2601
INITIAL
COMMENTS ON PROGNOSTIC FACTORS IN 35 CHILDREN WITH ACUTE LYMPHOBLASTIC
LEUKEMIA AT NATIONAL INSTITUTE OF PEDIATRIC OF HANOI - VIETNAM Tran Thi Hong Ha, Vo Thanh Huong, Nguyen Cong Khanh, Phan Thi
Phi Phi, Pham Quang Vinh National
Institute of Pediatric of Hanoi, Vietnam Objectives:
Initial study on prognotic factors in
children with acute lymphoblastic leukenia (ALL) in Vietnam. Materials
and methods: 35 children suffered from
ALL, 16 children were treated, 9 children were achieved complete remission
and 7 another were on the continuing treatment. All patients were
classified by morphology with FAB criteria and by immunology with
immunofluorescence indirect assay with anti-CD3, anti-CD4, anti-CD8,
anti-CD19. Analyse chromosomes of bone marrow cells by cells culture and
chromosomal banding technique. Results:
Age of onset, sex, morphology FAB,
labolatory findings: Age: 2-10 years old 74.2%-<2 years old 2.9% and
>10 years old 22.9%. Sex: Male 68.6%, female: 31.4%, WBC: <50.109/1:
62.8%-��100.109/1:8 cases (22.9%) all are
male. Morphology FAB: L1:
91.4%-L2: 8.6%. Hemoglobin level: <100g/l: 94.3%-��100g/l: 5.7%. Platelet
count: <50.109/l: 71.4%->100.109/l:5.7% -Immunophenotype:
Null-cell ALL 80.6% of cases, mainly in group 2-10 years old (80%) and
WBC<50.109/l (36%). All cases with T-cell All (9.7%) are
male, >10 years old and WBC >100.109/l. B-cell ALL (9.7%)
distributed more scatter among the age, sex, WBC morphology group. Cytogenetic: At
diagnosis: Normal 33.3%. Hyperploidy (47) 13.3%. Hypoploidy (44,45) 26.7%.
Pseudodiploidy 26.7%. In this number, some chromosomal abnormalities
associated with poor prognosis: 1 case philadelphia positive, 1 case had
both 9p and 14q+. In complete remission, 8
cases were analysed chromosomes, the chromosomal abnormalities were
disappeared in all cases. Conclusion: Age, sex, morphology FAB and labolatory
findings: Rate % patients in favorable prognostic group were high,
excluding sex and platelet count. Patients with T-cell ALL tend to be
higher initial leukocyte count, male and older age. At diagnosis,
chromosomal abnormalities were found 2/3 of cases, some in which associated
with poor prognosis (Phl-positive, 9q-, 14q+). In
complete remission, the chromosomal abnormalities were disappeared in all
cases analysed chromosomes.