Testosterone deficiency in men surviving childhood acute leukemia after treatment with hematopoietic stem cell transplantation or testicular radiation: an L.E.A. study

We included 255 patients from the L.E.A. French long-term follow-up cohort. All had received hematopoietic stem cell transplantation (HSCT) and/or testicular radiation for childhood acute leukemia and were older than 18 years at last L.E.A. evaluation. Total testosterone deficiency was defined as a...

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Published inBone marrow transplantation (Basingstoke) Vol. 56; no. 6; pp. 1422 - 1425
Main Authors Lopez, Romain, Plat, Geneviève, Bertrand, Yves, Ducassou, Stéphane, Saultier, Paul, Berbis, Julie, Pochon, Cécile, Hamidou, Zeinab, Poiree, Marilyne, Tabone, Marie-Dominique, Kanold, Justyna, Dalle, Jean-Hugues, Gandemer, Virginie, Paillard, Catherine, Sirvent, Nicolas, Plantaz, Dominique, Thouvenin, Sandrine, Pellier, Isabelle, Ansoborlo, Sophie, Leverger, Guy, Baruchel, André, Auquier, Pascal, Michel, Gérard
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.06.2021
Nature Publishing Group
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Summary:We included 255 patients from the L.E.A. French long-term follow-up cohort. All had received hematopoietic stem cell transplantation (HSCT) and/or testicular radiation for childhood acute leukemia and were older than 18 years at last L.E.A. evaluation. Total testosterone deficiency was defined as a <12 nmol/l level or by substitutive therapy, partial deficiency as normal testosterone with elevated luteinizing hormone (>10 UI/l). After myeloablative total body irradiation ( n = 178), 55.6% had total deficiency, 15.7% partial deficiency, and 28.7% were normal. A 4–6 Gy testicular boost and a younger age at HSCT increased significantly the risk. After a Busulfan-containing myeloablative conditioning regimen ( n = 53), 28.3% had total deficiency, 15.1% partial deficiency, 56.6% were normal (62.5% vs. 0% in patients without or with additional testicular radiation). A 24-Gy testicular radiation without HSCT induced total or partial deficiency in 71.4% and 28.6%, respectively ( n = 21). Total testosterone deficiency increased the risk of metabolic syndrome: 25% vs. 12.1% in men with partial testosterone deficiency and 8.8% when Leydig cell function was normal ( p = 0.031).
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ISSN:0268-3369
1476-5365
1476-5365
DOI:10.1038/s41409-020-01180-y