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Presentation on Leukemia
Introduction
A malignant progressive disease in which the bone marrow and other
blood-forming organs produce increased numbers of immature or
abnormal leucocytes. These suppress the production of normal blood
cells, leading to anaemia and other symptoms.
2
Types of leukemia
Acute Chronic
MyeloidorganLymphoidorgan
Acute myeloid
leukemia
(AML)
Acute lymphocytic
leukemia
(ALL)
Chronic lymphocytic
leukemia
(CLL)
Chronic myeloid
leukemia
(CML)
3
Generation of
Philadelphia chromosome
Chromosome 9
Chromosome 22
Chromosomal
breakage and
translocation
t(9;22)(q34;q11)
Derivative 9
Philadelphia
chromosome
abl
bcr
4
Philadelphia
chromosome
Inhibit DNA repair
ATP
Proliferation of Immature
cell/uncontrolled proliferation of cells
Bcr-Abl
fusion
protein
Variants of Bcr-Abl fusion protein :
p210 (CML)
p185
p190 (ALL )
p230
Increased tyrosine kinase activity
and interaction with Interleukine-3
receptor beta subunit.
Molecular mechanism
of ALL and CML
5
Fig : Pathophysiology of CML and ALL
ALL and CML in Bangladesh
0
20
40
60
80
100
Under 20 20-29 30-39 40-49
%ofoccurrence
Age
AML CML ALL Other HM
6
Fig : Age-group specific distribution of
hematological malignancies in Bangladesh
AML
CML
ALL
CLL
Others
DISTRIBUTION
AML CML ALL CLL Others
Fig : Distribution pattern of hematological
malignancies in Bangladesh
Source : Hossain et al. BMC Cancer 2014, 14:438
ALL and CML in global perspective
7
0 10 20 30 40 50 60 70 80
AML
CML
ALL
CLL
Median age
Hematologicalmalignancies
US India Bangladesh
Fig : Median age at diagnosis of hematological malignancies in Bangladesh as compared to India and US
Treatment
• Drugs : Imatinib (Glivec®) tablets
• Chemotherapy
• stem cell transplant (SCT)
• Elimination of the Ph chromosome.
• Supportive treatment :
Blood and platelet transfusions,
Antibiotic or antifungal medicines .
8
References
9

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Leukemia by Thosif Raza

  • 2. Introduction A malignant progressive disease in which the bone marrow and other blood-forming organs produce increased numbers of immature or abnormal leucocytes. These suppress the production of normal blood cells, leading to anaemia and other symptoms. 2
  • 3. Types of leukemia Acute Chronic MyeloidorganLymphoidorgan Acute myeloid leukemia (AML) Acute lymphocytic leukemia (ALL) Chronic lymphocytic leukemia (CLL) Chronic myeloid leukemia (CML) 3
  • 4. Generation of Philadelphia chromosome Chromosome 9 Chromosome 22 Chromosomal breakage and translocation t(9;22)(q34;q11) Derivative 9 Philadelphia chromosome abl bcr 4
  • 5. Philadelphia chromosome Inhibit DNA repair ATP Proliferation of Immature cell/uncontrolled proliferation of cells Bcr-Abl fusion protein Variants of Bcr-Abl fusion protein : p210 (CML) p185 p190 (ALL ) p230 Increased tyrosine kinase activity and interaction with Interleukine-3 receptor beta subunit. Molecular mechanism of ALL and CML 5 Fig : Pathophysiology of CML and ALL
  • 6. ALL and CML in Bangladesh 0 20 40 60 80 100 Under 20 20-29 30-39 40-49 %ofoccurrence Age AML CML ALL Other HM 6 Fig : Age-group specific distribution of hematological malignancies in Bangladesh AML CML ALL CLL Others DISTRIBUTION AML CML ALL CLL Others Fig : Distribution pattern of hematological malignancies in Bangladesh Source : Hossain et al. BMC Cancer 2014, 14:438
  • 7. ALL and CML in global perspective 7 0 10 20 30 40 50 60 70 80 AML CML ALL CLL Median age Hematologicalmalignancies US India Bangladesh Fig : Median age at diagnosis of hematological malignancies in Bangladesh as compared to India and US
  • 8. Treatment • Drugs : Imatinib (Glivec®) tablets • Chemotherapy • stem cell transplant (SCT) • Elimination of the Ph chromosome. • Supportive treatment : Blood and platelet transfusions, Antibiotic or antifungal medicines . 8