Department of Radiation Oncology, Allegheny General Hospital, Pittsburgh, United States.
Department of Radiation Oncology, University of Texas San Antonio, United States.
Radiother Oncol. 2018 Sep;128(3):492-497. doi: 10.1016/j.radonc.2018.06.011. Epub 2018 Jun 19.
Life expectancy of patients with limited-stage small cell lung cancer (LS-SCLC) continues to rise; thus, characterization of long-term toxicities is essential. Although there are emerging data linking cardiac irradiation doses with survival for non-small cell lung cancer, there are currently minimal data on cardiac-specific mortality (CSM) in LS-SCLC. The goal of this investigation was to evaluate CSM between left- and right-sided cases.
The Surveillance, Epidemiology, and End Results database was queried for stage I-III primary SCLC patients receiving radiotherapy; CSM was compared between left- and right-sided diseases. Accounting for mortality from other causes, Gray's test compared cumulative incidences of CSM between both groups. Multiple multivariate models examined the independent effect of laterality on CSM, including the Fine and Gray competing risk model and the Cox proportional hazards model.
Of 19,692 patients, 7991 (41%) were left-sided and 11,701 (59%) were right-sided. Left-sided patients experienced significantly higher CSM overall (3.3% vs. 2.6%, p = 0.004). Laterality was an independent predictor of CSM in the overall population in the Fine and Gray competing risk model (p = 0.006) as well as the Cox proportional hazards model (p = 0.007). The overall hazard ratio for CSM by disease laterality was 1.27 (95% confidence interval, 1.08-1.50). Laterality had no statistical association with non-cardiac mortality in the Fine and Gray competing risk model (p = 0.130).
Although causation between radiotherapy and CSM in LS-SCLC cannot be stated based on these data, we encourage clinical attentiveness to cardiac-sparing radiotherapy for LS-SCLC, along with further investigation evaluating dosimetric correlates for cardiotoxicity.
局限期小细胞肺癌(LS-SCLC)患者的预期寿命持续上升;因此,对长期毒性进行特征描述至关重要。尽管有新的数据表明非小细胞肺癌的心脏照射剂量与生存相关,但目前关于 LS-SCLC 中心脏特异性死亡率(CSM)的数据很少。本研究的目的是评估左侧和右侧病例之间的 CSM。
在监测、流行病学和最终结果数据库中查询接受放疗的 I-III 期原发性 SCLC 患者;比较左侧和右侧疾病之间的 CSM。考虑到其他原因导致的死亡率,Gray 检验比较了两组之间 CSM 的累积发生率。多个多变量模型研究了侧别对 CSM 的独立影响,包括 Fine 和 Gray 竞争风险模型和 Cox 比例风险模型。
在 19692 名患者中,7991 名(41%)为左侧,11701 名(59%)为右侧。左侧患者的 CSM 总体发生率显著较高(3.3%比 2.6%,p=0.004)。在 Fine 和 Gray 竞争风险模型(p=0.006)和 Cox 比例风险模型(p=0.007)中,侧别是全人群 CSM 的独立预测因子。疾病侧别的 CSM 总体风险比为 1.27(95%置信区间,1.08-1.50)。在 Fine 和 Gray 竞争风险模型中,侧别与非心脏死亡率无统计学关联(p=0.130)。
尽管基于这些数据不能说明 LS-SCLC 中放疗与 CSM 之间的因果关系,但我们鼓励对 LS-SCLC 进行心脏保护放疗,并进一步研究评估心脏毒性的剂量学相关性。