Background. Prevention of central nervous system (CNS) leukemia by early introduction of therapy to this sanctuary site is an essential component of modern treatment strategy for acute lymphoblastic leukemia (ALL). However, the optimal form of preventive CNS therapy remains debatable. Procedure. To
Treatment of high-risk acute lymphoblastic leukemia in children using the AL851 and ALHR88 protocols: A report from the Kyushu-Yamaguchi children cancer study group in Japan
โ Scribed by Matsuzaki, Akinobu; Ishii, Eiichi; Okamura, Jun; Eguchi, Haruhiko; Yoshida, Nobuyuki; Yanai, Fumio; Inoue, Toshiro; Miyake, Kazuaki; Ishihara, Takanobu; Tsuboi, Chizuru; Nibu, Keiko; Ueda, Kohji; Take, Hiromichi; Miyazaki, Sumio; Tasaka, Hideko
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 770 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
โฆ Synopsis
A total of 125 children, who were diagnosed as having high-risk acute lymphoblastic leukemia (ALL), were treated with two consecutive protocols designated as AL851 (1985( -1988( ) and ALHR88 (1988( -1990)). All patients received induction therapy consisting of vincristine (VCR), prednisolone (PSL), daunorubicin (DNR), and I-asparaginase (I-Asp). In the ALHR88 protocol, the patients whose blasts in the bone marrow (BM) were 225% on day 14 of induction therapy and who were classified into T-cell type received additional cytosine arabinoside (AraC). After consolidation with intermediate-dose methotrexate (MTX), reinduction therapy including VCR, dexamethasone, and adriamycin followed by high-dose AraC was done for all patients. lntrathecal MTX and 24Cy of cranial irradiation were used to prevent central nervous system leukemia. A maintenance ther-apy consisting of 6-mercaptopurine, cyclophosphamide, MTX, DNR, VCR, and AraC was administered for 3 years after achieving a complete remission (CR). CR was achieved in 51/55 (92.7%) for AL851 and 68/70 (97.1%) for ALHR88. The 5-year event-free survival rates were 49.1 f 6.7% in AL851 and 62.5 f 6.1% in ALHR88. The factors related to a poor prognosis were a high initial leukocyte count of greater than 50 x 109/L (P < O.OOl), an L2 morphology of leukemic cells by FAB classification (P = 0.009), the chromosomal abnormality (P = 0.004) and high residual leukemic cells in BM (225%) on day 14 of induction therapy ( P < 0.001).
Taking these factors into consideration, more intensive protocols were started in 1990 for the patients with high-risk ALL.
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