Long-term results of the MCL01 phase II trial of rituximab plus HyperCVAD alternating with high-dose cytarabine and methotrexate for the initial treatment of patients with mantle cell lymphoma

被引:2
|
作者
Massaro, Fulvio [1 ,2 ]
Stepanishyna, Yana [3 ]
Manni, Martina [4 ]
Luminari, Stefano [1 ,4 ]
Galimberti, Sara [5 ]
Marcheselli, Luigi [6 ]
Visco, Carlo [7 ,8 ]
Tecchio, Cristina [7 ,8 ]
Stelitano, Caterina [9 ]
Angrilli, Francesco [10 ]
Petrini, Mario [5 ]
Merli, Francesco [1 ]
Federico, Massimo [4 ]
机构
[1] AUSL IRCCS Reggio Emilia, Hematol, Reggio Emilia, Italy
[2] Univ Modena & Reggio Emilia, PhD Program Clin & Expt Med, Modena, Italy
[3] Natl Canc Inst, Res Dept Hemoblastosis Chemotherapy, Kiev, Ukraine
[4] Univ Modena & Reggio Emilia, CHIMOMO Dept, Modena, Italy
[5] Univ Pisa, Dept Clin & Expt Med, Div Hematol, Pisa, Italy
[6] Fdn Italiana Linf FIL Onlus, Modena, Italy
[7] Univ Verona, Dept Med, Sect Hematol, Verona, Italy
[8] Univ Verona, Bone Marrow Transplant Unit, Verona, Italy
[9] Azienda Osped Bianchi Melacrino Morelli, Div Haematol, Reggio Di Calabria, Italy
[10] Ematol Osped Civile Spirito Santo, Pescara, Italy
关键词
Hyper-CVAD-AM; long-term analysis; mantle cell lymphoma; second malignancies; survival; 15-YEAR FOLLOW-UP; OPEN-LABEL; MULTICENTER; IMMUNOCHEMOTHERAPY; TRANSPLANTATION; BENDAMUSTINE; SURVIVAL; THERAPY;
D O I
10.1111/bjh.16714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mantle cell lymphoma is a rare and incurable lymphoproliferative disorder. In the MCL01 trial, patients were treated with the R-HCVAD regimen [rituximab plus HyperCVAD (hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone; R-CVAD) alternating with high-dose methotrexate and cytarabine (AM)] for four cycles followed by autologous stem cell transplantation (ASCT) for those who reached only a partial response. After a median follow-up of 10 center dot 5 years, we reported 10-year progression-free and overall survival rates of 35% and 61% respectively, with a 10-years cumulative incidence rate of second malignancies of 10 center dot 6%. Mature results of the MCL01 trial confirmed the efficacy of HyperCVAD-AM as a frontline regimen for younger patients (<= 65 years).
引用
收藏
页码:1011 / 1014
页数:4
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