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Chemoradiotherapy Combined with Brachytherapy for the Definitive Treatment of Esophageal Carcinoma
SIMPLE SUMMARY: The aim of this retrospective study was to investigate whether dose escalation with additional intraluminal brachytherapy after definitive chemoradiotherapy can improve local control and survival in esophageal cancer. In the 71 patients who received additional brachytherapy, median l...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377190/ https://www.ncbi.nlm.nih.gov/pubmed/37509257 http://dx.doi.org/10.3390/cancers15143594 |
Sumario: | SIMPLE SUMMARY: The aim of this retrospective study was to investigate whether dose escalation with additional intraluminal brachytherapy after definitive chemoradiotherapy can improve local control and survival in esophageal cancer. In the 71 patients who received additional brachytherapy, median local progression-free survival, as well as overall survival, significantly improved in comparison to the 112 patients who received chemoradiotherapy alone. There was an increase in late toxicity with the addition of brachytherapy; however, no difference in life-threatening or lethal toxicities was observed. This concept can be a safe and effective option for dose escalation in chemoradiotherapy regarding esophageal cancer. ABSTRACT: This study aims to investigate the effect of dose escalation with brachytherapy (BT) as an addition to definitive chemoradiotherapy (CRT) on local control and survival in esophageal cancer. From 2001 to 2020, 183 patients with locally limited or locally advanced esophageal cancer received definitive CRT with or without brachytherapy in a two-center study. External-beam radiotherapy was delivered at 50.4 Gy in 1.8 Gy daily fractions, followed by a sequential boost to the primary tumor of 9 Gy in 1.8 Gy daily fractions if indicated. Intraluminal high dose rate (HDR) Ir-192 brachytherapy was performed on 71 patients at 10 Gy in two fractions, with one fraction per week. The combined systemic therapy schedules used included 5-fluorouracil/cisplatin or 5-fluorouracil alone. Cisplatin was not administered in patients receiving brachytherapy. The median local progression-free survival was significantly extended in the BT group (18.7 vs. 6.0 months; p < 0.0001), and the median local control was also significantly prolonged (30.5 vs. 11.3 months, p = 0.008). Overall survival (OS) significantly increased in the BT group (median OS 22.7 vs. 9.1 months, p < 0.0001). No significant difference in the overall rate of acute toxicities was observed; however, the rate of acute esophagitis was significantly higher in the BT group (94.4% vs. 81.2%). Likewise, the overall rate of late toxicities (43.7% vs. 18.8%) was significantly higher in the BT group, including the rate of esophageal stenosis (22.5% vs. 9.8%). There was no difference in the occurrence of life-threatening or lethal late toxicities (grades 4 and 5). Brachytherapy, after chemoradiation with single-agent 5-FU, represents a safe and effective alternative for dose escalation in the definitive treatment of esophageal cancer. |
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