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Chapter 60  Myelodysplastic Syndromes  969.e9


            366.  Broseus  J,  Alpermann  T,  Wulfert  M,  et al:  Age,  JAK2(V617F)  and   388.  Schouten HC, Vellenga E, van Rhenen DJ, et al: Recombinant human
                SF3B1  mutations  are  the  main  predicting  factors  for  survival  in   erythropoietin in patients with myelodysplastic syndromes. Leukemia
                refractory anaemia with ring sideroblasts and marked thrombocytosis.   5(5):432–436, 1991.
                Leukemia 27(9):1826–1831, 2013.                   389.  Hellstrom-Lindberg E, Gulbrandsen N, Lindberg G, et al: A validated
            367.  Ceesay MM, Lea NC, Ingram W, et al: The JAK2 V617F mutation is   decision model for treating the anaemia of myelodysplastic syndromes
                rare in RARS but common in RARS-T. Leukemia 20(11):2060–2061,   with erythropoietin + granulocyte colony-stimulating factor: significant
                2006.                                                 effects on quality of life. Br J Haematol 120(6):1037–1046, 2003.
            368.  Remacha A, Puget G, Nomdedéu JF, et al: Occurrence of the JAK2   390.  Park S, Grabar S, Kelaidi C, et al: Predictive factors of response and
                V617F  mutation  in  the  WHO  provisional  entity:  Myelodysplastic/  survival in myelodysplastic syndrome treated with erythropoietin and
                myeloproliferative disease, unclassifiable-refractory anemia with ringed   G-CSF: the GFM experience. Blood 111(2):574–582, 2008.
                sideroblasts  associated  with  marked  thrombocytosis.  Haematologica   391.  Rigolin GM, Porta MD, Ciccone M, et al: In patients with myelodys-
                91:719–720, 2006.                                     plastic syndromes response to rHuEPO and G-CSF treatment is related
            369.  Cheson BD, Bennett JM, Kantarjian H, et al: Report of an international   to  an  increase  of  cytogenetically  normal  CD34  cells.  Br  J  Haematol
                working  group  to  standardize  response  criteria  for  myelodysplastic   126(4):501–507, 2004.
                syndromes. Blood 96(12):3671–3674, 2000.          392.  Musto P, Matera R, Minervini MM, et al: Low serum levels of tumor
            370.  Jansen  AJG,  Essink-Bot  M-L,  Beckers  EAM,  et al:  Quality  of  life   necrosis  factor  and  interleukin-1  beta  in  myelodysplastic  syndromes
                measurement in patients with transfusion-dependent myelodysplastic   responsive  to  recombinant  erythropoietin.  Haematologica  79(3):265–
                syndromes. Br J Haematol 121(2):270–274, 2003.        268, 1994.
            371.  Abel GA, Klaassen R, Lee SJ, et al: Patient-reported outcomes for the   393.  Goy  A,  Belanger  C,  Casadevall  N,  et al:  High  doses  of  intravenous
                myelodysplastic syndromes: a new MDS-specific measure of quality of   recombinant erythropoietin for the treatment of anaemia in myelodys-
                life. Blood 123(3):451–452, 2014.                     plastic syndrome. Br J Haematol 84(2):232–237, 1993.
            372.  Hellstrom-Lindberg E, Malcovati L: Supportive care and use of hema-  394.  Stasi R, Abruzzese E, Lanzetta G, et al: Darbepoetin alfa for the treat-
                topoietic growth factors in myelodysplastic syndromes. Semin Hematol   ment of anemic patients with low- and intermediate-1-risk myelodys-
                45(1):14–22, 2008.                                    plastic syndromes. Ann Oncol 16(12):1921–1927, 2005.
            373.  Cazzola  M,  Malcovati  L:  Myelodysplastic  syndromes–coping  with   395.  Moyo V, Lefebvre P, Duh MS, et al: Erythropoiesis-stimulating agents
                ineffective hematopoiesis. N Engl J Med 352(6):536–538, 2005.  in  the  treatment  of  anemia  in  myelodysplastic  syndromes:  a  meta-
            374.  Hebert P, Wells G, Blajchman M, et al: A multicenter, randomized, con-  analysis. Ann Hematol 87(7):527–536, 2008.
                trolled clinical trial of transfusion requirements in critical care. Transfus   396.  Terpos E, Mougiou A, Kouraklis A, et al: Prolonged administration of
                Requir Crit Care Care Trials Group. N Engl J Med 340(6):409–417,   erythropoietin increases erythroid response rate in myelodysplastic syn-
                1999.                                                 dromes: a phase II trial in 281 patients. Br J Haematol 118(1):174–180,
            375.  Hajjar LA, Vincent J-L, Galas FRBG, et al: Transfusion requirements   2002.
                after cardiac surgery: the TRACS randomized controlled trial. JAMA   397.  Verhoef GE, Zachée P, Ferrant A, et al: Recombinant human erythro-
                304(14):1559–1567, 2010.                              poietin for the treatment of anemia in the myelodysplastic syndromes:
            376.  Fakhry S, Fata P: How low is too low? Cardiac risks with anemia. Crit   a  clinical  and  erythrokinetic  assessment.  Ann  Hematol  64(1):16–21,
                Care 8(Suppl 2):S11–S14, 2004.                        1992.
            377.  Oliva EN, Schey C, Hutchings AS: A review of anemia as a cardiovas-  398.  Kurzrock  R,  Talpaz  M,  Estey  E,  et al:  Erythropoietin  treatment  in
                cular risk factor in patients with myelodysplastic syndromes. Am J Blood   patients  with  myelodysplastic  syndrome  and  anemia.  Leukemia
                Res 1(2):160–166, 2011.                               5(11):985–990, 1991.
            378.  Anderson KC, Weinstein HJ: Transfusion-associated graft-versus-host   399.  Spiriti  MAA,  Latagliata  R,  Niscola  P,  et al:  Impact  of  a  new  dosing
                disease. N Engl J Med 323(5):315–321, 1990.           regimen of epoetin alfa on quality of life and anemia in patients with
            379.  Chacko J, Pennell DJ, Tanner MA, et al: Myocardial iron loading by   low-risk  myelodysplastic  syndrome.  Ann  Hematol  84(3):167–176,
                magnetic resonance imaging T2* in good prognostic myelodysplastic   2005.
                syndrome  patients  on  long-term  blood  transfusions.  Br  J  Haematol   400.  Jadersten  M,  Malcovati  L,  Dybedal  I,  et al:  Erythropoietin  and
                138(5):587–593, 2007.                                 granulocyte-colony  stimulating  factor  treatment  associated  with
            380.  Pascal L, Beyne-Rauzy O, Brechignac S, et al: Cardiac iron overload   improved  survival  in  myelodysplastic  syndrome.  J  Clin  Oncol
                assessed by T2* magnetic resonance imaging and cardiac function in   26(21):3607–3613, 2008.
                regularly transfused myelodysplastic syndrome patients. Br J Haematol   401.  Hellström-Lindberg E, Negrin R, Stein R, et al: Erythroid response to
                162(3):413–415, 2013.                                 treatment with G-CSF plus erythropoietin for the anaemia of patients
            381.  Malcovati  L:  Impact  of  transfusion  dependency  and  secondary  iron   with myelodysplastic syndromes: proposal for a predictive model. Br J
                overload on the survival of patients with myelodysplastic syndromes.   Haematol 99(2):344–351, 1997.
                Leuk Res 31(Suppl 3):S2–S6, 2007.                 402.  Rizzo JD, Brouwers M, Hurley P, et al: American Society of Hematology/
            382.  Chee CE, Steensma DP, Wu W, et al: Neither serum ferritin nor the   American  Society  of  Clinical  Oncology  clinical  practice  guideline
                number of red blood cell transfusions affect overall survival in refrac-  update on the use of epoetin and darbepoetin in adult patients with
                tory  anemia  with  ringed  sideroblasts.  Am  J  Hematol  83(8):611–613,   cancer. Blood 116(20):4045–4059, 2010.
                2008.                                             403.  Phrommintikul A, Haas SJ, Elsik M, et al: Mortality and target haemo-
            383.  Rose  EH,  Abels  RI,  Nelson  RA,  et al:  The  use  of  r-HuEpo  in  the   globin concentrations in anaemic patients with chronic kidney disease
                treatment of anaemia related to myelodysplasia (MDS). Br J Haematol   treated with erythropoietin: a meta-analysis. Lancet 369(9559):381–388,
                89(4):831–837, 1995.                                  2007.
            384.  Bessho  M,  Jinnai  I,  Matsuda  A,  et al:  Improvement  of  anemia  by   404.  NCCN  practice  guidelines  for  the  myelodysplastic  syndromes.  Natl
                recombinant erythropoietin in patients with myelodysplastic syndromes   Compr Cancer Netw Oncol Williston Park 12:53, 1998.
                and aplastic anemia. Int J Cell Cloning 8(6):445–458, 1990.  405.  Vadhan-Raj S, Keating M, LeMaistre A, et al: Effects of recombinant
            385.  Stebler C, Tichelli A, Dazzi H, et al: High-dose recombinant human   human granulocyte-macrophage colony-stimulating factor in patients
                erythropoietin for treatment of anemia in myelodysplastic syndromes   with myelodysplastic syndromes. N Engl J Med 317(25):1545–1552,
                and paroxysmal nocturnal hemoglobinuria: a pilot study. Exp Hematol   1987.
                18(11):1204–1208, 1990.                           406.  Antin  JH,  Smith  BR,  Holmes  W,  et al:  Phase  I/II  study  of  recom-
            386.  Bowen  D,  Culligan  D,  Jacobs  A: The  treatment  of  anaemia  in  the   binant  human  granulocyte-macrophage  colony-stimulating  factor  in
                myelodysplastic  syndromes  with  recombinant  human  erythropoietin.   aplastic anemia and myelodysplastic syndrome. Blood 72(2):705–713,
                Br J Haematol 77(3):419–423, 1991.                    1988.
            387.  Hellstrom  E,  Birgegard  G,  Lockner  D,  et al:  Treatment  of  myelo-  407.  Negrin RS, Haeuber DH, Nagler A, et al: Treatment of myelodysplastic
                dysplastic syndromes with recombinant human erythropoietin. Eur J   syndromes  with  recombinant  human  granulocyte  colony-stimulating
                Haematol 47(5):355–360, 1991.                         factor. A phase I-II trial. Ann Intern Med 110(12):976–984, 1989.
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