Induction-consolidation with an idarubicin-containing regimen, unpurged marrow autograft, and post-graft chemotherapy in adult acute lymphoblastic leukaemia

被引:16
作者
Bassan, R [1 ]
Lerede, T
Di Bona, E
Rambaldi, A
Rossi, G
Pogliani, E
Oriani, A
D'Emilio, A
Izzi, T
Lambertenghi-Deliliers, G
Corneo, G
Barbui, T
机构
[1] Osped Riuniti Bergamo, Div Ematol, Haematol Unit, I-24100 Bergamo, Italy
[2] Osped Riuniti Bergamo, Bone Marrow Transplant Unit, I-24100 Bergamo, Italy
[3] Osped Gen San Bortolo, Vicenza, Italy
[4] Spedali Civili, I-25125 Brescia, Italy
[5] Nuovo Osped San Gerardo, Monza, Italy
[6] Univ Milan, Med Clin, Milan, Italy
关键词
adult ALL; idarubicin; ABMT; risk factors; long-term analysis;
D O I
10.1046/j.1365-2141.1999.01258.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Between 1991 and 1993 we conducted a collaborative trial in adult acute lymphoblastic leukaemia, introducing an idarubicin (IDA)-containing regimen for induction and early consolidation, and increasing consolidation intensity with an autologous bone marrow transplantation phase (ABMT, patients aged <51 years) followed by further chemotherapy for 12 weeks and low-dose maintenance for 6 months (ABMT patients) or 18 months. 96 patients were evaluable for antileukaemic response after induction with vincristine-prednisone-L-asparaginase plus cumulative IDA 36 or 20 mg/m(2) (IVAP-1 and IVAP-2), and for disease-free survival (DFS) after a minimum follow-up >3.5 years with an off-therapy interval >1.5 years. The response rate was 44% (7/16) with IVAP-1 and 90% (72/80) with IVAP-2 (P = 0.0001), due to regimen-related toxicities. Post-remission therapy was administered as planned to most cases but protocol violation was registered in some patients eligible to ABMT and post-graft chemotherapy. The 5-year disease-free survival (DFS) rate was 31%. Multivariate analysis indicated that DFS was improved in patients receiving a transplant (II allogeneic, DFS 70%: 32 ABMT. 36%; 37 neither, 17%: P < 0.001) and was negatively affected by high-risk features such as blast cell count > 25 x 10(9)/l, T-cell or mature B-cell immunophenotype, and t(9;22)/t(4;11) (all P values < 0.05). The 5-year DFS rate was 54% for 26 patients with no high-risk factor, 26% for 35 patients with any one, and 6% for 18 patients with any two (P < 0.005), IVAP-2 brought about a high complete response rate and post-remission treatment including ABMT was feasible and modestly toxic. In spite of the short postgraft chemotherapy phase, the long-term DFS rate was good in cases with no high-risk feature. However, because autografting may be redundant in the standard-risk category, its role requires further investigation for high-risk cases.
引用
收藏
页码:755 / 762
页数:8
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