Endocrinopathies after Allogeneic and Autologous Transplantation of Hematopoietic Stem Cells
Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem cell transplant (HSCT). This review summarizes main endocrine disorders reported in literature and observed in our center as consequence of aut...
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Published in | TheScientificWorld Vol. 2014; no. 2014; pp. 1 - 13 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
01.01.2014
John Wiley & Sons, Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2356-6140 1537-744X 1537-744X |
DOI | 10.1155/2014/282147 |
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Abstract | Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem cell transplant (HSCT). This review summarizes main endocrine disorders reported in literature and observed in our center as consequence of auto- and allo-HSCT and outlines current options for their management. Gonadal impairment has been found early in approximately two-thirds of auto- and allo-HSCT patients: 90–99% of women and 60–90% of men. Dysfunctions of the hypothalamus-pituitary-growth hormone/insulin growth factor-I axis, hypothalamus-pituitary-thyroid axis, and hypothalamus-pituitary-adrenal axis were documented as later complicances, occurring in about 10, 30, and 40–50% of transplanted patients, respectively. Moreover, overt or subclinical thyroid complications (including persistent low-T3 syndrome, chronic thyroiditis, subclinical hypo- or hyperthyroidism, and thyroid carcinoma), gonadal failure, and adrenal insufficiency may persist many years after HSCT. Our analysis further provides evidence that main recognized risk factors for endocrine complications after HSCT are the underlying disease, previous pretransplant therapies, the age at HSCT, gender, total body irradiation, posttransplant derangement of immune system, and in the allogeneic setting, the presence of graft-versus-host disease requiring prolonged steroid treatment. Early identification of endocrine complications can greatly improve the quality of life of long-term survivors after HSCT. |
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AbstractList | Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem cell transplant (HSCT). This review summarizes main endocrine disorders reported in literature and observed in our center as consequence of auto- and allo-HSCT and outlines current options for their management. Gonadal impairment has been found early in approximately two-thirds of auto- and allo-HSCT patients: 90-99% of women and 60-90% of men. Dysfunctions of the hypothalamus-pituitary-growth hormone/insulin growth factor-I axis, hypothalamus-pituitary-thyroid axis, and hypothalamus-pituitary-adrenal axis were documented as later complicances, occurring in about 10, 30, and 40-50% of transplanted patients, respectively. Moreover, overt or subclinical thyroid complications (including persistent low-T3 syndrome, chronic thyroiditis, subclinical hypo- or hyperthyroidism, and thyroid carcinoma), gonadal failure, and adrenal insufficiency may persist many years after HSCT. Our analysis further provides evidence that main recognized risk factors for endocrine complications after HSCT are the underlying disease, previous pretransplant therapies, the age at HSCT, gender, total body irradiation, posttransplant derangement of immune system, and in the allogeneic setting, the presence of graft-versus-host disease requiring prolonged steroid treatment. Early identification of endocrine complications can greatly improve the quality of life of long-term survivors after HSCT. Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem cell transplant (HSCT). This review summarizes main endocrine disorders reported in literature and observed in our center as consequence of auto- and allo-HSCT and outlines current options for their management. Gonadal impairment has been found early in approximately two-thirds of auto- and allo-HSCT patients: 90-99% of women and 60-90% of men. Dysfunctions of the hypothalamus-pituitary-growth hormone/insulin growth factor-I axis, hypothalamus-pituitary-thyroid axis, and hypothalamus-pituitary-adrenal axis were documented as later complicances, occurring in about 10, 30, and 40-50% of transplanted patients, respectively. Moreover, overt or subclinical thyroid complications (including persistent low-T3 syndrome, chronic thyroiditis, subclinical hypo- or hyperthyroidism, and thyroid carcinoma), gonadal failure, and adrenal insufficiency may persist many years after HSCT. Our analysis further provides evidence that main recognized risk factors for endocrine complications after HSCT are the underlying disease, previous pretransplant therapies, the age at HSCT, gender, total body irradiation, posttransplant derangement of immune system, and in the allogeneic setting, the presence of graft-versus-host disease requiring prolonged steroid treatment. Early identification of endocrine complications can greatly improve the quality of life of long-term survivors after HSCT.Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem cell transplant (HSCT). This review summarizes main endocrine disorders reported in literature and observed in our center as consequence of auto- and allo-HSCT and outlines current options for their management. Gonadal impairment has been found early in approximately two-thirds of auto- and allo-HSCT patients: 90-99% of women and 60-90% of men. Dysfunctions of the hypothalamus-pituitary-growth hormone/insulin growth factor-I axis, hypothalamus-pituitary-thyroid axis, and hypothalamus-pituitary-adrenal axis were documented as later complicances, occurring in about 10, 30, and 40-50% of transplanted patients, respectively. Moreover, overt or subclinical thyroid complications (including persistent low-T3 syndrome, chronic thyroiditis, subclinical hypo- or hyperthyroidism, and thyroid carcinoma), gonadal failure, and adrenal insufficiency may persist many years after HSCT. Our analysis further provides evidence that main recognized risk factors for endocrine complications after HSCT are the underlying disease, previous pretransplant therapies, the age at HSCT, gender, total body irradiation, posttransplant derangement of immune system, and in the allogeneic setting, the presence of graft-versus-host disease requiring prolonged steroid treatment. Early identification of endocrine complications can greatly improve the quality of life of long-term survivors after HSCT. |
Audience | Academic |
Author | Giudice, Valentina Selleri, Carmine Ferrara, Idalucia Muscogiuri, Giovanna Serio, Bianca Sessa, Mariarosaria Colao, Annamaria Orio, Francesco Palomba, S. Tauchmanovà, Libuse |
AuthorAffiliation | 3 Department of Clinical Medicine and Surgery, University Federico II Naples, 80131 Naples, Italy 2 Sterile Techniques SSD, AOU “S. Giovanni di Dio e Ruggi d'Aragona” Salerno, Salerno, Italy 1 Department of Sports Science and Wellness, University “Parthenope” Naples, 80133 Naples, Italy 5 Hematology and Hematopoietic Stem Cell Transplant Center, Department of Medicine and Surgery, University of Salerno, 84131 Salerno, Italy 4 Unit of Obstetrics and Gynaecology, “Arcispedale Santa Maria Nuova”, IRCCS, 42123 Reggio Emilia, Italy |
AuthorAffiliation_xml | – name: 4 Unit of Obstetrics and Gynaecology, “Arcispedale Santa Maria Nuova”, IRCCS, 42123 Reggio Emilia, Italy – name: 3 Department of Clinical Medicine and Surgery, University Federico II Naples, 80131 Naples, Italy – name: 2 Sterile Techniques SSD, AOU “S. Giovanni di Dio e Ruggi d'Aragona” Salerno, Salerno, Italy – name: 1 Department of Sports Science and Wellness, University “Parthenope” Naples, 80133 Naples, Italy – name: 5 Hematology and Hematopoietic Stem Cell Transplant Center, Department of Medicine and Surgery, University of Salerno, 84131 Salerno, Italy |
Author_xml | – sequence: 1 fullname: Selleri, Carmine – sequence: 2 fullname: Tauchmanovà, Libuse – sequence: 3 fullname: Ferrara, Idalucia – sequence: 4 fullname: Giudice, Valentina – sequence: 5 fullname: Sessa, Mariarosaria – sequence: 6 fullname: Serio, Bianca – sequence: 7 fullname: Palomba, S. – sequence: 8 fullname: Muscogiuri, Giovanna – sequence: 9 fullname: Orio, Francesco – sequence: 10 fullname: Colao, Annamaria |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24883377$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Copyright © 2014 Francesco Orio et al. COPYRIGHT 2014 John Wiley & Sons, Inc. Copyright © 2014 Francesco Orio et al. Francesco Orio et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © 2014 Francesco Orio et al. 2014 |
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Snippet | Early and late endocrine disorders are among the most common complications in survivors after hematopoietic allogeneic- (allo-) and autologous- (auto-) stem... |
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SubjectTerms | Age Amenorrhea Blood diseases Chemotherapy Drug dosages Endocrine system Endocrine System Diseases - etiology Female Graft versus host disease Hematopoietic Stem Cell Transplantation - adverse effects Hematopoietic stem cells Humans Hypothalamic Diseases - etiology Immune system Infertility - etiology Irradiation Leukemia Lymphoma Male Ovaries Quality of life Radiation Review Risk Factors Sex Factors Stem cell transplantation Stem cells Thyroid Thyroid Diseases - etiology Transplantation Transplantation, Autologous - adverse effects Transplantation, Homologous - adverse effects Womens health |
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Title | Endocrinopathies after Allogeneic and Autologous Transplantation of Hematopoietic Stem Cells |
URI | https://search.emarefa.net/detail/BIM-1049060 https://dx.doi.org/10.1155/2014/282147 https://www.ncbi.nlm.nih.gov/pubmed/24883377 https://www.proquest.com/docview/1547777851 https://www.proquest.com/docview/1543680618 https://www.proquest.com/docview/1611641370 https://pubmed.ncbi.nlm.nih.gov/PMC4032698 https://doaj.org/article/328e9c778dbd49598497e471e7f64787 |
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