Baskent Department of Radiation Oncology, University Adana Medical Faculty, Adana, Turkey.
Baskent Department of Radiation Oncology, University Adana Medical Faculty, Adana, Turkey.
Int J Radiat Oncol Biol Phys. 2015 Mar 15;91(4):774-80. doi: 10.1016/j.ijrobp.2014.12.010.
To investigate the safety and efficacy of single-dose 8-Gy palliative chest reirradiation (CRI) in metastatic non-small cell lung cancer (M-NSCLC) patients with painful thoracic failures (TF) within the previous radiation portal.
We retrospectively analyzed the clinical data of 78 M-NSCLC patients who received single-dose 8-Gy CRI for painful TF after concurrent chemoradiation therapy to a total radiation dose of 52 to 66 Gy between 2007 and 2012. Primary endpoints included significant pain relief (SPR) defined as a ≥2 point decrement in the Visual Analogue Scale for Pain inventory (VAS-P), time to pain relief, and duration of pain control. Secondary objectives were survival and prognostic factors.
Treatment was well tolerated, with only 5.1% grade 3 pneumonitis and 1.3% grade 2 esophagitis. Pre-CRI median and post-CRI minimum VAS-P were 7 and 3 (P<.001), respectively. SPR was noted in 67 (85.9%) patients, and only 3 (3.9%) scored progressive pain. Median time to lowest VAS-P and duration of pain control were 27 days and 6.1 months, respectively. Median overall survival (OS) was 7.7 months, and the 1-year OS rate was 26.5%. On multivariate analyses, lower Eastern Cooperative Oncology group score (1-2; P<.001), absence of anemia (P=.001), and fewer metastatic sites (1-2; P<.001) were found to be associated with longer OS.
Single-dose 8-Gy CRI provides safe, effective, and durable pain palliation for TF in radically irradiated M-NSCLC patients. Because of its convenience, lower cost, and higher comfort, the present protocol can be considered an appropriate option for patients with limited life spans.
研究单次 8-Gy 姑息性胸部再放疗(CRI)在既往放疗野内出现疼痛性胸内复发(TF)的转移性非小细胞肺癌(M-NSCLC)患者中的安全性和疗效。
我们回顾性分析了 2007 年至 2012 年间,78 例接受同步放化疗后总剂量为 52-66Gy 的 M-NSCLC 患者,因 TF 接受单次 8-Gy CRI 的临床数据。主要终点包括明显疼痛缓解(SPR),定义为疼痛视觉模拟量表(VAS-P)评分降低≥2 分;疼痛缓解时间和疼痛控制时间。次要目标是生存和预后因素。
治疗耐受性良好,仅有 5.1%的患者发生 3 级肺炎,1.3%的患者发生 2 级食管炎。CRI 前和 CRI 后最小 VAS-P 的中位数分别为 7 和 3(P<.001)。67 例(85.9%)患者出现 SPR,仅 3 例(3.9%)出现进展性疼痛。最低 VAS-P 时间和疼痛控制时间的中位数分别为 27 天和 6.1 个月。中位总生存期(OS)为 7.7 个月,1 年 OS 率为 26.5%。多因素分析显示,Eastern Cooperative Oncology Group 评分较低(1-2 分;P<.001)、无贫血(P=.001)和转移灶较少(1-2 个;P<.001)与 OS 延长相关。
单次 8-Gy CRI 为根治性放疗后 M-NSCLC 患者的 TF 提供了安全、有效和持久的疼痛缓解。由于其方便、成本低和舒适性高,本方案可作为生命有限的患者的合适选择。