메뉴 건너뛰기




Volumn 48, Issue 9, 2013, Pages 1168-1172

Reduced intensity conditioning is effective for hematopoietic SCT in dyskeratosis congenita-related BM failure

Author keywords

CBT; DKC; EMRO; Hematopoietic SCT; MUD; Trends

Indexed keywords

BUSULFAN; CYCLOPHOSPHAMIDE; CYCLOSPORIN A; FLUDARABINE; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; METHOTREXATE; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; THYMOCYTE ANTIBODY;

EID: 84883742527     PISSN: 02683369     EISSN: 14765365     Source Type: Journal    
DOI: 10.1038/bmt.2013.35     Document Type: Article
Times cited : (52)

References (35)
  • 1
    • 0000605996 scopus 로고
    • Atrophia cutis reticularis cum pigmentations, dystrophia unguium et leukoplakis oris (Poikioodermia atrophicans vascularis Jacobi.)
    • Zinsser F. Atrophia cutis reticularis cum pigmentations, dystrophia unguium et leukoplakis oris (Poikioodermia atrophicans vascularis Jacobi.). Ikonogr Dermatol 1910; 5: 219-223.
    • (1910) Ikonogr Dermatol , vol.5 , pp. 219-223
    • Zinsser, F.1
  • 2
    • 84921685373 scopus 로고
    • Dyskeratosis congenita
    • In: Pagon RA, Bird TD, Dolan CR, Stephens K (eds). University of Washington: Seattle, WA, USA
    • Savage SA. Dyskeratosis Congenita. In: Pagon RA, Bird TD, Dolan CR, Stephens K (eds). Gene Reviews [Internet]. University of Washington: Seattle, WA, USA, 1993-2009.
    • (1993) Gene Reviews [Internet]
    • Savage, S.A.1
  • 4
    • 64249090973 scopus 로고    scopus 로고
    • Dyskeratosis congenita, stem cells and telomeres
    • Kirwan M, Dokal I. Dyskeratosis congenita, stem cells and telomeres. Biochim Biophys Acta 2009; 1792: 371-379.
    • (2009) Biochim Biophys Acta , vol.1792 , pp. 371-379
    • Kirwan, M.1    Dokal, I.2
  • 5
    • 34848872850 scopus 로고    scopus 로고
    • Dyskeratosis congenita. Report of a case with literature review
    • Auluck A. Dyskeratosis congenita. Report of a case with literature review. Med Oral Patol Oral Cir Bucal 2007; 12: E369-E373.
    • (2007) Med Oral Patol Oral Cir Bucal , vol.12
    • Auluck, A.1
  • 6
    • 0035002944 scopus 로고    scopus 로고
    • Identification of novel DKC1 mutations in patients with dyskeratosis congenita: Implications for pathophysiology and diagnosis
    • Knight SW, Vulliamy TJ, Morgan B, Devriendt K, Mason PJ, Dokal I. Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosis. Hum Genet 2001; 108: 299-303.
    • (2001) Hum Genet , vol.108 , pp. 299-303
    • Knight, S.W.1    Vulliamy, T.J.2    Morgan, B.3    Devriendt, K.4    Mason, P.J.5    Dokal, I.6
  • 7
    • 78549268108 scopus 로고    scopus 로고
    • Recent progress in dyskeratosis congenita
    • Nishio N, Kojima S. Recent progress in dyskeratosis congenita. Int J Hematol 2010; 92: 419-424.
    • (2010) Int J Hematol , vol.92 , pp. 419-424
    • Nishio, N.1    Kojima, S.2
  • 8
    • 34547410832 scopus 로고    scopus 로고
    • Dyskeratosis congenita: Advances in the understanding of the telomerase defect and the role of stem cell transplantation
    • De la Fuente J, Dokal I. Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantation. Pediatr Transplant 2007; 11: 584-594.
    • (2007) Pediatr Transplant , vol.11 , pp. 584-594
    • De La Fuente, J.1    Dokal, I.2
  • 9
    • 84885379730 scopus 로고    scopus 로고
    • Dyskeratosis congenita: Low regimen-related toxicity following hematopoietic cell transplantation (HCT) using a reduced intensity conditioning regimen
    • Tolar J, Orchard PJ, Miller JS, MacMillan ML, Wagner JE, Alter BP et al. Dyskeratosis congenita: low regimen-related toxicity following hematopoietic cell transplantation (HCT) using a reduced intensity conditioning regimen. Blood 2007; 110: 2005.
    • (2005) Blood 2007 , vol.110
    • Tolar, J.1    Orchard, P.J.2    Miller, J.S.3    MacMillan, M.L.4    Wagner, J.E.5    Alter, B.P.6
  • 10
    • 0038621756 scopus 로고    scopus 로고
    • Low-intensity hematopoietic stem-cell transplantation across human leucocyte antigen barriers in dyskeratosis congenita
    • Dror Y, Freedman MH, Leaker M, Verbeek J, Armstrong CA, Saunders FE et al. Low-intensity hematopoietic stem-cell transplantation across human leucocyte antigen barriers in dyskeratosis congenita. Bone Marrow Transplant 2003; 31: 847-850.
    • (2003) Bone Marrow Transplant , vol.31 , pp. 847-850
    • Dror, Y.1    Freedman, M.H.2    Leaker, M.3    Verbeek, J.4    Armstrong, C.A.5    Saunders, F.E.6
  • 12
    • 78651373073 scopus 로고    scopus 로고
    • Disease-specific hematopoietic cell transplantation: Nonmyeloablative conditioning regimen for dyskeratosis congenita
    • Dietz AC, Orchard PJ, Baker KS, Giller RH, Savage SA, Alter BP et al. Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita. Bone Marrow Transplant 2011; 46: 98-104.
    • (2011) Bone Marrow Transplant , vol.46 , pp. 98-104
    • Dietz, A.C.1    Orchard, P.J.2    Baker, K.S.3    Giller, R.H.4    Savage, S.A.5    Alter, B.P.6
  • 14
    • 84866004422 scopus 로고    scopus 로고
    • A reduced intensity conditioning regimen of fludarabine, cyclophosphamide, antithymocyte globulin, plus 2 Gy TBI facilitates successful hematopoietic cell engraftment in an adult with dyskeratosis congenita
    • Kharfan-Dabaja MA, Otrock ZK, Bacigalupo A, Mahfouz RA, Geara F, Bazarbachi A. A reduced intensity conditioning regimen of fludarabine, cyclophosphamide, antithymocyte globulin, plus 2 Gy TBI facilitates successful hematopoietic cell engraftment in an adult with dyskeratosis congenita. Bone Marrow Transplant 2012; 47: 1254-1255.
    • (2012) Bone Marrow Transplant , vol.47 , pp. 1254-1255
    • Kharfan-Dabaja, M.A.1    Otrock, Z.K.2    Bacigalupo, A.3    Mahfouz, R.A.4    Geara, F.5    Bazarbachi, A.6
  • 15
    • 34249792115 scopus 로고    scopus 로고
    • Allogeneic stem cell transplantation in a patient with dyskeratosis congenita after conditioning with low-dose cyclophosphamide and anti-thymocyte globulin
    • Ayas M, Al-Musa A, Al-Jefri A, Al-Seraihi A, Al-Mahr M, Rifai S et al. Allogeneic stem cell transplantation in a patient with dyskeratosis congenita after conditioning with low-dose cyclophosphamide and anti-thymocyte globulin. Pediatr Blood Cancer 2007; 49: 103-104.
    • (2007) Pediatr Blood Cancer , vol.49 , pp. 103-104
    • Ayas, M.1    Al-Musa, A.2    Al-Jefri, A.3    Al-Seraihi, A.4    Al-Mahr, M.5    Rifai, S.6
  • 16
    • 0344851536 scopus 로고    scopus 로고
    • Late presentation of dyskeratosis congenita as apparently acquired aplastic anemia due to mutations in telomerase RNA
    • Fogarty PF, Yamaguchi H, Wiestner A, Baerlocher GM, Sloand E, Zeng WS et al. Late presentation of dyskeratosis congenita as apparently acquired aplastic anemia due to mutations in telomerase RNA. Lancet 2003; 362: 1628-1630.
    • (2003) Lancet , vol.362 , pp. 1628-1630
    • Fogarty, P.F.1    Yamaguchi, H.2    Wiestner, A.3    Baerlocher, G.M.4    Sloand, E.5    Zeng, W.S.6
  • 17
    • 0028122239 scopus 로고
    • Dyskeratosis congenita is a chromosomal instability disorder
    • Dokal I, Luzzatto L. Dyskeratosis congenita is a chromosomal instability disorder. Leuk Lymphoma 1994; 15: 1-7.
    • (1994) Leuk Lymphoma , vol.15 , pp. 1-7
    • Dokal, I.1    Luzzatto, L.2
  • 18
    • 0031656541 scopus 로고    scopus 로고
    • Unusual complications after bone marrow transplantation for dyskeratosis congenita
    • Rocha V, Devergie A, Socié G, Ribaud P, Espérou H, Parquet N et al. Unusual complications after bone marrow transplantation for dyskeratosis congenita. Br J Haematol 1998; 103: 243-248.
    • (1998) Br J Haematol , vol.103 , pp. 243-248
    • Rocha, V.1    Devergie, A.2    Socié, G.3    Ribaud, P.4    Espérou, H.5    Parquet, N.6
  • 20
    • 30544453376 scopus 로고    scopus 로고
    • Fatal diffuse capillaritis after haematopoietic stem cell transplantation for dyskeratosis congenita despite low-intensity conditioningreg regimen
    • Brazzola P, Duval M, Fournet JC, Gauvin F, Dalle JH, Champagne MA et al. Fatal diffuse capillaritis after haematopoietic stem cell transplantation for dyskeratosis congenita despite low-intensity conditioningreg regimen. Bone Marrow Transplant 2005; 36: 1103-1105.
    • (2005) Bone Marrow Transplant , vol.36 , pp. 1103-1105
    • Brazzola, P.1    Duval, M.2    Fournet, J.C.3    Gauvin, F.4    Dalle, J.H.5    Champagne, M.A.6
  • 21
    • 35648971048 scopus 로고    scopus 로고
    • Late death after unrelated-BMT for dyskeratosis congenita following conditioning with alemtuzumab, fludarabine and melphalan
    • Amarasinghe K, Dalley C, Dokal I, Laurie A, Gupta V, Marsh J. Late death after unrelated-BMT for dyskeratosis congenita following conditioning with alemtuzumab, fludarabine and melphalan. Bone Marrow Transplant 2007; 40: 913-914.
    • (2007) Bone Marrow Transplant , vol.40 , pp. 913-914
    • Amarasinghe, K.1    Dalley, C.2    Dokal, I.3    Laurie, A.4    Gupta, V.5    Marsh, J.6
  • 22
    • 0031045320 scopus 로고    scopus 로고
    • Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation
    • Yabe M, Yabe H, Hattori K, Morimoto T, Hinohara T, Takakura I et al. Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation. Bone Marrow Transplant 1997; 19: 389-392.
    • (1997) Bone Marrow Transplant , vol.19 , pp. 389-392
    • Yabe, M.1    Yabe, H.2    Hattori, K.3    Morimoto, T.4    Hinohara, T.5    Takakura, I.6
  • 24
    • 78650978155 scopus 로고    scopus 로고
    • Eurocord and SAAWP from EBMT. Outcomes after related and unrelated umbilical cord blood transplantation for hereditary bone marrow failure syndromes other than Fanconi anemia
    • Bizzetto R, Bonfim C, Rocha V, Socié G, Locatelli F, Chan K et al. Eurocord and SAAWP from EBMT. Outcomes after related and unrelated umbilical cord blood transplantation for hereditary bone marrow failure syndromes other than Fanconi anemia. Haematologica 2011; 96: 134-141.
    • (2011) Haematologica , vol.96 , pp. 134-141
    • Bizzetto, R.1    Bonfim, C.2    Rocha, V.3    Socié, G.4    Locatelli, F.5    Chan, K.6
  • 25
    • 0007397245 scopus 로고
    • Elevated levels and multimer pattern of von Willebrand factor in patients with dyskeratosis congenita
    • Dokal I, Manning R, Laffan M. Elevated levels and multimer pattern of von Willebrand factor in patients with dyskeratosis congenita. Br J Haematol 1995; 89: 33.
    • (1995) Br J Haematol , vol.89 , pp. 33
    • Dokal, I.1    Manning, R.2    Laffan, M.3
  • 26
    • 0034663152 scopus 로고    scopus 로고
    • Nonmyeloablative stem cell transplantation for congenital immunodeficiencies
    • Amrolia P, Gaspar HB, Hassan A, Webb D, Jones A, Sturt N et al. Nonmyeloablative stem cell transplantation for congenital immunodeficiencies. Blood 2000; 96: 1239-1246.
    • (2000) Blood , vol.96 , pp. 1239-1246
    • Amrolia, P.1    Gaspar, H.B.2    Hassan, A.3    Webb, D.4    Jones, A.5    Sturt, N.6
  • 27
    • 0037356063 scopus 로고    scopus 로고
    • Nonmyeloablative allogeneic hematopoietic stem cell transplantation for treatment of dyskeratosis congenita
    • Gungor T, Corbacioglu S, Storb R, Seger RA. Nonmyeloablative allogeneic hematopoietic stem cell transplantation for treatment of dyskeratosis congenita. Bone Marrow Transplant 2003; 31: 407-410.
    • (2003) Bone Marrow Transplant , vol.31 , pp. 407-410
    • Gungor, T.1    Corbacioglu, S.2    Storb, R.3    Seger, R.A.4
  • 29
    • 20044379963 scopus 로고    scopus 로고
    • Usual interstitial pneumonia complicating dyskeratosis congenita
    • Utz JP, Ryu JH, Myers JL, Michels VV. Usual interstitial pneumonia complicating dyskeratosis congenita. Mayo Clin Proc 2005; 80: 817-821.
    • (2005) Mayo Clin Proc , vol.80 , pp. 817-821
    • Utz, J.P.1    Ryu, J.H.2    Myers, J.L.3    Michels, V.V.4
  • 30
    • 77954339095 scopus 로고    scopus 로고
    • Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
    • Alter BP, Giri N, Savage SA, Peters JA, Loud JT, Leathwood L et al. Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study. Br J Haematol 2010; 150: 179-188.
    • (2010) Br J Haematol , vol.150 , pp. 179-188
    • Alter, B.P.1    Giri, N.2    Savage, S.A.3    Peters, J.A.4    Loud, J.T.5    Leathwood, L.6
  • 31
    • 74049111326 scopus 로고    scopus 로고
    • Telomeres and telomerase in cancer
    • Artandi SE, DePinho RA. Telomeres and telomerase in cancer. Carcinogenesis 2010; 31: 9-18.
    • (2010) Carcinogenesis , vol.31 , pp. 9-18
    • Artandi, S.E.1    Depinho, R.A.2
  • 32
    • 0032717119 scopus 로고    scopus 로고
    • Hematopoietic stem-cell transplantation using unrelated cord-blood versus matched sibling marrow in pediatric bone marrow failure syndrome: One center's experience
    • Shaw PH, Haut PR, Olszewski M, Kletzel M. Hematopoietic stem-cell transplantation using unrelated cord-blood versus matched sibling marrow in pediatric bone marrow failure syndrome: one center's experience. Pediatr Transplant 1999; 3: 315-321.
    • (1999) Pediatr Transplant , vol.3 , pp. 315-321
    • Shaw, P.H.1    Haut, P.R.2    Olszewski, M.3    Kletzel, M.4
  • 33
    • 7244234131 scopus 로고    scopus 로고
    • Androgens and liver tumors: Fanconi's anemia and non-Fanconi's conditions
    • Velazquez I, Alter BP. Androgens and liver tumors: Fanconi's anemia and non-Fanconi's conditions. Am J Hematol 2004; 77: 257-267.
    • (2004) Am J Hematol , vol.77 , pp. 257-267
    • Velazquez, I.1    Alter, B.P.2
  • 34
    • 34548153469 scopus 로고    scopus 로고
    • Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor
    • Giri N, Pitel PA, Green D, Alter BP. Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor. Br J Haematol 2007; 138: 815-817.
    • (2007) Br J Haematol , vol.138 , pp. 815-817
    • Giri, N.1    Pitel, P.A.2    Green, D.3    Alter, B.P.4
  • 35
    • 77958533701 scopus 로고    scopus 로고
    • Reduced-intensity conditioning using fludarabine and antithymocyte globulin alone allows stable engraftment in a patient with dyskeratosis congenita
    • Vuong LG, Hemmati PG, Neuburger S, Terwey TH, Vulliamy T, Dokal I et al. Reduced-intensity conditioning using fludarabine and antithymocyte globulin alone allows stable engraftment in a patient with dyskeratosis congenita. Acta Haematol 2010; 124: 200-203.
    • (2010) Acta Haematol , vol.124 , pp. 200-203
    • Vuong, L.G.1    Hemmati, P.G.2    Neuburger, S.3    Terwey, T.H.4    Vulliamy, T.5    Dokal, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.