Prior treatment with gemtuzumab ozogamicin and the risk of veno-occlusive disease after allogeneic haematopoietic stem cell transplantation

被引:22
作者
Chevallier, P. [1 ,2 ]
Prebet, T. [3 ]
Turlure, P. [4 ]
Hunault, M. [5 ]
Vigouroux, S. [6 ]
Harousseau, J-L [7 ]
Blaise, D. [3 ]
Ifrah, N. [5 ]
Milpied, N. [6 ]
Mohty, M. [2 ,8 ]
机构
[1] CHU Nantes, Serv Hematol Clin, Ctr Invest Clin Cancerol CI2C, F-44093 Nantes 01, France
[2] CHU Hotel Dieu, Serv Hematol Clin, Nantes 01, France
[3] Inst J Paoli I Calmettes, Dept Hematol, F-13009 Marseille, France
[4] CHU Limoges, Serv Hematol, Limoges, France
[5] CHU Angers, Serv Hematol, Angers, France
[6] CHU Bordeaux, Serv Hematol Clin, Bordeaux, France
[7] Univ Nantes, Fac Med, CRCNA, Nantes, France
[8] CHU Nantes, INSERM, U892, F-44093 Nantes 01, France
关键词
Gemtuzumab; CD33; VOD; toxicity; allo-HSCT; ACUTE MYELOID-LEUKEMIA; BONE-MARROW-TRANSPLANTATION; INDUCTION CHEMOTHERAPY; PRIMARY RESISTANT; FREE SURVIVAL; EFFICACY; CYTARABINE; COMBINATION; MYLOTARG; SAFETY;
D O I
10.1038/bmt.2009.153
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This was a retrospective multicenter study including 44 acute leukaemia patients who have received allogeneic haematopoietic SCT (allo-HSCT) after prior exposure to Gemtuzumab Ozogamicin (GO) + chemotherapy. Median interval between last administration of GO and allo-HSCT was 4.2 (range, 0.8-26.3) months. At time of allo-HSCT, 33 patients were in CR. The majority of patients (n = 36) received a reduced-intensity conditioning (RIC) regimen before allo-HSCT. All but one patient received low-dose heparin for veno-occlusive disease (VOD) prophylaxis. With a median follow-up of 15 (range, 1.1-63) months, overall survival and disease-free survival after allo-HSCT were 45% (95% confidence interval (CI), 30-61%) and 38% (95% CI, 24-54%) at 2 years, respectively. The cumulative incidence of grade 3-4 hyperbilirubinemia was 13.5% (n = 6), with this being 21% in patients with a short (<= 3.5 months) GO-allo-HSCT interval (n = 4/19) vs 8% in all others (P = NS). Overall, the cumulative incidence of VOD was 7% (n = 3), with this being 10.5% (n = 2/19) in patients with a short GO-allograft interval (<= 3.5 months) vs 4% (n = 1/25) for all others (P = NS), and 5.5%(n = 2/36) in patients receiving an RIC regimen vs 12.5% for the others (n = 1/8) (P = NS). These results suggest that GO-based chemotherapy before allo-HSCT is feasible and does not result in an excessive rate of liver toxicity, especially VOD, after allo-HSCT. Bone Marrow Transplantation (2010) 45, 165-170; doi: 10.1038/bmt.2009.153; published online 6 July 2009
引用
收藏
页码:165 / 170
页数:6
相关论文
共 26 条
[1]   Safety and efficacy of gemtuzumab ozogamicin in combination with chemotherapy for pediatric acute myeloid leukemia: A report from the children's oncology group [J].
Aplenc, Richard ;
Alonzo, Todd A. ;
Gerbing, Robert B. ;
Lange, Beverly J. ;
Hurwitz, Craig A. ;
Wells, Robert J. ;
Bernstein, Irwin ;
Buckley, Patrick ;
Krimmel, Kathleen ;
Smith, Franklin O. ;
Sievers, Eric L. ;
Arceci, Robert J. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (14) :2390-2395
[2]   Safety and efficacy of gemtuzumab ozogamicin in pediatric patients with advanced CD33+ acute myeloid leukemia [J].
Arceci, RJ ;
Sande, J ;
Lange, B ;
Shannon, K ;
Franklin, J ;
Hutchinson, R ;
Vik, TA ;
Flowers, D ;
Aplenc, R ;
Berger, MS ;
Sherman, ML ;
Smith, FO ;
Bernstein, I ;
Sievers, EL .
BLOOD, 2005, 106 (04) :1183-1188
[3]  
ATTAL M, 1992, BLOOD, V79, P2834
[4]   Gemtuzumab ozogamicin as part of reduced-intensity conditioning for allogeneic hematopoietic cell transplantation in patients with relapsed acute myeloid leukemia [J].
Bornhaeuser, Martin ;
Illmer, Thomas ;
Elschlaegel, Uta ;
Schetelig, Johannes ;
Ordemann, Rainer ;
Schaich, Markus ;
Haenel, Mathias ;
Schuler, Ulrich ;
Thiede, Christian ;
Kiani, Alexander ;
Platzbecker, Uwe ;
Ehninger, Gerhard .
CLINICAL CANCER RESEARCH, 2008, 14 (17) :5585-5593
[5]   Efficacy of fractionated gemtuzumab ozogamicin combined with cytarabine in advanced childhood myeloid leukaemia [J].
Brethon, Benoit ;
Yakouben, Karima ;
Oudot, Caroline ;
Boutard, Patrick ;
Bruno, Benedicte ;
Jermoe, Cecile ;
Nelken, Brigitte ;
de Lumley, Lionel ;
Bertrand, Yves ;
Dalle, Jean-Hugues ;
Chevret, Sylvie ;
Leblanc, Thierry ;
Baruchel, Andre .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 143 (04) :541-547
[6]   The addition of gemtuzumab ozogamicin to induction chemotherapy for AML improves disease free survival without extra toxicity: Preliminary analysis of 1115 patients in the MRC AML15 trial. [J].
Burnett, Alan K. ;
Kell, William J. ;
Goldstone, Anthony H. ;
Milligan, Donald ;
Hunter, Ann ;
Prentice, Archie G. ;
Russell, Nigel H. ;
Gibson, Brenda ;
Wheatley, Keith ;
Hills, Robert K. .
BLOOD, 2006, 108 (11) :8A-8A
[7]   Gemtuzumab-ozogamicin in combination with fludarabine, cytarabine, idarubicin (FLAI-GO) as induction therapy in CD33-positive AML patients younger than 65 years [J].
Candoni, Anna ;
Martinelli, Giovanni ;
Toffoletti, Eleonora ;
Chiarvesio, Alexia ;
Tiribelli, Mario ;
Malagola, Michele ;
Piccaluga, Pier Paolo ;
Michelutti, Angela ;
Simeone, Erica ;
Damiani, Daniela ;
Russo, Domenico ;
Fanin, Renato .
LEUKEMIA RESEARCH, 2008, 32 (12) :1800-1808
[8]  
Carreras E, 1998, BLOOD, V92, P3599
[9]  
Cesaro S, 2005, HAEMATOLOGICA, V90, P1396
[10]   Administration of mylotarg 4 days after beginning of a chemotherapy including intermediate-dose aracytin and mitoxantrone (MIDAM regimen) produces a high rate of complete hematologic remission in patients with CD33+ primary resistant or relapsed acute myeloid leukemia [J].
Chevallier, P ;
Roland, V ;
Mahé, B ;
Juge-Morineau, N ;
Dubruille, V ;
Guillaume, T ;
Vigouroux, S ;
Moreau, P ;
Milpied, N ;
Garand, R ;
Avet-Loiseau, H ;
Harousseau, JL .
LEUKEMIA RESEARCH, 2005, 29 (09) :1003-1007