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Protocols - Hemorio

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CHRONIC MYELOID LEUKEMIA<br />

LABORATORIAL TESTS TO DIAGNOSIS<br />

Peripheral blood:<br />

- Complete blood count (with specific leukometry + platelet count)<br />

- Uric acid, calcium, creatinine, TGO, TGP, alkaline phosphatase, LDH, triglycerides<br />

- Neutrophils alkaline phosphatase<br />

- patient and siblings’ HLA study<br />

- qualitative RT-PCR to bcr-abl<br />

Bone marrow:<br />

- cytology<br />

- conventional cytogenetic ( 3- 5 ml of bone marrow in sodium heparin)<br />

- FISH in case of cytogenetic without mitosis<br />

- MO biopsy – histopatological test<br />

Suspend hydroxiurea for at least 5 days before collection for cytogenetic<br />

PROGNOSTIC CRITERION - Calculate Sokal index<br />

DIAGNOSIS CONFIRMATION:<br />

- Presence of Philadelphia chromosome (Cr Ph) t(9;22)(q34;q11) or presence of BCR-ABL<br />

PHASE DEFINITIONS:<br />

• Chronic Phase<br />

• Accelerated Phase<br />

• Blasts SP or MO 10 to 29%<br />

• Basophils SP > 20%<br />

• Platelets < 100000 (not by treatment)<br />

• Platelets > 1000000 (no response to treatment)<br />

• Spleen ongoing increase and leukometry<br />

• Clonal progress<br />

• Blastic Crisis<br />

• Blasts > 30 % SP or MO<br />

• Extra medullar proliferation<br />

• Blast nests on bone marrow biopsy<br />

TREATMENT:<br />

After diagnosis confirmation, request imatinib’s release<br />

Cytoreduction until leukometry gets to 15.000 /mm 3 :<br />

- hydroxiurea 15 to 40mg/kg/day in 2 to 3 PO administrations<br />

- alopurinol 300 -600 mg/day (children 10mg/kg/day)<br />

- oral hydration<br />

- hematological and biochemical control<br />

Hyperleukocitary patients, evaluate hospitalization:<br />

- aracythin 100mg/m 2 EV continuous infusion 24h<br />

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