Department of Otorhinolaryngology and Head & Neck surgery, Erasmus MC, Postbus 2040, 3000, Rotterdam, CA, Netherlands.
Department of Radiotherapy, Academic Medical Center, Postbus 22660, 1100, Amsterdam, DD, Netherlands.
Radiat Oncol. 2018 Dec 24;13(1):253. doi: 10.1186/s13014-018-1202-z.
Although stereotactic radiotherapy (SRT) for vestibular schwannoma has demonstrated excellent local control rates, hearing deterioration is often reported after treatment. We therefore wished to assess the change in hearing loss after SRT and to determine which patient, tumor and treatment-related factors influence deterioration.
We retrospectively analyzed progression of hearing loss in patients with vestibular schwannoma who had received stereotactic radiosurgery (SRS) or fractionated stereotactic radiotherapy (FSRT) as a primary treatment between 2000 and 2014. SRS had been delivered as a single fraction of 12 Gy, and patients treated with FSRT had received 30 fractions of 1.8 Gy. To compare the effects of SRS and FSRT, we converted cochlear doses into EQD. Primary outcomes were loss of functional hearing, Gardner Robertson (GR) classes I and II, and loss of baseline hearing class. These events were used in Kaplan Meier plots and Cox regression. We also calculated the rate of change in Pure Tone Average (PTA) in dB per month elapsed after radiation-a measure we use in linear regression-to assess the associations between the rate of change in PTA and age, pre-treatment hearing level, tumor size, dose scheme, cochlear dose, and time elapsed after treatment (time-to-first-audiogram).
The median follow-up was 36 months for 67 SRS patients and 63 months for 27 FSRT patients. Multivariate Cox regression and in linear regression both showed that the cochlear V90 was significantly associated with the progression of hearing loss. But although pre-treatment PTA correlated with rate of change in Cox regression, it did not correlate in linear regression. The time-to-first-audiogram was also significantly associated, indicating time dependency of the rate of change. None of the analysis showed a significant difference between dose schemes.
We found no significant difference between SRS and FSRT. As the deterioration in hearing after radiotherapy for vestibular schwannoma was associated with the cochlea V90, restricting the V90 may reduce progression of hearing loss. The association between loss of functional hearing and baseline PTA seems to be biased by the use of a categorized variable for hearing loss.
尽管立体定向放疗(SRT)治疗前庭神经鞘瘤已显示出优异的局部控制率,但治疗后常出现听力恶化。因此,我们希望评估 SRT 后听力损失的变化,并确定哪些患者、肿瘤和治疗相关因素会影响听力恶化。
我们回顾性分析了 2000 年至 2014 年间接受立体定向放射外科(SRS)或分割立体定向放疗(FSRT)作为主要治疗的前庭神经鞘瘤患者的听力损失进展情况。SRS 采用单次 12Gy 剂量,FSRT 患者则接受 30 次 1.8Gy 剂量。为了比较 SRS 和 FSRT 的效果,我们将耳蜗剂量转换为 EQD。主要结果是功能性听力丧失、Gardner Robertson(GR)分级 I 和 II 以及基线听力丧失分级。这些事件用于 Kaplan-Meier 图和 Cox 回归。我们还计算了辐射后纯音平均(PTA)每 1 个月的变化率,这是我们在线性回归中使用的一个指标,以评估 PTA 变化率与年龄、治疗前听力水平、肿瘤大小、剂量方案、耳蜗剂量和治疗后时间(首次听力测试时间)之间的关系。
67 例 SRS 患者的中位随访时间为 36 个月,27 例 FSRT 患者的中位随访时间为 63 个月。多变量 Cox 回归和线性回归均表明耳蜗 V90 与听力损失的进展显著相关。尽管治疗前 PTA 与 Cox 回归中的变化率相关,但在线性回归中不相关。首次听力测试时间也与变化率显著相关,表明变化率存在时间依赖性。两种分析均未显示剂量方案之间有显著差异。
我们发现 SRS 和 FSRT 之间没有显著差异。由于放疗后前庭神经鞘瘤的听力恶化与耳蜗 V90 相关,因此限制 V90 可能会减少听力损失的进展。功能性听力丧失与基线 PTA 之间的关联似乎受到听力损失分类变量的影响而存在偏差。