Literature DB >> 24038890

Pubertal development and fertility in survivors of childhood acute myeloid leukemia treated with chemotherapy only: a NOPHO-AML study.

Lene Molgaard-Hansen1, Anne-Sofie Skou, Anders Juul, Heidi Glosli, Kirsi Jahnukainen, Marianne Jarfelt, Guðmundur K Jónmundsson, Johan Malmros, Karsten Nysom, Henrik Hasle.   

Abstract

BACKGROUND: More than 60% of children with acute myeloid leukemia (AML) become long-term survivors. Most are cured using chemotherapy without hematopoietic stem cell transplantation (HSCT). We report on pubertal development and compare self-reported parenthood among AML survivors and their siblings. PROCEDURE: We included 137 children treated for AML according to the Nordic Society of Pediatric Hematology and Oncology (NOPHO)-AML-84, -88, and -93 trials, who were alive by June 2007. Patients with relapse or treated with HSCT were excluded. AML survivors participated in a physical and biochemical examination (n = 102) and completed a questionnaire (n = 101). One of their siblings completed an identical questionnaire (n = 84).
RESULTS: At a median follow-up of 11 years (range 5-25) after diagnosis of AML the survivors (median age 16 years, range 5-36) were either prepubertal or had entered puberty normally. Serum levels of FSH, LH, testosterone, estradiol, sex hormone binding globulin (SHBG), inhibin A and B, and testicular volumes were within normal ranges. Anti-Müllerian hormone (AMH) levels were decreased in 5 of 40 postpubertal females. Mean reported age at menarche was 13.1 (range 11-17) years. Among survivors 15 years of age or older 31% of females reported pregnancies and 9% of males reported pregnancies in their partners, rates comparable with the frequency reported by their siblings.
CONCLUSIONS: Most AML survivors treated with chemotherapy had normal pubertal development and fertility, however, AMH levels were decreased in 13% of postpubertal females. Longer follow-up is necessary to evaluate possible risk of premature ovarian failure.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  acute myeloid leukemia; children; fertility; late effects; premature ovarian failure; puberty

Mesh:

Substances:

Year:  2013        PMID: 24038890     DOI: 10.1002/pbc.24715

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  8 in total

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Journal:  Support Care Cancer       Date:  2017-02-02       Impact factor: 3.603

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Journal:  Clin Cancer Res       Date:  2016-09-20       Impact factor: 12.531

3.  Anti-Müllerian hormone and Inhibin B after stem cell transplant in childhood: a comparison of myeloablative, reduced intensity and treosulfan-based chemotherapy regimens.

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Journal:  Chin Med J (Engl)       Date:  2016-10-05       Impact factor: 2.628

6.  Late outcomes in survivors of childhood acute myeloid leukemia: a report from the St. Jude Lifetime Cohort Study.

Authors:  Neel S Bhatt; Malek J Baassiri; Wei Liu; Nickhill Bhakta; Wassim Chemaitilly; Matthew J Ehrhardt; Hiroto Inaba; Kevin Krull; Kirsten K Ness; Jeffrey E Rubnitz; Deokumar Srivastava; Leslie L Robison; Melissa M Hudson; Daniel A Mulrooney
Journal:  Leukemia       Date:  2021-01-25       Impact factor: 11.528

7.  Long-term health outcomes in survivors of childhood AML treated with allogeneic HSCT: a NOPHO-AML Study.

Authors:  Mari Wilhelmsson; Heidi Glosli; Marianne Ifversen; Jonas Abrahamsson; Jacek Winiarski; Kirsi Jahnukainen; Henrik Hasle
Journal:  Bone Marrow Transplant       Date:  2018-09-21       Impact factor: 5.483

8.  Efficacy of a Mer and Flt3 tyrosine kinase small molecule inhibitor, UNC1666, in acute myeloid leukemia.

Authors:  Alisa B Lee-Sherick; Weihe Zhang; Kelly K Menachof; Amanda A Hill; Sean Rinella; Gregory Kirkpatrick; Lauren S Page; Michael A Stashko; Craig T Jordan; Qi Wei; Jing Liu; Dehui Zhang; Deborah DeRyckere; Xiaodong Wang; Stephen Frye; H Shelton Earp; Douglas K Graham
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  8 in total

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