Leukemia - cancer

Leukemia

1. Dr.Sana AL Aqqad

2. Leukemia: Cancer that starts in blood forming cells in B.M.
Classified based on the cell of origin
Types (classifications):
1.Acute lymphoblastic(lymphocytic) leukaemia (ALL)
2.Chronic lymphocytic leukaemia (CLL)
3.Acute myeloid (myelogenous) (Myeloblastic)leukaemia
(AML)
4.Chronic myeloid (myelogenous) leukaemia (CML)

4. It is fatal within weeks to months if not treated.
Median age at diagnosis of pts. with AMLis about 67
years
The peak age for ALLpts. is 2 to 3 years(8-10 Y).
ALL account 30% of all malignancies in children.
About 75-80% of children with leukemia have ALLand 10-
15% AML(The 2 most common type of childhood leukemia)
The prognosisof adult acute leukemia is generally worse
than that of childhood leukemia
When all ages are included, the 5-year relative survival
rate in USA (2008) for ALL was 66% and 25% for AML
Aetiology unknown (Ionizing radiation and benzene exposure are
the only environmental risk factors strongly associated with ALL or
AML).

5. Symptoms:
Feeling unwell
Fatigue/weakness
Dizziness
Easy bleeding (gum,
epistaxis) andbruising.
Patients may have bone
pain(in arms, legs, joints)
from a hyperactive bone
marrow. (ALL)
SOB
Frequent infection
Temperature is often
elevated and may be
caused by disease or
infection
Unexplained weight loss

6. Note :
Symptomsdisease complications:
1.B.M failure:
↓WBC neutropenia infection
↓RBC anemia weakness, SOB, palpitation …..
↓Pltthrombocytopenia bleeding, bruising,
petechiae
2.Other organ involvement: CNS (In ALL)
3.Organ failure (kidney) TLS
Other symptoms:
Splenomegaly, hepatomegaly, and/or lymphadenopathy
are common in patients presenting with ALL
AMLmay present with gum hypertrophy & bleeding.

7. CBC 
Anaemia (normochromic and normocytic).
Thrombocytopenia
Leukocytosis or leukopenia (blood cell (WBC) count
≥50,000 cells/mm
3
, WBC <10,000 cells/mm
3
)
Bone marrow aspirate and biopsy (Confirm diagnosis)
Lymphoblast in bone marrow (>20%)
Lymphoblast in peripheral blood (smear/film)
Pts. with ALL should have a screening lumbar puncture
performed to assess CNS involvement

8. Aetiology: Unknown; atom bomb, children exposed to
radiation in utero, pesticides, cigarette smoking, maternal
use of alcohol.
Symptoms(discussed in previous slides)
Fever (61%)
Bleeding (48%)
Bone pain (23%) usually severe
ALL non specific symptoms; may share other childhood
disease (Juvenile R.A).
Physical examination:
Lymphadenopathy (50%)
Splenomegaly (63%)
hepatosplenomegaly(68%).

10. At diagnosis at least 59%of patients have a normal or low
WBC count;the remainder have elevated counts.
The WBC differential typically shows a low % of neutrophils
and bands, and a marked lymphocytosis.
Lymphoblastsmay be present in the peripheral blood even
with a low WBC count (e.g., 2,000–4,000 cells/μL), but
they are more likely when the WBC count is elevated.
Anemia (a normochromic, normocytic ), along with
thrombocytopenia, is present in most patients.
No stages

11. Diagnosis:
A bone marrow aspirate & biopsy usually necessary to
confirmthe diagnosis of ALL.
Patients with ↑ WBC counts, diagnosis can be confirmed by
studies of lymphoblastsin the peripheral blood.
The diagnosis of ALL is made when at least 20% of lymphoid
cells in the bone marrow are blasts.
Most ALL patients have far greater than 20% blasts, and
many have complete replacement of bone marrow with
lymphoblasts.

12. ALLpoorprognosis:
Male sex
Age (<2 years or > 12 years)
WBC ≥ 50.000 (increase risk of relapse)
CNS involvement
Philadelphia chromosome (Ph+)very high risk to relapse
Treatment: (over all period is 2.5 years)
Induction(induction of remission)typically last 28 days.
Consolidationphase (post-induction phase)
CNS prophylaxis
Maintenancetreatment/phase (2 years)

14. 1.Induction phase
3-4 weeks (28 days)
Goal is complete remission (blasts < 5%, normal Hband plt)
Corticosteroids, vincristine, and various asparaginase
products come closest to this ideal in terms of activity,
primarily against lymphocytic leukemia (these agents are
selectively toxic to the leukemia cells while sparing normal B.M
elements)
CVP other option
Plus
MTX 12 mg IT day 1,15, 29(CNS therapy)
Supportive bld, plt, antibiotics
Vincristinereduce GI motility stool softener
Dexamethasonebehaviour disturbance ; sleep
disturbance, depressed mood, listlessness 
Promethazine (PO)

16. Asparaginase S.E:
Acute pancreatitis
Hyper sensitivity reaction (20-35%), IgGmediated.
(Anaphylactoidrxnless common with IM
administration)
Thrombotic events

18. Early response, (measured by either clearance of blasts
from the peripheral blood or morphologic bone marrow
remission e.g.,<5% bone marrow blasts) on day 7 or
14 of therapy, is predictive of long-term disease-free
survival.
The rapid of response; marker of treatment sensitivity.
Children who were slow responders were 2.7 times
more likely to have a relapse than thosewith more
rapid clearance of blasts.

19. CNS prophylaxis
IT chemotherapy
Prevent CNS relapse.
MTX alone
Triple IT (MTX, cytarabine, Hydrocortisone)
WARNING:
Administration of vincristineinto IT space is fatal.
IT MTX acute arachnoiditis 12-24 hrafter injection
(N,V, headache)

20. 2.Consolidation phase
Usually uses combination approaches that are somewhat
different than induction therapy
Designed to kill leukemia cells in the cell cycle that were
not destroyed by induction therapy.
Prevent relapse
Produce event-free survival (80% in low risk pt.)
2-6 week treatment cycle.

21. Eg. For consolidation regimen:
Methotrexate 1 g/m
2
IV for 24 hours, every 3 weeks ×
6 doses
Vincristine 1.5 mg/m
2
IV on weeks 8, 9, 17, and 18
Prednisone 40 mg/m
2
PO daily ×7 days, weeks 8 & 17
Vincristine 1.5 mg/m
2
IV on days 0, 10, 20, 30, and 40
Dexamethasone 10 mg/m
2
PO daily, days 0–7, 14–20
Vincristine 1.5 mg/m
2
IV on days 0, 7, and 14
PEG-asparaginase2,500 units/m2 IM on day 3
Doxorubicin 25 mg/m
2
IV on days 0, 7, and 14

22. 3.Maintenance treatment (2 years)
Less intensive than previous phases.
Longest phase
Goal: sustains the complete remission achieved from
induction chemotherapy
Consists mostly of continuous oral chemotherapy with
infrequent intravenous and CNS therapy.
Most effective drugs: MTX , Mercaptopurine
Methotrexate: Methotrexate is most effective and least
toxic when administered intermittently, in oral doses of
20 mg/ m2 /week
Mercaptopurineis effective and well tolerated orally
when dosed daily, usually at a dose of 50 to 75 mg/ m2
/day.

23. Appears suddenly and progresses rapidly.
Death as a result of infection or bleeding within weeks
to months if pt. is not effectively treated
Most common acute leukemia in adults(80% of cases).
< 10% of acute leukemias in children younger than 10
years of age.
The incidence increases with age ( 1.3 cases/ 100,000
for those <65 and 12.2 cases/100,000 > 65 years)
At age 40 years, there is only 1 case of AML per
100,000, but the annual incidence increases to 15% at
age > 75 years
Male to female ratio 5: 3
Prognosis is directly related to age.

24. Treatment:
Induction phase
Most commonly is ‘’7+3” regimencombine a 7-day
continuous (IV) infusion of cytarabinewith a short
infusion or bolus of an anthracycline (daunorubicin) given
on days 1 through 3.
Eg: Daunorubicin90 mg/m2/day on days 1 to 3 as an IV bolus
injection, plus cytarabine100 mg/m2/day as a continuous IV
infusion on days 1 to 7.
Continuous infusions of cytarabineare preferred/higher
response rates.
60%-80% of adult pts. attain complete remission
Median duration of remission ONLY 12-18 months

25. 20-40% of ptshas DFS exceeding 5-years
Complications of induction: TLS, Myelosuppression
Very high WBC bldhyperviscosity(ringing ears, stroke,
headache, …)
Give hydroxyurea2-4 g PO/ leukapheresis
If plt< 10,000 cells/mlplttransfusion every 2-3 days
Hg < 8 mg/dl give packed RBC transfusion

26. Consolidation phase
High-dose cytarabinehas been the consolidation
chemotherapy of choice for younger patients with good
intermediate risk disease.
HiDAC alone (>1g/m
2
/day) or in combination with
other agents such as an anthracycline or etoposide.
Patients (60 to 75 years of age):
most clinicians will base induction and consolidation
therapy recommendations on a patient’s performance
status, patient’s wishes, and prognostic factors.
S.E:
Cytarabine normal dose : myelosuppression, fever, skin
rash.
High dose cytarabine: cerebellar toxicity (ataxia), ocular
toxicity, Hand-foot syndrome = plantar-palmar
erythrodysesthesia(PPE).

27. Less than 50% of patients achieving a second remission
Median survival ranging from 3 to 12 months
If relapsesalvage regimen
I.intermediate-dose cytarabineto HiDAC
II.combination regimens:
fludarabine, cytarabine, and G-CSF (FLAG)
cladribine, cytarabine, and G-CSF (CLAG)
followed by allogeneic HCT

28. The typical clinical presentation of the chronic leukemias is
an indolent course
Sing & symptoms:
40%-50% asymptomatic at presentation & are diagnosed
by routine CBC (lymphocytosis, anemia, or thrombocytopenia)
Fatigue
Weight loss
Fever
Anorexia
On physical examination: splenomegalyCML
Night sweats, painful lymphadenopathyCLL
Diagnosis: BM biopsy (hallmark Phchromosome in CML)
translocation t(9;22) create new protein BCR-ABL

29. Characterized by unregulated stem cell proliferation in B.M
and an increase in mature granulocytes in the peripheral
blood.
Increase WBC, differential normal, splenomegaly.
50-70% pts. Present with WBC > 100,000 cells/μl
The median age of diagnosis is 50 to 60 years.
Seldom seen in paediatric.
CML accounts for 15% of adult leukemia cases.
The estimated 7-to 10-year survival rate is 80% to 85%
since the introduction of TK inhibitors(stop regulating BCR-
ABL)
Bone marrow biopsy reveals the cytogenetic hallmark of
CML (Philadelphia chromosome), >95% cases

30. The natural history of CML can be divided into 3
distinct phases:
I.Chronic phase (earliest phase)
II.Accelerated phase
III.Blast phase.
> 90% of patients are diagnosed in chronic phase
The terminal stage of CML is characterized by rapid
accumulation of blast cells in the BM(Blast crisis)
and suppression of normal hematopoiesis that
ultimately leads to death (6-months).
Most problem: Transformation into acute leukaemia

31. phases:
1.chronic phase: patients exhibit leukocytosis & associated
symptoms (described previously), <10% blasts in BM and
peripheral blood.
The duration of the chronic phase may range from a few
months to many years
2.Accelerated phase: increased blast & leukocytosis,
anemia, increased splenomegaly, fever, and bone pain.
If not treated, accelerated phase will generally progress to the
blast phase in less than 6 weeks if not treated.
3.Blast phase (blast crisis): characterized by predominance
of immature cells. Blast crisis is defined as more than
20% blasts in the peripheral blood or BM
In blast crisis, patients often experience bone pain,
fatigue, fever, infections, and bleeding complications.
This phase is often refractory to conventional induction
chemotherapy regimens for AML, (median survival is 6 months)

32. Treatment:
Allogeneic Hematopoietic cell transplantation (HCT)
remains the only curative therapy for CML to datehigh
risk of morbidity & mortality
TK inhibitors are 1
st
line therapyin most patients (not
curative)
Goals of the TK inhibitors are to prolong survival,
prevent progression of disease, & attain a complete
hematologic or cytogenetic remission.
1.Imatinib
2.Nilotinib, approved for patients with resistant Ph+
chromosome chronic-or accelerated phase CML
Patients in accelerated or blast phase at presentation or
those progressing during TK inhibitor are generally
referred for HCT (achieved a 40% and 10% 5-year,
Leukemia free survival, respectively).

33. Newly diagnosed patients who present with very high
leukocyte counts (>100,000 cells/μL), the initial goal of
therapy is to immediately reduce leukocytosis and its
related symptoms.
Hhydroxyureais the most common agent used for
initial leukocyte reduction.
Dose is 2 g/day P, titrate the dose until leukocyte count
< 20,000 cells/ML
Use hydroxyurea 3 -5 days before transitioning to a TK
inhibitor. (Imatinab400mg PO daily with food)
Resistance can be seen at 6-months (rare, 15-25%), no
cytogenetic response.
In suboptimal response escalate imatinabeto 400mg
twice daily
If still no response, change to Nolitinib(400mg BID)

34. •The most common toxicities reported with imatinib
(Gleevec) are superficial edema (face, feet, hands),
nausea, muscle cramps, and rashes
•Nolotinib(Tasigna) demonstrate a higher incidence of
rash, headache, pruritus, and alopecia/hair loss and a
lower incidence of nausea, diarrhea, vomiting, edema,
and muscle spasm.
•Take Tasignaat least 1 hour before or 2 hours after
eating any food

35. IFN-α was the preferred agent in the treatment of CML.
(before TK-I)
IFN-αrelegated to pts. who fail TK-I and are not
candidates for allogeneic HSCT.
Associated with both short-term toxicities and potentially
dose-limiting long-term toxicities (so limited use)
Early toxicity is a flu-like syndrome (fever, chills, myalgia,
headache, and anorexia)
Cardiovascular toxicities (tachycardia, hypotension) 
15% of pts. in the first few weeks.
Long-term S.E:
weight loss, alopecia, neurologic effects (paresthesia,
cognitive impairment, depression)
immune-mediated complications (hemolysis,
thrombocytopenia, nephroticsyndrome, SLE, hypothyroidism) 5%
to 20% of patients

36. patients undergoing transplantation in the accelerated
and blast phases achieved a 40% and 10% 5-year,
leukemia-free survival, respectively.
For those who relapse after HCT, initiation of a TK
inhibitor has improved long-term outcome

37. Mature but not functional lymphocytes.
The most common type of leukemia in adults
Annually, 15,000 new cases and 4,400 deaths
CLL is a disease of the older population
90% of patients > age 50 at diagnosis (median age at
diagnosis is 65 years).
Characterized by overproduction of functionally
incompetent B-cell lymphocytes derived from a single stem
cell clone in B.M
These lymphocytes accumulate in the blood, B.M, lymph
nodes, and spleen.
Some patients experience an indolent course & maintain
good QoL, others experience more aggressive disease and
weakness.

38. 40% of patients are asymptomatic at presentation
Diagnosed by routine CBC (lymphocytosis, anemia, or
thrombocytopenia).
Usually, patient will seek medical check for infection, bleeding……
Symptomatic patients commonly experience:
Night sweats
Fatigue,
weight loss,
Fever
Painful lymphadenopathy
Survival is variable/ depends on the stage of disease at diagnosis.
CLL is staged based on peripheral lymphocyte counts;
enlargement of lymph nodes, liver, and spleen; and the presence
of anemia or thrombocytopenia.

39. Stages: (Binetclassification)
Stage A: no need to treat (watch-wait).
Stage B: depends on symptoms.
Stage C: Needs to treat.
StageLymphocytosis
(>5000 cells/μl)
Thrombocyto
penia
(<100,000)
Anaemia
(<10g/dl)
L.Ns
involve
Medium
Survival
A + _ _ <3 12 years
B + _ _ ≥3 7 years
C + + + Any2-4 years

40. Treatment (stage C):
1.Alkylating agent (oral chlorambucil or
cyclophosphamide) +/-prednisone
chlorambucil +/-prednisone is recommended for patients
older >= 70 years, or in younger patients if they have
significant comorbidities
2.Fludarabineis now considered the single most active
agent in the treatment of CLL.
Fludarabine monotherapy ( dose range of 25 to 30
mg/m2/dose IV ×5 days), orwith cyclophosphamide
and rituximabto increase the response .
Fludarabine my have improved OS compared with
chlorambucil
Fludarabine S.E: Typically mildinclude fever and
immunosuppression. Increased incidence of infection
and autoimmune hemolytic anemia can occur.

41. 4.Rituximab:
Anti-CD 20
The CD20 surface antigen is expressed on a high
percentage of CLL cells.
Rituximab monotherapy is reserved for patients with
significant comorbidity. (375 mg/m2 weekly, for 4
doses)
Generally it is used in combination therapy with
cytotoxic agents
4.Combination therapy:
FC-R:
Fludarabine25 mg/m2 IVon days 1 to 3,
cyclophosphamide 250 mg/m2 IV on days 1 to 3
rituximab 375 mg/m2 IV on day 1 of cycle.
FCR is recommended in patients younger than 70
years without significant comorbidities.

42. Indications for treatment initiation in CLL include:
significant anaemia or thrombocytopenia
progressive disease: demonstrated by
lymphadenopathy, hepatomegaly, splenomegaly, a
lymphocyte doubling time of less than 6 months
Persistent B symptoms (fever, night sweats, and weight
loss)
Threatened end-organ function
Recurrent infection.

43. Refractory/ Relapsed CLL
Classified as treatment-sensitiveif the disease
relapses > 3 years after treatment, or refractoryif the
disease relapses within 2 years of treatment
Treatment-sensitive: Same as treated before, unless
became >70 years or with significant comorbidities.
Treatment refractory: add at least one anti-cancer
agent did not used before.
Eg:
FCR + other agent
If > 70 with comorbidities : high dose
methylprednisolone + Rituximab ORchlorambucil+
prednisolone

44. Acute VS. Chronic leukaemia:
Acute Chronic
Age All ages Usuallyadults
Clinical onset Sudden Insidious
Grow grows & progress very
fast
More indolent/slow
Course (untreated) < 6-month 2-6 years
Leukemic cellImmature blast >20%More mature cells
Anaemia Prominent Mild
Thrombocytopenia Prominent Mild
Lymphadenopathy/
Splenomegaly
Mild Oftenprominent

45. THANKS