<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Eichinger A</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>2567-2576</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9613465</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(11)</volume><pubmed_abstract>Total body irradiation (TBI)-based conditioning is associated with superior leukemia-free survival in children with ALL undergoing HSCT. However, the risk for subsequent malignant neoplasms (SMN) remains a significant concern. We analyzed 705 pediatric patients enrolled in the prospective ALL-SCT-BFM-2003 trial and its subsequent registry. Patients &amp;gt;2 years received conditioning with TBI 12 Gy/etoposide (n = 558) and children ≤2 years of age or with contraindications for TBI received busulfan/cyclophosphamide/etoposide (n = 110). The 5- and 10-year cumulative incidence of SMN was 0.02 ± 0.01 and 0.13 ± 0.03, respectively. In total, 39 SMN (34 solid tumors, 5 MDS/AML) were diagnosed in 33 patients at a median of 5.8 years (1.7-13.4), exclusively in the TBI group. Of 33 affected patients,</pubmed_abstract><journal>Leukemia</journal><pubmed_title>Incidence of subsequent malignancies after total body irradiation-based allogeneic HSCT in children with ALL - long-term follow-up from the prospective ALL-SCT 2003 trial.</pubmed_title><pmcid>PMC9613465</pmcid><funding_grant_id>EI 1185/1-1</funding_grant_id><pubmed_authors>Peters C</pubmed_authors><pubmed_authors>Deubzer HE</pubmed_authors><pubmed_authors>Lang P</pubmed_authors><pubmed_authors>Schlegel PG</pubmed_authors><pubmed_authors>Schulz A</pubmed_authors><pubmed_authors>Bader P</pubmed_authors><pubmed_authors>Poetschger U</pubmed_authors><pubmed_authors>Eichinger A</pubmed_authors><pubmed_authors>Wawer A</pubmed_authors><pubmed_authors>Basu O</pubmed_authors><pubmed_authors>Kafa K</pubmed_authors><pubmed_authors>Kuhl JS</pubmed_authors><pubmed_authors>Lange BS</pubmed_authors><pubmed_authors>Gungor T</pubmed_authors><pubmed_authors>Corbacioglu S</pubmed_authors><pubmed_authors>Glogova E</pubmed_authors><pubmed_authors>Greil J</pubmed_authors><pubmed_authors>Beier R</pubmed_authors><pubmed_authors>Sauer MG</pubmed_authors><pubmed_authors>Strahm B</pubmed_authors><pubmed_authors>Claviez A</pubmed_authors><pubmed_authors>Gruhn B</pubmed_authors><pubmed_authors>Classen CF</pubmed_authors><pubmed_authors>Meisel R</pubmed_authors><pubmed_authors>Stachel D</pubmed_authors><pubmed_authors>Albert MH</pubmed_authors><pubmed_authors>Burkhardt B</pubmed_authors><pubmed_authors>Muller I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Incidence of subsequent malignancies after total body irradiation-based allogeneic HSCT in children with ALL - long-term follow-up from the prospective ALL-SCT 2003 trial.</name><description>Total body irradiation (TBI)-based conditioning is associated with superior leukemia-free survival in children with ALL undergoing HSCT. However, the risk for subsequent malignant neoplasms (SMN) remains a significant concern. We analyzed 705 pediatric patients enrolled in the prospective ALL-SCT-BFM-2003 trial and its subsequent registry. Patients &amp;gt;2 years received conditioning with TBI 12 Gy/etoposide (n = 558) and children ≤2 years of age or with contraindications for TBI received busulfan/cyclophosphamide/etoposide (n = 110). The 5- and 10-year cumulative incidence of SMN was 0.02 ± 0.01 and 0.13 ± 0.03, respectively. In total, 39 SMN (34 solid tumors, 5 MDS/AML) were diagnosed in 33 patients at a median of 5.8 years (1.7-13.4), exclusively in the TBI group. Of 33 affected patients,</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-07-14T15:52:05.809Z</modification><creation>2024-11-09T20:29:30.381Z</creation></dates><accession>S-EPMC9613465</accession><cross_references><pubmed>36097283</pubmed><doi>10.1038/s41375-022-01693-z</doi></cross_references></HashMap>