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Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy

Near‐infrared photoimmunotherapy (NIR‐PIT) is a novel cancer therapy that employs a combination of infrared light and tumor‐targeted monoclonal antibody‐photoabsorber conjugates to cause both direct tumor necrosis and immunogenic cell death. NIR‐PIT may have potential in the perioperative setting be...

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Autores principales: Rosenberg, Adrian, Inagaki, Fuyuki, Kato, Takuya, Okada, Ryuhei, Wakiyama, Hiroaki, Furusawa, Aki, Choyke, Peter L., Kobayashi, Hisataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433815/
https://www.ncbi.nlm.nih.gov/pubmed/32579795
http://dx.doi.org/10.1002/cam4.3247
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author Rosenberg, Adrian
Inagaki, Fuyuki
Kato, Takuya
Okada, Ryuhei
Wakiyama, Hiroaki
Furusawa, Aki
Choyke, Peter L.
Kobayashi, Hisataka
author_facet Rosenberg, Adrian
Inagaki, Fuyuki
Kato, Takuya
Okada, Ryuhei
Wakiyama, Hiroaki
Furusawa, Aki
Choyke, Peter L.
Kobayashi, Hisataka
author_sort Rosenberg, Adrian
collection PubMed
description Near‐infrared photoimmunotherapy (NIR‐PIT) is a novel cancer therapy that employs a combination of infrared light and tumor‐targeted monoclonal antibody‐photoabsorber conjugates to cause both direct tumor necrosis and immunogenic cell death. NIR‐PIT may have potential in the perioperative setting before surgery, and therefore it is important to know the effect of NIR‐PIT on wound healing. Fifty mice were implanted with subcutaneous xenografts of N87 human gastric cancer cells, and tumors were excised after reaching a predetermined size. After excision, 30 mice were split into three groups: Controls, NIR‐PIT 1 day prior to surgery and NIR‐PIT 3 days prior to surgery. The quantity of reactive oxygen species (ROS) in each wound was measured on Postoperative Days 2 and 4, and mice were monitored weekly for 4 weeks for evidence of local tumor recurrence as well as clinical evidence of wound healing complications (eg, dehiscence, infection). The remaining 20 mice (10 controls, 10 treated with NIR‐PIT 1 day prior to surgery) were sacrificed on either Postoperative Day 7 or 14, the skin around wounds were excised, and tensile strength was measured with a digital force gauge. There were no significant differences between treatment and control groups with respect to wound ROS levels, wound tensile strength, local tumor recurrence, or postoperative complication rates (P > .05). In conclusion, neoadjuvant (pre‐operative) NIR‐PIT shows no evidence of adverse wound healing effects, and it is likely a safe adjunctive treatment to surgery. Postoperative use of NIR‐PIT merits investigation.
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spelling pubmed-74338152020-08-20 Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy Rosenberg, Adrian Inagaki, Fuyuki Kato, Takuya Okada, Ryuhei Wakiyama, Hiroaki Furusawa, Aki Choyke, Peter L. Kobayashi, Hisataka Cancer Med Cancer Biology Near‐infrared photoimmunotherapy (NIR‐PIT) is a novel cancer therapy that employs a combination of infrared light and tumor‐targeted monoclonal antibody‐photoabsorber conjugates to cause both direct tumor necrosis and immunogenic cell death. NIR‐PIT may have potential in the perioperative setting before surgery, and therefore it is important to know the effect of NIR‐PIT on wound healing. Fifty mice were implanted with subcutaneous xenografts of N87 human gastric cancer cells, and tumors were excised after reaching a predetermined size. After excision, 30 mice were split into three groups: Controls, NIR‐PIT 1 day prior to surgery and NIR‐PIT 3 days prior to surgery. The quantity of reactive oxygen species (ROS) in each wound was measured on Postoperative Days 2 and 4, and mice were monitored weekly for 4 weeks for evidence of local tumor recurrence as well as clinical evidence of wound healing complications (eg, dehiscence, infection). The remaining 20 mice (10 controls, 10 treated with NIR‐PIT 1 day prior to surgery) were sacrificed on either Postoperative Day 7 or 14, the skin around wounds were excised, and tensile strength was measured with a digital force gauge. There were no significant differences between treatment and control groups with respect to wound ROS levels, wound tensile strength, local tumor recurrence, or postoperative complication rates (P > .05). In conclusion, neoadjuvant (pre‐operative) NIR‐PIT shows no evidence of adverse wound healing effects, and it is likely a safe adjunctive treatment to surgery. Postoperative use of NIR‐PIT merits investigation. John Wiley and Sons Inc. 2020-06-24 /pmc/articles/PMC7433815/ /pubmed/32579795 http://dx.doi.org/10.1002/cam4.3247 Text en © Published 2020. This article is a U.S. Government work and is in the public domain in the USA. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biology
Rosenberg, Adrian
Inagaki, Fuyuki
Kato, Takuya
Okada, Ryuhei
Wakiyama, Hiroaki
Furusawa, Aki
Choyke, Peter L.
Kobayashi, Hisataka
Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title_full Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title_fullStr Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title_full_unstemmed Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title_short Wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
title_sort wound healing after excision of subcutaneous tumors treated with near‐infrared photoimmunotherapy
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433815/
https://www.ncbi.nlm.nih.gov/pubmed/32579795
http://dx.doi.org/10.1002/cam4.3247
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