Achievement of at Least Very Good Partial Response Is a Simple and Robust Prognostic Factor in Patients With Multiple Myeloma Treated With High-Dose Therapy: Long-Term Analysis of the IFM 99-02 and 99-04 Trials

被引:142
作者
Harousseau, Jean-Luc [1 ]
Avet-Loiseau, Herve
Attal, Michel
Charbonnel, Catherine
Garban, Frederic
Hulin, Cyrille
Michallet, Mauricette
Facon, Thierry
Garderet, Laurent
Marit, Gerald
Ketterer, Nicolas
Lamy, Thierry
Voillat, Laurent
Guilhot, Francois
Doyen, Chantal
Mathiot, Claire
Moreau, Philippe
机构
[1] Ctr Rene Gauducheau, F-44035 Nantes, France
关键词
STEM-CELL TRANSPLANTATION; LENALIDOMIDE PLUS DEXAMETHASONE; PROGRESSION-FREE SURVIVAL; AUTOLOGOUS TRANSPLANTATION; MOLECULAR REMISSION; RANDOMIZED-TRIAL; ELDERLY-PATIENTS; ONCOLOGY-GROUP; FOLLOW-UP; MELPHALAN;
D O I
10.1200/JCO.2008.21.1060
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The prognostic impact of complete response (CR) achievement in multiple myeloma ( MM) has been shown mostly in the context of autologous stem-cell transplantation. Other levels of response have been defined because, even with high-dose therapy, CR is a relatively rare event. The purpose of this study was to analyze the prognostic impact of very good partial response (VGPR) in patients treated with high-dose therapy. Patients and Methods All patients were included in the Intergroupe Francophone du Myelome 99-02 and 99-04 trials and treated with vincristine, doxorubicin, and dexamethasone (VAD) induction therapy followed by double autologous stem-cell transplantation ( ASCT). Best post-ASCT response assessment was available for 802 patients. Results With a median follow-up of 67 months, median event-free survival (EFS) and 5-year EFS were 42 months and 34%, respectively, for 405 patients who achieved at least VGPR after ASCT versus 32 months and 26% in 288 patients who achieved only partial remission (P = .005). Five-year overall survival ( OS) was significantly superior in patients achieving at least VGPR (74% v 61% P = .0017). In multivariate analysis, achievement of less than VGPR was an independent factor predicting shorter EFS and OS. Response to VAD had no impact on EFS and OS. The impact of VGPR achievement on EFS and OS was significant in patients with International Staging System stages 2 to 3 and for patients with poor-risk cytogenetics t(4; 14) or del(17p). Conclusion In the context of ASCT, achievement of at least VGPR is a simple prognostic factor that has importance in intermediate and high-risk MM and can be informative in more patients than CR.
引用
收藏
页码:5720 / 5726
页数:7
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