<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Seftel MD</submitter><funding>HRSA/DHHS</funding><funding>National Cancer Institute (NCI)</funding><funding>National Heart, Lung and Blood Institute (NHLBI)</funding><funding>NCI</funding><funding>NHLBI NIH HHS</funding><funding>*Actinium Pharmaceuticals; Allos Therapeutics, Inc.; *Amgen, Inc</funding><funding>NCI NIH HHS</funding><funding>National Cancer Institute (NCI) (to SES)</funding><funding>PHS HHS</funding><funding>Office of Naval Research</funding><funding>the National Institute of Allergy and Infectious Diseases (NIAID)</funding><pagination>322-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4764423</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>91(3)</volume><pubmed_abstract>For adults with Philadelphia chromosome-negative (Ph-) acute lymphoblastic leukemia (ALL) in first complete remission (CR1), allogeneic hematopoietic cell transplantation (HCT) is an established curative strategy. However, pediatric-inspired chemotherapy may also offer durable leukemia-free survival in the absence of HCT. We compared 422 HCT recipients aged 18-50 years with Ph-ALL in CR1 reported to the CIBMTR with an age-matched concurrent cohort of 108 Ph- ALL CR1 patients who received a Dana-Farber Consortium pediatric-inspired non-HCT regimen. At 4 years of follow-up, incidence of relapse after HCT was 24% (95% CI 19-28) versus 23% (95% CI 15-32) for the non-HCT (chemo) cohort (P=0.97). Treatment-related mortality (TRM) was higher in the HCT cohort [HCT 37% (95% CI 31-42) versus chemo </pubmed_abstract><journal>American journal of hematology</journal><pubmed_title>Pediatric-inspired therapy compared to allografting for Philadelphia chromosome-negative adult ALL in first complete remission.</pubmed_title><pmcid>PMC4764423</pmcid><funding_grant_id>T32 CA009515</funding_grant_id><funding_grant_id>P01CA068484 (The DFCI ALL Consortium trials in younger adults)</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>U24-CA076518</funding_grant_id><funding_grant_id>Grant/Cooperative Agreement 5U10HL069294</funding_grant_id><funding_grant_id>P01 CA068484</funding_grant_id><funding_grant_id>N00014-13-1-0039</funding_grant_id><funding_grant_id>N00014-14-1-0028</funding_grant_id><funding_grant_id>HHSH250201200016C with Health Resources and Services Administration</funding_grant_id><funding_grant_id>U10 HL069294</funding_grant_id><funding_grant_id>HHSH250201200016C</funding_grant_id><funding_grant_id>U24 CA076518</funding_grant_id><funding_grant_id>5U10HL069294</funding_grant_id><funding_grant_id>Public Health Service Grant/Cooperative Agreement U24-CA076518 (CIBMTR)</funding_grant_id><pubmed_authors>Wang HL</pubmed_authors><pubmed_authors>Sallan SE</pubmed_authors><pubmed_authors>Zhang MJ</pubmed_authors><pubmed_authors>Bergeron J</pubmed_authors><pubmed_authors>Lazarus HM</pubmed_authors><pubmed_authors>Seftel MD</pubmed_authors><pubmed_authors>Couban S</pubmed_authors><pubmed_authors>Freytes CO</pubmed_authors><pubmed_authors>Saber W</pubmed_authors><pubmed_authors>Tallman MS</pubmed_authors><pubmed_authors>Woolfrey AE</pubmed_authors><pubmed_authors>Acute Leukemia Committee of the CIBMTR and the Dana Farber ALL Consortium</pubmed_authors><pubmed_authors>DeAngelo DJ</pubmed_authors><pubmed_authors>Kharfan-Dabaja MA</pubmed_authors><pubmed_authors>Soiffer R</pubmed_authors><pubmed_authors>Neuberg D</pubmed_authors><pubmed_authors>Hamadani M</pubmed_authors><pubmed_authors>Paulson K</pubmed_authors><pubmed_authors>Nishihori T</pubmed_authors><pubmed_authors>Weisdorf DJ</pubmed_authors><pubmed_authors>Ballen KK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pediatric-inspired therapy compared to allografting for Philadelphia chromosome-negative adult ALL in first complete remission.</name><description>For adults with Philadelphia chromosome-negative (Ph-) acute lymphoblastic leukemia (ALL) in first complete remission (CR1), allogeneic hematopoietic cell transplantation (HCT) is an established curative strategy. However, pediatric-inspired chemotherapy may also offer durable leukemia-free survival in the absence of HCT. We compared 422 HCT recipients aged 18-50 years with Ph-ALL in CR1 reported to the CIBMTR with an age-matched concurrent cohort of 108 Ph- ALL CR1 patients who received a Dana-Farber Consortium pediatric-inspired non-HCT regimen. At 4 years of follow-up, incidence of relapse after HCT was 24% (95% CI 19-28) versus 23% (95% CI 15-32) for the non-HCT (chemo) cohort (P=0.97). Treatment-related mortality (TRM) was higher in the HCT cohort [HCT 37% (95% CI 31-42) versus chemo </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-04-21T18:34:59.047Z</modification><creation>2019-03-27T02:09:42Z</creation></dates><accession>S-EPMC4764423</accession><cross_references><pubmed>26701142</pubmed><doi>10.1002/ajh.24285</doi></cross_references></HashMap>