首页> 美国卫生研究院文献>Neuro-Oncology >P06.09LONG TERM VISUAL OUTCOME AFTER RADIOSURGERY IN 97 PATIENTS AFFECTED BY ANTERIOR SKULL BASE BENIGN MENINGIOMAS
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P06.09LONG TERM VISUAL OUTCOME AFTER RADIOSURGERY IN 97 PATIENTS AFFECTED BY ANTERIOR SKULL BASE BENIGN MENINGIOMAS

机译:P06.09颅骨前根瘤对97例患者进行放射外科手术后的长期视觉结果

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摘要

INTRODUCTION. The concern about radiation induced optic neuropathy (RION) strongly characterized the recent past. This has probably been the main limit to a wider diffusion of radiotherapy and radiosurgery as treatment of meningiomas involving the anterior optic pathways. In spite of this consideration, during the last few years the radiotherapy activity for such lesions is continuously increasing. The aim of the present study is to define the risk of RION on a medium to long term follow-up period in a large series of patients treated by radiosurgery. The efficacy of the treatment is also investigated. MATERIALS AND METHODS: The visual outcome of 97 patients which underwent radiosurgery due to a meningioma involving the anterior optic pathways has been retrospectively evaluated. Patients with a minimum follow-up period longer than 12 months were included. Sixteen patients had a single session radiosurgery (sSRS) with a mean dose of 12 Gy (range 8-13 Gy; median 13 Gy). In these cases the mean tumour volume was 4,9 cc (range 0,3-10,5 cc; median 3.6 cc) Eighty-one patients underwent a multi-session radiosurgery (mSRS). The mean prescription dose was 24 Gy (range 15-30Gy; median 25Gy), the mean tumour volume was 9,5 cc (range 0,5-65 cc; median 6,5 cc) The visual outcome was evaluated in all cases. All the included patients had at least a pre-treatment and a last follow-up visual function assessment. Furthermore local control has been analyzed. RESULTS: The mean follow-up is 43 months (range 12-96 months; 56 patients f-up ≥ 36 monts; 23 patients f-up ≥ 60 months) Compared to the baseline the visual function improved in 24 patients (24 %) and was unchanged in 65 (68 %). Seven patients worsened 8 (8 %). Three out of these experienced a tumour progression. Only two patients with no progression disease developed a “de novo” visual deficit. At the analysis time, the overall local control was 94 %. Eighteen lesions (18%) showed a partial shrinkage, seventy-three (72%) were stable and 6 patients (6%) experienced a progression of the disease. When observed, the tumour progression always occurred later than 36 months post-treatment. CONCLUSIONS: The study confirms the low risk of radiation induced optic neuropathy both in case of sSRS and mSRS. Multisession radiosurgery makes also the larger lesions manageable. The high local control rate and the low toxicity suggest that radiosurgery could be proposed also as a primary treatment.
机译:介绍。对辐射诱发的视神经病变(RION)的关注强烈地表征了最近的过去。作为涉及前视路的脑膜瘤的治疗,这可能是放疗和放射外科广泛传播的主要限制。尽管有这种考虑,但是在最近几年中,针对这种病变的放射治疗活性正在持续增加。本研究的目的是确定在接受放射外科手术治疗的大量患者中长期随访期间发生RION的风险。还研究了治疗的功效。材料与方法:回顾性评估了97例因脑膜瘤涉及前视路的放射外科手术患者的视觉效果。最短随访时间超过12个月的患者也包括在内。 16例患者接受了一次单次放射外科手术(sSRS),平均剂量为12 Gy(范围8-13 Gy;中位数13 Gy)。在这些情况下,平均肿瘤体积为4.9 cc(范围为0.3 cc-5.5 cc;中位数为3.6 cc)八十一例患者接受了多期放射外科手术(mSRS)。平均处方剂量为24 Gy(范围为15-30Gy;中位数为25Gy),平均肿瘤体积为9.5 cc(范围为0.5-65 cc;中位数为6.5 cc)在所有情况下均评估了视觉效果。所有纳入的患者至少进行了治疗前和最后一次随访的视觉功能评估。此外,已经对本地控制进行了分析。结果:平均随访时间为43个月(范围12-96个月; 56例f-up≥36 monts; 23例f-up≥60个月)与基线相比,24例患者的视功能得到改善(24%)而在65(68%)中没有变化。七名患者恶化8(8%)。其中三个经历了肿瘤进展。仅两名没有进展性疾病的患者出现了“从头”视觉缺陷。在分析时,总体本地控制率为94%。有18个病灶(18%)表现出局部萎缩,有73个病灶(72%)稳定,有6名患者(6%)病情进展。当观察到时,肿瘤进展总是在治疗后36个月之后发生。结论:本研究证实,无论是sSRS还是mSRS,放射线诱发的视神经病变的风险均较低。多阶段放射外科也使较大的病灶易于管理。高局部控制率和低毒性表明放射外科也可以被建议作为主要治疗方法。

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