1972
DOI: 10.1002/1097-0142(197212)30:6<1480::aid-cncr2820300611>3.0.co;2-3
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Chemotherapy of acute lymphocytic leukemia of childhood

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Cited by 102 publications
(19 citation statements)
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“…' The lack of specificity of both chemotherapeutic agents and radiation therapy (RT) in terms of differentiating neoplastic cells from metabolically active normal cells might result in abnormalities of dental and facial development. [2][3][4][5][6] In addition to the direct effects of therapy on growing cells, an indirect effect might also occur due to altered hypothalmic-pituitary function resulting in diminished growth hormone produ~tion.~-" This in turn may also adversely effect odontogenesis and craniofacial development.…”
Section: S the Prognosis For Childhood Acute Lymphoblasticmentioning
confidence: 99%
“…' The lack of specificity of both chemotherapeutic agents and radiation therapy (RT) in terms of differentiating neoplastic cells from metabolically active normal cells might result in abnormalities of dental and facial development. [2][3][4][5][6] In addition to the direct effects of therapy on growing cells, an indirect effect might also occur due to altered hypothalmic-pituitary function resulting in diminished growth hormone produ~tion.~-" This in turn may also adversely effect odontogenesis and craniofacial development.…”
Section: S the Prognosis For Childhood Acute Lymphoblasticmentioning
confidence: 99%
“…1,2 Clinical studies performed in the 1970s and 1980s showed that treatment intensification during maintenance improved the outcome of nonintensive protocols. 3,4 Among the combinations added to the thiopurine-methotrexate basic continuation therapy, reinductions of vincristine (VCR) and prednisone (PRED) have often been used and have improved treatment outcome for some patients. 5 A large retrospective analysis by the Childhood ALL Collaborative Group 6 suggested that for patients at standard or intermediate risk of relapse receiving a treatment regimen of moderate intensity, the addition of VCR ϩ PRED pulses to continuation therapy did improve the disease-free survival (DFS) from 59.5% to 68.9%.…”
Section: Introductionmentioning
confidence: 99%
“…In Slovakia, an ALL treatment protocol was initiated in the early 70s when Čáp, Koza and Černý worked out the fi rst protocol (0171), based on the work of American authors Holand et al, in which the treatment was already divided into stages of induction (prednisone, vincristine), consolidation (methotrexate, mercaptopurine), intensifi cation (prednisone, vincristine, methotrexate, mercaptoputine, cyclophosphamide), maintenance (prednisone, vincristine, methotrexate, mercaptopurine) and prophylaxis/treatment of leukaemia CNS (methotrexate and cytarabine intrathecal, cranial radiotherapy 24 Gy) [1,2]. Five years later, the 0276 protocol was created with the addition of L-asparaginase for induction and with the maintenance treatment extended from 72 to 132 weeks.…”
Section: Introductionmentioning
confidence: 99%