Park Chul-Kee, Jung Hee-Won, Kim Jeong Eun, Paek Sun Ha, Kim Dong Gyu
Department of Neurosurgery, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, Seoul 110-744, South Korea.
Surg Neurol. 2006 Aug;66(2):160-5; discussion 165-6. doi: 10.1016/j.surneu.2005.12.024.
Broad experience with the management of petroclival meningiomas was analyzed to optimize therapeutic strategy.
The records of 75 patients with petroclival meningioma were reviewed. The population was divided into a microsurgery group (n = 49), a radiosurgery group (n = 12), a radiation therapy group (n = 5), and an observation group (n = 9) according to the modality of primary treatment. In the microsurgery group, the tumor was completely resected in 10 patients. Eleven of the 39 patients with incomplete resections sequentially underwent adjuvant radiation therapy or radiosurgery. The median follow-up period was 86 months (range, 48-210 months). The median follow-up period of the radiosurgery, the radiation therapy, and the observation group was 52 months (range, 48-71 months), 56 months (range, 51-72 months), and 63 months (range, 53-68 months), respectively. Management outcomes were evaluated with respect to tumor control rate, neurological deficit, and functional status assessed by the Karnofsky Performance Score.
In the microsurgery group, 11 (22.4%) patients eventually showed tumor progression. However, there was only one recurrence if adjuvant therapy was used after incomplete removal. The incidence of favorable outcomes for cranial neuropathies was better in the incomplete resection group (69.2%) than for patients in the complete resection group (20%, P = .032). Moreover, a favorable functional outcome predominated in the incomplete resection group (76.9%) compared with the complete resection group (30%, P = .049). The disease was stable in both the radiation therapy and the radiosurgery groups during the follow-up period, with functional status and cranial nerve function perfectly preserved in these patients. No predictive factor other than short symptom duration was found to be significant.
Because the growth rate of petroclival meningioma is low and good functional status can be guaranteed, intended incomplete resection should be considered as an acceptable treatment option. Adjuvant treatment after surgery is useful in the control of residual tumors. Radiosurgery may be appropriate as the primary treatment in asymptomatic patients with small tumor; however, more aggressive treatment is needed in young patients or patients with short symptom durations.
分析岩斜区脑膜瘤管理的广泛经验以优化治疗策略。
回顾75例岩斜区脑膜瘤患者的记录。根据初始治疗方式将患者分为显微手术组(n = 49)、放射外科组(n = 12)、放射治疗组(n = 5)和观察组(n = 9)。在显微手术组中,10例患者肿瘤完全切除。39例未完全切除的患者中有11例依次接受辅助放射治疗或放射外科治疗。中位随访期为86个月(范围48 - 210个月)。放射外科组、放射治疗组和观察组的中位随访期分别为52个月(范围48 - 71个月)、56个月(范围51 - 72个月)和63个月(范围53 - 68个月)。根据肿瘤控制率、神经功能缺损以及通过卡诺夫斯基性能评分评估的功能状态对治疗结果进行评估。
在显微手术组中,11例(22.4%)患者最终出现肿瘤进展。然而,不完全切除后使用辅助治疗时仅1例复发。不完全切除组颅神经病变良好结局的发生率(69.2%)高于完全切除组患者(20%,P = 0.032)。此外,与完全切除组(30%,P = 0.049)相比,不完全切除组功能良好结局占主导(76.9%)。在随访期间,放射治疗组和放射外科组疾病均稳定,这些患者的功能状态和颅神经功能得到完美保留。除症状持续时间短外,未发现其他显著的预测因素。
由于岩斜区脑膜瘤生长速度低且可保证良好的功能状态,有意的不完全切除应被视为可接受的治疗选择。术后辅助治疗对控制残留肿瘤有用。对于无症状的小肿瘤患者,放射外科可作为主要治疗方法;然而,年轻患者或症状持续时间短的患者需要更积极的治疗。