Comparison of outcomes after single or double cord blood transplantation in adults with acute leukemia using different types of myeloablative conditioning regimen, a retrospective study on behalf of Eurocord and the Acute Leukemia Working Party of EBMT


Por: Ruggeri, A, Sanz, G, Bittencourt, H, Sanz, J, Rambaldi, A, Volt, F, Yakoub-Agha, I, Ribera, JM, Mannone, L, Sierra, J, Mohty, M, Solano, C, Nabhan, S, Arcese, W, Gluckman, E, Labopin, M, Rocha, V

Publicada: 1 abr 2014
Resumen:
We report outcomes after single (s) and double (d) umbilical cord blood transplantation (UCBT) after myeloablative conditioning (MAC) regimen for 239 patients transplanted for acute leukemia in first complete remission (CR1). All sUCBT patients received a total nucleated cell dose >2.5 x 10(7)/kg. Conditioning regimen for sUCBT was total body irradiation (TBI) 12 Gy-or busulfan (BU)based +/- fludarabine (Flu) (n = 68, group 1), thiotepa + BU + Flu (TBF) (n = 88, group 2), and for dUCBT it was TBI12 Gycyclophosphamide +/- Flu (n = 83, group 3). dUCBT recipients were younger, received higher cell dose and less frequently antithymocyte globulin. In multivariate analysis, we found similar neutrophil recovery among the three groups; however, acute graft-versus-host disease II-IV was higher in dUCBT compared with others. Non-relapse mortality and relapse incidence were not statistically different among the three groups. Leukemia-free survival was 30% for sUCBT using TBI-or BU-based MAC compared with 48% for sUCBT TBF and 48% for dUCBT (P = 0.02 and P = 0.03, respectively), and it was not statistically different between sUCBT with TBF and dUCBT. In conclusion, use of sUCBT with adequate cell dose (42.5 +/- 107/kg) and a specific conditioning regimen in the MAC setting results in similar outcomes as dUCBT. The choice of TBF conditioning regimen for sUCBT may improve results, and whether this regimen may be effective in dUCBT should be further analyzed.

Filiaciones:
Ruggeri, A:
 Hop St Louis, AP HP, Eurocord, F-75010 Paris, France

 Univ Paris 07, IUH, Paris, France

 Univ Tor Vergata, Rome Transplant Network, Rome, Italy

Sanz, G:
 Hosp Univ La Fe, Valencia, Spain

Bittencourt, H:
 CHU St Justine, Montreal, PQ, Canada

Sanz, J:
 Hosp Univ La Fe, Valencia, Spain

Rambaldi, A:
 Osped Riuniti Bergamo, I-24100 Bergamo, Italy

Volt, F:
 Hop St Louis, AP HP, Eurocord, F-75010 Paris, France

 Univ Paris 07, IUH, Paris, France

Yakoub-Agha, I:
 Hop Claude Huriez, Lille, France

Ribera, JM:
 Hosp Badalona Germans Trias & Pujol, ICO, Jose Carreras Res Inst, Badalona, Spain

Mannone, L:
 Hop Archet, Nice, France

Sierra, J:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Mohty, M:
 UPMC, Hosp St Antoine, AP HP, Serv Hematol & Therapie Cellulaire,UMR S 938,CERE, Paris, France

Solano, C:
 Hosp Clin Univ, Valencia, Spain

Nabhan, S:
 Hop St Louis, AP HP, Eurocord, F-75010 Paris, France

 Univ Paris 07, IUH, Paris, France

Arcese, W:
 Univ Tor Vergata, Rome Transplant Network, Rome, Italy

Gluckman, E:
 Hop St Louis, AP HP, Eurocord, F-75010 Paris, France

 Univ Paris 07, IUH, Paris, France

Labopin, M:
 UPMC, Hosp St Antoine, AP HP, Serv Hematol & Therapie Cellulaire,UMR S 938,CERE, Paris, France

Rocha, V:
 Hop St Louis, AP HP, Eurocord, F-75010 Paris, France

 Univ Paris 07, IUH, Paris, France

 Churchill Hosp, Oxford Univ Hosp, Oxford OX3 7LJ, England
ISSN: 08876924





LEUKEMIA
Editorial
SPRINGERNATURE, CAMPUS, 4 CRINAN ST, LONDON, N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 28 Número: 4
Páginas: 779-786
WOS Id: 000334350900008
ID de PubMed: 24005245
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