...
首页> 外文期刊>Radiation oncology >Predicting per-lesion local recurrence in locally advanced non-small cell lung cancer?following?definitive radiation therapy using pre- and mid-treatment metabolic tumor volume
【24h】

Predicting per-lesion local recurrence in locally advanced non-small cell lung cancer?following?definitive radiation therapy using pre- and mid-treatment metabolic tumor volume

机译:在局部晚期非小细胞肺癌中预测局部病变局部复发?以下?使用预治疗的代谢肿瘤体积进行明确的放射治疗

获取原文
           

摘要

We evaluated whether pre- and mid-treatment metabolic tumor volume (MTV) predicts per lesion local recurrence (LR) in patients treated with definitive radiation therapy (RT, dose≥60?Gy) for locally advanced non-small cell lung cancer (NSCLC). We retrospectively reviewed records of patients with stage III NSCLC treated from 2006 to 2018 with pre- and mid-RT PET-CT. We measured the?MTV of treated lesions on the pre-RT (MTVpre) and mid-RT (MTVmid) PET-CT. LR was defined per lesion as recurrence within the planning target volume. Receiver operating characteristic (ROC) curves, cumulative incidence rates, and uni- and multivariable (MVA) competing risk regressions were used to evaluate the association between MTV and LR. We identified 111 patients with 387 lesions (112 lung tumors and 275 lymph nodes). Median age was 68?years, 69.4% were male, 46.8% had adenocarcinoma, 39.6% had squamous cell carcinoma, and 95.5% received concurrent chemotherapy. Median follow-up was 38.7?months. 3-year overall survival was 42.3%. 3-year cumulative incidence of LR was 26.8% per patient and 11.9% per lesion. Both MTVpre and MTVmid were predictive of LR by ROC (AUC?=?0.71 and 0.76, respectively) and were significantly associated with LR on MVA (P?=?0.004 and P?=?7.1e-5, respectively). Among lesions at lower risk of LR based on MTVpre, higher MTVmid was associated with LR (P?=?0.001). Per-lesion, larger MTVpre and MTVmid predicted for increased risk of LR. MTVmid was more highly predictive of LR than MTVpre and if validated may allow for further discrimination of high-risk lesions at mid-RT informing dose painting strategies.
机译:我们评估了在治疗局部晚期非小细胞肺癌(NSCLC)治疗的患者治疗患者的患者局部复发(MTV)预测和中期的代谢肿瘤体积(MTV)是否预测)。我们回顾性地审查了从2006年至2018年治疗的III阶段NSCLC患者的记录,并在中期和中期PET-CT。我们测量了在RT(MTVPRE)和RT(MTVMID)PET-CT中的治疗病变的MTV。 LR在规划目标体积内为每种病变定义为复发。接收器操作特征(ROC)曲线,累积发射率和单级和多变量(MVA)竞争风险回归用于评估MTV和LR之间的关联。我们确定了111名患者387例病变(112肺肿瘤和275个淋巴结)。中位年龄为68岁?岁月,69.4%是男性,46.8%腺癌,39.6%有鳞状细胞癌,95.5%接受同时化疗。中位后续时间为38.7?几个月。 3年整体生存率为42.3%。每位患者的3年累积发病率为26.8%,每病灶为11.9%。 MTVPRE和MTVMID都是通过ROC(AUC?= 0.71和0.76)的LR预测的,并且与MVA上的LR显着相关(P?= 0.004和P?7.1e-5)。基于MTVPRE的LR风险较低的病变中,较高的MTVMID与LR相关(P?= 0.001)。每病变,较大的MTVPRE和MTVMID预测LR的风险增加。 MTVMID比MTVPRE更高度预测,并且如果验证可以允许在中期通知剂量绘画策略中进一步辨别高风险病变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号