
Schroers, Roland [5 ]
Reiser, Marcel [2 ]
Dreyling, Martin [6 ]
Eucker, Jan [1 ]
Scholz, Christian [1 ]
Metzner, Bernd [7 ]
Roeth, Alexander [8 ]
Birkmann, Josef [9 ]
Schlegel, Uwe [10 ]
Martus, Peter [11 ,12 ]
Illerhaus, Gerard [13 ]
Fischer, Lars [1 ]
机构
[1] Charite Univ Med Berlin, Dept Hematol & Oncol, Berlin, Germany
[2] Univ Hosp, Dept Hematol & Oncol, Cologne, Germany
[3] Klinikum Chemnitz, Dept Hematol & Oncol, Chemnitz, Germany
[4] Univ Tubingen Hosp, Dept Hematol & Oncol, Tubingen, Germany
[5] Ruhr Univ Bochum, Dept Med Hematol & Oncol, Knappschaftskrankenkenhaus, Bochum, Germany
[6] Univ Hosp Grosshadern, Dept Hematol & Oncol, Munich, Germany
[7] Klinikum Oldenburg, Dept Hematol & Oncol, Oldenburg, Germany
[8] Univ Hosp, Dept Hematol & Oncol, Essen, Germany
[9] Klinikum Nurnberg, Dept Hematol & Oncol, Nurnberg, Germany
[10] Ruhr Univ Bochum, Dept Neurol, Knappschaftskrankenkenhaus, Bochum, Germany
[11] Charite, Inst Biostat & Clin Epidemiol, Berlin, Germany
[12] Univ Tubingen Hosp, Inst Clin Epidemiol & Appl Biostat, Tubingen, Germany
[13] Univ Hosp, Dept Hematol & Oncol, Freiburg, Germany
关键词
NON-HODGKIN-LYMPHOMA; RISK-FACTORS; RESPONSE CRITERIA; ELDERLY-PATIENTS; MARROW-TRANSPLANTATION; INTERNATIONAL WORKSHOP; PROGNOSTIC-FACTORS; METHOTREXATE; INVOLVEMENT; GRADE;
D O I
10.3324/haematol.2012.077917
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The prognosis of patients with central nervous system relapse of aggressive lymphoma is very poor with no therapy established so far. In a prospective multicenter phase II study, we evaluated a potentially curative chemotherapy-only regimen in these patients. Adult immunocompetent patients 65 years of age or under received induction chemotherapy with MTX/IFO/DEP (methotrexate 4 g/m(2) intravenously (i.v.) Day 1, ifosfamide 2 g/m(2) i.v. Days 3-5 and liposomal cytarabine 50 mg intrathecally (i.th) Day 6) and AraC/TT/DEP (cytarabine 3g/m(2) i.v. Days 1-2, thiotepa 40 mg/m(2) i.v. Day 2 and i.th.. liposomal cytarabine 50 mg i.th. Day 3) followed by high-dose chemotherapy with carmustine 400 mg/m(2) i.v. Day -5, thiotepa 2x5 mg/kg i.v. Days -4 to -3 and etoposide 150 mg/m(2) i.v. Days -5 to -3, and autologous stem cell transplantation Day 0 (HD-ASCT). Thirty eligible patients (median age 58 years) were enrolled. After HD-ASCT (n=24), there was a complete remission in 15 (63%), partial remission in 2 (8%) and progressive disease in 7 (29%) patients. Myelotmdcity was the most adverse event with CTC grade 3/4 infections in 12% of MTX/IFO/DEP courses, 21% of AraC/TT/DEP courses and 46% of HD-ASCT courses. The 2-year time to treatment failure was 49 +/- 19% for all patients and 58 +/- 22% for patients completing HD-ASCT. The protocol assessed proved feasible and highly active with long-lasting remissions in a large proportion of patients. (ClinicalTrials.gov Identifier NCT01148173)
引用
收藏
页码:364 / 370
页数:7
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