Niu Shaoqing, Li Yiyang, Shao Han, Hu Jiang, Wang Jijin, Wang Hanyu, Zhang Yujing
Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, China; Department of Radiation Oncology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, China; Department of Oncology, First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, China.
Int J Radiat Oncol Biol Phys. 2024 Mar 1;118(3):770-780. doi: 10.1016/j.ijrobp.2023.09.031. Epub 2023 Nov 7.
The aim of this study was to investigate the treatment results and long-term quality of life in patients with early-stage extranodal natural killer/T-cell lymphoma who were prospectively treated with simultaneous boost intensity modulated radiation therapy (SIB-IMRT) with 3 dose gradients.
Sixty patients with stage I-II nasal cavity natural killer/T-cell lymphoma (NKTCL) and Waldeyer's ring NKTCL were enrolled in a single-arm, prospective, phase 2 clinical trial from August 2011 to April 2015. All patients were treated with definitive radiation therapy combined with short-course induction chemotherapy. A newly designed SIB-IMRT scheme was uniformly adopted, with 54.6 Gy for the gross tumor volume (GTV) of the primary tumor and GTV of the positive lymph nodes, 50.7 Gy for the high-risk clinical target volume (CTV), and 45.5 Gy for the low-risk CTV, all delivered in 26 daily fractions. Before SIB-IMRT, L-asparaginase-based induction chemotherapy was used in 95.0% (57/60) of patients.
With a median follow-up time of 95.8 months, the 5-year locoregional recurrence-free survival, progression-free survival, and overall survival rates were 83.3%, 81.7%, and 88.3%, respectively. Dosimetric analysis in the first 21 patients showed satisfying conformality for planning target volume of GTV, high-risk CTV, and low-risk CTV, while the organs at risk were well protected. The results of long-term quality-of-life investigations in patients without progression were favorable, and nasal discomfort was the most common symptom. No grade 3 or 4 acute or late toxicities were observed.
The scheme of target volume delineation and dose setting that we designed has favorable clinical effects with mild side effects in treating patients with stage I-II nasal cavity NKTCL and Waldeyer's ring NKTCL.
本研究旨在调查接受具有3个剂量梯度的同步推量调强放射治疗(SIB-IMRT)的早期结外自然杀伤/T细胞淋巴瘤患者的治疗结果和长期生活质量。
2011年8月至2015年4月,60例I-II期鼻腔自然杀伤/T细胞淋巴瘤(NKTCL)和韦氏环NKTCL患者入组一项单臂、前瞻性2期临床试验。所有患者均接受根治性放疗联合短程诱导化疗。统一采用新设计的SIB-IMRT方案,原发肿瘤大体肿瘤体积(GTV)和阳性淋巴结GTV给予54.6 Gy,高危临床靶区(CTV)给予50.7 Gy,低危CTV给予45.5 Gy,均分26次每日照射。在SIB-IMRT之前,95.0%(57/60)的患者使用了基于左旋门冬酰胺酶的诱导化疗。
中位随访时间为95.8个月,5年局部区域无复发生存率、无进展生存率和总生存率分别为83.3%、81.7%和88.3%。对前21例患者的剂量学分析显示,GTV、高危CTV和低危CTV的计划靶区具有令人满意的适形性,同时危及器官得到了很好的保护。无进展患者的长期生活质量调查结果良好,鼻腔不适是最常见的症状。未观察到3级或4级急性或晚期毒性反应。
我们设计的靶区勾画和剂量设定方案在治疗I-II期鼻腔NKTCL和韦氏环NKTCL患者时具有良好的临床效果,副作用轻微。