Randomized comparison of ACVBP and m-BACOD in the treatment of patients with low-risk aggressive lymphoma:: The LNH87-1 study

被引:52
作者
Tilly, H
Mounier, N
Lederlin, P
Brière, J
Dupriez, B
Sebban, C
Bosly, A
Biron, P
Nouvel, C
Herbrecht, R
Bordessoule, D
Coiffier, B
机构
[1] Ctr Henri Becquerel, F-76038 Rouen, France
[2] Hop St Louis, Paris, France
[3] Hop Laennec, F-75340 Paris, France
[4] Ctr Hosp Reg, Vandoeuvre Les Nancy, France
[5] Ctr Hosp Reg, Lille, France
[6] Hop Edouard Herriot, Lyon, France
[7] Ctr Leon Berard, F-69373 Lyon, France
[8] Ctr Hosp Purpan, Toulouse, France
[9] Hop Hautepierre, Strasbourg, France
[10] CHU Limoges, Limoges, France
[11] Ctr Hosp Lyon Sud, F-69310 Pierre Benite, France
[12] Clin Univ Mt Godinne, Yvoir, Belgium
关键词
D O I
10.1200/JCO.2000.18.6.1309
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To compare ct short intensified regimen followed by sequential consolidation therapy (doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone [ACVBP]) to the standard regimen of methotrexate, bleomycin, cyclophosphamide, and etoposide (m-BACOD) in patients with low-risk aggressive lymphoma. Patients and Methods: A total of 752 patients with intermediate or high-grade lymphoma and no adverse prognostic factors (Eastern Cooperative Oncology Group performance status of 2 to 4, greater than or equal to two extranodal sites of disease, tumor burden greater than or equal to 10 cm in largest dimension, bone marrow or CNS involvement, Burkitt's or lymphoblastic subtypes) were registered. Of 673 eligible patients, 332 received ACVBP and 341 received m-BACOD. Results: The complete remission rate wets identical (86%) in the two groups. With a median follow-up duration of 7 years, the 5-year failure-free survival (FFS) rate wets 65% in the ACVBP group and 61% in the m-BACOD group (P = .16), The 5-year overall survival rate wets 75% in the ACVBP group and 73% in the m-BACOD group (P = .47). ACVBP was responsible for more severe and life-threatening infections (P < .01), but m-BACOD caused more pulmonary toxicity (P < .001). The number of treatment-related deaths did not differ between the two regimens. A multivariate analysis indicated that ACVBP wets associated with a longer FFS in patients with two or three risk factors of the International Prognostic Index. Conclusion: In this population of patients with low-risk aggressive lymphoma, toxicities of the regimens are different, but the rates of response and survival are identical. The survival advantage of ACVBP over standard regimen in patients with advanced disease is suggested by this analysis but remains to be assessed in prospective studies specifically designed for this purpose. (C) 2000 by American Society of Clinical Oncology,
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页码:1309 / 1315
页数:7
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