Addition of melphalan to fludarabine/busulfan (FLU/BU4/MEL) provides survival benefit for patients with myeloid malignancy following allogeneic bone-marrow transplantation/peripheral blood stem-cell transplantation

被引:14
作者
Ueda, Tomoaki [1 ]
Maeda, Tetsuo [1 ]
Kusakabe, Shinsuke [1 ]
Fujita, Jiro [1 ]
Fukushima, Kentaro [1 ]
Yokota, Takafumi [1 ]
Shibayama, Hirohiko [1 ]
Tomiyama, Yoshiaki [2 ]
Kanakura, Yuzuru [1 ]
机构
[1] Osaka Univ, Dept Hematol & Oncol, Grad Sch Med, 2-2 Yamada Oka, Suita, Osaka 5650871, Japan
[2] Osaka Univ Hosp, Dept Blood Transfus, Suita, Osaka, Japan
关键词
Allogeneic bone-marrow transplantation; peripheral blood stem-cell transplantation; Conditioning regimen; Myeloid malignancy; Intravenous busulfan; Melphalan; DAILY INTRAVENOUS BUSULFAN; LEUKEMIA WORKING PARTY; VERSUS-HOST-DISEASE; CONDITIONING REGIMEN; MYCOPHENOLATE-MOFETIL; ACUTE GVHD; INTENSITY; AML; CHIMERISM; CYCLOPHOSPHAMIDE;
D O I
10.1007/s12185-018-2562-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A conditioning regimen with fludarabine and myeloablative dose of busulfan (FLU/BU4) has been commonly used in allogeneic hematopoietic cell transplantation (allo-HCT). However, there are two major problems with this regimen: insufficient anti-leukemic effect, especially in advanced cases, and slow time to complete donor-type chimerism, especially T-cell chimerism. To overcome these issues, we designed a combination regimen with FLU (150mg/m(2)), intravenous BU (12.8mg/kg), and melphalan (100mg/m(2)) (FLU/BU4/MEL) and conducted retrospective analyses of treatment outcomes at our institute. Forty-two patients with myeloid malignancies received allogeneic bone-marrow transplantation or peripheral blood stem-cell transplantation (allo-BMT/PBSCT) with FLU/BU4/MEL regimen. The median age of patients was 46.5years (20-63years). Thirteen patients (31%) did not achieve complete hematological remission at transplantation. All patients examined achieved complete whole and T-cell chimerism within 1 month after allo-HCT. The 4-year overall survival and disease-free survival rates were 66.0% [95% confidence interval (CI) 49.4-78.3%] and 59.5% (95% CI 43.2-72.6%) in all patients, and 49.4% (95% CI 19.7-73.6%) and 38.5% (95% CI 14.1-62.8%) in patients who were not in remission. In conclusion, FLU/BU4/MEL showed curative potential, even in patients with advanced myeloid malignancies, accompanied by achievement of rapid complete chimerism after allo-BMT/PBSCT.
引用
收藏
页码:197 / 205
页数:9
相关论文
共 32 条
[1]   Myeloablative Reduced-Toxicity i.v. Busulfan-Fludarabine and Allogeneic Hematopoietic Stem Cell Transplant for Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome in the Sixth through Eighth Decades of Life [J].
Alatrash, Gheath ;
de Lima, Marcos ;
Hamerschlak, Nelson ;
Pelosini, Matteo ;
Wang, Xuemei ;
Xiao, Lianchun ;
Kerbauy, Fabio ;
Chiattone, Alexandre ;
Rondon, Gabriela ;
Qazilbash, Muzaffar H. ;
Giralt, Sergio A. ;
Silva, Leandro de Padua ;
Hosing, Chitra ;
Kebriaei, Partow ;
Zhang, Weiqing ;
Nieto, Yago ;
Saliba, Rima M. ;
Champlin, Richard E. ;
Andersson, Borje S. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2011, 17 (10) :1490-1496
[2]   Validation and refinement of the Disease Risk Index for allogeneic stem cell transplantation [J].
Armand, Philippe ;
Kim, Haesook T. ;
Logan, Brent R. ;
Wang, Zhiwei ;
Alyea, Edwin P. ;
Kalaycio, Matt E. ;
Maziarz, Richard T. ;
Antin, Joseph H. ;
Soiffer, Robert J. ;
Weisdorf, Daniel J. ;
Rizzo, J. Douglas ;
Horowitz, Mary M. ;
Saber, Wael .
BLOOD, 2014, 123 (23) :3664-3671
[3]   Reduced-Intensity Conditioning With Fludarabine and Busulfan Versus Fludarabine and Melphalan for Patients With Acute Myeloid Leukemia: A Report From the Acute Leukemia Working Party of the European Group for Blood and Marrow Transplantation [J].
Baron, Frederic ;
Labopin, Myriam ;
Peniket, Andy ;
Jindra, Pavel ;
Afanasyev, Boris ;
Sanz, Miguel A. ;
Deconinck, Eric ;
Nagler, Arnon ;
Mohty, Mohamad .
CANCER, 2015, 121 (07) :1048-1055
[4]   Busulfan fludarabine vs busulfan cyclophosphamide as a preparative regimen before allogeneic hematopoietic cell transplantation: systematic review and meta-analysis [J].
Ben-Barouch, S. ;
Cohen, O. ;
Vidal, L. ;
Avivi, I. ;
Ram, R. .
BONE MARROW TRANSPLANTATION, 2016, 51 (02) :232-240
[5]   Prognostic impact of c-KIT mutations in core binding factor leukemas:: an Italian retrospective study [J].
Cairoli, R ;
Beghini, A ;
Grillo, G ;
Nadali, G ;
Elice, F ;
Ripamonti, CB ;
Colapietro, P ;
Nichelatti, M ;
Pezzetti, L ;
Lunghi, M ;
Cuneo, A ;
Viola, A ;
Ferrara, F ;
Lazzarino, M ;
Rodeghiero, F ;
Pizzolo, G ;
Larizza, L ;
Morra, E .
BLOOD, 2006, 107 (09) :3463-3468
[6]   Fludarabine/i.v. BU conditioning regimen: myeloablative, reduced intensity or both? [J].
Chunduri, S. ;
Dobogai, L. C. ;
Peace, D. ;
Saunthararajah, Y. ;
Quigley, J. ;
Chen, Y-H ;
Mahmud, N. ;
Hurter, E. ;
Beri, R. ;
Rondelli, D. .
BONE MARROW TRANSPLANTATION, 2008, 41 (11) :935-940
[7]   Once-daily intravenous busulfan and fludarabine: clinical and pharmacokinetic results of a myeloablative, reduced-toxicity conditioning regimen for allogeneic stem cell transplantation in AML and MDS [J].
de Lima, M ;
Couriel, D ;
Thall, PF ;
Wang, XM ;
Madden, T ;
Jones, R ;
Shpall, EJ ;
Shahjahan, M ;
Pierre, B ;
Giralt, S ;
Korbling, M ;
Russell, JA ;
Champlin, RE ;
Andersson, BS .
BLOOD, 2004, 104 (03) :857-864
[8]   Hematopoietic cell transplant for acute myeloid leukemia and myelodysplastic syndrome: conditioning regimen intensity [J].
Eapen, Mary ;
Brazauskas, Ruta ;
Hemmer, Michael ;
Perez, Waleska S. ;
Steinert, Patricia ;
Horowitz, Mary M. ;
Deeg, H. Joachim .
BLOOD ADVANCES, 2018, 2 (16) :2095-2103
[9]   Acute GVHD is a strong predictor of full donor CD3+ T cell chimerism after reduced intensity conditioning allogeneic stem cell transplantation [J].
El-Cheikh, Jean ;
Vazquez, Alberto ;
Crocchiolo, Roberto ;
Furst, Sabine ;
Calmels, Boris ;
Castagna, Luca ;
Lemarie, Claude ;
Granata, Angela ;
Ladaique, Patrick ;
Oudin, Claire ;
Faucher, Catherine ;
Chabannon, Christian ;
Blaise, Didier .
AMERICAN JOURNAL OF HEMATOLOGY, 2012, 87 (12) :1074-1078
[10]   National Institutes of Health consensus development project on criteria for clinical trials in chronic graft-versus-host disease: I. Diagnosis and staging working group report [J].
Filipovich, AH ;
Weisdorf, D ;
Pavletic, S ;
Socie, G ;
Wingard, JR ;
Lee, SJ ;
Martin, P ;
Chien, J ;
Przepiorka, D ;
Couriel, D ;
Cowen, EW ;
Dinndorf, P ;
Farrell, A ;
Hartzman, R ;
Henslee-Downey, J ;
Jacobsohn, D ;
McDonald, G ;
Mittleman, B ;
Rizzo, JD ;
Robinson, M ;
Schubert, M ;
Schultz, K ;
Shulman, H ;
Turner, M ;
Vogelsang, G ;
Flowers, MED .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (12) :945-956