메뉴 건너뛰기




Volumn 13, Issue SUPPL. 1, 2007, Pages 64-72

Philadelphia Chromosome-Negative Myeloproliferative Disorders: Biology and Treatment

Author keywords

Essential thrombocythemia; Idiopathic myelofibrosis; JAK2; Myeloproliferative disorders; Polycythemiavera; Stem cell transplantation

Indexed keywords

ACETYLSALICYLIC ACID; ANAGRELIDE; BUSULFAN; CYCLOPHOSPHAMIDE; DANAZOL; ERYTHROPOIETIN; FLUDARABINE; HYDROXYUREA; INTERFERON; JANUS KINASE 2; LENALIDOMIDE; MELPHALAN; PEGINTERFERON; STAT PROTEIN; THALIDOMIDE; THIOTEPA; THROMBOPOIETIN RECEPTOR; THYMOCYTE ANTIBODY;

EID: 33846028528     PISSN: 10838791     EISSN: 15236536     Source Type: Journal    
DOI: 10.1016/j.bbmt.2006.11.003     Document Type: Article
Times cited : (39)

References (68)
  • 1
    • 0001639195 scopus 로고
    • Some speculations on the myeloproliferative syndromes
    • Dameshek W. Some speculations on the myeloproliferative syndromes. Blood 6 (1951) 372-375
    • (1951) Blood , vol.6 , pp. 372-375
    • Dameshek, W.1
  • 2
    • 17844383458 scopus 로고    scopus 로고
    • A unique JAK2 mutation leading to constitute signaling causes polycythaemia vera
    • James C., Ugo V., Le Couedic J.P., et al. A unique JAK2 mutation leading to constitute signaling causes polycythaemia vera. Nature 434 (2005) 1144-1148
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couedic, J.P.3
  • 3
    • 33746437130 scopus 로고    scopus 로고
    • MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia
    • [epub ahead of print]
    • Pikman Y., Lee B.H., Mercher T., et al. MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med 3 (2006) e270 [epub ahead of print]
    • (2006) PLoS Med , vol.3
    • Pikman, Y.1    Lee, B.H.2    Mercher, T.3
  • 4
    • 0016391236 scopus 로고
    • Bone marrow responses in polycythemia vera
    • (letter)
    • Prchal J.F., and Axelrad A.A. Bone marrow responses in polycythemia vera. N Engl J Med 290 (1974) 1382 (letter)
    • (1974) N Engl J Med , vol.290 , pp. 1382
    • Prchal, J.F.1    Axelrad, A.A.2
  • 5
    • 0028045069 scopus 로고
    • Circulating erythroid progenitors in polycythemia vera are hypersensitive to insulin-like growth factor-1 in vitro: studies in an improved serum-free medium
    • Correa P.N., Eskinazi D., and Axelrad A.A. Circulating erythroid progenitors in polycythemia vera are hypersensitive to insulin-like growth factor-1 in vitro: studies in an improved serum-free medium. Blood 83 (1994) 99-112
    • (1994) Blood , vol.83 , pp. 99-112
    • Correa, P.N.1    Eskinazi, D.2    Axelrad, A.A.3
  • 6
    • 0026667283 scopus 로고
    • Polycythemia vera, II: hypersensitivity of bone marrow erythroid, granulocyte-macrophage, and megakaryocyte progenitor cells to interleukin-3 and granulocytes macrophage colony-stimulating factor
    • Dai C.H., Krantz S.B., Dessypris E.N., et al. Polycythemia vera, II: hypersensitivity of bone marrow erythroid, granulocyte-macrophage, and megakaryocyte progenitor cells to interleukin-3 and granulocytes macrophage colony-stimulating factor. Blood 80 (1992) 891-899
    • (1992) Blood , vol.80 , pp. 891-899
    • Dai, C.H.1    Krantz, S.B.2    Dessypris, E.N.3
  • 7
    • 13144256114 scopus 로고
    • Differences in gene expression between normal and polycythemia vera CD34 cells
    • (abstr.)
    • Kralovics R., Guan Y., and Prchal J.T. Differences in gene expression between normal and polycythemia vera CD34 cells. Blood 86 (1995) 733a (abstr.)
    • (1995) Blood , vol.86
    • Kralovics, R.1    Guan, Y.2    Prchal, J.T.3
  • 8
    • 0031010122 scopus 로고    scopus 로고
    • Selective expression of mRNA coding for the truncated form of erythropoietin receptor in hematopoietic cells and its decrease in patients with polycythemia vera
    • Chiba S., Takahashi T., Takeshita K., et al. Selective expression of mRNA coding for the truncated form of erythropoietin receptor in hematopoietic cells and its decrease in patients with polycythemia vera. Blood 90 (1997) 97-104
    • (1997) Blood , vol.90 , pp. 97-104
    • Chiba, S.1    Takahashi, T.2    Takeshita, K.3
  • 9
    • 0034656066 scopus 로고    scopus 로고
    • Cloning of PRV-1, a novel member of the uPAR receptor superfamily, which is overexpressed in polycythemia rubra vera
    • Temerinac S., Klippel S., Strunck E., et al. Cloning of PRV-1, a novel member of the uPAR receptor superfamily, which is overexpressed in polycythemia rubra vera. Blood 95 (2000) 2569-2576
    • (2000) Blood , vol.95 , pp. 2569-2576
    • Temerinac, S.1    Klippel, S.2    Strunck, E.3
  • 10
    • 0032568003 scopus 로고    scopus 로고
    • Expression of Bcl-x in erythroid precursors from patients with polycythemia vera
    • Silva M., Richard C., Benito A., et al. Expression of Bcl-x in erythroid precursors from patients with polycythemia vera. N Engl J Med 338 (1998) 564-567
    • (1998) N Engl J Med , vol.338 , pp. 564-567
    • Silva, M.1    Richard, C.2    Benito, A.3
  • 11
    • 0035383807 scopus 로고    scopus 로고
    • Increased expression of the INK4a/ARF locus in polycythemia vera
    • 3424-332
    • Dai C., and Krantz S.B. Increased expression of the INK4a/ARF locus in polycythemia vera. Blood 97 (2001) 3424-332
    • (2001) Blood , vol.97
    • Dai, C.1    Krantz, S.B.2
  • 12
    • 0030791577 scopus 로고    scopus 로고
    • Identification of increased protein tyrosine phosphatase activity in polycythemia vera erythroid progenitor cells
    • Sui X., Krantz S.B., and Zhao Z. Identification of increased protein tyrosine phosphatase activity in polycythemia vera erythroid progenitor cells. Blood 90 (1997) 651-657
    • (1997) Blood , vol.90 , pp. 651-657
    • Sui, X.1    Krantz, S.B.2    Zhao, Z.3
  • 13
    • 0036191941 scopus 로고    scopus 로고
    • Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
    • Kralovics R., Guan Y., and Prchal J.T. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 30 (2002) 229-236
    • (2002) Exp Hematol , vol.30 , pp. 229-236
    • Kralovics, R.1    Guan, Y.2    Prchal, J.T.3
  • 14
    • 33845969986 scopus 로고    scopus 로고
    • The polycythemia vera and other polycythemic disorders: biological aspects
    • Melo J.V., and Goldman J.M. (Eds), Springer-Verlag, New York
    • Ang S.O., and Prchal J.T. The polycythemia vera and other polycythemic disorders: biological aspects. In: Melo J.V., and Goldman J.M. (Eds). Myeloproliferative Diseases (2006), Springer-Verlag, New York 297-319
    • (2006) Myeloproliferative Diseases , pp. 297-319
    • Ang, S.O.1    Prchal, J.T.2
  • 15
    • 0035694582 scopus 로고    scopus 로고
    • The N-terminal domain of Janus kinase 2 is required for golgi processing and cell surface expression of erythropoietin receptor
    • Huang L.J., Constantinescu S.N., and Lodish H.F. The N-terminal domain of Janus kinase 2 is required for golgi processing and cell surface expression of erythropoietin receptor. Mol Cell 8 (2001) 1327-1338
    • (2001) Mol Cell , vol.8 , pp. 1327-1338
    • Huang, L.J.1    Constantinescu, S.N.2    Lodish, H.F.3
  • 16
    • 0842309105 scopus 로고    scopus 로고
    • Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera
    • Ugo V., Marzac C., Teyssandier I., et al. Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera. Exp Hematol 32 (2004) 179-187
    • (2004) Exp Hematol , vol.32 , pp. 179-187
    • Ugo, V.1    Marzac, C.2    Teyssandier, I.3
  • 17
    • 33645450223 scopus 로고    scopus 로고
    • The effect of the JAK2 V617F mutation of PRV-1 expression
    • Mnjoyan Z., Yoon D., Li J., et al. The effect of the JAK2 V617F mutation of PRV-1 expression. Haematologica 91 (2006) 411-412
    • (2006) Haematologica , vol.91 , pp. 411-412
    • Mnjoyan, Z.1    Yoon, D.2    Li, J.3
  • 18
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Baxter E.J., Scott L.M., Campbell P.J., et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365 (2005) 1054-1061
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scott, L.M.2    Campbell, P.J.3
  • 19
    • 17644424955 scopus 로고    scopus 로고
    • A gain-of-function mutation of JAK2 in myeloproliferative disorders
    • Kralovics R., Passamonti F., Buser A.S., et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 352 (2005) 1779-1790
    • (2005) N Engl J Med , vol.352 , pp. 1779-1790
    • Kralovics, R.1    Passamonti, F.2    Buser, A.S.3
  • 20
    • 33646400413 scopus 로고    scopus 로고
    • The molecular basis of polycythemia vera unraveled?
    • Emanuel P., and Prchal J.T. The molecular basis of polycythemia vera unraveled?. The Hematologist 2 (2005) 1-2
    • (2005) The Hematologist , vol.2 , pp. 1-2
    • Emanuel, P.1    Prchal, J.T.2
  • 21
    • 20244369569 scopus 로고    scopus 로고
    • Activating mutation in the tyrosine kinase JAK2 in polycythaemia vera, essential thrombocythemia and myeloid metaplasia with myelofibrosis
    • Levine R.L., Wadleigh M., Cools J., et al. Activating mutation in the tyrosine kinase JAK2 in polycythaemia vera, essential thrombocythemia and myeloid metaplasia with myelofibrosis. Cancer Cell 7 (2005) 387-397
    • (2005) Cancer Cell , vol.7 , pp. 387-397
    • Levine, R.L.1    Wadleigh, M.2    Cools, J.3
  • 22
    • 21344440357 scopus 로고    scopus 로고
    • The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
    • Steensma D.P., Dewald G.W., Lasho T.L., et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood 106 (2005) 1207-1209
    • (2005) Blood , vol.106 , pp. 1207-1209
    • Steensma, D.P.1    Dewald, G.W.2    Lasho, T.L.3
  • 23
    • 25844447519 scopus 로고    scopus 로고
    • JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
    • Jelinek J., Oki Y., Gharibyan V., et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. Blood 106 (2005) 3370-3373
    • (2005) Blood , vol.106 , pp. 3370-3373
    • Jelinek, J.1    Oki, Y.2    Gharibyan, V.3
  • 24
    • 31544477194 scopus 로고    scopus 로고
    • The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera
    • Tefferi A., Lasho T.L., Schwager S.M., et al. The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera. Cancer 106 (2006) 631-635
    • (2006) Cancer , vol.106 , pp. 631-635
    • Tefferi, A.1    Lasho, T.L.2    Schwager, S.M.3
  • 25
    • 33646405714 scopus 로고    scopus 로고
    • High levels of circulating CD34 cells, dacrocytes, clonal hematopoiesis, and JAK2 mutation differentiate myelofibrosis with myeloid metaplasia from secondary myelofibrosis associated with pulmonary hypertension
    • Popat U., Frost A., Liu E., et al. High levels of circulating CD34 cells, dacrocytes, clonal hematopoiesis, and JAK2 mutation differentiate myelofibrosis with myeloid metaplasia from secondary myelofibrosis associated with pulmonary hypertension. Blood 107 (2006) 3486-3488
    • (2006) Blood , vol.107 , pp. 3486-3488
    • Popat, U.1    Frost, A.2    Liu, E.3
  • 26
    • 33750534561 scopus 로고    scopus 로고
    • MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients
    • Jul 25 [epub ahead of print]
    • Pardanani A.D., Levine R.L., Lasho T., et al. MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood (2006) Jul 25 [epub ahead of print]
    • (2006) Blood
    • Pardanani, A.D.1    Levine, R.L.2    Lasho, T.3
  • 27
    • 32144461605 scopus 로고    scopus 로고
    • Essential thrombocythemia beyond the first decade: life expectancy, long-term complication rates, and prognostic factors
    • Wolanskyj A.P., Schwager S.M., McClure R.F., et al. Essential thrombocythemia beyond the first decade: life expectancy, long-term complication rates, and prognostic factors. Mayo Clin Proc 81 (2006) 159-166
    • (2006) Mayo Clin Proc , vol.81 , pp. 159-166
    • Wolanskyj, A.P.1    Schwager, S.M.2    McClure, R.F.3
  • 28
    • 28944455594 scopus 로고    scopus 로고
    • Long-term outcome of 231 patients with essential thrombocythemia: prognostic factors for thrombosis, bleeding, myelofibrosis and leukemia
    • Chim C.S., Kwong Y.L., Kwok-Wei Lie A., et al. Long-term outcome of 231 patients with essential thrombocythemia: prognostic factors for thrombosis, bleeding, myelofibrosis and leukemia. Arch Intern Med 165 (2005) 2651-2658
    • (2005) Arch Intern Med , vol.165 , pp. 2651-2658
    • Chim, C.S.1    Kwong, Y.L.2    Kwok-Wei Lie, A.3
  • 29
    • 33744505451 scopus 로고    scopus 로고
    • Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome
    • Patel R.K., Lea N.C., Heneghan M.A., et al. Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome. Gastroenterology 130 (2006) 2031-2038
    • (2006) Gastroenterology , vol.130 , pp. 2031-2038
    • Patel, R.K.1    Lea, N.C.2    Heneghan, M.A.3
  • 31
    • 28244442441 scopus 로고    scopus 로고
    • Definition of subtypes of essential thrombocythemia and relation to polycythemia vera based on JAK2V617F mutation status: a prospective study
    • 1995-1953
    • Campbell P.J., Scott L.M., Buck G., et al. Definition of subtypes of essential thrombocythemia and relation to polycythemia vera based on JAK2V617F mutation status: a prospective study. Lancet 366 (2005) 1995-1953
    • (2005) Lancet , vol.366
    • Campbell, P.J.1    Scott, L.M.2    Buck, G.3
  • 32
    • 33749434271 scopus 로고    scopus 로고
    • Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations and role in leukemic transformation
    • Jul 27 [epub ahead of print]
    • Campbell P.J., Baxter E.J., Beer P.A., et al. Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations and role in leukemic transformation. Blood (2006) Jul 27 [epub ahead of print]
    • (2006) Blood
    • Campbell, P.J.1    Baxter, E.J.2    Beer, P.A.3
  • 33
    • 84888732788 scopus 로고    scopus 로고
    • Risk-adapted therapy in essential thrombocythemia and polycythemia vera
    • Finazzi G., and Barbui T. Risk-adapted therapy in essential thrombocythemia and polycythemia vera. Blood Rev 74 (2005) 489-495
    • (2005) Blood Rev , vol.74 , pp. 489-495
    • Finazzi, G.1    Barbui, T.2
  • 34
    • 33746059048 scopus 로고    scopus 로고
    • High molecular response rate of polycythemia vera patients treated with pegylated interferon alpha-2a
    • May 18 [epub ahead of print]
    • Kiladjian J.J., Cassinat B., Turlure P., et al. High molecular response rate of polycythemia vera patients treated with pegylated interferon alpha-2a. Blood (2006) May 18 [epub ahead of print]
    • (2006) Blood
    • Kiladjian, J.J.1    Cassinat, B.2    Turlure, P.3
  • 35
    • 20144389274 scopus 로고    scopus 로고
    • Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study
    • Finazzi G., Caruso V., Marchioli R., et al. Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study. Blood 105 (2005) 2664-2670
    • (2005) Blood , vol.105 , pp. 2664-2670
    • Finazzi, G.1    Caruso, V.2    Marchioli, R.3
  • 36
    • 21444434751 scopus 로고    scopus 로고
    • United Kingdom Medical Research Council Primary Thrombocythemia 1 Study. Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia
    • Harrison C.N., Campbell P.J., Buck G., et al. United Kingdom Medical Research Council Primary Thrombocythemia 1 Study. Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia. N Engl J Med 353 (2005) 33-45
    • (2005) N Engl J Med , vol.353 , pp. 33-45
    • Harrison, C.N.1    Campbell, P.J.2    Buck, G.3
  • 37
    • 13544254271 scopus 로고    scopus 로고
    • The constitutive mobilization of bone marrow-repopulation cells into the peripheral blood in idiopathic myelofibrosis
    • Xu M., Bruno E., Chao J., et al. The constitutive mobilization of bone marrow-repopulation cells into the peripheral blood in idiopathic myelofibrosis. Blood 105 (2005) 1699-1705
    • (2005) Blood , vol.105 , pp. 1699-1705
    • Xu, M.1    Bruno, E.2    Chao, J.3
  • 38
    • 24944563475 scopus 로고    scopus 로고
    • +, and vascular endothelial growth factor receptor 2-positive endothelial progenitor cells in myelofibrosis with myeloid metaplasia
    • +, and vascular endothelial growth factor receptor 2-positive endothelial progenitor cells in myelofibrosis with myeloid metaplasia. J Clin Oncol 23 (2005) 5688-5695
    • (2005) J Clin Oncol , vol.23 , pp. 5688-5695
    • Massa, M.1    Rosti, V.2    Ramajoli, I.3
  • 39
    • 21144457074 scopus 로고    scopus 로고
    • + cells into the peripheral blood in idiopathic myelofibrosis may be due to the action of a number of proteases
    • + cells into the peripheral blood in idiopathic myelofibrosis may be due to the action of a number of proteases. Blood 105 (2005) 4508-4515
    • (2005) Blood , vol.105 , pp. 4508-4515
    • Xu, M.1    Bruno, E.2    Chao, J.3
  • 40
    • 20844457922 scopus 로고    scopus 로고
    • Myeloproliferative Diseases Research Consortium. Allogeneic hematopoietic stem cell transplantation with reduced-intensity conditioning in intermediate- or high-risk patients with myelofibrosis with myeloid metaplasia
    • Rondelli D., Barosi G., Bacigalupo A., et al. Myeloproliferative Diseases Research Consortium. Allogeneic hematopoietic stem cell transplantation with reduced-intensity conditioning in intermediate- or high-risk patients with myelofibrosis with myeloid metaplasia. Blood 105 (2005) 4115-4119
    • (2005) Blood , vol.105 , pp. 4115-4119
    • Rondelli, D.1    Barosi, G.2    Bacigalupo, A.3
  • 41
    • 0029767865 scopus 로고    scopus 로고
    • Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system
    • Dupriez B., Morel P., Demory J.L., et al. Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system. Blood 88 (1996) 1013-1018
    • (1996) Blood , vol.88 , pp. 1013-1018
    • Dupriez, B.1    Morel, P.2    Demory, J.L.3
  • 42
    • 31544454193 scopus 로고    scopus 로고
    • Prognosis in transplant-eligible patients with agnogenic myeloid metaplasia: a simple CBC-based scoring system
    • Dingli D., Schwager S.M., Mesa R.A., et al. Prognosis in transplant-eligible patients with agnogenic myeloid metaplasia: a simple CBC-based scoring system. Cancer 106 (2006) 623-630
    • (2006) Cancer , vol.106 , pp. 623-630
    • Dingli, D.1    Schwager, S.M.2    Mesa, R.A.3
  • 43
    • 30844463437 scopus 로고    scopus 로고
    • Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis
    • Dingli D., Schwager S.M., Mesa R.A., et al. Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis. Cancer 106 (2006) 1985-1989
    • (2006) Cancer , vol.106 , pp. 1985-1989
    • Dingli, D.1    Schwager, S.M.2    Mesa, R.A.3
  • 44
    • 0030756292 scopus 로고    scopus 로고
    • Allogeneic marrow transplantation for primary myelofibrosis and myelofibrosis secondary to polycythaemia vera or essential thrombocytosis
    • Anderson J., Sale G., Appelbaum F., et al. Allogeneic marrow transplantation for primary myelofibrosis and myelofibrosis secondary to polycythaemia vera or essential thrombocytosis. Br J Haematol 98 (1997) 1010-1016
    • (1997) Br J Haematol , vol.98 , pp. 1010-1016
    • Anderson, J.1    Sale, G.2    Appelbaum, F.3
  • 45
    • 0027082150 scopus 로고
    • Allogeneic bone marrow transplantation for primary myelofibrosis
    • Creemers G., Lowenberg B., and Hagenbeek A. Allogeneic bone marrow transplantation for primary myelofibrosis. Br J Haematol 82 (1992) 158-162
    • (1992) Br J Haematol , vol.82 , pp. 158-162
    • Creemers, G.1    Lowenberg, B.2    Hagenbeek, A.3
  • 46
    • 0029618855 scopus 로고
    • Allogeneic bone marrow transplantation for primary myelofibrosis
    • Singhal S., Powles R., Treleaven J., et al. Allogeneic bone marrow transplantation for primary myelofibrosis. Bone Marrow Transplant 16 (1995) 743-746
    • (1995) Bone Marrow Transplant , vol.16 , pp. 743-746
    • Singhal, S.1    Powles, R.2    Treleaven, J.3
  • 47
    • 0031963620 scopus 로고    scopus 로고
    • Allogeneic marrow transplantation for myeloproliferative disorders other than chronic myelogenous leukemia: review of forty cases
    • Przepiorka D., Giralt S., Khouri I., et al. Allogeneic marrow transplantation for myeloproliferative disorders other than chronic myelogenous leukemia: review of forty cases. Am J Hematol 57 (1998) 24-29
    • (1998) Am J Hematol , vol.57 , pp. 24-29
    • Przepiorka, D.1    Giralt, S.2    Khouri, I.3
  • 48
    • 0033135848 scopus 로고    scopus 로고
    • Allogeneic stem cell transplantation for agnogenic myeloid metaplasia
    • A European Group for Blood and Marrow Transplantation, Sociate Francaise de Greffe de Moelle, Gruppo Italiano per il Trapianto di Midollo Osseo and Fred Hutchinson Cancer Research Center Collaborative Study
    • Guardiola P., Anderson J.E., Bandini G., et al., A European Group for Blood and Marrow Transplantation, Sociate Francaise de Greffe de Moelle, Gruppo Italiano per il Trapianto di Midollo Osseo and Fred Hutchinson Cancer Research Center Collaborative Study. Allogeneic stem cell transplantation for agnogenic myeloid metaplasia. Blood 93 (1999) 2831-2838
    • (1999) Blood , vol.93 , pp. 2831-2838
    • Guardiola, P.1    Anderson, J.E.2    Bandini, G.3
  • 49
    • 10744225447 scopus 로고    scopus 로고
    • Stem cell transplantation for myelofibrosis: a report from two Canadian centers
    • Daly A., Song K., Nevill T., et al. Stem cell transplantation for myelofibrosis: a report from two Canadian centers. Bone Marrow Transplant 32 (2003) 35-40
    • (2003) Bone Marrow Transplant , vol.32 , pp. 35-40
    • Daly, A.1    Song, K.2    Nevill, T.3
  • 50
    • 10744230038 scopus 로고    scopus 로고
    • Allogeneic hematopoietic stem cell transplantation for myelofibrosis
    • Deeg H.J., Gooley T.A., Flowers M.E., et al. Allogeneic hematopoietic stem cell transplantation for myelofibrosis. Blood 102 (2003) 3912-3918
    • (2003) Blood , vol.102 , pp. 3912-3918
    • Deeg, H.J.1    Gooley, T.A.2    Flowers, M.E.3
  • 51
    • 0034057313 scopus 로고    scopus 로고
    • Induction of remission after donor leukocyte infusion for the treatment of relapsed chronic idiopathic myelofibrosis following allogenic transplantation: evidence for a "graft vs myelofibrosis" effect
    • Byrne J.L., Beshti H., Clark D., et al. Induction of remission after donor leukocyte infusion for the treatment of relapsed chronic idiopathic myelofibrosis following allogenic transplantation: evidence for a "graft vs myelofibrosis" effect. Br J Haematol 108 (2000) 430-433
    • (2000) Br J Haematol , vol.108 , pp. 430-433
    • Byrne, J.L.1    Beshti, H.2    Clark, D.3
  • 52
    • 0034739223 scopus 로고    scopus 로고
    • Myelofibrosis with myeloid metaplasia
    • (letter)
    • Guardiola P., Anderson J.E., and Gluckman E. Myelofibrosis with myeloid metaplasia. N Engl J Med 343 (2000) 659-660 (letter)
    • (2000) N Engl J Med , vol.343 , pp. 659-660
    • Guardiola, P.1    Anderson, J.E.2    Gluckman, E.3
  • 53
    • 0035437162 scopus 로고    scopus 로고
    • Myeloablation and autologous peripheral blood stem cell rescue results in hematologic and clinical responses in patients with myelofibrosis
    • Anderson J.E., Tefferi A., Craig F., et al. Myeloablation and autologous peripheral blood stem cell rescue results in hematologic and clinical responses in patients with myelofibrosis. Blood 98 (2001) 586-593
    • (2001) Blood , vol.98 , pp. 586-593
    • Anderson, J.E.1    Tefferi, A.2    Craig, F.3
  • 54
    • 33750081766 scopus 로고    scopus 로고
    • Stem cell transplantation with reduced-intensity conditioning regimens: a review of ten years experience with new transplant concepts and new therapeutic agents
    • Jul 27 [epub ahead of print]
    • Barrett A.J., and Savani B.N. Stem cell transplantation with reduced-intensity conditioning regimens: a review of ten years experience with new transplant concepts and new therapeutic agents. Leukemia (2006) Jul 27 [epub ahead of print]
    • (2006) Leukemia
    • Barrett, A.J.1    Savani, B.N.2
  • 55
    • 0037085757 scopus 로고    scopus 로고
    • Allogeneic blood cell transplantation following reduced-intensity conditioning is effective therapy for older patients with myelofibrosis with myeloid metaplasia
    • Devine S.M., Hoffman R., Verma A., et al. Allogeneic blood cell transplantation following reduced-intensity conditioning is effective therapy for older patients with myelofibrosis with myeloid metaplasia. Blood 99 (2002) 2255-2258
    • (2002) Blood , vol.99 , pp. 2255-2258
    • Devine, S.M.1    Hoffman, R.2    Verma, A.3
  • 56
    • 20044391419 scopus 로고    scopus 로고
    • Pilot study of reduced-intensity conditioning followed by allogeneic stem cell transplantation from related and unrelated donors in patients with myelofibrosis
    • Kroger N., Zabelina T., Schieder H., et al. Pilot study of reduced-intensity conditioning followed by allogeneic stem cell transplantation from related and unrelated donors in patients with myelofibrosis. Br J Haematol 128 (2005) 690-697
    • (2005) Br J Haematol , vol.128 , pp. 690-697
    • Kroger, N.1    Zabelina, T.2    Schieder, H.3
  • 58
    • 0034567061 scopus 로고    scopus 로고
    • Acute safety and pharmacokinetics of intravenous busulfan when used with oral busulfan and cyclophosphamide as pretransplantation conditioning therapy: a phase I study
    • Andersson B.S., Madden T., Tran H.T., et al. Acute safety and pharmacokinetics of intravenous busulfan when used with oral busulfan and cyclophosphamide as pretransplantation conditioning therapy: a phase I study. Biol Blood Marrow Transplant 6 (2000) 548-554
    • (2000) Biol Blood Marrow Transplant , vol.6 , pp. 548-554
    • Andersson, B.S.1    Madden, T.2    Tran, H.T.3
  • 59
    • 0036401558 scopus 로고    scopus 로고
    • Once-daily intravenous busulfan given with fludarabine as conditioning for allogeneic stem cell transplantation: study of pharmacokinetics and early clinical outcomes
    • Russell J.A., Tran H.T., Quinlan D., et al. Once-daily intravenous busulfan given with fludarabine as conditioning for allogeneic stem cell transplantation: study of pharmacokinetics and early clinical outcomes. Biol Blood Marrow Transplant 8 (2002) 468-476
    • (2002) Biol Blood Marrow Transplant , vol.8 , pp. 468-476
    • Russell, J.A.1    Tran, H.T.2    Quinlan, D.3
  • 60
    • 3242810563 scopus 로고    scopus 로고
    • Once-daily intravenous busulfan and fludarabine: clinical and pharmacokinetic results of a myeloablative, reduced-toxicity conditioning regimen for allogeneic stem cell transplantation in AML and MDS
    • de Lima M., Couriel D., Thall P.F., et al. Once-daily intravenous busulfan and fludarabine: clinical and pharmacokinetic results of a myeloablative, reduced-toxicity conditioning regimen for allogeneic stem cell transplantation in AML and MDS. Blood 104 (2004) 857-864
    • (2004) Blood , vol.104 , pp. 857-864
    • de Lima, M.1    Couriel, D.2    Thall, P.F.3
  • 61
    • 33749028469 scopus 로고    scopus 로고
    • Comparable kinetics of myeloablation between fludarabine/full-dose busulfan and fludarabine/melphalan conditioning regimens in allogeneic peripheral blood stem cell transplantation
    • Chunduri S., Dobogai L., Peace D., et al. Comparable kinetics of myeloablation between fludarabine/full-dose busulfan and fludarabine/melphalan conditioning regimens in allogeneic peripheral blood stem cell transplantation. Bone Marrow Transplant 38 (2006) 477-482
    • (2006) Bone Marrow Transplant , vol.38 , pp. 477-482
    • Chunduri, S.1    Dobogai, L.2    Peace, D.3
  • 62
    • 0027534832 scopus 로고
    • Splenectomy for patients with myelofibrosis with myeloid metaplasia: pretreatment variables and outcome prediction
    • Barosi G., Ambrosetti A., Buratti A., et al. Splenectomy for patients with myelofibrosis with myeloid metaplasia: pretreatment variables and outcome prediction. Leukemia 7 (1993) 200-206
    • (1993) Leukemia , vol.7 , pp. 200-206
    • Barosi, G.1    Ambrosetti, A.2    Buratti, A.3
  • 63
    • 0034176014 scopus 로고    scopus 로고
    • Splenectomy in myelofibrosis with myeloid metaplasia: a single-institution experience with 223 patients
    • Tefferi A., Mesa R.A., Nagorney D.N., et al. Splenectomy in myelofibrosis with myeloid metaplasia: a single-institution experience with 223 patients. Blood 95 (2000) 2226-2233
    • (2000) Blood , vol.95 , pp. 2226-2233
    • Tefferi, A.1    Mesa, R.A.2    Nagorney, D.N.3
  • 64
    • 18544413070 scopus 로고    scopus 로고
    • Splenectomy and risk of blast transformation in myelofibrosis with myeloid metaplasia
    • Barosi G., Ambrosetti A., Centra A., et al. Splenectomy and risk of blast transformation in myelofibrosis with myeloid metaplasia. Blood 91 (1998) 3630-3636
    • (1998) Blood , vol.91 , pp. 3630-3636
    • Barosi, G.1    Ambrosetti, A.2    Centra, A.3
  • 65
    • 0035312989 scopus 로고    scopus 로고
    • Splenectomy and hemopoietic stem cell transplantation for myelofibrosis
    • Li Z., Gooley T., Applebaum F.R., et al. Splenectomy and hemopoietic stem cell transplantation for myelofibrosis. Blood 97 (2001) 2180-2181
    • (2001) Blood , vol.97 , pp. 2180-2181
    • Li, Z.1    Gooley, T.2    Applebaum, F.R.3
  • 66
    • 27144485409 scopus 로고    scopus 로고
    • Response criteria for myelofibrosis with myeloid metaplasia: results of an initiative of the European Myelofibrosis Network (EUMNET)
    • Barosi G., Bordessoule D., Briere J., et al. Response criteria for myelofibrosis with myeloid metaplasia: results of an initiative of the European Myelofibrosis Network (EUMNET). Blood 106 (2005) 2849-2853
    • (2005) Blood , vol.106 , pp. 2849-2853
    • Barosi, G.1    Bordessoule, D.2    Briere, J.3
  • 67
    • 33748205495 scopus 로고    scopus 로고
    • International Working Group (IWG) consensus criteria for treatment response in myelofibrosis with myeloid metaplasia
    • International Working Group for Myelofibrosis Research and Treatment (IWG-MRT)
    • Tefferi A., Barosi G., Mesa R.A., et al., International Working Group for Myelofibrosis Research and Treatment (IWG-MRT). International Working Group (IWG) consensus criteria for treatment response in myelofibrosis with myeloid metaplasia. Blood 108 (2006) 1497-1503
    • (2006) Blood , vol.108 , pp. 1497-1503
    • Tefferi, A.1    Barosi, G.2    Mesa, R.A.3
  • 68
    • 33750524290 scopus 로고    scopus 로고
    • Allogeneic Hematopoietic Cell Transplantation following Reduced Intensity Conditioning for Treatment of Myelofibrosis
    • Snyder D.S., Palmer J., Stein A.S., et al. Allogeneic Hematopoietic Cell Transplantation following Reduced Intensity Conditioning for Treatment of Myelofibrosis. Biol Blood Marrow Transplant 12 (2006) 1161-1168
    • (2006) Biol Blood Marrow Transplant , vol.12 , pp. 1161-1168
    • Snyder, D.S.1    Palmer, J.2    Stein, A.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.