Intensive methotrexate and cytarabine followed by high-dose chemotherapy with autologous stem-cell rescue in patients with newly diagnosed primary CNS lymphoma: An intent-to-treat analysis

被引:210
作者
Abrey, LE
Moskowitz, CH
Mason, WP
Crump, M
Stewart, D
Forsyth, P
Paleologos, N
Correa, DD
Anderson, ND
Caron, D
Zelenetz, A
Nimer, SD
DeAngelis, LM
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Neurol, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Off Clin Res, New York, NY 10021 USA
[4] Univ Toronto, Princess Margaret Hosp, Toronto, ON, Canada
[5] Univ Calgary, Tom Baker Canc Ctr, Calgary, AB, Canada
[6] Northwestern Univ, Evanston Hosp, Dept Neurol, Chicago, IL 60611 USA
关键词
D O I
10.1200/JCO.2003.05.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the safety and efficacy of intensive methotrexate-based chemotherapy followed by high-dose chemotherapy (HDT) with autologous stem-cell rescue in patients with newly diagnosed primary CNS lymphoma (PCNSL). Patients and Methods: Twenty-eight patients received induction chemotherapy using high-dose systemic methotrexate (3.5 g/m(2)) and cytarabine (3 g/m(2) daily for 2 days). Fourteen patients with chemosensitive disease evident on neuroimaging then received high-dose therapy using carmustine, etoposide, cytarabine, and melphalan with autologous stem-cell rescue. Results: The objective response rate to the induction-phase chemotherapy was 57%, and median overall survival is not yet assessable, with a median follow-up time of 28 months. The overall median event-free survival time is 5.6 months for all patients and 9.3 months for 14 patients who underwent transplantation. Six of these 14 patients (43%) remained disease-free at last follow-up. Treatment was well tolerated; there was one transplantation-related death. Prospective neuropsychologic evaluations have revealed no evidence of treatment-related neurotoxicity. Conclusion: This treatment approach is feasible in patients with newly diagnosed PCNSL without evidence of significant related neurotoxicity. Although the transplantation results are similar to those achieved in patients with aggressive or poor-prognosis systemic lymphoma, the low response rate to induction chemotherapy and the significant number of patients who experienced relapse soon after HDT suggest that more aggressive induction chemotherapy may be warranted. (C) 2003 by American Society of Clinical Oncology.
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收藏
页码:4151 / 4156
页数:6
相关论文
共 25 条
[1]   Long-term survival in primary CNS lymphoma [J].
Abrey, LE ;
DeAngelis, LM ;
Yahalom, J .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (03) :859-863
[2]   Treatment for primary CNS lymphoma: The next step [J].
Abrey, LE ;
Yahalom, J ;
DeAngelis, LM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (17) :3144-3150
[3]  
Abrey LE, 1997, NEUROLOGY, V48, pV1003
[4]   Treatment of primary CNS lymphoma with methotrexate and deferred radiotherapy: A report of NABTT 96-07 [J].
Batchelor, T ;
Carson, K ;
O'Neill, A ;
Grossman, SA ;
Alavi, J ;
New, P ;
Hochberg, F ;
Priet, R .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (06) :1044-1049
[5]   MECHANISM OF SYNERGISTIC CELL KILLING WHEN METHOTREXATE PRECEDES CYTOSINE-ARABINOSIDE - STUDY OF L1210 AND HUMAN-LEUKEMIC CELLS [J].
CADMAN, E ;
EIFERMAN, F .
JOURNAL OF CLINICAL INVESTIGATION, 1979, 64 (03) :788-797
[6]  
Cairncross G, 2000, NEURO-ONCOLOGY, V2, P114, DOI 10.1093/neuonc/2.2.114
[7]   High-dose thiotepa, busulfan, cyclophosphamide and ASCT without whole-brain radiotherapy for poor prognosis primary CNS lymphoma [J].
Cheng, G ;
Forsyth, P ;
Chaudhry, A ;
Morris, D ;
Gluck, S ;
Russell, JA ;
Stewart, DA .
BONE MARROW TRANSPLANTATION, 2003, 31 (08) :679-685
[8]  
COLTMAN AC, 1986, UPDATE TREATMENT DIF, P71
[9]  
Deangelis L M, 1995, Oncology (Williston Park), V9, P63
[10]   Combination chemotherapy and radiotherapy for primary central nervous system lymphoma: Radiation Therapy Oncology Group study 93-10 [J].
DeAngelis, LM ;
Seiferheld, W ;
Schold, SC ;
Fisher, B ;
Schultz, CJ .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (24) :4643-4648