Mangesius Julian, Hörmandinger Katharina, Jäger Robert, Skvortsov Sergej, Plankensteiner Marlen, Maffei Martin, Seppi Thomas, Dejaco Daniel, Santer Matthias, Sarcletti Manuel, Ganswindt Ute
Department of Radiation Oncology, Medical University of Innsbruck, 6020 Innsbruck, Austria.
Comprehensive Cancer Center Innsbruck (CCCI), 6020 Innsbruck, Austria.
Cancers (Basel). 2023 Jul 12;15(14):3594. doi: 10.3390/cancers15143594.
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; < 0.0001), and the median local control was also significantly prolonged (30.5 vs. 11.3 months, = 0.008). Overall survival (OS) significantly increased in the BT group (median OS 22.7 vs. 9.1 months, < 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.
本研究旨在探讨近距离放射治疗(BT)剂量递增作为确定性放化疗(CRT)的补充对食管癌局部控制和生存的影响。在一项两中心研究中,2001年至2020年期间,183例局部局限或局部晚期食管癌患者接受了有或无近距离放射治疗的确定性CRT。外照射放疗剂量为50.4 Gy,每日分次剂量为1.8 Gy;如果有指征,随后对原发肿瘤进行序贯增敏,每日分次剂量为1.8 Gy,总剂量为9 Gy。71例患者接受腔内高剂量率(HDR)铱-192近距离放射治疗,分两次给予10 Gy,每周一次。联合使用的全身治疗方案包括5-氟尿嘧啶/顺铂或单纯5-氟尿嘧啶。接受近距离放射治疗的患者未使用顺铂。BT组的中位局部无进展生存期显著延长(18.7个月对6.0个月;P<0.0001),中位局部控制期也显著延长(30.5个月对11.3个月,P = 0.008)。BT组的总生存期(OS)显著提高(中位OS 22.7个月对9.1个月,P<0.0001)。急性毒性总发生率无显著差异;然而,BT组的急性食管炎发生率显著更高(94.4%对81.2%)。同样,BT组晚期毒性总发生率(43.7%对18.8%)显著更高,包括食管狭窄发生率(22.5%对9.8%)。危及生命或致命的晚期毒性(4级和5级)发生率无差异。在单药5-氟尿嘧啶同步放化疗后进行近距离放射治疗,是食管癌确定性治疗中剂量递增的一种安全有效的替代方法。