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调强放疗联合化疗在T1-2N1M0期鼻咽癌患者中的作用回顾性研究
引用本文:李佩静,金厅,陈媛媛,陈明,田野. 调强放疗联合化疗在T1-2N1M0期鼻咽癌患者中的作用回顾性研究[J]. 中华放射肿瘤学杂志, 2021, 30(12): 1227-1232. DOI: 10.3760/cma.j.cn113030-20210412-00155
作者姓名:李佩静  金厅  陈媛媛  陈明  田野
作者单位:苏州大学附属第二医院放射治疗科,苏州大学放射肿瘤治疗学研究所,苏州市肿瘤放射治疗学重点实验室 215004;中国科学院大学附属肿瘤医院(浙江省肿瘤医院)放疗科,中国科学院肿瘤与基础医学研究所,杭州310022;中山大学肿瘤防治中心放疗科,华南肿瘤学国家重点实验室,肿瘤医学协同创新中心,广州 510060
摘    要:
目的 探索调强放疗(IMRT)联合化疗在治疗T1-2N1M0期鼻咽癌患者中的作用。方法 收集2008—2016年间浙江省肿瘤医院和中山大学肿瘤防治中心接受根治性治疗的T1-2N1M0期鼻咽癌患者343例。所有患者均接受IMRT,分为单纯放疗组(RT组)和放化疗组(CRT组),后者又分为同步放化疗组(CCRT组)、诱导化疗+同步放化疗组(IC+CCRT组)和同步放化疗+辅助化疗组(CCRT+AC组)。采用Kaplan-Meier法评价局部区域无复发生存率(LRFFS)、远处无转移生存率(DMFS)、无进展生存率(PFS)、肿瘤特异生存率(CSS)和总生存率(OS)。Cox模型多因素预后分析。结果 303例存活患者的中位随访时间为91个月(49~138个月)。CRT组∶RT组的5年OS、CSS、PFS、LRFFS、DMFS均相近(93.7%∶93.9%、93.7%∶93.9%、89.0%∶87.7%、93.8%∶92.8%、93.8%∶91.2%,均P>0.05)。T1N1期和T2N1期亚组分析也显示CRT组与RT组的治疗结果均相近(均P>0.05)。多因素分析显示只有年龄是OS、PFS、CSS和DMFS的独立预后因素,随年龄增长与上述结局呈负相关。CCRT组、IC+CCRT组、CCRT+AC组与RT组的治疗结局均未给患者带来生存获益,且上述3种联合治疗方式之间的疗效也相近(均P>0.05)。结论 T1-2N1M0期鼻咽癌患者接受单纯IMRT获得了满意的治疗效果,预后与联合化疗相当。但未来是否可在T1-2N1M0期人群中取消化疗仍需要前瞻性随机对照临床试验的进一步证实。

关 键 词:鼻咽肿瘤/调强放射疗法  鼻咽肿瘤/化学疗法  诱导化疗  同步放化疗  预后  
收稿时间:2021-04-12

Role of intensity-modulated radiation therapy combined with chemotherapy in patients with stage T1-2N1M0 nasopharyngeal carcinoma:a retrospective study
Li Peijing,Jin Ting,Chen Yuanyuan,Chen Ming,Tian Ye. Role of intensity-modulated radiation therapy combined with chemotherapy in patients with stage T1-2N1M0 nasopharyngeal carcinoma:a retrospective study[J]. Chinese Journal of Radiation Oncology, 2021, 30(12): 1227-1232. DOI: 10.3760/cma.j.cn113030-20210412-00155
Authors:Li Peijing  Jin Ting  Chen Yuanyuan  Chen Ming  Tian Ye
Abstract:
Objective To evaluate the efficacy of intensity-modulated radiation therapy (IMRT) combined with chemotherapy for treating patients with T1-2N1M0 nasopharyngeal carcinoma (NPC). Methods 343 patients diagnosed with T1-2N1M0 NPC in Zhejiang Cancer Hospital and Sun Yat-sen University Cancer Center from January 2008 to December 2016 were recruited in this study. All patients received IMRT and divided into the radiotherapy (RT) and chemoradiotherapy (CRT) groups. Patients in the CRT group were further assigned into the concurrent chemoradiotherapy (CCRT), induction chemotherapy+ CCRT (IC+CCRT) and CCRT+ adjuvant chemotherapy (AC) groups. Locoregional failure-free survival (LRFFS), distant metastasis-free survival (DMFS), progression-free survival (PFS), cancer-specific survival (CSS) and overall survival (OS) were estimated by Kaplan-Meier method. Multivariate prognostic analysis was performed by Cox models. Results The median follow-up time for surviving patients (303/343) was 91(range:49-138) months. The 5-year OS, CSS, PFS, LRFFS, and DMFS rates in the CRT group were not superior to those of the RT group (93.7%:93.9%,93.7%:93.9%,89.0%:87.7%,93.8%:92.8%,93.8%:91.2%, all P>0.05). No significant difference was found in treatment outcomes of patients with T1N1 or T2N1 NPC between two groups (all P>0.05). In multivariable analyses, only age was an independent prognostic factor for OS, PFS, CSS and DMFS, and negative correlation was found between them. No survival benefits were achieved in the CCRT, IC+CCRT, CCRT+AC and RT groups, and no significant differences were found in clinical efficacy among the three combined (all P>0.05). Conclusions IMRT alone yields comparable clinical efficacy to CRT in treating patients with T1-2N1M0 NPC. However, whether CT can be eliminated in the T1-2N1M0 population still needs further confirmation by prospective, randomized and controlled clinical trials.
Keywords:Nasopharyngeal neoplasm/intensity-modulated radiation therapy  Nasopharyngeal neoplasm/adjuvant chemotherapy  Induction chemotherapy  Concurrent chemoradiotherapy  Prognosis  
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