Zhang Jing, Fan Min, Liu Di, Zhao Kuai-Le, Wu Kai-Liang, Zhao Wei-Xin, Zhu Zheng-Fei, Fu Xiao-Long
Department of Radiation Oncology, Fudan University Shanghai Cancer Center, 270 Dong an Road, Shanghai, 200032, China.
Radiat Oncol. 2017 Mar 11;12(1):51. doi: 10.1186/s13014-017-0788-x.
Previous data from our institution showed that hypofractionated thoracic radiotherapy (HypoTRT) with concurrent etoposide/platinum chemotherapy yielded favorable survival in patients with limited-stage small cell lung cancer (LS-SCLC). The present study retrospectively compared the survival outcomes, failure patterns and toxicities between groups of LS-SCLC patients treated with conventionally fractionated thoracic radiotherapy (ConvTRT) or HypoTRT combined with chemotherapy.
Medical records of LS-SCLC patients between January 2010 and December 2013 at Fudan University Shanghai Cancer Center were retrospectively reviewed. All patients treated with chemotherapy and ConvTRT (2 Gy per fraction daily, DT ≥ 56 Gy) or HypoTRT (2.5 Gy per fraction daily, DT = 55 Gy) were eligible for analysis. Progression-free survival (PFS) and overall survival (OS) were generated for different populations using the Kaplan-Meier method and compared using the log-rank test. Comparisons of failure patterns and toxicity were analyzed using the χ test.
A total of 170 patients treated with HypoTRT (n = 69) or ConvTRT (n = 101) were eligible for analysis. The median PFS and OS were 13.7 and 25.3 months, respectively, in the ConvTRT cohort, which was similar to the HypoTRT cohort (PFS 18.2 months, p = 0.991, and OS 27.2 months, p = 0.698), with a median follow-up of 30 months. Multivariate analysis revealed that PCI and TNM stage were prognostic factors for PFS and that PCI was prognostic for OS. The patterns of failure (stratified by local-regional recurrence, distant metastasis or both as first relapse) were similar between the dose cohorts (p = 0.693, p = 0.330, p = 0.572). Distant metastasis remained the main failure pattern. The brain was the most frequent remote failure site, followed by bone, liver and adrenal gland. PCI improved the 2-year survival rate from 46.1% to 70.0% and the 2-year PFS rate from 20.9% to 45.3%, respectively (p < 0.001). Grade ≥3 esophagitis and pneumonitis occurred in 9.9% and 11.9%, respectively, of the patients in the ConvTRT cohort and in 11.6% and 10.0%, respectively, of those in the HypoTRT cohort (p = 0.815).
This retrospective analysis demonstrated that HypoTRT or ConvTRT combined with etoposide/platinum chemotherapy yielded statistically similar survival, treatment failure outcomes, and toxicity profiles. PCI correlated with improved PFS and OS.
我们机构之前的数据显示,超分割胸部放疗(HypoTRT)联合依托泊苷/铂类化疗可使局限期小细胞肺癌(LS-SCLC)患者获得良好的生存率。本研究回顾性比较了接受常规分割胸部放疗(ConvTRT)或HypoTRT联合化疗的LS-SCLC患者组之间的生存结果、失败模式和毒性。
回顾性分析了2010年1月至2013年12月在复旦大学附属上海肿瘤中心就诊的LS-SCLC患者的病历。所有接受化疗和ConvTRT(每日每次分割2 Gy,总剂量≥56 Gy)或HypoTRT(每日每次分割2.5 Gy,总剂量=55 Gy)治疗的患者均纳入分析。采用Kaplan-Meier方法计算不同人群的无进展生存期(PFS)和总生存期(OS),并使用对数秩检验进行比较。采用χ检验分析失败模式和毒性的比较。
共有170例接受HypoTRT(n = 69)或ConvTRT(n = 101)治疗的患者符合分析条件。ConvTRT队列的中位PFS和OS分别为13.7个月和25.3个月,与HypoTRT队列相似(PFS为18.2个月,p = 0.991;OS为27.2个月,p = 0.698),中位随访时间为30个月。多因素分析显示,PCI和TNM分期是PFS的预后因素,PCI是OS的预后因素。剂量组之间的失败模式(按局部区域复发、远处转移或两者均为首次复发分层)相似(p = 0.693,p = 0.330,p = 0.572)。远处转移仍然是主要的失败模式。脑是最常见的远处失败部位,其次是骨、肝和肾上腺。PCI分别将2年生存率从46.1%提高到70.0%,将2年PFS率从20.9%提高到45.3%(p < 0.001)。ConvTRT队列中分别有9.9%和11.9%的患者发生≥3级食管炎和肺炎,HypoTRT队列中分别有11.6%和10.0%的患者发生≥3级食管炎和肺炎(p = 0.815)。
这项回顾性分析表明,HypoTRT或ConvTRT联合依托泊苷/铂类化疗在生存、治疗失败结果和毒性方面具有统计学上的相似性。PCI与PFS和OS的改善相关。