{"title":"Do Breast Cancer Patients With Chemotherapy-induced Peripheral Neuropathy Have an Increased Risk of Radiation Dermatitis?","authors":"Dirk Rades, Martin Ballegaard","doi":"10.21873/invivo.14019","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aim: </strong>Patients with breast cancer scheduled for irradiation may present with peripheral neuropathy (PNP) caused by preceding taxane-based chemotherapy. Chemotherapy-related toxicity was suggested to be associated with a lower individual DNA repair capacity. A similar association was described for radiation-related toxicity. We investigated whether patients with taxane-induced PNP have an increased risk of radiation dermatitis.</p><p><strong>Patients and methods: </strong>In a retrospective cohort of 129 patients irradiated for breast cancer following taxane-based chemotherapy, PNP plus 14 characteristics were evaluated for associations with grade ≥2 radiation dermatitis.</p><p><strong>Results: </strong>No, mild, and moderate to severe PNP were associated with grade ≥2 dermatitis rates of 22.2%, 27.7%, and 37.8% (<i>p</i>=0.123). On multivariate analysis, grade ≥2 dermatitis was significantly associated with normo-fractionated radiotherapy (<i>p</i>=0.032) and a body mass index ≥30 kg/m<sup>2</sup> (<i>p</i><0.001).</p><p><strong>Conclusion: </strong>A significant association between severity of PNP and grade ≥2 radiation dermatitis was not found, although grade ≥2 dermatitis occurred more frequently in patients with moderate to severe PNP.</p>","PeriodicalId":13364,"journal":{"name":"In vivo","volume":"39 4","pages":"2236-2242"},"PeriodicalIF":1.8000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12223629/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"In vivo","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.21873/invivo.14019","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background/aim: Patients with breast cancer scheduled for irradiation may present with peripheral neuropathy (PNP) caused by preceding taxane-based chemotherapy. Chemotherapy-related toxicity was suggested to be associated with a lower individual DNA repair capacity. A similar association was described for radiation-related toxicity. We investigated whether patients with taxane-induced PNP have an increased risk of radiation dermatitis.
Patients and methods: In a retrospective cohort of 129 patients irradiated for breast cancer following taxane-based chemotherapy, PNP plus 14 characteristics were evaluated for associations with grade ≥2 radiation dermatitis.
Results: No, mild, and moderate to severe PNP were associated with grade ≥2 dermatitis rates of 22.2%, 27.7%, and 37.8% (p=0.123). On multivariate analysis, grade ≥2 dermatitis was significantly associated with normo-fractionated radiotherapy (p=0.032) and a body mass index ≥30 kg/m2 (p<0.001).
Conclusion: A significant association between severity of PNP and grade ≥2 radiation dermatitis was not found, although grade ≥2 dermatitis occurred more frequently in patients with moderate to severe PNP.
期刊介绍:
IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management.
The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.