scholarly journals Advanced parental age as risk factor for childhood acute lymphoblastic leukemia: results from studies of the Childhood Leukemia International Consortium

2018 ◽  
Vol 33 (10) ◽  
pp. 965-976 ◽  
Author(s):  
Eleni Th. Petridou ◽  
Marios K. Georgakis ◽  
Friederike Erdmann ◽  
Xiaomei Ma ◽  
Julia E. Heck ◽  
...  
2015 ◽  
Vol 26 (9) ◽  
pp. 1257-1270 ◽  
Author(s):  
Helen D. Bailey ◽  
Catherine Metayer ◽  
Elizabeth Milne ◽  
Eleni Th. Petridou ◽  
Claire Infante-Rivard ◽  
...  

2018 ◽  
Vol 36 (9) ◽  
pp. 900-907 ◽  
Author(s):  
Kenichi Sakamoto ◽  
Toshihiko Imamura ◽  
Kentaro Kihira ◽  
Koji Suzuki ◽  
Hisashi Ishida ◽  
...  

Purpose Osteonecrosis (ON) is a serious complication of the treatment of childhood acute lymphoblastic leukemia (ALL); however, data relating to ON in Asian pediatric patients with ALL are scarce. Therefore, we performed a retrospective analysis of cohorts of Japanese patients with ALL to clarify the incidence, clinical characteristics, and risk factors of ON. Patients and Methods The incidence and characteristics of ON were determined in patients with ALL (n = 1,662) enrolled in two studies from the Japan Association of Childhood Leukemia Study (JACLS) group (n = 635 and n = 1,027 patients treated with the ALL-97 and ALL-02 protocols, respectively). Results In total, 24 of 1,662 patients suffered from ON, of which 12 of 635 and 12 of 1,027 patients were treated with the ALL-97 and the ALL-02 protocol, respectively. Of the 24 patients, 23 were older than 10 years. In multivariate analysis, age (≥ 10 years) was the sole significant risk factor for ON ( P < .001). Separate evaluation of patients ≥ 10 years of age indicated a 5-year cumulative incidence of ON of 7.2% (95% CI, 4.0% to 12.6%) and 5.9% (95% CI, 3.3% to 10.4%) in the ALL-97 and the ALL-02 protocol, respectively, which was lower than reported previously, despite an administration of dexamethasone (DEX) similar to that in comparable studies; however, concomitant administration of DEX and l-asparaginase was reduced in the JACLS protocols. Conclusion We identified a low frequency of ON in the JACLS ALL-97 and ALL-02 studies. Although the sole risk factor for ON was age (≥ 10 years), even among high-risk patients, ON incidence was significantly lower than that reported in previous studies. These results suggest that, not only the total amount of DEX, but also how DEX and l-asparaginase are administered, which affects the clearance of DEX, may be associated with ON incidence in patients with ALL.


2011 ◽  
Vol 57 (1) ◽  
pp. 160-162 ◽  
Author(s):  
Agata Pastorczak ◽  
Malgorzata Stolarska ◽  
Joanna Trelińska ◽  
Joanna Zawitkowska ◽  
Jerzy Kowalczyk ◽  
...  

Blood ◽  
1999 ◽  
Vol 94 (11) ◽  
pp. 3957-3958 ◽  
Author(s):  
M. Tevfik Dorak ◽  
Alan K. Burnett ◽  
Mark Worwood ◽  
Anne M. Sproul ◽  
Brenda E.S. Gibson

1987 ◽  
Vol 5 (7) ◽  
pp. 1015-1021 ◽  
Author(s):  
G V Dahl ◽  
G K Rivera ◽  
A T Look ◽  
H O Hustu ◽  
D K Kalwinsky ◽  
...  

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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