Impact of cyclophosphamide on the morphological and histological changes in polyglycolic acid spacers

Abstract In radiotherapy for pediatric abdominal tumors, determining the effect of concurrent chemotherapy on polyglycolic acid (PGA) spacers is crucial; yet this effect has not been validated. Therefore, we aimed to evaluate the impact of cyclophosphamide (CPA) chemotherapy on the PGA spacer using...

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Veröffentlicht in:Journal of radiation research 2024-09, Vol.65 (5), p.725-732
Hauptverfasser: Tsuzuki, Yusuke, Kamei, Michi, Iwata, Hiromitsu, Takeda, Risa, Kimura, Hiroaki, Aiba, Hisaki, Murase, Takayuki, Tsuchiya, Takahiro, Sasaki, Ryohei, Hiwatashi, Akio
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Sprache:eng
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Zusammenfassung:Abstract In radiotherapy for pediatric abdominal tumors, determining the effect of concurrent chemotherapy on polyglycolic acid (PGA) spacers is crucial; yet this effect has not been validated. Therefore, we aimed to evaluate the impact of cyclophosphamide (CPA) chemotherapy on the PGA spacer using a rat model. Twenty-four rats were implanted with the spacer, and morphological changes in the spacer were assessed on CT for both the CPA-dosed group (40 mg/kg) and the control group. The size and volume of the spacer were quantified using CT, while the degree of adhesion and microscopic examination of the tissue were determined using pathology specimens. Morphologically, the size of the spacer decreased over time in both the CPA-dosed and control groups, with no significant differences observed between groups. No significant differences in adhesion were observed between the two groups. Macrophages were observed around the PGA fibers, suggesting their involvement in the degradation of the PGA spacer. These results suggest that CPA does not cause significant clinically problematic degradation or adverse tissue reactions to the PGA spacer. This study reinforced the benefits of PGA spacers; however, future research focusing on in vivo longitudinal monitoring of individual rats, as well as on humans, is required.
ISSN:0449-3060
1349-9157
1349-9157
DOI:10.1093/jrr/rrae070