acute myeloid leukaemia— phenotype and genotype barbara j. bain department of haematology st...
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Acute Myeloid Leukaemia—phenotype and genotype
Barbara J. Bain
Department of Haematology
St Mary’s Hospital, London
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The phenotypic diagnosis
• A case of leukaemia was first clearly described in 1845 by John Hughes Bennett and another, 6 weeks later, by Rudolf Virchow
• These were phenotypic diagnoses at autopsy, the blood being examined microscopically
• A few years later Virchow was the first to use the term “Leukhemia”
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Things moved on
The next one and a half centuries saw advances in the phenotypic diagnosis of leukaemia based on
• Better stains and microscopes
• Examination of the blood and, later, the bone marrow during life
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Things moved on further
Further advances improved the phenotypic diagnosis. These were
• Cytochemical stains
• Immunophenotyping
• Integration and codification of phenotypic diagnoses
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And further still
The FAB classifications from the last quarter of the 20th century can be seen as the culmination of phenotypic diagnosis
• The FAB group defined, and categorized and gave haematologists and, later, cytogeneticists throughout the world a common language
• Phenotypic diagnosis had become quite sophisticated
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But meanwhile —
Cytogenetic techniques were improving and with the introduction of chromosome banding there was a quantum leap in what could be recognized
• The incorporation of cytogenetic information into leukaemia classification started, e.g. MIC Group 1986.
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And furthermore —
Molecular genetics was invented
Now we have
• FISH, SKY, spectral karyotyping, CGH
• PCR and RT-PCR
• Microarray analysis
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What does this mean for leukaemia diagnosis and
classification?
• Can we move from a MIC to a MIC-M approach
• Should we do so?
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The WHO classification
The WHO classification has taken an approach which is partly based on cytogenetic and molecular genetic analysis
• First, antecedent factors are considered
• Secondly, genetic features are considered
• Thirdly, phenotype is used to categorize the remaining patients
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The WHO classification
• When appropriate, patients are first assigned to the category of therapy-related AML, regardless of whether they have recurring cytogenetic abnormalities
• These cases are further categorized as– Alkylating agent-related– Topoisomerase II-interactive drug-related– Other
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WHO and therapy-related AML
This is, in part, a genetic classification
• Alkylating agent-related AML is characterized by abnormalities of chromosomes 5 and 7, inv(3), t(3;3), t(6;9), t(8;16) and complex rearrangements
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WHO and therapy-related AML
Topoisomerase II-inhibitor-related AML is characterized by balanced translocations with 21q22 (AML1) and 11q23 (MLL) breakpoints including t(3;21), t(8;21), t(4;11), t(9;11) and t(11;19)(q23;p13.1) [but not t(11;19)(q23;p13.3)]
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WHO and therapy-related AML
• Topoisomerase II-inhibitor-related AML is associated not only with t(8;21)(q22;q22) but also with other translocations usually found in de novo AML, e.g. t(15;17)(q22;q12) and inv(16)(p13q22)
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Where does therapy-related AML with recurrent
cytogenetic abnormality belong?
It may be important to classify such cases as therapy-related in order to accurately judge the magnitude of the problem of therapy-induced AML (and ALL)
These cases might also be prognostically worse than de novo cases
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Where does therapy-related AML with recurrent
cytogenetic abnormality belong?
However—t-AML and de novo AML with the same cytogenetic abnormality have a lot of features in common and maybe the prognosis is not so very different
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Therapy-related AML with t(8;21)(q22;q22)
Slovak et al. (2002) reported a median survival of < 3 years and a 5 year survival of < 30%
However the treatment was not standardized and in the larger group of AML patients with a 21q22 bp a quarter of patients were untreated or undertreated
Slovak et al. (2002) Genes Chromosomes Cancer, 33, 379.
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Therapy-related AML with t(15;17)(q22;q21)
Andersen et al. (2002) reported, for intensively treated patients, that there was:
• a 69% CR rate• a median survival of 29 months• a 5-year survival of 45%
Andersen et al. (2002) Genes Chromosomes Cancer, 33, 395.
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Therapy-related AML with t(15;17)(q22;q21)
n CR rate 4-yr EFS 4-yr OS
34 97% 65% 85%
‘secondary’
642 93% 68% 78%
de novo‘Secondary’ = 15 surgery, 17 RT, 10 Chemo, 10 Chemo + RT
Pulsoni et al. (2002) Blood, 100, 1972
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Therapy-related AML with inv(16)(p13q22)
Andersen et al (2002) reported , with intensive treatment:
• 85% CR
• 29 months median survival
• 45% 5-year survival• Andersen et al. (2002) Genes Chromosomes Cancer, 33, 395.
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What should we do?
• We should follow the WHO classification but should note the presence of relevant cytogenetic abnormalities
• We should recognize that topoisomerase II-inhibitor-related secondary AML is quite a different matter from t-AML related to alkylating agents
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WHO classification AML — with recurrent cytogenetic
abnormalitiesAdvantages
• Certain cytogenetic/molecular genetic categories are recognized
• AML, e.g. with t(8;21) and inv(16) with less than 30% blasts is recognized
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WHO classification AML — with recurrent cytogenetic
abnormalitiesDisadvantages
• Acute promyelocytic leukaemia with classical and variant translocations are lumped together
• All cases of AML with all 11q23 breakpoint and MLL rearrangement are lumped together
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Acute promyelocytic leukaemia and “variants” (i)
Subtype Gene ATRA PML response distrib
M3/M3v/t(15;17)PML-RARA Yes AbnormalM3-like/t(11;17) PLZF-RARA No Normal
(q23;q21)M3-like/t(11;17) NuMA-RARA Probably Normal
(q13;q21)M3-like/t(1;17) NPM-RARA Probably Normal
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Acute promyelocytic leukaemia and “variants” (ii)
RARA and the normal cell
RAR binds to RXR. In the absence of RA, RAR-RXR binds to RARE in the promoter of target genes, interacts with co-repressors, attracts HDACs, leading to chromatin condensation and repression of transcription
In the presence of RA, RAR-RXR is converted from a repressor to an activator since it now binds to co-activators and fails to bind to co-repressors
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Acute promyelocytic leukaemia and “variants” (iii)
RARA and the promyelocytic leukaemia cell
• PML-RAR binds more strongly to co-repressors and does not dissociate in the presence of physiological levels of RA
• However, pharmacological levels of ATRA correct the situation
• HDAC inhibitors should enhance the action of ATRA and appear to do so
Jones and Saha (2002) Br J Haematol, 118, 714
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Acute promyelocytic leukaemia and “variants” (iv)
RARA and the leukaemia cell of M3-like/t(15;17)/PLZF-RARA AML
• PLZF is a transfer factor that binds to co-repressors• PLZF-RAR therefore binds to corepressors through two
binding sites —dependent on RARA and independent of it• Pharmacological doses of ATRA don’t break the second bond
and therefore cases are refractory to this therapy• However HDAC inhibitors should enhance and appear to do so
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Acute promyelocytic leukaemia and “variants” (v)
Conclusion• Not all acute leukaemias involving the RARA gene
represent the same disease– Some respond to ATRA and some do not
– Some respond to arsenic trioxide and some do not
– A molecular classification can help us to predict or understand response to therapy
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Acute myeloid leukaemia with 11q23 breakpoints and MLL
rearrangement
Is this one disease or many?
The results of the European 11q23 workshop and other published data suggest that this is many diseases
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Acute myeloid leukaemia with 11q23/MLL rearrangement
n < 1 y ALL
t(4;11) 183 34 % 95 %
t(6;11) 30 7 % 10 %
t(9;11) 125 17 % 7 %
t(10;11) 20 32 % 20 %
t(11;19)/MLL-ELL 21 14 % nil
t(11;19)/MLL-ENL 32 41 % 66 %
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Acute myeloid leukaemia with 11q23/MLL rearrangement
FAB t-AML/MDS
t(4;11) M4 5.5 %
t(6;11) M4/M5a nil
t(9;11) M5a 10 %
t(10;11) M5a 1 %
t(11;19)/MLL-ELL M4 7 %
t(11;19)/MLL-ENL M4/M5a nil
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Acute myeloid leukaemia with 11q23/MLL rearrangement
Conclusion
• Acute leukaemia with 11q23/MLL involvement is many disease not one
• This does not yet have much therapeutic significance but maybe it will have in the future
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Are there other cytogenetic/ molecular genetic categories of
AML we should recognize?M1/t(9;22)/BCR-ABL fusion
• FAB: M1 (occasionally M0, M2, M4)• Usually no Auer rods• Mainly de novo but occasionally after topoisomerase-II-
interactive drugs• Poor prognosis
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Are there other cytogenetic/ molecular genetic categories of
AML we should recognize?
M2 or M4Baso/t(6;9)/DEK-CAN fusion• FAB: M2 (occasionally M4 or M1)• May show basophilic differentiation and Auer rods• Mainly de novo but occasionally after topoisomerase-
II-interactive drugs or alkylating agents• Poor prognosis
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Are there other cytogenetic/ molecular genetic categories of
AML we should recognize?
M5/t(8;16)/MOZ-CBP fusion• FAB: M5 or M4 with haemophagocytosis• Abnormal coagulation• de novo or secondary (topoisomerase-II-
interactive drugs or alkylating agents) • Poor prognosis
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Are there other cytogenetic/ molecular genetic categories of
AML we should recognize?
M7/t(1;22)/OTT-MAL fusion• FAB: M7• Mainly infants
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Are there other cytogenetic/ molecular genetic categories of
AML we should recognize?Various/inv(3) or t(3;3)/EVI1 dysregulation• Any category except M3; M7 over-represented• Platelet count often normal or even increased• Trilineage myelodysplasia• De novo, secondary to alkylating agents or
transformation of a MPD
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Can we recognize any purely molecular categories of AML?
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Can we recognize any purely molecular categories of AML?
Yes
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AML with CEBPA mutations (i)
Mutations in the CEBPA gene, encoding the CCAAT/enhancer binding protein have now been identified in 7-10% of AML
CEBP is exclusively expressed in myelomonocytic cells and is essential for neutrophilic differentiation
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AML with CEBPA mutations (ii)
CEBP negatively regulates MYC and positively regulates the genes encoding the receptors for M-CSF, G-CSF and GM-CSF
CEBPdeficient mice have granulopoiesis arrested at the myeloblast stage
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AML with CEBPA mutations (iii)
CEBP mutations were found in 15 of 134 patients studied prospectively and were an independent good prognostic feature
Such mutations, in the absence of FLT3 ITD, could lead to a patient being classified and treated as ‘good prognosis’
Preudhomme et al (2002) Blood, 100, 2717
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What does the future hold?
Is the future micro-arrays?
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What does the future hold?• Clinical assessment and morphology will
remain crucial, particularly for diagnosis• Cytochemistry will continue to decline in
importance, but should not be neglected• Immunophenotyping will hang on• Molecular diagnosis will lead to more
accurate classification and scientifically-based more effective treatment