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分次质子束放疗对不适用于立体定向放射外科治疗的颅神经鞘瘤的有效性和毒性

Effectiveness and Toxicity of Fractionated Proton Beam Radiotherapy for Cranial Nerve Schwannoma Unsuitable for Stereotactic Radiosurgery.

作者信息

Eichkorn Tanja, Regnery Sebastian, Held Thomas, Kronsteiner Dorothea, Hörner-Rieber Juliane, El Shafie Rami A, Herfarth Klaus, Debus Jürgen, König Laila

机构信息

Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.

National Center for Radiation Oncology (NCRO), Heidelberg Institute for Radiation Oncology (HIRO), Heidelberg, Germany.

出版信息

Front Oncol. 2021 Nov 17;11:772831. doi: 10.3389/fonc.2021.772831. eCollection 2021.

Abstract

PURPOSE

In this benign tumor entity, preservation of cranial nerve function is of special importance. Due to its advantageous physical properties, proton beam radiotherapy (PRT) is a promising approach that spares healthy tissue. Could PRT go along with satisfactory preservation rates for cranial nerve function without compromising tumor control in patients with cranial nerve schwannoma unsuitable for stereotactic radiosurgery?

METHODS

We analyzed 45 patients with cranial nerve schwannomas who underwent PRT between 2012 and 2020 at our institution. Response assessment was performed by MRI according to RECIST 1.1, and toxicity was graded following CTCAE 5.0.

RESULTS

The most common schwannoma origin was the vestibulocochlear nerve with 82.2%, followed by the trigeminal nerve with 8.9% and the glossopharyngeal nerve as well as the vagal nerve, both with each 4.4%. At radiotherapy start, 58% of cranial nerve schwannomas were progressive and 95.6% were symptomatic. Patients were treated with a median total dose of 54 Gy RBE in 1.8 Gy RBE per fraction. MRI during the median follow-up period of 42 months (IQR 26-61) revealed stable disease in 93.3% of the patients and partial regression in 6.7%. There was no case of progressive disease. New or worsening cranial nerve dysfunction was found in 20.0% of all patients, but always graded as CTCAE °I-II. In seven cases (16%), radiation-induced contrast enhancements (RICE) were detected after a median time of 14 months (range 2-26 months). RICE were asymptomatic (71%) or transient symptomatic (CTCAE °II; 29%). No CTCAE °III/IV toxicities were observed. Lesions regressed during the follow-up period in three of the seven cases, and no lesion progressed during the follow-up period.

CONCLUSION

These data demonstrate excellent effectiveness with 100% local control in a median follow-up period of 3.6 years with a promising cranial nerve functional protection rate of 80%. RICE occurred in 16% of the patients after PRT and were not or only mildly symptomatic.

摘要

目的

在这种良性肿瘤实体中,保留颅神经功能尤为重要。由于其有利的物理特性,质子束放疗(PRT)是一种有前景的可减少健康组织受照的方法。对于不适合立体定向放射外科治疗的颅神经鞘瘤患者,PRT能否在不影响肿瘤控制的情况下实现令人满意的颅神经功能保留率?

方法

我们分析了2012年至2020年间在我院接受PRT治疗的45例颅神经鞘瘤患者。根据RECIST 1.1标准通过MRI进行疗效评估,并按照CTCAE 5.0对毒性进行分级。

结果

最常见的鞘瘤起源于前庭蜗神经,占82.2%,其次是三叉神经,占8.9%,舌咽神经和迷走神经均占4.4%。放疗开始时,58%的颅神经鞘瘤处于进展期,95.6%有症状。患者接受的中位总剂量为54 Gy RBE,每次分割剂量为1.8 Gy RBE。在中位随访期42个月(IQR 26 - 61)期间,MRI显示93.3%的患者病情稳定,6.7%部分缓解。无疾病进展病例。在所有患者中,20.0%出现新的或加重的颅神经功能障碍,但均为CTCAE °I - II级。7例(16%)患者在中位时间14个月(范围2 - 26个月)后检测到放射诱导的对比增强(RICE)。RICE无症状(71%)或短暂有症状(CTCAE °II;29%)。未观察到CTCAE °III/IV级毒性反应。7例中有3例病变在随访期间消退,随访期间无病变进展。

结论

这些数据表明,在中位随访期3.6年时,局部控制率达100%,颅神经功能保护率有望达到80%,疗效极佳。PRT后16%的患者出现RICE,且无症状或仅轻微有症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf6b/8635775/823413bf7457/fonc-11-772831-g001.jpg

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