1. Jensen PD. Iron overload in patients with myelodysplastic syndromes. Curr Hematol Malig Rep. 2007; 2:13–21. PMID:
20425384.
Article
2. Shenoy N, Vallumsetla N, Rachmilewitz E, Verma A, Ginzburg Y. Impact of iron overload and potential benefit from iron chelation in low-risk myelodysplastic syndrome. Blood. 2014; 124:873–881. PMID:
24923296.
Article
3. Kumar A, List AF, Hozo I, Komrokji R, Djulbegovic B. Decitabine versus 5-azacitidine for the treatment of myelodysplastic syndrome: adjusted indirect meta-analysis. Haematologica. 2010; 95:340–342. author reply 343-4PMID:
19850902.
Article
4. Silverman LR, Demakos EP, Peterson BL, et al. Randomized controlled trial of azacitidine in patients with the myelodysplastic syndrome: a study of the cancer and leukemia group B. J Clin Oncol. 2002; 20:2429–2440. PMID:
12011120.
Article
5. Musto P, Maurillo L, Spagnoli A, et al. Azacitidine for the treatment of lower risk myelodysplastic syndromes : a retrospective study of 74 patients enrolled in an Italian named patient program. Cancer. 2010; 116:1485–1494. PMID:
20151429.
6. Sohn SK, Moon JH. When is the optimal timing for allogeneic transplantation in the case of MDS patients treated with hypomethylating agents? Expert Rev Hematol. 2013; 6:389–395. PMID:
23991925.
Article
7. Bird RJ, Kenealy M, Forsyth C, et al. When should iron chelation therapy be considered in patients with myelodysplasia and other bone marrow failure syndromes with iron overload? Intern Med J. 2012; 42:450–455. PMID:
22498118.
Article
8. Alessandrino EP, Della Porta MG, Bacigalupo A, et al. Prognostic impact of pre-transplantation transfusion history and secondary iron overload in patients with myelodysplastic syndrome undergoing allogeneic stem cell transplantation: a GITMO study. Haematologica. 2010; 95:476–484. PMID:
19903678.
Article
9. Temraz S, Santini V, Musallam K, Taher A. Iron overload and chelation therapy in myelodysplastic syndromes. Crit Rev Oncol Hematol. 2014; 91:64–73. PMID:
24529413.
Article
10. Delforge M, Selleslag D, Beguin Y, et al. Adequate iron chelation therapy for at least six months improves survival in transfusiondependent patients with lower risk myelodysplastic syndromes. Leuk Res. 2014; 38:557–563. PMID:
24661630.
Article
11. Gattermann N. Overview of guidelines on iron chelation therapy in patients with myelodysplastic syndromes and transfusional iron overload. Int J Hematol. 2008; 88:24–29. PMID:
18581200.
Article
12. Greenberg PL. Myelodysplastic syndromes: iron overload consequences and current chelating therapies. J Natl Compr Canc Netw. 2006; 4:91–96. PMID:
16403408.
Article
13. Fenaux P, Adès L. How we treat lower-risk myelodysplastic syndromes. Blood. 2013; 121:4280–4286. PMID:
23575446.
Article
14. Silverman LR, Fenaux P, Mufti GJ, et al. Continued azacitidine therapy beyond time of first response improves quality of response in patients with higher-risk myelodysplastic syndromes. Cancer. 2011; 117:2697–2702. PMID:
21656747.
Article
15. Gerds AT, Gooley TA, Estey EH, Appelbaum FR, Deeg HJ, Scott BL. Pretransplantation therapy with azacitidine vs induction chemotherapy and posttransplantation outcome in patients with MDS. Biol Blood Marrow Transplant. 2012; 18:1211–1218. PMID:
22252125.
Article
16. Damaj G, Duhamel A, Robin M, et al. Impact of azacitidine before allogeneic stem-cell transplantation for myelodysplastic syndromes: a study by the Société Francaise de Greffe de Moelle et
de Thérapie-Cellulaire and the Groupe-Francophone des Myélodysplasies. J Clin Oncol. 2012; 30:4533–4540. PMID:
23109707.
17. Zeidan AM, Lee JW, Prebet T, et al. Platelet count doubling after the first cycle of azacitidine therapy predicts eventual response and survival in patients with myelodysplastic syndromes and oligoblastic acute myeloid leukaemia but does not add to prognostic utility of the revised IPSS. Br J Haematol. 2014; 167:62–68. PMID:
24995683.
Article
18. Alessandrino EP, Porta MG, Malcovati L, et al. Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome. Am J Hematol. 2013; 88:581–588. PMID:
23606215.
Article
19. Oran B, Popat U, Andersson B, Champlin R. Allogeneic hematopoietic stem cell transplantation for myelodysplastic syndromes. Clin Lymphoma Myeloma Leuk. 2013; 13(Suppl 2):S282–S288. PMID:
24290213.
Article
20. Yahng SA, Yoon JH, Shin SH, et al. Response to pretransplant hypomethylating agents influences the outcome of allogeneic hematopoietic stem cell transplantation in adults with myelodysplastic syndromes. Eur J Haematol. 2013; 90:111–120. PMID:
23113470.
Article
21. Prébet T, Gore SD, Esterni B, et al. Outcome of high-risk myelodysplastic syndrome after azacitidine treatment failure. J Clin Oncol. 2011; 29:3322–3327. PMID:
21788559.
Article
22. Della Porta MG, Alessandrino EP, Bacigalupo A, et al. Predictive factors for the outcome of allogeneic transplantation in patients with MDS stratified according to the revised IPSS-R. Blood. 2014; 123:2333–2342. PMID:
24558201.
Article
23. Jabbour E, Kantarjian HM, Qiao W, et al. Impact of the achievement of a complete cytogenetic response (CCyR) on outcome in patients (pts) with myelodysplastic syndromes (MDS) treated with hypomethylating agents (HMA). Blood (ASH Annual Meeting Abstracts). 2013; 122(Suppl):2801.
Article
24. Bejar R, Stevenson KE, Caughey B, et al. Somatic mutations predict poor outcome in patients with myelodysplastic syndrome after hematopoietic stem-cell transplantation. J Clin Oncol. 2014; 32:2691–2698. PMID:
25092778.
Article
25. Lee KH, Lee JH, Lee JH, et al. Reduced-intensity conditioning therapy with busulfan, fludarabine, and antithymocyte globulin for HLA-haploidentical hematopoietic cell transplantation in acute leukemia and myelodysplastic syndrome. Blood. 2011; 118:2609–2617. PMID:
21715313.
Article
26. Martino R, Iacobelli S, Brand R, et al. Retrospective comparison of reduced-intensity conditioning and conventional high-dose conditioning for allogeneic hematopoietic stem cell transplantation using HLA-identical sibling donors in myelodysplastic syndromes. Blood. 2006; 108:836–846. PMID:
16597592.
Article
27. Martino R, de Wreede L, Fiocco M, et al. Comparison of conditioning regimens of various intensities for allogeneic hematopoietic SCT using HLA-identical sibling donors in AML and MDS with <10% BM blasts: a report from EBMT. Bone Marrow Transplant. 2013; 48:761–770. PMID:
23208314.
28. Bacigalupo A, Socié G, Schrezenmeier H, et al. Bone marrow versus peripheral blood as the stem cell source for sibling transplants in acquired aplastic anemia: survival advantage for bone marrow in all age groups. Haematologica. 2012; 97:1142–1148. PMID:
22315497.
Article
29. Servais S, Porcher R, Robin M, et al. Donor characteristics as pretransplant predictive factors of long-term outcomes after allogeneic peripheral blood stem cell transplantation from HLA-matched related and unrelated donors in patients with hematologic malignancies. Blood (ASH Annual Meeting Abstracts). 2012; 120(Suppl):2000.
Article
30. Ayuk F, Zabelina T, Wortmann F, et al. Donor choice according to age for allo-SCT for AML in complete remission. Bone Marrow Transplant. 2013; 48:1028–1032. PMID:
23419435.
Article