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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003302naa a2200469 4500
001oai:DiVA.org:uu-246896
003SwePub
008150311s2014 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:129831070
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2468962 URI
024a https://doi.org/10.1182/blood-2013-03-4903342 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1298310702 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Aplenc, Richard4 aut
2451 0a Effect of body mass in children with hematologic malignancies undergoing allogeneic bone marrow transplantation.
264 1b American Society of Hematology,c 2014
338 a print2 rdacarrier
520 a The rising incidence of pediatric obesity may significantly affect bone marrow transplantation (BMT) outcomes. We analyzed outcomes in 3687 children worldwide who received cyclophosphamide-based BMT regimens for leukemias between 1990 and 2007. Recipients were classified according to age-adjusted body mass index (BMI) percentiles as underweight (UW), at risk of UW (RUW), normal, overweight (OW), or obese (OB). Median age and race were similar in all groups. Sixty-one percent of OB children were from the United States/Canada. Three-year relapse-free and overall survival ranged from 48% to 52% (P = .54) and 55% to 58% (P = .81) across BMI groups. Three-year leukemia relapses were 33%, 33%, 29%, 25%, and 21% in the UW, RUW, normal, OW, and OB groups, respectively (P < .001). Corresponding cumulative incidences for transplant-related mortality (TRM) were 18%, 19%, 21%, 22%, and 28% (P < .01). Multivariate analysis demonstrated a decreased risk of relapse compared with normal BMI (relative risk [RR] = 0.73; P < .01) and a trend toward higher TRM (RR = 1.28; P = .014). BMI in children is not significantly associated with different survival after BMT for hematologic malignancies. Obese children experience less relapse posttransplant compared with children with normal BMI; however, this benefit is offset by excess in TRM.
700a Zhang, Mei-Jie4 aut
700a Sung, Lillian4 aut
700a Zhu, Xiaochun4 aut
700a Ho, Vincent T4 aut
700a Cooke, Kenneth4 aut
700a Dvorak, Christopher4 aut
700a Hale, Gregory4 aut
700a Isola, Luis M4 aut
700a Lazarus, Hillard M4 aut
700a McCarthy, Philip L4 aut
700a Olsson, Richardu Karolinska Institutet,Uppsala universitet,Centrum för klinisk forskning i Sörmland (CKFD)4 aut0 (Swepub:uu)riols677
700a Pulsipher, Michael4 aut
700a Pasquini, Marcelo C4 aut
700a Bunin, Nancy4 aut
710a Uppsala universitetb Centrum för klinisk forskning i Sörmland (CKFD)4 org
773t Bloodd : American Society of Hematologyg 123:22, s. 3504-11q 123:22<3504-11x 0006-4971x 1528-0020
856u https://europepmc.org/articles/pmc4041168
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-246896
8564 8u https://doi.org/10.1182/blood-2013-03-490334
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:129831070

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