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

Author:

Tsuzuki Yusuke123,Kamei Michi4,Iwata Hiromitsu12,Takeda Risa4,Kimura Hiroaki5,Aiba Hisaki5,Murase Takayuki6,Tsuchiya Takahiro7,Sasaki Ryohei8,Hiwatashi Akio3

Affiliation:

1. Department of Radiation Oncology , Nagoya Proton Therapy Center, , 1-1-1 Hirate-cho, Kita-ku, Nagoya 462-8508, Japan

2. Nagoya City University West Medical Center , Nagoya Proton Therapy Center, , 1-1-1 Hirate-cho, Kita-ku, Nagoya 462-8508, Japan

3. Department of Radiology, Nagoya City University Graduate School of Medical Sciences , 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan

4. Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences , 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan

5. Department of Orthopedic Surgery, Nagoya City University Graduate School of Medical Sciences , 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan

6. Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences , 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan

7. Central Department of Radiology, Nagoya City University Hospital , 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8602, Japan

8. Division of Radiation Oncology, Kobe University Graduate School of Medicine , 7-5-2 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan

Abstract

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.

Funder

Japan Society for the Promotion of Science

Publisher

Oxford University Press (OUP)

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