CHOD/BVAM CHEMOTHERAPY AND WHOLE-BRAIN RADIOTHERAPY FOR NEWLY DIAGNOSED PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA

被引:15
作者
Laack, Nadia N. [1 ]
O'Neill, Brian Patrick [2 ]
Ballman, Karla V. [3 ]
O'Fallon, Judith Rich [3 ]
Carrero, Xiomara W. [3 ]
Kurtin, Paul J. [4 ]
Scheithauer, Bernd W. [4 ]
Brown, Paul D. [1 ]
Habermann, Thomas M. [10 ]
Colgan, Joseph P. [10 ]
Gilbert, Mark R. [5 ]
Hawkins, Roland B. [6 ]
Morton, Roscoe F. [7 ]
Windschitl, Harry E. [8 ]
Fitch, Tom R. [10 ]
Pajon, Eduardo R., Jr. [9 ]
机构
[1] Mayo Clin & Mayo Fdn, Dept Radiat Oncol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Div Biostat, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Pathol, Rochester, MN 55905 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX 77030 USA
[6] Oschner CCOP, New Orleans, LA USA
[7] Iowa Oncol Res Assoc CCOP, Des Moines, IA USA
[8] CentraCare Clin, St Cloud, MN USA
[9] Colorado Canc Res Program, Denver, CO USA
[10] Mayo Clin & Mayo Fdn, Div Hematol, Rochester, MN 55905 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2011年 / 81卷 / 02期
关键词
Primary central nervous system lymphoma; Chemotherapy; Whole-brain radiotherapy; PRIMARY CNS LYMPHOMA; NON-HODGKINS-LYMPHOMA; TREATMENT GROUP NCCTG; TO-TREAT ANALYSIS; LONG-TERM; ONCOLOGY-GROUP; THERAPY; METHOTREXATE; CANCER; SURVIVAL;
D O I
10.1016/j.ijrobp.2010.06.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the efficacy and toxicity of chemotherapy consisting of cyclophosphamide, doxorubicin (Adriamycin), vincristine, and dexamethasone (CHOD) plus bis-chloronitrosourea (BCNU), cytosine arabinoside, and methotrexate (BVAM) followed by whole-brain irradiation (WBRT) for patients with primary central nervous system lymphoma (PCNSL). Methods and Materials: Patients 70 years old and younger with newly diagnosed, biopsy-proven PCNSL received one cycle of CHOD followed by two cycles of BVAM. Patients then received WBRT, 30.6 Gy, if a complete response was evoked, or 50.4 Gy if the response was less than complete; both doses were given in 1.8-Gy daily fractions. The primary efficacy endpoint was 1-year survival. Results: Thirty-six patients (19 men, 17 women) enrolled between 1995 and 2000. Median age was 60.5 years (range, 34 to 69 years). Thirty (83%) patients had baseline Eastern Cooperative Oncology Group performance scores of 0 to 1. All 36 patients were eligible for survival and response evaluations. Median time to progression was 12.3 months, and median survival was 18.5 months. The percentages of patients alive at 1, 2, and 3 years were 64%, 36%, and 33%, respectively. The best response was complete response in 10 patients and immediate progression in 7 patients. Ten (28%) patients had at least one grade 3 or higher neurologic toxicity. Conclusions: This regimen did improve the survival of PCNSL patients but also caused substantial toxicity. The improvement in survival is less than that reported with high-dose methotrexate-based therapies. (C) 2011 Elsevier Inc.
引用
收藏
页码:476 / 482
页数:7
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