Salvage re-irradiation in non-melanoma skin cancers: A multicenter analysis

We conducted a multicentre real-world study to assess the outcomes of radical salvage re-irradiation for non-melanoma skin cancer (nMSC) recurrences following definitive or postoperative radiotherapy. Data on patients treated between 2006 and 2022 with re-irradiation for nMSCs were retrospectively c...

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Veröffentlicht in:Radiotherapy and oncology 2023-12, Vol.189, p.109945-109945, Article 109945
Hauptverfasser: Miszczyk, Marcin, Suleja, Agata, Sobel, Szymon, Stec, Maria, Chyrek, Artur Jan, Kolbusz, Mirosław, Spałek, Mateusz, Nasiek, Aleksandra, Stankiewicz, Magdalena, Lelek, Piotr, Moll, Matthias, Kluska, Adam, Kazalski, Damian, Saniewski, Piotr, Kaminiów, Konrad, Burchardt, Wojciech Maria, Wojcieszek, Piotr, Chicheł, Adam, Cichoń, Piotr, Krzysztofiak, Tomasz
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Sprache:eng
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Zusammenfassung:We conducted a multicentre real-world study to assess the outcomes of radical salvage re-irradiation for non-melanoma skin cancer (nMSC) recurrences following definitive or postoperative radiotherapy. Data on patients treated between 2006 and 2022 with re-irradiation for nMSCs were retrospectively collected from five high-volume brachytherapy centers. The primary endpoint was local control (LC). Secondary endpoints included overall survival, progression-free survival, and adverse events (AEs). The Kaplan-Meier estimator and Cox Proportional-Hazards Model were utilised in the analysis. A total of 58 patients with a median age of 78.4 years with recurrences of previously irradiated nMSC in the head and neck region were included in the analysis. The majority had cutaneous basal cell carcinoma (BCC; 91.4%), and were irradiated with high-dose-rate brachytherapy (HDR-BT; 91.4%). The most common locations included the nasal region (36.2%) and external ear (18.9%). The 1-year LC was 73.1% and decreased to 41.7% at three years. The size of the re-irradiated lesion was the single independent prognostic factor in Cox analysis (per mm; HR 1.07; 95% CI 1.04–1.11; p 
ISSN:0167-8140
1879-0887
DOI:10.1016/j.radonc.2023.109945