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Outcome of dose-escalated intensity-modulated radiotherapy for limited disease small cell lung cancer. 剂量递增调强放疗治疗局限性小细胞肺癌癌症的疗效。
Pub Date : 2023-09-01 Epub Date: 2023-09-26 DOI: 10.3857/roj.2023.00591
Eunyeong Yang, Young Seob Shin, Ji Hyeon Joo, Wonsik Choi, Su Ssan Kim, Eun Kyung Choi, Jaeha Lee, Si Yeol Song

Purpose: An optimal once-daily radiotherapy (RT) regimen is under investigation for definitive concurrent chemoradiotherapy (CCRT) in limited disease small cell lung cancer (LD-SCLC). We compared the efficacy and safety of dose escalation with intensity-modulated radiotherapy (IMRT).

Materials and methods: Between January 2016 and March 2021, patients treated with definitive CCRT for LD-SCLC with IMRT were retrospectively reviewed. Patients who received a total dose <50 Gy or those with a history of thoracic RT or surgery were excluded. The patients were divided into two groups (standard and dose-escalated) based on the total biologically effective dose (BED, α/β = 10) of 70 Gy. The chemotherapeutic regimen comprised four cycles of etoposide and cisplatin.

Results: One hundred and twenty-two patients were analyzed and the median follow-up was 27.8 months (range, 4.4 to 76.9 months). The median age of the patients was 63 years (range, 35 to 78 years) and the majority had a history of smoking (86.0%). The 1- and 3-year overall survival rates of the escalated dose group were significantly higher than those of the standard group (93.5% and 50.5% vs. 76.7% and 33.3%, respectively; p = 0.008), as were the 1- and 3-year freedom from in-field failure rates (91.4% and 66.5% vs. 73.8% and 46.9%, respectively; p = 0.018). The incidence of grade 2 or higher acute and late pneumonitis was not significantly different between the two groups (p = 0.062, 0.185).

Conclusion: Dose-escalated once-daily CCRT with IMRT led to improved locoregional control and survival, with no increase in toxicity.

目的:正在研究一种最佳的每日一次放射治疗(RT)方案,用于限制性疾病小细胞肺癌癌症(LD-SCLC)的最终并发放化疗(CCRT)。我们比较了剂量递增与调强放疗(IMRT)的疗效和安全性。材料和方法:在2016年1月至2021年3月期间,对接受明确CCRT治疗的LD-SCLC伴IMRT的患者进行了回顾性审查。接受总剂量治疗的患者结果:对122名患者进行了分析,中位随访时间为27.8个月(范围为4.4至76.9个月)。患者的中位年龄为63岁(范围为35-78岁),大多数患者有吸烟史(86.0%)。递增剂量组的1年和3年总生存率显著高于标准组(分别为93.5%和50.5%,76.7%和33.3%;p=0.008),1年和3年无现场失败率(分别为91.4%和66.5%,73.8%和46.9%;p=0.018)。两组之间2级或更高级别急性和晚期肺炎的发生率没有显著差异(p=0.062,0.185)。
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Radiation oncology journal
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