1. CHRONIC MYELOID LEUKEMIA (CML)
By:
Dr Waqar
Asst. Professor
Maarefa Medical College

2. NORMAL WBC FORMATION

3. CML DEFINITION
It is a cancer of WBCs in which there is excess production of granulocytes (neutros.,basophils & eosinophils) & their precursors( myeloid cells). The cells are mature looking but functionally abnormal.

4. REMEMBER !
AML is also a malignancy of myeloid cells but:
It runs an acute course ( rapid)
The leukemic cells are immature looking “blasts”

5. SOME GENERAL POINTS It has an insidious and gradual onset.
Occurs in middle to old age
The cells contain an abnormal chromosome called “Philadelphia chromosome”
In most cases, it is curable
The drug IMATINIB has revolutionized the treatment & prognosis

6. EPIDEMIOLOGY Age group : Middle to old age. Rare in children
Gender: Slightly more in males
Accounts for 8% of all leukemias in U.K.

7. PHASES OF CML
CML is classified into 3 phases , based on clinical features and lab findings: Chronic Accelarated Blast phase phase crisis

8. CHRONIC PHASE
* This is the initial phase & lasts for 3-4 yrs, if no treatment is given * Tumour grows slowly & gradually * Patients often asymptomatic & discovered on routine CBC ( v. high WBC) * May be fatigue, wt. loss, night sweats, huge spleen causing abdominal heaviness. * Fever, night sweats * If treatment is not given, this progresses into the next phase.

9. ACCELERATED PHASE * The cancer grows faster during this phase &
WBC count rises fast
* There are specific W.H.O. criteria for diagnosis
of accelerated phase ( increased no. of
basophils & blast cells, spleen size etc)
* Patients may present with features of anemia,
bleeding or infections

10. BLAST CRISIS
* Final phase in the course of CML * Cancer progresses very rapidly and quick death occurs (behaves like acute leukemia) * Excess blast cells in the marrow and blood * Patients present with fever, anemia, bleeding, & infections (more severe now.)

11. If treatment is given during the chronic phase, it may stop the tumor progression into the next phases

12. S/S Depend on the phase of the disease at the time of diagnosis :
Asymptomatic
Fatigue, weakness, wt. loss, pain or heaviness
in the left hypochondrium ( splenomegaly)
Features of anemia, bleeding & infections
Fever, night sweats
Massive splenomegaly, hepatomegaly

13. DIAGNOSIS
1) Blood: * Very high WBC count 30, 000 and more) * High neutros., basophils & eosinophils ( myeloid cells) * Anemia, low platelets ( may be normal also) 2) Bone Marrow : * Hypercellular, with very high number of myeloid cells

14. BLOOD FILM

15. BLOOD FILM

16. BONE MARROW
Note the excess myeloid series cells

17. Diagnosis (contd)
3) Cytogenetics ( gene analysis of the cells) * Leukemic cells have the Philadelphia chromosome (Ph chromosome)

18. TREATMENT
1) Chronic phase : * Tyrosine kinase inhibitors (eg Imatinib) * Introduced in the 2000s. Very good survival rates with this drug (response in more than 95% cases) 2) Accelerated & blast phase: * Imatinib not very effective * These phases treated like acute leukemia( more aggressive treatment with other chemo drugs)

19. PROGNOSIS
*Greatly improved after “tyrosine kinase inhibitors” * 5 yr survival is around 89%

20. How to remember leukemia drugs
1) AML: Cytarabine, Daunorubicin ( C.D.) 2) ALL: Very Dark And Dirty Clothes (Vincristine, Dexa., Asparaginase, Daunorubicin, Cytarabine) 3) CLL: Chocolate Cake From Riyadh ( Chlorambucil, Cyclophosphamide, Fluda- -rabine,Rituximab) 4) CML : Imatinib

21. Quick Points Most common leukemia in children: ALL Auer Rods: AML
Philadelphia Chromosome: CML
Massive splenomegaly: CML

22. THANK YOU & ENJOY YOUR DAY