TY - JOUR
T1 - Late toxicity of a novel allogeneic stem cell transplant using single fraction total body irradiation for hematologic malignancies in children
AU - Madden, Lisa M.
AU - Ngwube, Alexander I.
AU - Shenoy, Shalini
AU - Druley, Todd E.
AU - Hayashi, Robert J.
N1 - Publisher Copyright:
© 2014 Wolters Kluwer Health, Inc.
PY - 2015/3/6
Y1 - 2015/3/6
N2 - Summary: Single fraction total body irradiation (SFTBI) as part of a myeloablative preparative regimen in allogeneic hematopoietic stem cell transplantation (HSCT) for hematopoietic malignancies was shown to have similar survival compared with fractionated total body irradiation (FTBI)-containing regimens, with less acute toxicity. The objective of this study was to determine long-term toxicity >2 years following SFTBI-based HSCT. Twenty-one patients were evaluated at a median follow-up of 6.8 years. Thyroid dysfunction was found in 21% of patients, 1 of whom (5.2%) was symptomatic; 23% had gonadal failure; 50% of patients with growth potential had linear growth disturbance; 27% had mild to moderate pulmonary disease; and 25% had cataracts. Intelligence quotient was stable. cGVHD was present in 28%, and 4 patients (19%) were on immune suppression 2 years posttransplant. Overall survival subsequent to 2 years posttransplant was 76% in this cohort of patients. No secondary malignancies were observed. In conclusion, the toxicities of SFTBI occurred at similar or reduced frequency compared with FTBI. SFTBI should be considered for patients who may benefit from a radiation-containing HSCT preparative regimen.
AB - Summary: Single fraction total body irradiation (SFTBI) as part of a myeloablative preparative regimen in allogeneic hematopoietic stem cell transplantation (HSCT) for hematopoietic malignancies was shown to have similar survival compared with fractionated total body irradiation (FTBI)-containing regimens, with less acute toxicity. The objective of this study was to determine long-term toxicity >2 years following SFTBI-based HSCT. Twenty-one patients were evaluated at a median follow-up of 6.8 years. Thyroid dysfunction was found in 21% of patients, 1 of whom (5.2%) was symptomatic; 23% had gonadal failure; 50% of patients with growth potential had linear growth disturbance; 27% had mild to moderate pulmonary disease; and 25% had cataracts. Intelligence quotient was stable. cGVHD was present in 28%, and 4 patients (19%) were on immune suppression 2 years posttransplant. Overall survival subsequent to 2 years posttransplant was 76% in this cohort of patients. No secondary malignancies were observed. In conclusion, the toxicities of SFTBI occurred at similar or reduced frequency compared with FTBI. SFTBI should be considered for patients who may benefit from a radiation-containing HSCT preparative regimen.
KW - hematopoietic malignancy
KW - late effects
KW - pediatric allogeneic hematopoietic stem cell transplant
KW - total body irradiation
KW - toxicity
UR - http://www.scopus.com/inward/record.url?scp=84924277710&partnerID=8YFLogxK
U2 - 10.1097/MPH.0000000000000272
DO - 10.1097/MPH.0000000000000272
M3 - Article
C2 - 25333837
AN - SCOPUS:84924277710
SN - 1077-4114
VL - 37
SP - e94-e101
JO - Journal of Pediatric Hematology/Oncology
JF - Journal of Pediatric Hematology/Oncology
IS - 2
ER -