Reduction of adult height in childhood acute lymphoblastic leukemia survivors after prophylactic cranial irradiation

2005 ◽  
Vol 45 (2) ◽  
pp. 139-143 ◽  
Author(s):  
M.E.J. Bongers ◽  
A.B. Francken ◽  
C. Rouwé ◽  
W.A. Kamps ◽  
A. Postma
Keyword(s):  
Acute Lymphoblastic Leukemia ◽  
Adult Height ◽  
Lymphoblastic Leukemia ◽  
Cranial Irradiation ◽  
Prophylactic Cranial Irradiation ◽  
Childhood Acute Lymphoblastic Leukemia

Teniposide plus cytarabine improves outcome in childhood acute lymphoblastic leukemia presenting with a leukocyte count greater than or equal to 100 x 10(9)/L.

1987 ◽  
Vol 5 (7) ◽  
pp. 1015-1021 ◽  
Author(s):  
G V Dahl ◽  
G K Rivera ◽  
A T Look ◽  
H O Hustu ◽  
D K Kalwinsky ◽  
...  
Keyword(s):  
Acute Lymphoblastic Leukemia ◽  
Childhood Leukemia ◽  
Leukocyte Count ◽  
Lymphoblastic Leukemia ◽  
Cranial Irradiation ◽  
Childhood Acute Lymphoblastic Leukemia ◽  
Remission Induction ◽  
First Year ◽  
P 16 ◽  
Continuation Treatment

Childhood acute lymphoblastic leukemia with an initial leukocyte count greater than or equal to 100 X 10(9)/L responds poorly to conventional chemotherapy. To extend event-free survival (EFS) in this disease, we devised a protocol that specifies intensive 2-week courses of teniposide (VM-26, 165 mg/m2) plus cytarabine (ara-C, 300 mg/m2), before and immediately after standard 4-week remission induction therapy with prednisone, vincristine, and L-asparaginase. The VM-26 and ara-C combination was also administered intermittently for the first year of continuation treatment with oral 6-mercaptopurine and methotrexate. CNS prophylaxis consisted of periodic intrathecal (IT) injections of methotrexate and delayed cranial irradiation. At a median follow-up of 4 years, the estimated EFS rate for 57 consecutive patients with leukocyte counts of 100 to 1,000 X 10(9)/L was 44%, compared with 10% for matched controls (P less than .001). Remission induction rates in the two groups were similar (82% v 72%, P = .16). Twenty-five patients in the VM-26/ara-C group have survived without adverse events for 2.7 to 6.8 years, whereas only nine of the controls achieved more than a year of EFS. The most common complications during early treatment were acute hyperkalemia from rapid tumor cell lysis and infections due to prolonged marrow aplasia. Continuation chemotherapy was well tolerated. We conclude that VM-26 plus ara-C, added to each phase of an otherwise basic regimen of chemotherapy, will substantially improve prognosis in this high-risk form of childhood leukemia.

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