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Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome
M. Erlacher, F. Andresen, M. Sukova, J. Stary, B. De Moerloose, JVWT. Bosch, M. Dworzak, MG. Seidel, S. Polychronopoulou, R. Beier, CP. Kratz, M. Nathrath, MC. Frühwald, G. Göhring, AK. Bergmann, C. Mayerhofer, D. Lebrecht, S. Ramamoorthy, A....
Jazyk angličtina Země Itálie
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1994
Free Medical Journals
od 1994
Freely Accessible Science Journals
od 1994
PubMed Central
od 2009
Europe PubMed Central
od 2009
Open Access Digital Library
od 1994-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1996
- MeSH
- chromozomální delece * MeSH
- dítě MeSH
- intracelulární signální peptidy a proteiny genetika MeSH
- kojenec MeSH
- lidé MeSH
- lidské chromozomy, pár 7 genetika MeSH
- monozomie MeSH
- myelodysplastické syndromy * diagnóza genetika terapie MeSH
- předškolní dítě MeSH
- progrese nemoci MeSH
- spontánní remise MeSH
- transkripční faktory genetika MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
Monosomy 7 is the most common cytogenetic abnormality in pediatric myelodysplastic syndrome (MDS) and associated with a high risk of disease progression. However, in young children, spontaneous loss of monosomy 7 with concomitant hematologic recovery has been described, especially in the presence of germline mutations in SAMD9 and SAMD9L genes. Here, we report on our experience of close surveillance instead of upfront hematopoietic stem cell transplantation (HSCT) in seven patients diagnosed with SAMD9L syndrome and monosomy 7 at a median age of 0.6 years (range, 0.4-2.9). Within 14 months from diagnosis, three children experienced spontaneous hematological remission accompanied by a decrease in monosomy 7 clone size. Subclones with somatic SAMD9L mutations in cis were identified in five patients, three of whom attained hematological remission. Two patients acquired RUNX1 and EZH2 mutations during the observation period, of whom one progressed to myelodysplastic syndrome with excess of blasts (MDS-EB). Four patients underwent allogeneic HSCT at a median time of 26 months (range, 14-40) from diagnosis for MDSEB, necrotizing granulomatous lymphadenitis, persistent monosomy 7, and severe neutropenia. At last follow-up, six patients were alive, while one passed away due to transplant-related causes. These data confirm previous observations that monosomy 7 can be transient in young children with SAMD9L syndrome. However, they also indicate that delaying HSCT poses a substantial risk of severe infection and disease progression. Finally, surveillance of patients with SAMD9L syndrome and monosomy 7 is critical to define the evolving genetic landscape and to determine the appropriate timing of HSCT (clinicaltrials gov. Identifier: NCT00662090).
Department of Hematology St Jude Children's Research Hospital Memphis TN
Department of Human Genetics Hannover Medical School Hannover
Department of Pediatric Hematology and Oncology Hannover Medical School Hannover
Department of Pediatric Hematology and Oncology Klinikum Kassel Kassel Germany
Department of Pediatric Hematology Oncology Aghia Sophia Children's Hospital Athens Greece
Department of Pediatric Hematology Oncology University Hospital Brussel Brussels
German Cancer Consortium Partner Site Freiburg
Pediatrics and Adolescent Medicine University Medical Center Augsburg Augsburg
Citace poskytuje Crossref.org
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- $a Erlacher, Miriam $u Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany; German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Partner Site Freiburg. Miriam.erlacher@uniklinik-freiburg.de
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- $a Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome / $c M. Erlacher, F. Andresen, M. Sukova, J. Stary, B. De Moerloose, JVWT. Bosch, M. Dworzak, MG. Seidel, S. Polychronopoulou, R. Beier, CP. Kratz, M. Nathrath, MC. Frühwald, G. Göhring, AK. Bergmann, C. Mayerhofer, D. Lebrecht, S. Ramamoorthy, A. Yoshimi, B. Strahm, MW. Wlodarski, CM. Niemeyer
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- $a Monosomy 7 is the most common cytogenetic abnormality in pediatric myelodysplastic syndrome (MDS) and associated with a high risk of disease progression. However, in young children, spontaneous loss of monosomy 7 with concomitant hematologic recovery has been described, especially in the presence of germline mutations in SAMD9 and SAMD9L genes. Here, we report on our experience of close surveillance instead of upfront hematopoietic stem cell transplantation (HSCT) in seven patients diagnosed with SAMD9L syndrome and monosomy 7 at a median age of 0.6 years (range, 0.4-2.9). Within 14 months from diagnosis, three children experienced spontaneous hematological remission accompanied by a decrease in monosomy 7 clone size. Subclones with somatic SAMD9L mutations in cis were identified in five patients, three of whom attained hematological remission. Two patients acquired RUNX1 and EZH2 mutations during the observation period, of whom one progressed to myelodysplastic syndrome with excess of blasts (MDS-EB). Four patients underwent allogeneic HSCT at a median time of 26 months (range, 14-40) from diagnosis for MDSEB, necrotizing granulomatous lymphadenitis, persistent monosomy 7, and severe neutropenia. At last follow-up, six patients were alive, while one passed away due to transplant-related causes. These data confirm previous observations that monosomy 7 can be transient in young children with SAMD9L syndrome. However, they also indicate that delaying HSCT poses a substantial risk of severe infection and disease progression. Finally, surveillance of patients with SAMD9L syndrome and monosomy 7 is critical to define the evolving genetic landscape and to determine the appropriate timing of HSCT (clinicaltrials gov. Identifier: NCT00662090).
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