Lee Carrie B, Stinchcombe Thomas E, Moore Dominic T, Morris David E, Hayes D Neil, Halle Jan, Rosenman Julian G, Rivera M Patricia, Socinski Mark A
Division of Hematology/Oncology, Multidisciplinary Thoracic Oncology Program, Lineberger Comprehensive Cancer Center at University of North Carolina at Chapel Hill, North Carolina, USA.
J Thorac Oncol. 2009 Jan;4(1):74-9. doi: 10.1097/JTO.0b013e3181915028.
Combined modality treatment is the standard of care for patients (pts) with unresectable stage III non-small cell lung cancer. Dose escalation of radiotherapy is one strategy used to improve locoregional control and survival, but it increases the risk of both early and late treatment related toxicities.
From May 1996 to August 2004, a total of 112 stage III non-small cell lung cancer pts were treated on 4 phase I/II or phase II trials to assess the safety and feasibility of high-dose (60-90 Gy) thoracic conformal radiotherapy. Patients who received >/=66 Gy (n = 88) were included in an analysis of late complications. Late complications were defined as complications that developed or persisted >/=90 days postradiotherapy. The classic lung toxicities of radiation pneumonitis and fibrosis were not included in this analysis.
Of the 88 patients included in this analysis of late complications, 21 patients (24%) developed a late complication and a total of 28 late complications were observed. The late complications were: pulmonary (n = 5; bronchial stenosis [n = 3] and fatal pulmonary hemoptysis [n = 2]), esophageal (n = 6), cardiac (n = 9), osseous (n = 6), and second primary tumor (n = 2). The median survival for all patients enrolled on the 4 trials (with 95% confidence interval [CI]) was 24.7 months (18.1-30.4 months), and the 5-year overall survival (with 95% CI) was 24% (16-32%). Data to assess for radiographic evidence of local progression were available for 99 patients, and the rate of local progression was 43% (95% CI 34-53%).
High-dose thoracic conformal radiotherapy is feasible and results in promising survival outcomes. Late complications occur in a minority of patients.
综合治疗是不可切除的Ⅲ期非小细胞肺癌患者的标准治疗方法。放疗剂量递增是用于改善局部区域控制和生存的一种策略,但它会增加早期和晚期治疗相关毒性的风险。
从1996年5月至2004年8月,共有112例Ⅲ期非小细胞肺癌患者在4项Ⅰ/Ⅱ期或Ⅱ期试验中接受治疗,以评估高剂量(60 - 90 Gy)胸部适形放疗的安全性和可行性。接受≥66 Gy(n = 88)的患者被纳入晚期并发症分析。晚期并发症定义为放疗后≥90天出现或持续存在的并发症。本分析未包括放射性肺炎和肺纤维化等典型的肺部毒性。
在本次晚期并发症分析纳入的88例患者中,21例(24%)发生了晚期并发症,共观察到28例晚期并发症。晚期并发症包括:肺部(n = 5;支气管狭窄[n = 3]和致命性肺咯血[n = 2])、食管(n = 6)、心脏(n = 9)、骨骼(n = 6)和第二原发肿瘤(n = 2)。4项试验中所有入组患者的中位生存期(95%置信区间[CI])为24.7个月(18.1 - 30.4个月),5年总生存率(95% CI)为24%(16 - 32%)。99例患者有评估局部进展影像学证据的数据,局部进展率为43%(95% CI 34 - 53%)。
高剂量胸部适形放疗是可行的,并且能带来有前景的生存结果。少数患者会发生晚期并发症。