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Volumn 23, Issue 6, 2016, Pages 508-514

Matched sibling donor hematopoietic stem cell transplantation for thalassemia

Author keywords

class 3; matched sibling donor bone marrow transplantation; novel conditioning; thalassemia

Indexed keywords

AZATHIOPRINE; BUSULFAN; CYCLOPHOSPHAMIDE; DEXAMETHASONE; FLUDARABINE; HYDROXYUREA; THIOTEPA; THYMOCYTE ANTIBODY; HLA ANTIGEN;

EID: 84981714779     PISSN: 10656251     EISSN: 15317048     Source Type: Journal    
DOI: 10.1097/MOH.0000000000000286     Document Type: Review
Times cited : (7)

References (32)
  • 2
    • 0019630298 scopus 로고
    • Haemoglobinopathies including thalassaemia.Part 1: Tropical Asia
    • Wasi P. Haemoglobinopathies including thalassaemia. Part 1: Tropical Asia. Clin Haematol 1981; 10:707-729.
    • (1981) Clin Haematol , vol.10 , pp. 707-729
    • Wasi, P.1
  • 3
    • 0033953189 scopus 로고    scopus 로고
    • Clinical and hematologic aspects of hemoglobin e beta-thalassemia
    • Fucharoen S, Winichagoon P. Clinical and hematologic aspects of hemoglobin E beta-thalassemia. Curr Opin Hematol 2000; 7:106-112.
    • (2000) Curr Opin Hematol , vol.7 , pp. 106-112
    • Fucharoen, S.1    Winichagoon, P.2
  • 4
    • 20844460608 scopus 로고    scopus 로고
    • Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine
    • Borgna-Pignatti C, Rugolotto S, De Stefano P, et al. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica 2004; 89:1187-1193.
    • (2004) Haematologica , vol.89 , pp. 1187-1193
    • Borgna-Pignatti, C.1    Rugolotto, S.2    De Stefano, P.3
  • 5
    • 79961008228 scopus 로고    scopus 로고
    • Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: Efficacy and safety during 5 years' follow-up
    • Cappellini MD, Bejaoui M, Agaoglu L, et al. Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: Efficacy and safety during 5 years' follow-up. Blood 2011; 118:884-893.
    • (2011) Blood , vol.118 , pp. 884-893
    • Cappellini, M.D.1    Bejaoui, M.2    Agaoglu, L.3
  • 6
    • 0019967483 scopus 로고
    • Marrow transplantation for thalassaemia
    • Thomas ED, Buckner CD, Sanders JE, et al. Marrow transplantation for thalassaemia. Lancet 1982; 2:227-229.
    • (1982) Lancet , vol.2 , pp. 227-229
    • Thomas, E.D.1    Buckner, C.D.2    Sanders, J.E.3
  • 7
    • 0025070260 scopus 로고
    • Bone marrow transplantation in patients with thalassemia
    • Lucarelli G, Galimberti M, Polchi P, et al. Bone marrow transplantation in patients with thalassemia. N Engl J Med 1990; 322:417-421.
    • (1990) N Engl J Med , vol.322 , pp. 417-421
    • Lucarelli, G.1    Galimberti, M.2    Polchi, P.3
  • 8
    • 0027184519 scopus 로고
    • Marrow transplantation in patients with thalassemia responsive to iron chelation therapy
    • Lucarelli G, Galimberti M, Polchi P, et al. Marrow transplantation in patients with thalassemia responsive to iron chelation therapy. N Engl J Med 1993; 329:840-844.
    • (1993) N Engl J Med , vol.329 , pp. 840-844
    • Lucarelli, G.1    Galimberti, M.2    Polchi, P.3
  • 9
    • 0036301696 scopus 로고    scopus 로고
    • The cure of thalassemia by bone marrow transplantation
    • Lucarelli G, Andreani M, Angelucci E. The cure of thalassemia by bone marrow transplantation. Blood Rev 2002; 16:81-85.
    • (2002) Blood Rev , vol.16 , pp. 81-85
    • Lucarelli, G.1    Andreani, M.2    Angelucci, E.3
  • 10
    • 13344276567 scopus 로고    scopus 로고
    • Marrow transplantation for patients with thalassemia: Results in class 3 patients
    • Lucarelli G, Clift RA, Galimberti M, et al. Marrow transplantation for patients with thalassemia: Results in class 3 patients. Blood 1996; 87:2082-2088.
    • (1996) Blood , vol.87 , pp. 2082-2088
    • Lucarelli, G.1    Clift, R.A.2    Galimberti, M.3
  • 11
    • 84899721999 scopus 로고    scopus 로고
    • Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel
    • Angelucci E, Matthes-Martin S, Baronciani D, et al. Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel. Haematologica 2014; 99:811-820.
    • (2014) Haematologica , vol.99 , pp. 811-820
    • Angelucci, E.1    Matthes-Martin, S.2    Baronciani, D.3
  • 12
    • 34447318137 scopus 로고    scopus 로고
    • A new stratification strategy that identifies a subset of class III patients with an adverse prognosis among children with beta thalassemia major undergoing a matched related allogeneic stem cell transplantation
    • Mathews V, George B, Deotare U, et al. A new stratification strategy that identifies a subset of class III patients with an adverse prognosis among children with beta thalassemia major undergoing a matched related allogeneic stem cell transplantation. Biol Blood Marrow Transplant 2007; 13:889-894.
    • (2007) Biol Blood Marrow Transplant , vol.13 , pp. 889-894
    • Mathews, V.1    George, B.2    Deotare, U.3
  • 13
    • 79551639277 scopus 로고    scopus 로고
    • HLA-matched sibling bone marrow transplantation for beta-thalassemia major
    • Sabloff M, Chandy M, Wang Z, et al. HLA-matched sibling bone marrow transplantation for beta-thalassemia major. Blood 2011; 117:1745-1750.
    • (2011) Blood , vol.117 , pp. 1745-1750
    • Sabloff, M.1    Chandy, M.2    Wang, Z.3
  • 14
    • 19244366141 scopus 로고    scopus 로고
    • New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years
    • Sodani P, Gaziev D, Polchi P, et al. New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years. Blood 2004; 104:1201-1203.
    • (2004) Blood , vol.104 , pp. 1201-1203
    • Sodani, P.1    Gaziev, D.2    Polchi, P.3
  • 15
    • 84944338667 scopus 로고    scopus 로고
    • Optimal outcomes in young class 3 patients with thalassemia undergoing HLA-identical sibling bone marrow transplantation
    • Gaziev J, Isgro A, Sodani P, et al. Optimal outcomes in young class 3 patients with thalassemia undergoing HLA-identical sibling bone marrow transplantation. Transplantation 2016; 100:925-932.
    • (2016) Transplantation , vol.100 , pp. 925-932
    • Gaziev, J.1    Isgro, A.2    Sodani, P.3
  • 16
    • 84876834095 scopus 로고    scopus 로고
    • Improved clinical outcomes of high risk beta thalassemia major patients undergoing a HLA matched related allogeneic stem cell transplant with a treosulfan based conditioning regimen and peripheral blood stem cell grafts
    • Mathews V, George B, Viswabandya A, et al. Improved clinical outcomes of high risk beta thalassemia major patients undergoing a HLA matched related allogeneic stem cell transplant with a treosulfan based conditioning regimen and peripheral blood stem cell grafts. PloS One 2013; 8:e61637.
    • (2013) PloS One , vol.8 , pp. e61637
    • Mathews, V.1    George, B.2    Viswabandya, A.3
  • 17
    • 84880435286 scopus 로고    scopus 로고
    • Pretransplant immunosuppression followed by reduced-toxicity conditioning and stem cell transplantation in high-risk thalassemia: A safe approach to disease control
    • Anurathapan U, Pakakasama S, Rujkijyanont P, et al. Pretransplant immunosuppression followed by reduced-toxicity conditioning and stem cell transplantation in high-risk thalassemia: A safe approach to disease control. Biol Blood Marrow Transplant 2013; 19:1259-1262.
    • (2013) Biol Blood Marrow Transplant , vol.19 , pp. 1259-1262
    • Anurathapan, U.1    Pakakasama, S.2    Rujkijyanont, P.3
  • 18
    • 84912110334 scopus 로고    scopus 로고
    • Outcomes of thalassemia patients undergoing hematopoietic stem cell transplantation by using a standard myeloablative versus a novel reduced-toxicity conditioning regimen according to a new risk stratification
    • Anurathapan U, Pakakasama S, Mekjaruskul P, et al. Outcomes of thalassemia patients undergoing hematopoietic stem cell transplantation by using a standard myeloablative versus a novel reduced-toxicity conditioning regimen according to a new risk stratification. Biol Blood Marrow Transplant 2014; 20:2066-2071.
    • (2014) Biol Blood Marrow Transplant , vol.20 , pp. 2066-2071
    • Anurathapan, U.1    Pakakasama, S.2    Mekjaruskul, P.3
  • 19
    • 0033558264 scopus 로고    scopus 로고
    • Bone marrow transplantation in adult thalassemic patients
    • Lucarelli G, Clift RA, Galimberti M, et al. Bone marrow transplantation in adult thalassemic patients. Blood 1999; 93:1164-1167.
    • (1999) Blood , vol.93 , pp. 1164-1167
    • Lucarelli, G.1    Clift, R.A.2    Galimberti, M.3
  • 20
    • 0028821145 scopus 로고
    • Transplantation of cord-blood stem cells into a patient with severe thalassemia
    • Issaragrisil S, Visuthisakchai S, Suvatte V, et al. Transplantation of cord-blood stem cells into a patient with severe thalassemia. N Engl J Med 1995; 332:367-369.
    • (1995) N Engl J Med , vol.332 , pp. 367-369
    • Issaragrisil, S.1    Visuthisakchai, S.2    Suvatte, V.3
  • 21
    • 0037443543 scopus 로고    scopus 로고
    • Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease
    • Locatelli F, Rocha V, ReedW, et al. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. Blood 2003; 101:2137-2143.
    • (2003) Blood , vol.101 , pp. 2137-2143
    • Locatelli, F.1    Rocha, V.2    ReedW3
  • 22
    • 84886897873 scopus 로고    scopus 로고
    • Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling
    • Locatelli F, Kabbara N, Ruggeri A, et al. Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling. Blood 2013; 122:1072-1078.
    • (2013) Blood , vol.122 , pp. 1072-1078
    • Locatelli, F.1    Kabbara, N.2    Ruggeri, A.3
  • 23
    • 84954526227 scopus 로고    scopus 로고
    • Hemopoietic stem cell transplantation in thalassemia: A report from the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry, 2000-2010
    • Baronciani D, Angelucci E, Potschger U, et al. Hemopoietic stem cell transplantation in thalassemia: A report from the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry, 2000-2010. Bone Marrow Transplant 2016; 51:536-541
    • (2016) Bone Marrow Transplant , vol.51 , pp. 536-541
    • Baronciani, D.1    Angelucci, E.2    Potschger, U.3
  • 24
    • 29744438595 scopus 로고    scopus 로고
    • Bone marrow transplantation in adults with thalassemia: Treatment and long-term follow-up
    • Gaziev J, Sodani P, Polchi P, et al. Bone marrow transplantation in adults with thalassemia: Treatment and long-term follow-up. Ann N Y Acad Sci 2005; 1054:196-205.
    • (2005) Ann N y Acad Sci , vol.1054 , pp. 196-205
    • Gaziev, J.1    Sodani, P.2    Polchi, P.3
  • 25
    • 84864866509 scopus 로고    scopus 로고
    • HLA-matched sibling stem cell transplantation in children with beta-thalassemia with anti-thymocyte globulin as part of the preparative regimen: The Greek experience
    • Goussetis E, Peristeri I, Kitra V, et al. HLA-matched sibling stem cell transplantation in children with beta-thalassemia with anti-thymocyte globulin as part of the preparative regimen: The Greek experience. Bone Marrow Transplant 2012; 47:1061-1066.
    • (2012) Bone Marrow Transplant , vol.47 , pp. 1061-1066
    • Goussetis, E.1    Peristeri, I.2    Kitra, V.3
  • 26
    • 84871922030 scopus 로고    scopus 로고
    • French multicenter 22-year experience in stem cell transplantation for beta-thalassemia major: Lessons and future directions
    • Galambrun C, Pondarre C, Bertrand Y, et al. French multicenter 22-year experience in stem cell transplantation for beta-thalassemia major: Lessons and future directions. Biol Blood Marrow Transplant 2013; 19:62-68.
    • (2013) Biol Blood Marrow Transplant , vol.19 , pp. 62-68
    • Galambrun, C.1    Pondarre, C.2    Bertrand, Y.3
  • 27
    • 84958073437 scopus 로고    scopus 로고
    • Hematopoietic stem cell transplantation for homozygous beta-thalassemia and beta-thalassemia/hemoglobin e patients from haploidentical donors
    • Anurathapan U, Hongeng S, Pakakasama S, et al. Hematopoietic stem cell transplantation for homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients from haploidentical donors. Bone Marrow Transplant 2016; 51:813-818.
    • (2016) Bone Marrow Transplant , vol.51 , pp. 813-818
    • Anurathapan, U.1    Hongeng, S.2    Pakakasama, S.3
  • 28
    • 0033996420 scopus 로고    scopus 로고
    • Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation
    • Andreani M, Nesci S, Lucarelli G, et al. Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation. Bone Marrow Transplant 2000; 25:401-404.
    • (2000) Bone Marrow Transplant , vol.25 , pp. 401-404
    • Andreani, M.1    Nesci, S.2    Lucarelli, G.3
  • 29
    • 47749098306 scopus 로고    scopus 로고
    • Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia
    • Andreani M, Testi M, Battarra M, et al. Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia. Blood Transfus 2008; 6:143-149.
    • (2008) Blood Transfus , vol.6 , pp. 143-149
    • Andreani, M.1    Testi, M.2    Battarra, M.3
  • 30
    • 84894269854 scopus 로고    scopus 로고
    • Mixed chimerism in haemoglobinopathies: From risk of graft rejection to immune tolerance
    • Andreani M, Testi M, Lucarelli G. Mixed chimerism in haemoglobinopathies: From risk of graft rejection to immune tolerance. Tissue Antigens 2014; 83:137-146.
    • (2014) Tissue Antigens , vol.83 , pp. 137-146
    • Andreani, M.1    Testi, M.2    Lucarelli, G.3
  • 31
    • 84962204190 scopus 로고    scopus 로고
    • Management of iron overload before, during, and after hematopoietic stem cell transplantation for thalassemia major
    • Angelucci E, Pilo F. Management of iron overload before, during, and after hematopoietic stem cell transplantation for thalassemia major. Ann N Y Acad Sci 2016; 1368:115-121.
    • (2016) Ann N y Acad Sci , vol.1368 , pp. 115-121
    • Angelucci, E.1    Pilo, F.2
  • 32
    • 0029080340 scopus 로고
    • Intravenous chelation therapy during transplantation for thalassemia
    • Gaziev D, Giardini C, Angelucci E, et al. Intravenous chelation therapy during transplantation for thalassemia. Haematologica 1995; 80:300-304.
    • (1995) Haematologica , vol.80 , pp. 300-304
    • Gaziev, D.1    Giardini, C.2    Angelucci, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.