Radiotherapy Combined with Immune Checkpoint Inhibitor on Murine Fibrosarcoma and a Narrative Review of Clinical Studies

<b>Purpose:</b> The objective of this study was to evaluate the synergistic effect of combining an immune checkpoint inhibitor (ICI) with radiotherapy (RT) on murine fibrosarcoma and to conduct a narrative review of clinical studies on soft tissue sarcoma (STS). <b>Materials and Methods:</b> Forty male C3H mice (aged 5 weeks) were injected intramuscularly with 2 × 10<sup>5</sup> FSaII cells into the right thigh and randomly assigned to four groups: (1) control; (2) RT; (3) InVivoMab™ (CD279) (mouse anti-PD-1 antibody) (ICI group); and (4) combined treatment with InVivoMab™ (CD279) and RT (combination group). On day -1, ICI was administered intraperitoneally. On day 0, RT (10 Gy, single fraction) was delivered locally to the tumors in the right hind limb. Subsequently, ICI was injected twice weekly (a total of 8 times). On day 26, all mice were euthanized, and the results were analyzed. In addition, a narrative review was conducted to identify clinical evidence. <b>Results:</b> On day 26, mean gross tumor volumes were 3578.13 ± 407.32 mm<sup>3</sup> in the control group, 1995.72 ± 970.46 mm<sup>3</sup> in the RT group, 2729.96 ± 286.47 mm<sup>3</sup> in the ICI group, and 1007.92 ± 197.36 mm<sup>3</sup> in the combination group. Gross tumor growth delay was most pronounced in the combination group. Moreover, the TUNEL assay demonstrated a significant increase in apoptosis in the combination group. Analysis of the underlying immune system revealed significantly higher expression of CD4+, CD8+, and IFN-γ in the combination group. The literature search identified only 12 case reports and 3 prospective studies involving patients with STS treated with the combined treatment of ICI and RT, suggesting potential synergism with acceptable toxicity. <b>Conclusions:</b> The current study demonstrated a synergistic effect of combining an ICI with RT in murine fibrosarcoma. There was limited data in the clinical setting. Further investigations are warranted to determine the optimal combination strategy of ICI and RT for STS.

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Publication Details

Journal
Current Issues in Molecular Biology
Published
2025-12-24
DOI
https://doi.org/10.3390/cimb48010020
Primary Topic
Cancer Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Radiotherapy Combined with Immune Checkpoint Inhibitor on Murine Fibrosarcoma and a Narrative Review of Clinical Studies

Sun Hyun Bae, M. S. Kim, Won Il Jang, Hyunkyung Kim et al.
Current Issues in Molecular Biology
Cancer Research and Treatments
article

Radiotherapy Combined with Immune Checkpoint Inhibitor on Murine Fibrosarcoma and a Narrative Review of Clinical Studies

Sun Hyun Bae, M. S. Kim, Won Il Jang, Hyunkyung Kim, Wonwoo Kim
article en

Abstract

<b>Purpose:</b> The objective of this study was to evaluate the synergistic effect of combining an immune checkpoint inhibitor (ICI) with radiotherapy (RT) on murine fibrosarcoma and to conduct a narrative review of clinical studies on soft tissue sarcoma (STS). <b>Materials and Methods:</b> Forty male C3H mice (aged 5 weeks) were injected intramuscularly with 2 × 10<sup>5</sup> FSaII cells into the right thigh and randomly assigned to four groups: (1) control; (2) RT; (3) InVivoMab™ (CD279) (mouse anti-PD-1 antibody) (ICI group); and (4) combined treatment with InVivoMab™ (CD279) and RT (combination group). On day -1, ICI was administered intraperitoneally. On day 0, RT (10 Gy, single fraction) was delivered locally to the tumors in the right hind limb. Subsequently, ICI was injected twice weekly (a total of 8 times). On day 26, all mice were euthanized, and the results were analyzed. In addition, a narrative review was conducted to identify clinical evidence. <b>Results:</b> On day 26, mean gross tumor volumes were 3578.13 ± 407.32 mm<sup>3</sup> in the control group, 1995.72 ± 970.46 mm<sup>3</sup> in the RT group, 2729.96 ± 286.47 mm<sup>3</sup> in the ICI group, and 1007.92 ± 197.36 mm<sup>3</sup> in the combination group. Gross tumor growth delay was most pronounced in the combination group. Moreover, the TUNEL assay demonstrated a significant increase in apoptosis in the combination group. Analysis of the underlying immune system revealed significantly higher expression of CD4+, CD8+, and IFN-γ in the combination group. The literature search identified only 12 case reports and 3 prospective studies involving patients with STS treated with the combined treatment of ICI and RT, suggesting potential synergism with acceptable toxicity. <b>Conclusions:</b> The current study demonstrated a synergistic effect of combining an ICI with RT in murine fibrosarcoma. There was limited data in the clinical setting. Further investigations are warranted to determine the optimal combination strategy of ICI and RT for STS.

Current Issues in Molecular BiologyVol. 48(1)
Soonchunhyang University (KR), Korea Institute of Radiological and Medical Sciences (KR), Korea Pharma (South Korea) (KR), Korea Pharmaceutical and Bio-Pharma Manufacturers Association (KR)
Soonchunhyang University, Korea Institute of Radiological and Medical Sciences, Ministry of Science and ICT, South Korea
Good health and well-being
Openalex Percentile: Top 32%
Cancer Research and Treatments
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