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MYELODYSPLASTIC SYNDROME: prognosis & treatment options

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Presentation on theme: "MYELODYSPLASTIC SYNDROME: prognosis & treatment options"— Presentation transcript:

1 MYELODYSPLASTIC SYNDROME: prognosis & treatment options
JILL Fulcher MD PhD FRCP(UK) 13th oct 2018

2 Normal blood smear 1. Red cells - Contain Hb Anemia when low
2. White cells - neutrophils - Infection when low 3. Platelets Clot formation Bleeding when low

3 Normal hematopoiesis Blood cells are made in the bone marrow
Hematopoietic stem cell (HSC) Undergo a series of developmental steps resulting in mature red cells, neutrophils and platelets Released into bloodstream

4 Myelodysplastic syndrome
Chung SS & Park YP Blood Advances;1(26):2572-8

5 MDS: Abnormal haematopoiesis
Myelodysplastic Syndrome Anemia, infection, bleeding

6 Prognostic Scoring System for MDS

7

8 Steensma Blood Cancer Journal (2018) 8:47

9 Symptomatic MDS bleeding Infections fatigue, SOB +/- Iron chelation
Medications: Tranexamic acid Antibiotics Antiviral agent Anti-fungal agent (TPO receptor agonists) bleeding Infections fatigue, SOB +/- Iron chelation

10 Anemia – Trial of Erythropoietin Replacement Therapy (ERT)
Response rate predicted from: Serum EPO level Transfusion requirements 74% chance of responding when EPO < 500 U/L, <2 units RBC/mth 7% if EPO > 500, >2 units RBC/mth Target Hb g/L Synergy with GCSF

11 Steensma Blood Cancer Journal (2018) 8:47

12 Other therapies for lower-risk mds
Lenalidomide Immuno-modulating agent MDS with del(5q) with anemia 10mg/d for 21d out of 28d Response in 4-6 weeks Rise in Hb of 32 g/L % achieve transfusion independence, 30-40% cytogenetic remission Improves survival (2y OS 90%v74%) S/E: low neutrophils, low platelets, rash, GI, ? secondary malignancy Immunosuppressive therapy (IST) ATG + cyclosporine More likely to work in patients: 60y/o or younger Low-risk disease BM blasts < 5% Bone marrow hypoplasia Normal cytogenetics HLA-DR15 PNH clone

13 Steensma Blood Cancer Journal (2018) 8:47

14 The only cure for MDS is Hematopoietic Stem Cell Transplantation

15 Myelodysplastic Syndrome: a disease mostly of the elderly
Mean age at diagnosis 70-75y Incidence : 4.9 per 100,000/year <40y per 100,000/year 70-79y per 100,000/year >80y per 100,000/year Buckstein R. Leuk Res 2009;33:1313-8 Williamson PJ, et al. Br J Haematol. 1994;87:743

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17 Co-morbidities affect transplant outcomes
Sorror et al, Blood; 106(5):

18 Steensma Blood Cancer Journal (2018) 8:47

19 Hypomethylating agents

20 Effect of Azacitidine in Higher-risk MDS (>/= IPSS-2)
Fenaux et al, Lancet Oncol 2009 358 patients Median OS: vs 15 mths Alive at 2 years: % vs. 26% Transformation to AML: 11.5 vs. 17.8%

21 Agents iN clinical trial
Hypomethylating agents (HMAs) Decitabine iv Guadecitabine (SGI-110) Oral azacitidine (CC486) Oral decitabine (Cedurazine) Erythroid Stimulating Agents Luspatercept Thrombopoiesis Stimulating Agents TPO mimetics Romiplostin (intectable) Eltrombopag (oral)

22 Timing of Transplant in Lower-risk MDS
De Witte et al Blood;127(13):

23 Thank you QUESTIONS?


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