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Risk and predictors for early radiation pneumonitis in patients with stage III non-small cell lung cancer treated with concurrent or sequential chemoradiotherapy

机译:同期或序贯放化疗治疗III期非小细胞肺癌患者早期放射性肺炎的风险和预测因素

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Background The rate of radiation pneumonitis (RP) for patients receiving chemoradiotherapy has been various across studies. Whether it is related to different chemotherapy schedules used in combination with radiation therapy were evaluated in this study. New factors associated with RP were also investigated. Methods and materials A total of 369 consecutive patients with Stage III non small cell lung cancer treated with chemoradiotherapy were followed after radiotherapy (RT). Among them 262 patients received concurrent chemoradiotherapy followed by consolidation chemotherapy and 107 patients received only sequential chemotherapy after RT. RP was graded according to Common Terminology Criteria for Adverse Events version 4.0. Results The rate of grade?≥?2 were 39.7%, 31% and 33.6% in the concurrent DP (docetaxel/cisplatin), concurrent NP (vinorelbine/cisplatin) and sequential group, and grade?≥?3 RP were 18.4%, 9.5%, and 11.2% respectively. The rate of grade?≥?3 RP was significantly higher in concurrent DP group than that in concurrent NP group (p?=?0.04). RP occurred earlier in concurrent DP group than that in the other two groups. There were no significant differences in response rate among the three groups. In the multivariate analysis, age (OR?=?1.99, p?=?0.038 and OR?=?8.90, p?
机译:背景技术在接受放化疗的患者中,放射性肺炎(RP)的发生率在各个研究中都有所不同。在这项研究中评估了是否与放疗联合使用的不同化疗方案有关。还研究了与RP相关的新因素。方法和材料放疗(RT)后,共追踪了369例接受放化疗的III期非小细胞肺癌患者。其中262例接受同步放化疗,然后进行巩固化疗,107例仅接受RT后序贯化疗。 RP是根据《不良事件通用术语标准》 4.0版进行评分的。结果并发DP(多西他赛/顺铂),并发NP(长春瑞滨/顺铂)和序贯组的≥≥2级分别为39.7%,31%和33.6%,≥≥3级RP为18.4%。分别为9.5%和11.2%。并发DP组RP≥3级的比率显着高于并发NP组(p≥0.04)。并发DP组中的RP发生早于其他两组。三组之间的回应率无显着差异。在多变量分析中,年龄(OR = 1.99,p = 0.038,OR = 8.90,P <0.001),化疗方案(OR = 1.45,p = 0.041,OR = 0.41,OR = 0.45,OR = 0.001)。 1.98,p <= 0.013),平均肺部剂量(OR <= 1.42,p 0.001,OR <= 1.64,p 0.001),计划目标体积(OR <= 1.004, p≥0.001,OR≥1.005,p≥0.021)是RP≥2和≥≥3的预测指标。对治疗的反应仅是≥3级RP的新预测因子(OR≥4.39,p≥0.034)。结论发现对治疗的反应是≥3级RP的新预测指标。与同时进行的NP治疗方案相比,同时进行的DP治疗方案对治疗的反应相似,但是导致≥3级RP的风险更高。

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