Twenty years of experience of a tertiary cancer center in total body irradiation with focus on oncological outcome and secondary malignancies.
Graft vs Host Disease
/ epidemiology
Hematopoietic Stem Cell Transplantation
/ adverse effects
Humans
Leukemia, Myeloid, Acute
/ complications
Middle Aged
Neoplasms, Second Primary
/ etiology
Retrospective Studies
Transplantation Conditioning
/ adverse effects
Whole-Body Irradiation
/ adverse effects
Hematopoietic stem cell transplant
Long-term follow-up
Sequelae
TBI
Toxicity
Journal
Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]
ISSN: 1439-099X
Titre abrégé: Strahlenther Onkol
Pays: Germany
ID NLM: 8603469
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
08
11
2021
accepted:
20
02
2022
pubmed:
24
3
2022
medline:
26
5
2022
entrez:
23
3
2022
Statut:
ppublish
Résumé
Total body irradiation (TBI) is a common part of the myelo- and immuno-ablative conditioning regimen prior to an allogeneic hematopoietic stem cell transplantation (allo-HSCT). Due to concerns regarding acute and long-term complications, there is currently a decline in otherwise successfully established TBI-based conditioning regimens. Here we present an analysis of patient and treatment data with focus on survival and long-term toxicity. Patients with hematologic diseases who received TBI as part of their conditioning regimen prior to allo-HSCT at Frankfurt University Hospital between 1997 and 2015 were identified and retrospectively analyzed. In all, 285 patients with a median age of 45 years were identified. Median radiotherapy dose applied was 10.5 Gy. Overall survival at 1, 2, 5, and 10 years was 72.6, 64.6, 54.4, and 51.6%, respectively. Median follow-up of patients alive was 102 months. The cumulative incidence of secondary malignancies was 12.3% (n = 35), with hematologic malignancies and skin cancer predominating. A TBI dose ≥ 8 Gy resulted in significantly improved event-free (p = 0.030) and overall survival (p = 0.025), whereas a total dose ≤ 8 Gy and acute myeloid leukemia (AML) diagnosis were associated with significantly increased rates of secondary malignancies (p = 0.003, p = 0.048) in univariate analysis. No significant correlation was observed between impaired renal or pulmonary function and TBI dose. TBI remains an effective and well-established treatment, associated with distinct late-toxicity. However, in the present study we cannot confirm a dose-response relationship in intermediate dose ranges. Survival, occurrence of secondary malignancies, and late toxicities appear to be subject to substantial confounding in this context.
Identifiants
pubmed: 35318487
doi: 10.1007/s00066-022-01914-5
pii: 10.1007/s00066-022-01914-5
pmc: PMC9165288
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
547-557Informations de copyright
© 2022. The Author(s).
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