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对于根治性放化疗治疗后的 IV 期非小细胞肺癌患者,单次 8Gy 再放疗治疗局部疼痛失败的安全性和姑息疗效。

Safety and palliative efficacy of single-dose 8-Gy reirradiation for painful local failure in patients with stage IV non-small cell lung cancer previously treated with radical chemoradiation therapy.

机构信息

Baskent Department of Radiation Oncology, University Adana Medical Faculty, Adana, Turkey.

Baskent Department of Radiation Oncology, University Adana Medical Faculty, Adana, Turkey.

出版信息

Int J Radiat Oncol Biol Phys. 2015 Mar 15;91(4):774-80. doi: 10.1016/j.ijrobp.2014.12.010.

Abstract

PURPOSE

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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