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Erschienen in: Annals of Hematology 12/2008

01.12.2008 | Original Article

Influence of conditioning regimens and stem cell sources on donor-type chimerism early after stem cell transplantation

verfasst von: Junichi Sugita, Junji Tanaka, Aya Hashimoto, Souichi Shiratori, Atsushi Yasumoto, Kentaro Wakasa, Misato Kikuchi, Akio Shigematsu, Yoko Miura, Yutaka Tsutsumi, Takeshi Kondo, Masahiro Asaka, Masahiro Imamura

Erschienen in: Annals of Hematology | Ausgabe 12/2008

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Abstract

We retrospectively analyzed very early chimerism before and ongoing neutrophil engraftment (days 7, 14, 21, 28) and investigated the influence of conditioning regimens and stem cell sources on donor-type chimerism in 59 Japanese patients who had received allogeneic hematopoietic stem cell transplantation. The percentage of donor-type chimerism increased before engraftment in all patients who achieved engraftment. The average percentage of donor-type chimerism in patients who had received reduced-intensity stem cell transplantation (RIST) with total body irradiation (TBI) was significantly higher than that in patients who had received RIST without TBI (98.8% vs 87.5% on day 21, P < 0.01; 99.3% vs 84.3% on day 28, P < 0.01). The average percentage of donor-type chimerism after peripheral blood stem cell transplantation was significantly higher than that after bone marrow transplantation on day 7 (81.5% vs 43.1%, P < 0.01), and the average percentage of donor-type chimerism after cord blood transplantation was significantly lower on day 14 (55.8% vs 84.8%, P < 0.05). Compared with the average percentage of donor-type chimerism in patients who achieved engraftment with each stem cell source, a notable decrease in donor-type chimerism was observed in patients who failed to achieve engraftment. This study suggests that differences in conditioning regimens and stem cell sources should be taken into account when considering donor-type chimerism.
Literatur
1.
Zurück zum Zitat Balon J, Halaburda K, Bieniaszewska M, Reichert M, Bieniaszewski L, Piekarska A et al (2005) Early complete donor hematopoietic chimerism in peripheral blood indicates the risk of extensive graft-versus-host disease. Bone Marrow Transplant 35:1083–1088 doi:10.1038/sj.bmt.1704962 PubMedCrossRef Balon J, Halaburda K, Bieniaszewska M, Reichert M, Bieniaszewski L, Piekarska A et al (2005) Early complete donor hematopoietic chimerism in peripheral blood indicates the risk of extensive graft-versus-host disease. Bone Marrow Transplant 35:1083–1088 doi:10.​1038/​sj.​bmt.​1704962 PubMedCrossRef
2.
Zurück zum Zitat Barker JN, Weisdorf DJ, DeFor TE, Blazar BR, Miller JS, Wagner JE (2003) Rapid and complete donor chimerism in adult recipients of unrelated donor umbilical cord blood transplantation after reduced-intensity conditioning. Blood 102:1915–1919 doi:10.1182/blood-2002-11-3337 PubMedCrossRef Barker JN, Weisdorf DJ, DeFor TE, Blazar BR, Miller JS, Wagner JE (2003) Rapid and complete donor chimerism in adult recipients of unrelated donor umbilical cord blood transplantation after reduced-intensity conditioning. Blood 102:1915–1919 doi:10.​1182/​blood-2002-11-3337 PubMedCrossRef
4.
Zurück zum Zitat Champlin R, Khouri I, Shimoni A, Gajewski J, Kornblau S, Molldrem J et al (2000) Harnessing graft-versus-malignancy: non-myeloablative preparative regimens for allogeneic haematopoietic transplantation, an evolving strategy for adoptive immunotherapy. Br J Haematol 111:18–29 doi:10.1046/j.1365-2141.2000.02196.x PubMedCrossRef Champlin R, Khouri I, Shimoni A, Gajewski J, Kornblau S, Molldrem J et al (2000) Harnessing graft-versus-malignancy: non-myeloablative preparative regimens for allogeneic haematopoietic transplantation, an evolving strategy for adoptive immunotherapy. Br J Haematol 111:18–29 doi:10.​1046/​j.​1365-2141.​2000.​02196.​x PubMedCrossRef
5.
Zurück zum Zitat Childs R, Clave E, Contentin N, Jayasekera D, Hensel N, Leitman S et al (1999) Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: full donor T-cell chimerism precedes alloimmune responses. Blood 94:3234–3241PubMed Childs R, Clave E, Contentin N, Jayasekera D, Hensel N, Leitman S et al (1999) Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: full donor T-cell chimerism precedes alloimmune responses. Blood 94:3234–3241PubMed
6.
7.
Zurück zum Zitat Giralt S, Thall PF, Khouri I, Wang X, Braunschweig I, Ippolitti C et al (2001) Melphalan and purine analog-containing preparative regimens: reduced-intensity conditioning for patients with hematologic malignancies undergoing allogeneic progenitor cell transplantation. Blood 97:631–637 doi:10.1182/blood.V97.3.631 PubMedCrossRef Giralt S, Thall PF, Khouri I, Wang X, Braunschweig I, Ippolitti C et al (2001) Melphalan and purine analog-containing preparative regimens: reduced-intensity conditioning for patients with hematologic malignancies undergoing allogeneic progenitor cell transplantation. Blood 97:631–637 doi:10.​1182/​blood.​V97.​3.​631 PubMedCrossRef
9.
Zurück zum Zitat Huisman C, de Weger RA, de Vries L, Tilanus MG, Verdonck LF (2007) Chimerism analysis within 6 months of allogeneic stem cell transplantation predicts relapse in acute myeloid leukemia. Bone Marrow Transplant 39:285–291 doi:10.1038/sj.bmt.1705582 PubMedCrossRef Huisman C, de Weger RA, de Vries L, Tilanus MG, Verdonck LF (2007) Chimerism analysis within 6 months of allogeneic stem cell transplantation predicts relapse in acute myeloid leukemia. Bone Marrow Transplant 39:285–291 doi:10.​1038/​sj.​bmt.​1705582 PubMedCrossRef
11.
Zurück zum Zitat Keil F, Prinz E, Moser K, Mannhalter C, Kalhs P, Worel N et al (2003) Rapid establishment of long-term culture-initiating cells of donor origin after nonmyeloablative allogeneic hematopoietic stem-cell transplantation, and significant prognostic impact of donor T-cell chimerism on stable engraftment and progression-free survival. Transplantation 76:230–236 doi:10.1097/01.TP.0000071862.42835.76 PubMedCrossRef Keil F, Prinz E, Moser K, Mannhalter C, Kalhs P, Worel N et al (2003) Rapid establishment of long-term culture-initiating cells of donor origin after nonmyeloablative allogeneic hematopoietic stem-cell transplantation, and significant prognostic impact of donor T-cell chimerism on stable engraftment and progression-free survival. Transplantation 76:230–236 doi:10.​1097/​01.​TP.​0000071862.​42835.​76 PubMedCrossRef
12.
Zurück zum Zitat Kusumi E, Kami M, Yuji K, Hamaki T, Murashige N, Hori A et al (2004) Feasibility of reduced intensity hematopoietic stem cell transplantation from an HLA-matched unrelated donor. Bone Marrow Transplant 33:697–702 doi:10.1038/sj.bmt.1704425 PubMedCrossRef Kusumi E, Kami M, Yuji K, Hamaki T, Murashige N, Hori A et al (2004) Feasibility of reduced intensity hematopoietic stem cell transplantation from an HLA-matched unrelated donor. Bone Marrow Transplant 33:697–702 doi:10.​1038/​sj.​bmt.​1704425 PubMedCrossRef
13.
Zurück zum Zitat Lassaletta A, Ramirez M, Montero JM, Gonzalez-Vicent M, Balas A, Madero L et al (2005) Full donor chimerism by day 30 after allogeneic peripheral blood progenitor cell transplantation is associated with a low risk of relapse in pediatric patients with hematological malignancies. Leukemia 19:504–506PubMed Lassaletta A, Ramirez M, Montero JM, Gonzalez-Vicent M, Balas A, Madero L et al (2005) Full donor chimerism by day 30 after allogeneic peripheral blood progenitor cell transplantation is associated with a low risk of relapse in pediatric patients with hematological malignancies. Leukemia 19:504–506PubMed
14.
Zurück zum Zitat Laughlin MJ, Eapen M, Rubinstein P, Wagner JE, Zhang MJ, Champlin RE et al (2004) Outcomes after transplantation of cord blood or bone marrow from unrelated donors in adults with leukemia. N Engl J Med 351:2265–2275 doi:10.1056/NEJMoa041276 PubMedCrossRef Laughlin MJ, Eapen M, Rubinstein P, Wagner JE, Zhang MJ, Champlin RE et al (2004) Outcomes after transplantation of cord blood or bone marrow from unrelated donors in adults with leukemia. N Engl J Med 351:2265–2275 doi:10.​1056/​NEJMoa041276 PubMedCrossRef
15.
Zurück zum Zitat McSweeney PA, Niederwieser D, Shizuru JA, Sandmaier BM, Molina AJ, Maloney DG et al (2001) Hematopoietic cell transplantation in older patients with hematologic malignancies: replacing high-dose cytotoxic therapy with graft-versus-tumor effects. Blood 97:3390–3400 doi:10.1182/blood.V97.11.3390 PubMedCrossRef McSweeney PA, Niederwieser D, Shizuru JA, Sandmaier BM, Molina AJ, Maloney DG et al (2001) Hematopoietic cell transplantation in older patients with hematologic malignancies: replacing high-dose cytotoxic therapy with graft-versus-tumor effects. Blood 97:3390–3400 doi:10.​1182/​blood.​V97.​11.​3390 PubMedCrossRef
16.
Zurück zum Zitat Miura Y, Tanaka J, Toubai T, Tsutsumi Y, Kato N, Hirate D et al (2006) Analysis of donor-type chimerism in lineage-specific cell populations after allogeneic myeloablative and non-myeloablative stem cell transplantation. Bone Marrow Transplant 37:837–843 doi:10.1038/sj.bmt.1705352 PubMedCrossRef Miura Y, Tanaka J, Toubai T, Tsutsumi Y, Kato N, Hirate D et al (2006) Analysis of donor-type chimerism in lineage-specific cell populations after allogeneic myeloablative and non-myeloablative stem cell transplantation. Bone Marrow Transplant 37:837–843 doi:10.​1038/​sj.​bmt.​1705352 PubMedCrossRef
17.
Zurück zum Zitat Petersen SL, Madsen HO, Ryder LP, Svejgaard A, Masmas TN, Dickmeiss E et al (2004) Chimerism studies in HLA-identical nonmyeloablative hematopoietic stem cell transplantation point to the donor CD8(+) T-cell count on day + 14 as a predictor of acute graft-versus-host disease. Biol Blood Marrow Transplant 10:337–346 doi:10.1016/j.bbmt.2004.01.003 PubMedCrossRef Petersen SL, Madsen HO, Ryder LP, Svejgaard A, Masmas TN, Dickmeiss E et al (2004) Chimerism studies in HLA-identical nonmyeloablative hematopoietic stem cell transplantation point to the donor CD8(+) T-cell count on day + 14 as a predictor of acute graft-versus-host disease. Biol Blood Marrow Transplant 10:337–346 doi:10.​1016/​j.​bbmt.​2004.​01.​003 PubMedCrossRef
18.
Zurück zum Zitat Ritchie DS, Morton J, Szer J, Roberts AW, Durrant S, Shuttleworth P et al (2003) Graft-versus-host disease, donor chimerism, and organ toxicity in stem cell transplantation after conditioning with fludarabine and melphalan. Biol Blood Marrow Transplant 9:435–442 doi:10.1016/S1083-8791(03)00128-9 PubMedCrossRef Ritchie DS, Morton J, Szer J, Roberts AW, Durrant S, Shuttleworth P et al (2003) Graft-versus-host disease, donor chimerism, and organ toxicity in stem cell transplantation after conditioning with fludarabine and melphalan. Biol Blood Marrow Transplant 9:435–442 doi:10.​1016/​S1083-8791(03)00128-9 PubMedCrossRef
19.
Zurück zum Zitat Rocha V, Labopin M, Sanz G, Arcese W, Schwerdtfeger R, Bosi A et al (2004) Transplants of umbilical-cord blood or bone marrow from unrelated donors in adults with acute leukemia. N Engl J Med 351:2276–2285 doi:10.1056/NEJMoa041469 PubMedCrossRef Rocha V, Labopin M, Sanz G, Arcese W, Schwerdtfeger R, Bosi A et al (2004) Transplants of umbilical-cord blood or bone marrow from unrelated donors in adults with acute leukemia. N Engl J Med 351:2276–2285 doi:10.​1056/​NEJMoa041469 PubMedCrossRef
20.
Zurück zum Zitat Slavin S, Nagler A, Naparstek E, Kapelushnik Y, Aker M, Cividalli G et al (1998) Nonmyeloablative stem cell transplantation and cell therapy as an alternative to conventional bone marrow transplantation with lethal cytoreduction for the treatment of malignant and nonmalignant hematologic diseases. Blood 91:756–763PubMed Slavin S, Nagler A, Naparstek E, Kapelushnik Y, Aker M, Cividalli G et al (1998) Nonmyeloablative stem cell transplantation and cell therapy as an alternative to conventional bone marrow transplantation with lethal cytoreduction for the treatment of malignant and nonmalignant hematologic diseases. Blood 91:756–763PubMed
21.
Zurück zum Zitat Stem cell Trialists’ Collaborative Group (2005) Allogeneic peripheral blood stem-cell compared with bone marrow transplantation in the management of hematologic malignancies: an individual patient data meta-analysis of nine randomized trials. J Clin Oncol 23:5074–5087CrossRef Stem cell Trialists’ Collaborative Group (2005) Allogeneic peripheral blood stem-cell compared with bone marrow transplantation in the management of hematologic malignancies: an individual patient data meta-analysis of nine randomized trials. J Clin Oncol 23:5074–5087CrossRef
22.
Zurück zum Zitat Takahashi S, Iseki T, Ooi J, Tomonari A, Takasugi K, Shimohakamada Y et al (2004) Single-institute comparative analysis of unrelated bone marrow transplantation and cord blood transplantation for adult patients with hematologic malignancies. Blood 104:3813–3820 doi:10.1182/blood-2004-03-1001 PubMedCrossRef Takahashi S, Iseki T, Ooi J, Tomonari A, Takasugi K, Shimohakamada Y et al (2004) Single-institute comparative analysis of unrelated bone marrow transplantation and cord blood transplantation for adult patients with hematologic malignancies. Blood 104:3813–3820 doi:10.​1182/​blood-2004-03-1001 PubMedCrossRef
23.
Zurück zum Zitat Tsutsumi Y, Tanaka J, Kato N, Zhang L, Mori A, Kobayasi R et al (2002) Analysis of mixed chimerism in patients after allogeneic stem cell transplantation using a capillary electrophoresis system. Acta Haematol 107:195–202 doi:10.1159/000058314 PubMedCrossRef Tsutsumi Y, Tanaka J, Kato N, Zhang L, Mori A, Kobayasi R et al (2002) Analysis of mixed chimerism in patients after allogeneic stem cell transplantation using a capillary electrophoresis system. Acta Haematol 107:195–202 doi:10.​1159/​000058314 PubMedCrossRef
25.
Zurück zum Zitat Valcarcel D, Martino R, Caballero D, Mateos MV, Perez-Simon JA, Canals C et al (2003) Chimerism analysis following allogeneic peripheral blood stem cell transplantation with reduced-intensity conditioning. Bone Marrow Transplant 31:387–392 doi:10.1038/sj.bmt.1703846 PubMedCrossRef Valcarcel D, Martino R, Caballero D, Mateos MV, Perez-Simon JA, Canals C et al (2003) Chimerism analysis following allogeneic peripheral blood stem cell transplantation with reduced-intensity conditioning. Bone Marrow Transplant 31:387–392 doi:10.​1038/​sj.​bmt.​1703846 PubMedCrossRef
Metadaten
Titel
Influence of conditioning regimens and stem cell sources on donor-type chimerism early after stem cell transplantation
verfasst von
Junichi Sugita
Junji Tanaka
Aya Hashimoto
Souichi Shiratori
Atsushi Yasumoto
Kentaro Wakasa
Misato Kikuchi
Akio Shigematsu
Yoko Miura
Yutaka Tsutsumi
Takeshi Kondo
Masahiro Asaka
Masahiro Imamura
Publikationsdatum
01.12.2008
Verlag
Springer-Verlag
Erschienen in
Annals of Hematology / Ausgabe 12/2008
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-008-0542-4

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