摘要
[目的]比较局部晚期非小细胞肺癌(NSCLC)常规静态调强(step-and-shoot intensity-modulated radiation therapy,s IMRT)和容积旋转调强(volumetric modulated arc therapy,VMAT)的临床效果。[方法]回顾性分析68例分别行IMRT和VMAT的NSCLC患者资料,IMRT组38例,VMAT组30例。比较两组患者的近期、远期疗效及急性不良反应。[结果]IMRT组和VMAT组的有效率分别为76.3%和80.0%。除放射性食管损伤外(P=0.045),其他急性不良反应两组均无显著性差异(P〉0.05)。IMRT组和VMAT组中位OS分别为23.0个月(95%CI:20.4-25.5)和24.3个月(95%CI:21.6-26.9);PFS分别为15.5个月(95%CI:13.5-17.6)和16.2个月(95%CI:13.5-18.9);局部复发时间分别为17.1个月(95%CI:14.6-19.6)和18.4个月(95%CI:15.8-21.1);远处转移时间分别为20.3个月(95%CI:17.5-23.1)和20.8个月(95%CI:17.5-24.1),差异均无统计学意义(P〉0.05)。[结论 ]VMAT能够获得与IMRT相同的临床疗效,且可降低放射性食管损伤的发生率。
[Purpose] To compare the clinical effect of step-and-shoot intensity modulated radio- therapy(slMRT) and volumetric modulated arc therapy(VMAT) for locally advanced non-small cell lung cancer(NSCLC). [Methods] The data of 68 cases with advanced NSCLC received IMRT(n=38) or VMAT (n=30) were included and analyzed retrospectively. The short-term and long-term clinical efficacy and acute toxicity between the two groups were evaluated. [Results] The total efficacy for IMRT and VMAT group was 76.3% and 80.0% respectively. Except fo radiation esophagitis (P= 0.045 ), there was no significant difference for acute toxicity between the two groups (P〉0.05). The median time to OS for IMRT and VMAT group were 23.0 months(95%CI:20.4-25.5) and 24.3 months (95%CI:21.6-26.9) respectively,the median time to PFS was 15.5 months(95%CI: 13.5-17.6) and 16.2 months (95%CI: 13.5-18.9),the median time of local-regional recurrence (LRR) was 17.1 months(95%CI: 14.6-19.6) and 18.4 months(95%CI:15.8-21.1),the median time of distant metas- tasis(DM) was 20.3 months(95%CI:17.5-23.1) and 20.8 months(95%CI: 17.5-24.1) respectively, there were no statistical differences between two groups for above 4 indexes(all P〉0.05). [ Conclusion ] VMAT achieves the same clinical efficacy as IMRT and can reduce the incidence of radia- tion esophagitis in locally advanced NSCLC.
出处
《中国肿瘤》
CAS
2016年第9期742-746,共5页
China Cancer
基金
江苏省第十二批六大人才高峰项目(WSW-024)
关键词
非小细胞肺癌
容积旋转调强
适形调强放疗
non-small cell cancer
volumetric modulated are therapy
intensity-modulated radiation therapy