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Late effects in survivors of tandem peripheral blood stem cell transplant for high‐risk neuroblastoma
Author(s) -
Hobbie Wendy L.,
Moshang Thomas,
Carlson Claire A.,
Goldmuntz Elizabeth,
Sacks Nancy,
Goldfarb Samuel B.,
Grupp Stephan A.,
Ginsberg Jill P.
Publication year - 2008
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.21683
Subject(s) - medicine , neuroblastoma , survivorship curve , blood cancer , quality of life (healthcare) , pediatric cancer , cohort , pediatrics , late effect , disease , medical record , prospective cohort study , cancer , genetics , biology , cell culture , nursing
Background Increasing numbers of children with advanced neuroblastoma are achieving cure. We describe the clinical late effects specific to survivors of stage IV neuroblastoma all similarly treated using tandem autologous peripheral blood stem cell rescue with TBI. Method The medical records of 35 neuroblastoma patients treated at CHOP between 1997 and 2001 were examined. Eighteen of the 35 patients died of progressive disease, and 4 were lost to follow‐up. Thirteen patients continue to follow‐up in our Multidisciplinary Cancer Survivorship Clinic where they are evaluated and monitored by a consistent group of subspecialists that evaluate long‐term sequelae. Data on treatment exposures including TBI and treatment related sequelae identified by clinician assessment and/or diagnostic testing were collected. Results Results indicate late effects were present in all 13 subjects, 12 of whom suffered from multiple negative sequelae, including issues with growth hormone deficiency, dental problems, osteochondromas and hearing deficiencies, among others, most at higher rates than reported previously. Conclusions The findings in this small cohort indicate the need for future prospective studies of this intensive pediatric cancer treatment, and underscore the importance of medical intervention and long‐term monitoring of these at‐risk subjects to increase overall quality‐of‐life. Pediatr Blood Cancer 2008;51:679–683. © 2008 Wiley‐Liss, Inc.