Ultra-hypofractionated one-week locoregional radiotherapy for patients with early breast cancer: Acute toxicity results

•One of the largest real-world cohorts using 5-fractionfor breast cancer patients.•The acute toxicity of adjuvant locoregional 5-fraction irradiation is well tolerated.•No increased toxicity for patients with breast reconstruction.•No increased toxicity for patients with irradiation to the internal...

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Veröffentlicht in:Clinical and translational radiation oncology 2024-05, Vol.46, p.100764-100764, Article 100764
Hauptverfasser: Ratosa, Ivica, Montero, Angel, Ciervide, Raquel, Alvarez, Beatriz, García-Aranda, Mariola, Valero, Jeannette, Chen-Zhao, Xin, Lopez, Mercedes, Zucca, Daniel, Hernando, Ovidio, Sánchez, Emilio, de la Casa, Miguel Angel, Alonso, Rosa, Fernandez-Leton, Pedro, Rubio, Carmen
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Sprache:eng
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Zusammenfassung:•One of the largest real-world cohorts using 5-fractionfor breast cancer patients.•The acute toxicity of adjuvant locoregional 5-fraction irradiation is well tolerated.•No increased toxicity for patients with breast reconstruction.•No increased toxicity for patients with irradiation to the internal mammary lymph nodes. Moderate hypofractionated radiotherapy is the standard of care for all patients with breast cancer, irrespective of stage or prior treatments. While extreme hypofractionation is accepted for early-stage tumours, its application in irradiating locoregional lymph nodes remains controversial. A prospective registry analysis from July 2020 to September 2023 included 276 patients with early-stage breast cancer treated with one-week ultra-hypofractionation (UHF) at 26 Gy in 5 fractions on the whole breast (58.3 %) or thoracic wall (41.7 %) and ipsilateral regional lymph nodes and simultaneous integrated boost (58.3 %). Primary endpoint was assessment of acute adverse events (AEs). Secondarily, onset of early-delayed toxicity was assessed. A minimum 6-month follow-up was required for assessing potential treatment-related early-delayed complications. Acute or late complications attributable to treatment were assessed at inclusion using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 criteria. With a median follow-up of 19 months (range 1–49 months), 159 (57.6 %) patients reported AEs, predominantly grade (G) 1 (n = 139, 50.4 %) and G2 (n = 20, 7.8 %). Skin acute toxicity was common (G1/2: 134, G3: 14), while breast oedema occurred in 10 patients (G1: 9, G2: 1), and 15.9 % reported breast pain (G1: 42, G2: 2). Ipsilateral arm oedema was observed in 1.8 % patients. For patients with a follow-up beyond 6 months (n = 213), 23.4 % patients reported G1/G2 skin AEs, 8.8 % had G1/G2 breast/chest wall oedema, and 8.9 % experienced arm lymphedema. There were no cases of brachial plexopathy or G3 toxicity in this group of patients. One-week UHF adjuvant locoregional radiation is well-tolerated, displaying low-toxicity profiles comparable to other studies using similar irradiation schedules.
ISSN:2405-6308
2405-6308
DOI:10.1016/j.ctro.2024.100764