Long-term Outcomes Following Individualized Elective Primary Tumor CTV Delineation Based on Stepwise Spread Patterns of Nasopharyngeal Carcinoma Treated with Intensity-modulated Radiotherapy.

IF 6.4 1区 医学 Q1 ONCOLOGY
Rui Guo, Wei-Wei Zhang, Jia-Wei Lv, Jia-Yi Lin, Cheng Xu, Jing Li, Yan-Ling Wu, Xiao-Min Zhang, Ling-Long Tang, Ying Sun, Jun Ma
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引用次数: 0

Abstract

Purpose: Our institution has developed an individualized elective primary tumor clinical target volume (CTVp) delineation protocol for nasopharyngeal carcinoma (NPC) based on stepwise tumor spread patterns in intensity-modulated radiotherapy (IMRT) for over ten years. Herein, we report the long-term efficacy and toxicities in NPC patients treated under this protocol.

Methods and materials: A total of 7,262 histologically proven, nonmetastatic NPC patients treated with IMRT following this individualized delineation protocol were retrospectively evaluated. The 5-year rates for local relapse-free survival (LRFS), regional relapse-free survival (RRFS), distant metastasis-free survival (DMFS), progression-free survival (PFS), and overall survival (OS) were estimated. Dose-volume histogram (DVH) parameters for patients with local relapse were compared to those of propensity score-matched (PSM) without local relapse. Dosimetric comparisons of our delineation protocol with the 2018 International Guideline (2018-IG) were conducted on representative early- and advanced-stage NPC cases.

Results: The 5-year LRFS, RRFS, DMFS, PFS and OS were 93.6%, 94.4%, 86.8%, 77.8%, and 86.0%, respectively. 92.3% of local relapses and 86.0% of regional relapses occurred within the 95% isodose lines and were considered GTV in-field failures. No significant differences in DVH parameters were observed between the local relapse group and the propensity score-matched non-relapse group. Compared with the 2018-IG, our contouring protocol resulted in a 58.4% and 48.3% reduction in PTV70, and an 80.8% and 62.8% reduction in PTV60 for early and advanced-stage disease, respectively. Late grade 3 toxicities included ototoxicity (1.8%), xerostomia (0.2%), dysphagia (0.2%), temporal lobe injury (0.2%), and trismus (0.1%).

Conclusion: Individualized elective CTVp delineation based on the stepwise spread patterns of nasopharyngeal carcinoma achieved excellent long-term outcomes and reduced the irradiated volumes at equivalent dose levels compared to the 2018-IG.

基于调强放疗鼻咽癌逐步扩散模式的个体化选择性原发肿瘤CTV划定后的长期结果。
目的:十多年来,我们的机构根据调强放疗(IMRT)中逐步扩散的肿瘤模式,制定了鼻咽癌(NPC)的个体化选择性原发肿瘤临床靶体积(CTVp)划定方案。在此,我们报告了在该方案下治疗的鼻咽癌患者的长期疗效和毒性。方法和材料:共有7262例组织学证实的非转移性鼻咽癌患者接受了IMRT治疗,并按照这种个体化划定方案进行了回顾性评估。评估局部无复发生存期(LRFS)、区域无复发生存期(RRFS)、远处无转移生存期(DMFS)、无进展生存期(PFS)和总生存期(OS)的5年生存率。将局部复发患者的剂量-体积直方图(DVH)参数与没有局部复发的倾向评分匹配(PSM)参数进行比较。对代表性的早期和晚期鼻咽癌病例进行了我们的划定方案与2018年国际指南(2018- ig)的剂量学比较。结果:5年LRFS、RRFS、DMFS、PFS和OS分别为93.6%、94.4%、86.8%、77.8%和86.0%。92.3%的局部复发和86.0%的区域复发发生在95%等剂量线内,被认为是GTV现场失效。局部复发组与倾向评分匹配的非复发组DVH参数无显著差异。与2018-IG相比,我们的轮廓化方案导致早期和晚期疾病的PTV70分别降低58.4%和48.3%,PTV60分别降低80.8%和62.8%。晚期3级毒性包括耳毒性(1.8%)、口干(0.2%)、吞咽困难(0.2%)、颞叶损伤(0.2%)和咬牙(0.1%)。结论:与2018-IG相比,基于鼻咽癌逐步扩散模式的个体化选择性CTVp划定取得了良好的长期预后,并减少了同等剂量水平下的辐照体积。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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