Myelodysplasia.
This is the second in our series of clinical articles that discuss everyday presentations. Each emphasises practical aspects of teambased care that are relevant for general practitioners, specialists and paramedical professionals. Disorders arising in blood and bone marrow result in some of the commonest presenting symptoms and signs. A careful history and physical examination, complemented by rational use of laboratory tests, provides the clinical basis for a working diagnosis. If further investigation is needed into bone marrow or plasma, then supplementary imaging and radionuclide technology may be necessary under the guidance of an experienced haematologist.These clinical syndromes occur commonly in everyday practice and have variable and often subtle manifestations. The myelodysplasias are a heterogeneous group of malignant stem cell disorders that differ widely in haematological presentation and natural history. The characteristic features are:
* cytomorphological dysplasia
* hypercellular bone marrow in the face of pancytopenia, reflecting ineffective blood cell production
* a variable risk of transformation to acute leukaemia.
These neoplasms may arise de novo or after exposure to potentially mutagenic therapy. They are more common in older adults, but are increasingly recognised in children or young adults. Affected individuals are often underdiagnosed and may be treated inappropriately or unnecessarily. This is avoidable given current, and improving, understanding of these fluid-phase tumours.
Background
More than 50 years ago cases of anaemia that did not respond to available therapy were recognised, of which about twothirds defied diagnosis. Shortly thereafter some cases of refractory cytopenia were noted to develop into leukaemia, giving rise to the term pre-leukaemia. It was, however, not until 1970 that a classification was attempted, which was refined in 1976 by European, American and British investigators (Table 1). (1)
Table 1. French-American-British Co-operative Group Classification
Percentage
blasts
Type Bone Peripheral Monocytes Ringed
marrow blood 1x[10.sup.9]/1 sideroblasts
Refractory >5 [less than -- -
anaemia (RA) or equal
to]1
Refractory >5 [less than -- +
anaemia with or equal
ringed to]1
sideroblasts
(RARS)
Refractory 5--20 <5 -- [+ or -]
anaemia with
excess blasts
(RAEB)
Chronic [less <5 + [+ or -]
myelomonocytic than or
leukaemia equal
(CMML) to]20
RAEB in 21-- [greater [+ or -] [+ or -]
transformation 30 than or
(RAEB-T) equal to]5
Bennett, et al. (1)
This was the initial approach to providing
unification of these heterogeneous stem cell disorders. Ringed
sideroblasts exceeding 15% of nucleated erythroid series
classically in RARS but variably present in CMML and RAEB.
Subtypes with an excess of primitive marrow precursors have a higher transformation rate to acute leukaemia; this is a feature noted also in chronic myelomonocytic variants. Systematic research has resulted in the current recommendations from the World Health Organization that focus on the number of leukaemic blasts in the marrow and associated cytogenetic abnormalities (Table 2). (2), (3)
Table 2. World Health Organization Classification, 2008
Clinical Cytogenetic Marrow Disease
presentation abnormalities blasts
(%) (%)
Anaemia-- 25 <5 RA
isolated
[greater than or 5--20 <5 RARS--with ring
equal to]15% sideroblasts
ringed
sideroblasts
Anaemia--normal 100 <5 5q-syndrome
platelets
Bicytopenia or 50 <5 Refractory cytopenia
pancytopenia [+ with multilineage
or -]15 ring dysplasia (RCMD)
sideroblasts
Cytopenias Blood 30--50 5--9 Refractory anaemia with
blasts <5% excess blasts (RAEB1)
Cytopenias, 50--70 10-- Refractory anaemia with
peripheral blood 19 excess blasts (RAEB2)
blasts present
Neutropenia or 50 <5 Myelodysplastic
thrombocytopenia syndrome, unclassified
Swerdlow, et al (2)
Initially in 2001 the World Health Organization
proposed an update that largely replaced the earlier classification.
This has undergone extensive review and represents a worldwide
consensus for approaching haematological neoplasms.
These features are combined in an international scoring system that has predictive value for survival (Table 3). (4) However, in addition to disease status, there is recent recognition that non-leukaemic deaths may reflect extra-haematological co-morbidity and independently worsen survival patterns. This is particularly so in older patients and should be explained to the patient and the family (Table 4). (5)
Table 3. International prognostic scoring system
Criteria Score value
Prognostic risk 0 0.5 1 1.5 2
factor
Bone marrow <5 5--10 NA 11-- 21--30
blasts (%) 20
Karyotype Good Intermediate Poor NA NA
Cytopenias 0/1 2/3 NA NA NA
Median survival
by age group
(years)
IPSS [greater >60 [greater than >70
classification than or (n=611) or equal (n=371)
equal to]70(n=445)
to]60
(n=205)
Low (n=267) 11.8 4.8 9 3.9
Intermediate-1 5.2 2.7 4.4 2.4
(n=314)
Intermediate-2 1.8 1.1 1.3 1.2
(n=176)
High (n=59) 0.3 0.5 0.4 0.4
Greenberg, et al. (4)
This widely accepted approach is a useful basis
to explain to patients and their families how management may have
benefit and balance information against risk.
Table 4. Myelodysplasia-specific comorbidity index (MDS-CI)
Variable Score
Cardiac disease 2
Moderate-to-severe 1
hepatic disease
Severe pulmonary 1
disease
Renal disease 1
Solid tumour 1
Risk Total Distribution
scores (%)
Low 0 65
Intermediate 1--2 29
High >2 6
Della Porta, et al. (5)
Risk stratification based on both disease
status and extra-haematological comorbidity in patients with
myelodysplastic syndrome.
Prevalence
This is currently unknown, but males predominate with a median age of 65 years and incidence increases with increasing age.
Aetiology
Genetic factors may have a role in predisposition resulting from genes or polymorphic variants which increase the possibility of developing these entities. There may be a link with marrow injury and possible oxidative stress that accumulates with age, which may lead to mitochondrial damage with mutations in DNA. However, this is controversial.
An association with environmental or occupational factors is documented in relatively large case-control studies, but there is no proof of causation. Possible risk factors are tobacco smoking, alcohol, pesticides and a range of organic solvents. Better recognised correlations are the late consequences of cytotoxic chemotherapy and ionising radiation with both high and low concentration of exposure to benzene injurious via marrow damage. Notable is the occurrence after stem cell transplantation and in the course of aplastic anaemia, paroxysmal nocturnal haemoglobinuria and the chronic myeloproliferative syndrome neoplasms.
Children are increasingly recognised as having these disorders, particularly in the setting of Fanconi anaemia, ataxia telangiectasia and Bloom's syndrome. Juvenile myelomonocytic leukaemia and the monosomy-7 syndrome are relatively common; therefore the index of suspicion must be high when faced with otherwise unexplained signs and haematological abnormalities. (3)
Clinical features
Anaemia is present in more than threequarters of cases and is often symptomatic because of falling haemoglobin levels and coexisting cardiac and respiratory conditions. Erythropoiesis is ineffective and may be compounded by autoimmune haemolysis or pure red cell aplasia. Iron overload frequently occurs as a result of transfusions and increased absorption leading to hepatic, cardiac and endocrine dysfunction.
Thrombocytopenia occurs in more than half of the patients and explains easy bruising and inappropriate mucocutaneous bleeding (Fig. 1). This may be more severe and even lethal in 10--15% of cases, particularly in patients who have a poor prognosis according to the international scoring index.
[FIGURE 1 OMITTED]
Neutropenic bacterial sepsis, exacerbated by granulocyte dysfunction, responds poorly to standard therapy and remains a major cause of death in 20--40% of individuals.
Less frequent occurrences are autoimmune disorders, changes in the skin, inflammatory bowel disease and relapsing polychondritis, splenomegaly and haemostatic disorders. (3), (6)
Laboratory findings
Cell morphology is similar to that in nutritional deficiencies such as vitamin [B.sub.12] and folate deficiency, so a careful diagnostic algorithm is vital.
Red cells are macrocytic (Fig. 2) with wide-ranging morphological distortions. (2) Also present are small cells found in acquired haemoglobin H disease--or alpha thalassaemia. A fast migrating band seen on electrophoresis and golf-ball like inclusions of the abnormal haemoglobin are shown with supra-vital staining using methylene blue. (2), (3)
[FIGURE 2 OMITTED]
In the hypercellular marrow dyserythropoiesis is recognised by abnormal nuclear lobulation, irregular cytoplasmic haemoglobinisation together with basophilic stippling. An appropriate iron stain is needed to demonstrate the distinctive and diagnostically important ringed sideroblasts (Fig. 3).
[FIGURE 3 OMITTED]
White cells show morphological dysplasia in the form of poor granule formation in the cytoplasm and hyper- or hypo-lobulation of the nucleus (Fig. 4), often resulting in the typical pseudo-Pelger-Huet anomaly. A minimum of 10% dysplastic cells for each lineage is necessary to confidently diagnose these disorders. Monocytes are increased and there are also distinctively abnormal nuclei. A careful cell count is mandatory to record numbers and variations in the leukaemic blast population.
[FIGURE 4 OMITTED]
Platelets are typically reduced, although large forms and considerable variation in size are seen. In the trephine biopsy the increased numbers and small size of megakaryocytes, generally mononuclear, are characteristic (Fig. 5). It is important to recognise variants in which fibrous tissue is increased and, conversely, total cellularity is decreased, differentiating from primary myelofibrosis and aplasia respectively.
[FIGURE 5 OMITTED]
Making the diagnosis
Unexplained cytopenia, particularly in the elderly and when accompanied by monocytosis, requires a meticulous history aimed at excluding viral infections and nutritional deprivation.
Relatively insignificant bruising and bleeding, unexplained and recurrent infections as well as a broad range of autoimmune manifestations add to the difficulties in recognising this possibility in otherwise well individuals.
However, once considered, the cytomorphology in the peripheral blood and bone marrow is a reliable diagnostic starting point for an experienced haematologist. Vitamin B12 and folate deficiency, toxins, particularly including alcohol and a wide range of medications, as well as HIV infection, need to be excluded. The diagnosis is confirmed by flow cytometry and molecular genetics using fluorescent in situ hybridisation and conventional metaphase karyotyping. This information secures the diagnosis and classification as a basis for risk-stratified treatment using the international prognostic scoring system (Table 3). (4) The possible effects of any non-haemopoietic comorbidity also need to be discussed with the patient (Table 4).5
Molecular genetics is now an important part of haematology. In the elderly, management needs to take comorbidity into account. (6)
Management
These patients need to be treated only in a properly structured, experienced and effectively functioning multidisciplinary group in a major centre. Therapy should be individualised, based on risk stratification and, where possible, clinical trials. (4), (7)
First determine if treatment is necessary, or in an asymptomatic patient decide whether or not a conservative approach is appropriate. Standard supportive care is suitable in all those with a confirmed diagnosis. This is defined as red cell transfusion if symptomatic anaemia is present, with iron chelation, culture-directed antibiotics for documented infection and platelets. There may also be benefit in the simultaneous use of an antifibrinolytic agent such as cyclokapron.
Erythropoietin or similar agents are given, possibly combined with granulocyte stimulating peptides, independent of plasma levels. An adequate trial of therapy is important, probably not for less than 6 months. Thrombopoietin analogues, particularly romiplostim, may be useful.
Where more aggressive intervention is indicated those in the 5q category are treated with lenalidomide. (6), (7) The remainder are risk stratified by score on the IPSS. (4) Selected cases with bone marrow failure, rather than leukaemia and particularly when HLA-D 15 positive, may respond to immunosuppression including antilymphocyte globulin. This treatment carries risks of infection and infusion-related sideeffects that should not be underestimated. (7)
Persisting symptoms raise the possibility of allogeneic immunohaematopoietic stem cell transplantation if clinically appropriate and if a donor is available. (8)
In individuals eligible for this intervention it is still uncertain whether fully myeloablative or reduced intensity preparation, also known as conditioning, should be undertaken first. The benefits of diminishing leukaemic blast count before this procedure are still being debated. The debate is whether such chemotherapy can delay or prevent subsequent disease recurrence. Choice of donor, including possible umbilical cord units, is also under debate.
In those disqualified from this option the lowrisk category may qualify for lenalidomide, while more aggressive disease is amenable to DNA methyltransferase inhibition. This approach, together with either newer histone deacetylase agents such as a specific inhibitor, promotes the transcription of genes whose expression has been silenced--the epigenetic approach, which is being investigated by a number of cancer research centres worldwide.(5)
Conclusion
These syndromes are increasingly recognised. It is important that early and accurate diagnosis, with proper risk stratification, is the first step in management.
This crucial initial evaluation is the basis for a carefully defined proactive therapeutic algorithm designed to use all the available resources in an appropriate sequence and setting. It is no longer appropriate to manage these patients outside a comprehensive specialist group that accepts responsibility for all-inclusive care.
Acknowledgements. Supported by the Haematological Research Trust, with grants from the Louis Shill Foundation. Christine Dolling helped with the bibliographical review and Natasha Gordon typed the manuscript: appreciation is expressed to our research assistants. The photomicrographs are published with the permission of Professor Barbara Bain, who retains the copyright for them.
References available at www.cmej.org.za
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On 22 July 2011, Breivik killed 77 people and wounded 242 others. He said his actions were a protest against a left-wing government that was destroying Norway by promoting multiculturalism.
Many claimed the killings made sense only if Breivik was insane--indeed, an initial psychiatric report diagnosed him as having paranoid schizophrenia. But that highlights misconceptions about mental health, says Tad Tietze of the University of New South Wales in Sydney, Australia, an editor of a book on the attacks. 'People imply that mentalhealth patients are capable of these acts,' says Tietze. 'They don't deserve to be associated with a fascist mass killer.'
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References
(1.) Bennett JM, Catovsky D, Daniel MT, et al. Proposals for the classification of the myelodysplastic syndromes. The French-American-British (FAB) Co-operative Group. Br J Haematol 1982;51:190-199.
(2.) Swerdlow SH, Campo E, Harris NL, et al., eds. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th ed. Lyon: IARC, 2008
(3.) Doll DC, Landaw SA. Clinical manifestations and diagnosis of the myelodysplastic syndromes. www.uptodate.com, 2010.
(4.) Greenberg P, Cox C, LeBeau MM, et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997;89:2079-2088.
(5.) Della Porta MG, Malcovati L, Strupp C, et al. Risk stratification based on both disease status and extra-hematologic comorbidities in patients with myelodysplastic syndrome. Haematologica 2011;96:441-449.
(6.) Hellstrom-Lindberg E, ed. Myelodysplastic Syndromes. Chicago: Remedica, 2008.
(7.) Stone RM. How I treat patients with myelodysplastic syndromes. Blood 2009;113:6296-6303.
(8.) Blood Marrow Transplant Rev 2008;18(1).
Peter Jacobs, MB BCh, MD, PhD (Med), DSc (Med Sci), FRCP (Edin), MACP, FCP (SA), FRCPath (UK), IFCAP, MASSAf, FRSSAf
Emeritus Professor of Haematology, University of Cape Town, Honorary Consultant Physician, Groote Schuur Hospital Teaching Group, Professor of Internal Medicine, College of Medicine, University of Nebraska Medical Centre, Professor Extraordinaire in Haematological Pathology, Stellenbosch University and Tygerberg Academic Hospital, and Haematology Research Group, PathCare
Lucille Wood, FRCP (Edin), BA (Nursing Science), MSc (Med) (Haematol), RN, RM, Diploma in Intensive Nursing Care, Ward Administration and Clinical Teaching
Medical Biological Scientist, Senior Lecturer Extraordinaire in Clinical Haematology, Stellenbosch University and Tygerberg Academic Hospital, and Haematology Research Group, PathCare
Correspondence to: Natasha Gordon (natasha.gordon@pathcare.co.za)
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| Title Annotation: | Practical haematology |
|---|---|
| Author: | Jacobs, Peter; Wood, Lucille |
| Publication: | CME: Your SA Journal of CPD |
| Date: | Nov 1, 2012 |
| Words: | 2555 |
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