<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Winick N</submitter><funding>NCI NIH HHS</funding><pagination>1006-1016</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7749787</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>34(4)</volume><pubmed_abstract>The delayed intensification (DI) enhanced outcome for patients with acute lymphoblastic leukemia (ALL) treated on BFM 76/79 and CCG 105 after a prednisone-based induction. Childrens Oncology Group protocols P9904/9905 evaluated DI via a post-induction randomization for eligible National Cancer Institute (NCI) standard (SR) and high-risk (HR) patients. A second randomization compared intravenous methotrexate (IV MTX) as a 24- (1 g/m&lt;sup>2&lt;/sup>) vs. 4-h (2 g/m&lt;sup>2&lt;/sup>) infusion. NCI SR patients received a dexamethasone-based three-drug and NCI HR/CNS 3 SR patients a prednisone-based four-drug induction. End induction MRD (minimal residual disease) was obtained but did not impact treatment. DI improved the 10-year continuous complete remission (CCR) rate; 75.5 ± 2.5% vs. 81.8 ± 2.2% p = </pubmed_abstract><journal>Leukemia</journal><pubmed_title>Randomized assessment of delayed intensification and two methods for parenteral methotrexate delivery in childhood B-ALL: Children's Oncology Group Studies P9904 and P9905.</pubmed_title><pmcid>PMC7749787</pmcid><funding_grant_id>U10 CA098543</funding_grant_id><funding_grant_id>U10 CA180886</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><funding_grant_id>U10 CA098413</funding_grant_id><pubmed_authors>Carroll WL</pubmed_authors><pubmed_authors>Larsen E</pubmed_authors><pubmed_authors>Shuster J</pubmed_authors><pubmed_authors>Carroll A</pubmed_authors><pubmed_authors>Borowitz MJ</pubmed_authors><pubmed_authors>Paul Bowman W</pubmed_authors><pubmed_authors>Devidas M</pubmed_authors><pubmed_authors>Camitta BM</pubmed_authors><pubmed_authors>Hunger SP</pubmed_authors><pubmed_authors>Martin PL</pubmed_authors><pubmed_authors>Pullen J</pubmed_authors><pubmed_authors>Winick N</pubmed_authors><pubmed_authors>Willman C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Randomized assessment of delayed intensification and two methods for parenteral methotrexate delivery in childhood B-ALL: Children's Oncology Group Studies P9904 and P9905.</name><description>The delayed intensification (DI) enhanced outcome for patients with acute lymphoblastic leukemia (ALL) treated on BFM 76/79 and CCG 105 after a prednisone-based induction. Childrens Oncology Group protocols P9904/9905 evaluated DI via a post-induction randomization for eligible National Cancer Institute (NCI) standard (SR) and high-risk (HR) patients. A second randomization compared intravenous methotrexate (IV MTX) as a 24- (1 g/m&lt;sup>2&lt;/sup>) vs. 4-h (2 g/m&lt;sup>2&lt;/sup>) infusion. NCI SR patients received a dexamethasone-based three-drug and NCI HR/CNS 3 SR patients a prednisone-based four-drug induction. End induction MRD (minimal residual disease) was obtained but did not impact treatment. DI improved the 10-year continuous complete remission (CCR) rate; 75.5 ± 2.5% vs. 81.8 ± 2.2% p = </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2025-04-26T10:10:02.137Z</modification><creation>2022-02-09T10:54:02.652Z</creation></dates><accession>S-EPMC7749787</accession><cross_references><pubmed>31728054</pubmed><doi>10.1038/s41375-019-0642-2</doi></cross_references></HashMap>