Department of Oncology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Department of Medical Oncology, The First Affiliated Hospital of University of South China, Hengyang, China.
Biomed Res Int. 2021 Feb 8;2021:3834040. doi: 10.1155/2021/3834040. eCollection 2021.
To analyze the outcomes and adverse events of patients with esophageal squamous cell carcinoma (ESCC) treated with definitive chemoradiation with modified radiotherapy volume and increased radiation dose. This was a retrospective analysis of patients with ESCC treated with definitive chemoradiotherapy at the Sun Yat-sen University Cancer Center (02/2015 to 02/2017). The dose to the planning gross tumor volume (PGTV) and planning clinical tumor volume (PTV1) was 66-68 Gy (2.0-2.2 Gy/fraction). The dose to the planning regional lymph node drainage area volume (PTV2) was 46 Gy (2.0 Gy/fraction). Treatment response, adverse events, progression-free survival (PFS), overall survival (OS), and locoregional failure-free survival (LRFFS) were analyzed. Twenty-six patients were included. The median follow-up was 31 (range, 4.3-51.3) months. Sixteen (61.5%) patients had a complete response, and four (15.4%) achieved a partial response. The objective response rate was 76.9%, and the disease control rate was 80.8%. The median PFS and OS were not achieved. The 4-year PFS was 63.9%, and the 4-year OS was 71.0%. Grade 1-2 and 3-4 radiation-related esophagitis was observed in 15 (57.7%) and one (4.5%) patients, respectively. Grade 1-2 and 3-4 radiation-related pneumonitis was observed in 12 (46.2%) and one (4.5%) patients, respectively. No patients developed radiation-related heart or skin damage. The modified target volume definition and increased dose of definitive radiotherapy combined with chemotherapy in patients with ESCC had low toxicity and might improve survival, but additional trials are necessary to prove the superiority of this strategy.
分析采用改良放疗靶区容积和增加放射剂量的根治性放化疗治疗食管鳞癌(ESCC)患者的结局和不良反应。这是一项对中山大学肿瘤防治中心(2015 年 2 月至 2017 年 2 月)接受根治性放化疗的 ESCC 患者进行的回顾性分析。计划大体肿瘤体积(PGTV)和计划临床肿瘤体积(PTV1)的剂量为 66-68Gy(2.0-2.2Gy/分次)。计划区域淋巴结引流区体积(PTV2)的剂量为 46Gy(2.0Gy/分次)。分析治疗反应、不良反应、无进展生存期(PFS)、总生存期(OS)和局部区域失败无复发生存率(LRFFS)。共纳入 26 例患者。中位随访时间为 31 个月(范围 4.3-51.3 个月)。16 例(61.5%)患者完全缓解,4 例(15.4%)部分缓解。客观缓解率为 76.9%,疾病控制率为 80.8%。中位 PFS 和 OS 未达到。4 年 PFS 为 63.9%,4 年 OS 为 71.0%。15 例(57.7%)和 1 例(4.5%)患者分别出现 1-2 级和 3-4 级放射性食管炎。12 例(46.2%)和 1 例(4.5%)患者分别出现 1-2 级和 3-4 级放射性肺炎。无患者发生放射性心脏或皮肤损伤。改良的 ESCC 根治性放疗靶区定义和增加剂量联合化疗具有低毒性,可能提高生存率,但需要进一步的临床试验来证明这种策略的优越性。