Kinase inhibitors increase individual radiation sensitivity in normal cells of cancer patients.
Blood
Chromosomal aberrations
Fluorescence in situ hybridization
Small molecules
Targeted therapy
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:
09 2022
09 2022
Historique:
received:
12
01
2022
accepted:
03
04
2022
pubmed:
27
4
2022
medline:
27
8
2022
entrez:
26
4
2022
Statut:
ppublish
Résumé
Kinase inhibitors (KI) are known to increase radiosensitivity, which can lead to increased risk of side effects. Data about interactions of commonly used KI with ionizing radiation on healthy tissue are rare. Freshly drawn blood samples were analyzed using three-color FISH (fluorescence in situ hybridization) to measure individual radiosensitivity via chromosomal aberrations after irradiation (2 Gy). Thresholds of 0.5 and 0.6 breaks/metaphase (B/M) indicate moderate or clearly increased radiosensitivity. The cohorts consisted of healthy individuals (NEG, n = 219), radiosensitive patients (POS, n = 24), cancer patients (n = 452) and cancer patients during KI therapy (n = 49). In healthy individuals radiosensitivity (≥ 0.6 B/M) was clearly increased in 5% of all cases, while in the radiosensitive cohort 79% were elevated. KI therapy increased the rate of sensitive patients (≥ 0.6 B/M) to 35% significantly compared to 19% in cancer patients without KI (p = 0.014). Increased radiosensitivity of peripheral blood mononuclear cells (PBMCs) among patients occurred in six of seven KI subgroups. The mean B/M values significantly increased during KI therapy (0.47 ± 0.20 B/M without compared to 0.50 ± 0.19 B/M with KI, p = 0.047). Kinase inhibitors can intensify individual radiosensitivity of PBMCs distinctly in 85% of tested drugs.
Identifiants
pubmed: 35471558
doi: 10.1007/s00066-022-01945-y
pii: 10.1007/s00066-022-01945-y
pmc: PMC9402507
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
838-848Informations de copyright
© 2022. The Author(s).
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