TY - JOUR
T1 - Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS)
T2 - Successful management by allogeneic hematopoietic stem cell transplant (HSCT)
AU - Troubaugh-Lotrario, A. D.
AU - Kletzel, M.
AU - Quinones, R. R.
AU - McGavran, L.
AU - Proytcheva, M. A.
AU - Hunger, S. P.
AU - Malcolm, J.
AU - Schissel, D.
AU - Hild, E.
AU - Giller, Roger H.
PY - 2005/1
Y1 - 2005/1
N2 - Pediatric acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) with monosomy 7 is associated with poor disease-free survival when treated by conventional chemotherapy, immunosuppression or supportive measures. Hematopoietic stem cell transplant (HSCT) may improve outcomes; however, data to support this are limited. To better understand the curative potential of HSCT in these patients, all cases of AML and MDS with monosomy 7 treated by two transplant programs (1992 to present) were reviewed. A total of 16 patients were treated, all by allogeneic HSCT. Primary diagnoses were MDS (N=5), therapy-related MDS (N=3), AML (N=5) and therapy-related AML (N=3). In all, 11 patients (69%) survive event-free at 2 years with median follow-up of 986 days (range 330-2011 days). Toxicity caused deaths of the five nonsurviving patients, four of whom were transplanted with active leukemia. Allogeneic HSCT is effective therapy for childhood AML and MDS associated with monosomy 7, particularly for patients with AML in complete remission and MDS.
AB - Pediatric acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) with monosomy 7 is associated with poor disease-free survival when treated by conventional chemotherapy, immunosuppression or supportive measures. Hematopoietic stem cell transplant (HSCT) may improve outcomes; however, data to support this are limited. To better understand the curative potential of HSCT in these patients, all cases of AML and MDS with monosomy 7 treated by two transplant programs (1992 to present) were reviewed. A total of 16 patients were treated, all by allogeneic HSCT. Primary diagnoses were MDS (N=5), therapy-related MDS (N=3), AML (N=5) and therapy-related AML (N=3). In all, 11 patients (69%) survive event-free at 2 years with median follow-up of 986 days (range 330-2011 days). Toxicity caused deaths of the five nonsurviving patients, four of whom were transplanted with active leukemia. Allogeneic HSCT is effective therapy for childhood AML and MDS associated with monosomy 7, particularly for patients with AML in complete remission and MDS.
KW - Acute myeloid leukemia
KW - Monosomy 7
KW - Myelodysplastic syndrome
KW - Pediatric
UR - http://www.scopus.com/inward/record.url?scp=19944433683&partnerID=8YFLogxK
U2 - 10.1038/sj.bmt.1704753
DO - 10.1038/sj.bmt.1704753
M3 - Article
C2 - 15558042
AN - SCOPUS:19944433683
SN - 0268-3369
VL - 35
SP - 143
EP - 149
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 2
ER -