Treosulfan-fludarabine-thiotepa conditioning before allogeneic haemopoietic stem cell transplantation for patients with advanced lympho-proliferative disease. A single centre study

被引:6
作者
Baronciani, Donatella [1 ,2 ]
Depau, Cristina [1 ,2 ]
Targhetta, Clara [1 ,2 ]
Derudas, Daniele [1 ,2 ]
Culurgioni, Fabio [1 ,2 ]
Tandurella, Igor [1 ,2 ]
Latte, Giancarlo [3 ]
Palmas, Angelo [3 ]
Angelucci, Emanuele [1 ,2 ]
机构
[1] Osped Oncol Riferimento Reg Armando Businco, Unite Operat Ematol, Via Edward Jenner, I-09121 Cagliari, Italy
[2] Osped Oncol Riferimento Reg Armando Businco, Ctr Trapianti, Via Edward Jenner, I-09121 Cagliari, Italy
[3] ASL Nuoro, Unita Operat Ematol, Nuoro, Italy
关键词
conditioning; HSCT; toxicity; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; HIGH-DOSE THIOTEPA; PREPARATIVE REGIMEN; RISK; CYCLOPHOSPHAMIDE; TOXICITY; BLOOD; PHARMACOKINETICS; MELPHALAN;
D O I
10.1002/hon.2187
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, with the aim of reducing transplant-related mortality, new conditioning regimens have been explored in patients not eligible for conventional haemopoietic stem cell transplantation. In this setting, we investigated safety and feasibility of the treosulfan-fludarabine-thiotepa combination prior to allogeneic haemopoietic stem cell transplantation in patients with advanced lympho-proliferative diseases and at high transplant risk. Twenty-seven consecutive patients, median age 43years (range 19-60), entered this study. All of them were affected by lympho-proliferative disease in advanced phase and have been heavily pre-treated. The median haemopoietic stem cell transplant co-morbidity index was 1 (range 0-3). Twenty-five patients had regular engraftment, while the remaining two patients were not evaluable for early deaths. Non-haematological toxicity was limited. No patient developed veno-occlusive disease. The estimated probability of overall survival and progression-free survival with a median follow-up of 40months was 52% (95% confidence interval 33-73) and 50% (95% confidence interval 30-70) respectively. Six patients have relapsed; all of them were not in remission before transplantation. The treosulfan-fludarabine-thiotepa combination is a reduced toxicity but myeloablative regimen that can be proposed to patients not fitting criteria for conventional myeloablative transplant regimens. Longer follow-up and prospective randomized studies are necessary to evaluate this regimen. Copyright (c) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:17 / 21
页数:5
相关论文
共 25 条
[1]   HUMAN-PLASMA PHARMACOKINETICS OF THIOTEPA FOLLOWING ADMINISTRATION OF HIGH-DOSE THIOTEPA AND CYCLOPHOSPHAMIDE [J].
ACKLAND, SP ;
CHOI, KE ;
RATAIN, MJ ;
EGORIN, MJ ;
WILLIAMS, SF ;
SINKULE, JA ;
BITRAN, JD .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (07) :1192-1196
[2]   Graft-versus-tumor effects after allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning [J].
Baron, F ;
Maris, MB ;
Sandmaier, BM ;
Storer, BE ;
Sorror, M ;
Diaconescu, R ;
Woolfrey, AE ;
Chauncey, TR ;
Flowers, MED ;
Mielcarck, M ;
Maloney, DG ;
Storb, R .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (09) :1993-2003
[3]   Treosulfan/fludarabine as an allogeneic hematopoietic stem cell transplant conditioning regimen for high-risk patients [J].
Baronciani, Donatella ;
Rambaldi, Alessandro ;
Iori, Anna Paola ;
Di Bartolomeo, Paolo ;
Pilo, Federica ;
Pettinau, Martina ;
Depau, Cristina ;
Mico, Caterina ;
Santarone, Stella ;
Angelucci, Emanuele .
AMERICAN JOURNAL OF HEMATOLOGY, 2008, 83 (09) :717-720
[4]   Dose-escalated treosulphan in combination with cyclophosphamide as a new preparative regimen for allogeneic haematopoietic stem cell transplantation in patients with an increased risk for regimen-related complications [J].
Beelen, DW ;
Trenschel, R ;
Casper, J ;
Freund, M ;
Hilger, RA ;
Scheulen, ME ;
Basara, N ;
Fauser, AA ;
Hertenstein, B ;
Mylius, HA ;
Baumgart, J ;
Pichlmeier, U ;
Hahn, JR ;
Holler, E .
BONE MARROW TRANSPLANTATION, 2005, 35 (03) :233-241
[5]   Treosulfan and fludarabine:: a new toxicity-reduced conditioning regimen for allogeneic hematopoietic stem cell transplantation [J].
Casper, J ;
Knauf, W ;
Kiefer, T ;
Wolff, D ;
Steiner, B ;
Hammer, U ;
Wegener, R ;
Kleine, HD ;
Wilhelm, S ;
Knopp, A ;
Hartung, G ;
Dölken, G ;
Freund, M .
BLOOD, 2004, 103 (02) :725-731
[6]   The use of high-dose cyclophosphamide, carmustine, and thiotepa plus autologous hematopoietic stem cell transplantation as consolidation therapy for high-risk primary breast cancer after primary surgery or neoadjuvant chemothermpy [J].
Cheng, YC ;
Rondón, G ;
Yang, Y ;
Smith, TL ;
Gajewski, JL ;
Donato, ML ;
Shpall, EJ ;
Jones, R ;
Hortobagyi, GN ;
Champlin, RE ;
Ueno, NT .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2004, 10 (11) :794-804
[7]   High-dose thiotepa, melphalan and carboplatin (TMCb) followed by autologous peripheral blood stem cell transplantation in patients with lymphoma - a retrospective evaluation [J].
Demirer, T ;
Ayli, M ;
Fen, T ;
Ozcan, M ;
Arat, M ;
Buyukberber, S ;
Arslan, O ;
Gurman, G ;
Akan, H ;
Ilhan, O .
BONE MARROW TRANSPLANTATION, 2004, 34 (09) :781-786
[8]   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
[9]   Reduced-intensity conditioning for unrelated donor progenitor cell transplantation: Long-term follow-up of the first 285 reported to the National Marrow Donor Program [J].
Giralt, Sergio ;
Logan, Brent ;
Rizzo, Douglas ;
Zhang, Mei-Je ;
Ballen, Karen ;
Emmanouilides, Christos ;
Nath, Rajneesh ;
Parker, Pablo ;
Porter, David ;
Sandmaier, Brenda ;
Waller, Edmund K. ;
Barker, Juliet ;
Pavletic, Steven ;
Weisdorf, Daniel .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (07) :844-852
[10]   Reduced-Intensity Conditioning Regimen Workshop: Defining the Dose Spectrum. Report of a Workshop Convened by the Center for International Blood and Marrow Transplant Research [J].
Giralt, Sergio ;
Ballen, Karen ;
Rizzo, Douglas ;
Bacigalupo, Andreas ;
Horowitz, Mary ;
Pasquini, Marcelo ;
Sandmaier, Brenda .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2009, 15 (03) :367-369