Original Research ARTICLE

Front. Neurol., 13 May 2020 | https://doi.org/10.3389/fneur.2020.00355

Fractionated Radiation Therapy for Large and Giant Cavernous Sinus Hemangioma: A Retrospective Study

Zengfeng Xin1,2, Yihan Yao3, Guodi Chen1, Liancong Wang1, Meibao Shu1, Qinghua Lv3, Haifeng Yu4 and Ting Zhang1,3*
  • 1Department of Radiation Oncology, Zhejiang University School of Medicine, The Second Affiliated Hospital, Zhejiang University, Hangzhou, China
  • 2Department of Orthopedic Surgery, Zhejiang University School of Medicine, The Second Affiliated Hospital, Zhejiang University, Hangzhou, China
  • 3Key Laboratory of Tumor Microenvironment and Immune Therapy of Zhejiang Province, Hangzhou, China
  • 4Department of Chemotherapy Center, Zhejiang Cancer Hospital, Hangzhou, China

Purpose: Surgical resection has been traditionally used as a treatment for cavernous sinus hemangioma (CSH). However, this is usually difficult due to tumor vascularity and results in complications especially in large and giant CSH (volume >20 cm3). Previous studies have reported that radiotherapy (RT) provides an alternative treatment modality for hemangiomas. However, the optimized dose and fractions which control CSH and also protect the cognitive function remain unclear. This study reports our experience in the management of symptomatic large and giant CSH.

Methods: Fifty-four patients with symptomatic large (20 cm3 <tumor volume ≤ 40 cm3, 3–4 cm in diameter) and giant (tumor volume>40 cm3, >4 cm in diameter) CSH were enrolled in a retrospective study between January 2007 and December 2018. The prescription dose to the target margin was 50 Gy in 25 fractions.

Results: The mean pre-RT tumor volume was 60.9 cm3 which ranged from 20.2 to 230.5 cm3. The clinical data obtained was analyzed retrospectively following a mean follow-up period of 35.0 months which ranged from 1 to 140 months. All patients experienced tumor shrinkage within 3 months after radiotherapy. There was an average mean tumor reduction of 79.7% (range, 48.4–98.5%) with no patients experiencing tumor progression and recurrence. All the 54 patients experienced symptomatic improvement within 1 month to 12 months after radiotherapy. Within the entire follow up period, no patients experienced any form of permanent complications or symptomatic radiation toxicity. Neurocognitive impairment studies were conducted before and after radiotherapy on 28 patients while the studies were conducted after the last follow up in 40 patients. The cognitive function of all the participants had normal MoCA-scores of 28.25 pre-radiotherapy. The post-treatment MoCA-scores were also clinically stable (28.04, p = 0.78), and the average MoCA-score did not show any decline until the last follow-up (27.61, p = 0.13).

Conclusion: The optimal dose and fractions of radiotherapy treatment for symptomatic large and giant cavernous sinus hemangioma remain unclear. This study, therefore, used a marginal dose of 50 Gy in 25 fractions in radiotherapy and this was proven to be effective and relatively safe in the treatment of symptomatic large and giant CSHs.

Introduction

Hemangioma is a benign vascular tumor which causes clinical symptoms due to its progressive tumor growth and large size (1). Cavernous sinus hemangioma (CSH) is a rare benign tumor arising from the cavernous sinus and constitutes <3% of sellar or para sellar tumors, and tend to occur mostly in middle-aged females (2). CSHs can develop with no elaborate symptoms in the cavernous sinus (CS). Nonetheless, large (20 cm3 <tumor volume ≤ 40 cm3,3–4 cm in diameter) and giant (tumor volume>40 cm3, >4 cm in diameter) CSHs may present with a variety of neurologic symptoms, such as blurred vision, diplopia, headache, seizures, and neurological deficit (3). The fatality rate in the case of a rupture or bleeding is extremely high.

For this type of benign tumor, treatment can be achieved through the complete removal of CSH. Currently, the available treatments for CSH include microsurgical resection, embolization, stereotactic radiosurgery (SRS) such as Gamma Knife radiosurgery (GKRS), and fractionated radiotherapy (4, 5). The resection of large and giant CSHs is challenging due to the complex natural anatomic structures around the tumor (6). Surgical management of this lesion is also associated with extremely high risks due to the possibilities of significant blood loss and cranial neuropathies, hence, it is difficult to achieve total resection. Despite the recent advances in neurosurgical techniques, the total resection rate of CSHs by surgical excision is 64%, and cranial neuropathies-related symptoms deteriorate after surgical treatment in ~71% of the patients (7, 8).

Similar to the high risks of surgical treatment, radiotherapy (RT) for CSHs management has been extensively studied and reported. For example, in 1999, a postoperative patient with a residual lesion after resection was treated using GKRS. The postoperative results showed that the tumor markedly decreased and the preoperative clinical symptoms improved (9). Radiosurgery is currently an optimal choice for primary or postoperative treatment of CSH since it has demonstrated favorable clinical results. However, radiosurgery such as GKRS is suitable for small lesions (10, 11). Yamamoto et al. described their experiences of the successful treatment of about 30 cases of CSHs using radiosurgery. In their study, the average tumor volume was 11.5 cm3 (12). Due to the high morbidity of radiation complications, the size and location of the tumor limit the usage of GKRS for large CSHs, especially those adjacent to critical anatomic structures. Large lesions, therefore, require a larger target area and this may also lead to critical complications during irradiation for example on normal structures such as cerebral tissue and important nerves. Therefore, the use of fractionated stereotactic irradiation is increasing. In a previous study, hypofractionated stereotactic radiotherapy (H-SRT) was proven to effectively reduce the volume of CSH without causing severe radiation complications, even in large tumors with a median tumor volume of 19.3 cm3 (the range was from 15.8 cm3 to 69.3 cm3) (13). In another study, 14 large cavernous sinus hemangioma (volume >20 cm3) patients were treated using H-SRT, and the reported reduction rate of the tumor volume was 77%, and with no radiotherapy-induced complications observed. These studies have confirmed the effectiveness and safety of H-SRT (14). The reduction in the damage of normal structures while decreasing the volume of neoplasms is the main biological benefit of fractionated RT (15). For the current study, to achieve favorable reduction as well as to protect the optic pathway and other normal tissue from irradiation, this study's regimen of RT was used to deal with large and giant CSHs. In this retrospective study, the experience of 54 patients with large and giant CSHs in our institution was described. Therefore, the aim of this study was to evaluate the efficacy and safety of our regimen of RT as a treatment modality for large and giant CSHs.

Methods and Materials

Patients

Patients diagnosed with large and giant CSHs (tumor volume>20 cm3) and treated with RT at the Second Affiliated Hospital of Zhejiang University from January 2007 to December 2018 were recruited in the study. There were 54 patients diagnosed during the stipulated period and their characteristics are presented in Table 1. This study was approved by the Ethics Committee of the Second Affiliated Hospital of Zhejiang University School of Medicine (No. 2019–220).

TABLE 1
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Table 1. Baseline demographic and clinical factors of patients with large and giant CSHs.

Diagnosis

A brain magnetic resonance imaging (MRI) and/or computed tomography (CT) study was used as the primary diagnostic tool in all the patients. CSHs were mainly diagnosed based on some specific imaging characteristics using MRI where the CSHs had well-defined boundaries in the MRI images (16). On T1-weighted images, the tumor was uniformly hypointense compared with the brain parenchyma, and also showed significantly brighter hyperintensity on T2-weighted images. The lesions became significantly enhanced after a contrast agent injection (17). The diagnosis was confirmed through pathological diagnosis or typical neuroimaging diagnosis. In this study, a total of 5 patients were pathologically diagnosed, while 49 patients were diagnosed through MRI with or without digital subtraction angiography (DSA).

Treatment Strategy

The Eclipse treatment planning system was used to fuse the CT and MRI scan with enhanced T1-weighted sequence to improve the target identification. The gross tumor volume (GTV) was defined as the enhanced tumor area according to the images. Expansion of the GTV margin by 5 mm in all directions was used to obtain the planning target volume (PTV). As shown in Table 2, evaluation of the target coverage, dose heterogeneity, and conformity were used to assess the quality of the treatment plans. 6-MV X-ray was used to deliver a total dose of 50 Gy in 25 fractions in 45 patients. However, 5 patients received 46 Gy in 23 fractions, whereas 2 patients received 40 Gy in 20 fractions and 1 patient received 45 Gy in 15 fractions. Plan normalized at 100% prescription cover 95% target volume. RT was performed using intensity modulated three-dimensional treatment plan across several different non-coplanar fixed fields in a linear accelerator (Varian).

TABLE 2
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Table 2. Treatment characteristics and dose volume analyses of 54 patients.

Neurocognitive Function

The Montreal Cognitive Assessment (MoCA) was used to assess the neurocognitive performance of the patients (18). This assessment results were presented in the form of a total score and seven scores in seven different aspects: naming, memory, attention, language, executive and visuospatial functioning, abstraction and orientation (score 0–30). In this study, a score of <26 was used to define neurocognitive impairment (NCI) (19).

Follow Up Period

The first follow-up was conducted 3 months after the completion of RT, and subsequent follow-ups were conducted annually after the treatment. During each follow-up, a questionnaire was administered to obtain the patients clinical status and any other relevant physical examination, as well as brain MRI or CT scan, were performed. Based on MRI or CT results, the Eclipse planning system (version 13.6, Varian Medical Systems, Palo Alto, CA, USA) was used to estimate the tumor volumes. The National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0. was used to score and document all treatment-induced toxicities.

Statistical Analysis

Basic descriptive statistics were used to demonstrate the baseline characteristics of patients, treatment information, and other variables measured during treatment and the follow-up period. For binary results, univariable analyses were conducted using a logistic regression model whereas linear regression was used for continuous variables. t-tests were used to analyze the difference between pre-treatment mean MoCA scores and post-treatment mean MoCA scores. All the statistical analyses were performed using SPSS software, version 20.0.

Results

Patients Characteristics and Treatment Modalities

A total of 54 patients with CSH and treated between January 2007 and December 2018 were included in the study. As shown in Table 1, the majority of the patients were female (77.8%, 42) with a median age of 47.8 years old (age range was from 22 to 64 years) at diagnosis. Prior to RT, five patients received operations, 4 of them underwent lesion biopsy while another one received partial resection. The most common initial symptoms among the patients were blurred vision (61.1%, 33), dizziness (38.9%, 21), headache (33.3%, 18), vomit (11.1%, 6), proptosis (9.3%, 5), ptosis (5.6%, 3), vertigo (7.4%, 4), and weakness in upper extremities (1.9%, 1). The mean hemangioma volume was 61.3 cm3 (the range was between 20.2 to 230.5 cm3) before treatment.

Treatment characteristics of each patient are presented in Table 2. The RT was performed at the median 95% isodose line. The mean tumor coverage receiving the entire prescribed dose was 94.7% (ranging from 91.7 to 97.8%), and the mean conformity index was 0.82 (ranging from 0.76 to 0.88). In addition, the average tumor maximum dose was 53.36 Gy (ranging from 46.97 to 58.09 Gy), while the mean minimal dose of the tumor was 45.74 Gy (ranging from 37.60 to 49.15 Gy). Furthermore, the average maximum dose irradiating to the ipsilateral optic nerve, optic chiasm, and brainstem were 43.58Gy (range was between 21.03 and 53.60Gy), 46.67 Gy (range was between 21.18 and 53.62 Gy), and 44.19 Gy (range was between 25.11 and 53.67 Gy), respectively. Figure 1 shows one of the treatment plans.

FIGURE 1
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Figure 1. A mass occupying the left cavernous sinus of a 24-year-old woman (patient 1) was shrunk gradually after RT. (A) Treatment plan based on CT scan. (B) The 3D imaging of the mass before RT and at a different time of follow up after RT. (C) MRI scan before RT, the day after RT completion and 3 months, 9 months, and 2 years after RT.

Imaging Response

The average follow-up period for all the patients was 35.0 months (ranging from 1 to 140 months). The MRI or CT images demonstrated significant tumor shrinkage in all the patients and the tumors control rate was 100%. Shrinkage of the CSHs was seen immediately after the completion of RT. The tumor volume was about 65.7% of their initial volume at the end of the RT and kept decreasing during the follow-up period. Three months post RT, the masses had reduced in size to 42.9% of the original volume (Figures 3A,B). At 1-year post RT, they reduced further to 29.7% and 23.6% at 2 years post-RT. In some patients, the tumor sizes remained stable without any change in size while on others, they kept decreasing even after 5 years follow-up (Figures 2A,B). The MRI results indicated a 98.7% tumor volume reduction 2 years after RT (Figure 1). However, no transient tumor enlargement was observed in participants after RT.

FIGURE 2
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Figure 2. CSH of patient 7 kept decreasing even 5 years later. (A) The 3D imaging of the mass before RT and at different times of follow up after RT. (B) MRI scan before RT, the day after RT completion and at a different time of follow up after RT.

FIGURE 3
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Figure 3. The tumor volume reduced over the entire follow-up period without transient enlargement in all the patients. (A) The volume of the CSHs decreased in all patients. (B) The percentage of tumor volume during the follow-up intervals to their initial volume. (C) The MoCA score of participants at three-time points (pre-treatment, post-treatment and the last follow-up).

Clinical Response

All the patients had favorable neurological outcomes after the treatment. The neurologic symptoms changes after treatment are shown in Table 1. All pretreatment symptoms had recovered or improved within 1 month to 1 year after RT. Fifty-one patients (94.4%) experienced symptoms recovery after the treatment, while three patients (5.6%) had their symptoms improved which lasted for many years. During the final follow-up, all the participating patients showed favorable RT neurological outcomes. Only one patient expressed feelings of dizziness.

Toxicity

There was no patient who suffered severe acute or delayed complications associated with RT. All the observed side effects were mild and transient. Grade 1 nausea and anorexia developed in only two patients (3.7%). While Grade 2 nausea occurred in three patients (5.6%) during the course of RT. However, these symptoms of RT-related side effects were managed with corticosteroids and they completely disappeared. MRI showed that some patients had encephaledema about 2 years after RT, but they had no clinical symptoms. There were no other acute or early delayed side effects from RT observed both during the treatment and follow-up period.

Neurocognitive Assessment

Among 54 participating patients, 40 patients had the neurocognitive test done and they completed the MoCA at least once. Among them, 28 patients had the neurocognitive impairment study before and after RT while 40 patients did the study during the last follow-up. The cognitive functions of the participants were in the normal range (total MoCA-scores of 28.25) pre-RT. In comparison, post-treatment MoCA-scores were clinically stable (28.04, p = 0.78) and the average MoCA-score was not decreased at the last follow-up (27.61, p = 0.13) (Figure 3C).

Discussion

In this retrospective study, the efficacy of radiotherapy as a treatment modality for patients with large and giant CSHs was evaluated. RT of a marginal dose of 50 Gy in 25 fractions at the median 95% prescription isodose line was used. The results of this study demonstrated an average 79.7% tumor reduction. Moreover, the pretreatment symptoms such as visual disturbance and headache could be cured or improve after RT. In all the patients there was no severe radiotherapy-induced complications observed during the treatment and neither during the subsequent follow-up period. The cognitive function of the patients did not also change during the entire treatment and follow-up period. These results revealed the efficacy and safety of our regimen of RT for large and giant CSHs.

Surgery is a traditional treatment for CSHs, however, in spite of there being several advanced surgical techniques, it is difficult to completely remove large and giant CSHs through surgery. This is due to the complex and critical anatomic structures in the cavernous sinus and the possible risk of excessive bleeding during the operation. Previous studies have demonstrated a low total surgical removal rate and high morbidity of complications after surgery in CSH (1, 17). Majority of the cases reported arose from the neurosurgery department.

Radiotherapy has become an emerging approach for CHS treatment for patients with residual tumors after surgery as well as those with great intraoperative risk. This is due to its efficacy and safety compared with surgical treatment. As early as the 1980s, radiosurgery was used for the treatment of high surgical risk CSH and has been successfully used as adjuvant therapy in CSH patients having residual lesions after surgical removal (9, 20). Subsequently, more studies have been conducted on the function of radiotherapy for CSHs due to its remarkable tumor shrinkage effect. Gamma Knife surgery is one of the radiotherapy techniques which has been proven to be safe and is being used for primary as well as postoperative management of CSH patients. A retrospective study analyzing the effect of Gamma Knife surgery in patients with CSH reported an average tumor volume reduction of 82%, and most of the pretreatment symptoms had been improved (21). In another meta-analysis, by Wang et al. 59 patients with a mean follow-up period of 49.2 months (range between 6 and 156 months) was studied. The results supported stereotactic radiosurgery as an alternative treatment for CSHs because of its reduction in traditional surgery-associated complications (22). However, the treatment outcomes of GKRS were associated with the tumor volume, underdosed tumor volume and total treated volume (23). Single-shot radiosurgery was reported to be effective for patients with small- or middle-sized CSHs. The high risk of radiation-induced optic neuropathy (RION) limits the usage of single-shot stereotactic radiosurgery for the patients with large CSHs (23). However, for large and giant cavernous sinus hemangiomas, Gamma Knife radiosurgery may not the optimal treatment. Previous studies, indicate that the risk of radiation-induced complications such as cranial nerve palsies and cognitive damage, could be higher if fractionation is not performed (24). Wang X. reported hypofractionated stereotactic radiosurgery using CyberKnife with 21 Gy in 3 fractions or 22 Gy in 4 fractions for the treatment of giant CSHs (volume>40 cm3, >4 cm in diameter) in 31 patients. Compared with pretreatment tumor volume, the results demonstrated a median tumor volume reduction of 88.1% (62.3–99.4%) during the last follow-up (3), with a mean follow-up period of 30 months. However, there was a concern about cognitive impairment as a long-term side effect.

It has been reported that cognitive impairment is one of the radiation encephalopathies which may significantly affect a patient's quality of life (25, 26). Radiation-induced cognitive impairment can be divided as acute, early delayed and late effects, with late effects being considered to be irreversible (27). The mechanism of the effect of RT on cognitive function has been reported in previous studies (25). Radiotherapy induces vascular damage and changes in white matter, including demyelination and coagulative necrosis (28). One of the essential regions of cognition is the hippocampus which has been found to be damaged after radiation. In some preclinical studies, neurogenesis inhibition following brain radiotherapy was demonstrated which caused cognitive impairment (29, 30). In this study, we followed up on the long-term effect of RT, however, no cognitive impairment was observed.

Fractionated stereotactic radiotherapy is another alternative treatment modality for large and giant CSHs especially those showing great risk through traditional surgery and radiosurgery. However, studies about conventional radiotherapy performed for CSH are rare with most of those available being case reports. In these relevant studies, the radiation dose varied from 30 Gy to 50 Gy (31). A phase II study focusing on hypofractionated stereotactic radiotherapy for large (volume> 20 cm3) CSH reported a mean of 77% tumor volume reduction (range, 44–99%), 14 patients included, and the radiotherapy dose was 21 Gy delivered in 3 fractions, however the mean follow-up period was 15 months (range, 6–36 months) (14). The current study focused on large and giant CSHs and has a longer follow-up period. As a benign tumor, long-term survival is expected, and it is necessary to minimize the toxicity of RT such as RION (32, 33).

This study, however, had a number of limitations. First, it was a retrospective and single-centered study with a small number of patients to make a definitive conclusion. Therefore, this needs further research and the inclusion of larger sample size in a multicenter study. Besides, for observing long-term cognitive deficits, the follow-up time period was relatively short, longer and more extensive follow-up is needed. The assessment of neurocognitive function involves many factors which have an effect on the MoCA scores, therefore, it was difficult to balance the factors due to the limited sample size. In addition, MoCA score is not the optimal tool for neurocognitive assessment in brain tumor patients. Furthermore, this study did not include a control group, and both the patients and investigators were aware of the treatment, which may exert influence on symptom reporting. Overall, further research on radiotherapy on CSH is required.

Conclusions

MRI helps clinicians to make a diagnosis in large and giant cavernous sinus hemangioma, but the optimal treatment for symptomatic CSHs remain unclear. Although longer follow-up is needed, RT using a marginal dose of 50 Gy in 25 fractions was found to be effective and relatively safe in the treatment of symptomatic large and giant CSHs.

Data Availability Statement

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Ethics Statement

This study was approved by the Ethics Committee of the Second Affiliated Hospital of Zhejiang University School of Medicine (No. 2019–220).

Author Contributions

TZ and YY designed this study and wrote the manuscript. GC, LW, and MS analyzed the clinical data and participated in the manuscript writing. TZ, YY, and GC interpreted the clinical data. HY and QL read and interpreted the radiology images. YY and LW collected the clinical data of surgery and radiotherapy. ZX and YY conceived the study and wrote the manuscript. All authors had read and approved the final manuscript.

Funding

This work was supported by grants from The Natural Science Foundation of Zhejiang Province (LY12H10006, LY17C080002, LY19C080002, LY19C080001), The Department of Health of Zhejiang Province (2017KY365, 2018KY424) and The National Natural Science Foundation of China (31200652).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors would like to thank Dr. Guangwei Yu, Dr. Chao Li, Dr. Kui Wu from Department of Radiation Oncology and Dr. Bing Pan from Department of psychiatry department, The Second Affiliated Hospital, Zhejiang University School of Medicine.

References

1. Linskey ME, Sekhar LN. Cavernous sinus hemangiomas: a series, a review, and an hypothesis. Neurosurgery. (1992) 30:101–8. doi: 10.1097/00006123-199201000-00018

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Bakhsheshian J, Zada G, Pham MH. Cavernous sinus hemangioma: rare vascular tumor of cavernous sinus. World Neurosurg. (2018) 110:432–3. doi: 10.1016/j.wneu.2017.11.177

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Wang X, Zhu H, Knisely J, Mei G, Liu X, Dai J, et al. Hypofractionated stereotactic radiosurgery: a new treatment strategy for giant cavernous sinus hemangiomas. J Neurosurg. (2018) 128:60–7. doi: 10.3171/2016.10.JNS16693

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Khan AA, Niranjan A, Kano H, Kondziolka D, Flickinger JC, Lunsford LD. Stereotactic radiosurgery for cavernous sinus or orbital hemangiomas. Neurosurgery. (2009) 65:914–8 discussion 8. doi: 10.1227/01.NEU.0000356987.98197.71

CrossRef Full Text | Google Scholar

5. Lee CC, Sheehan JP, Kano H, Akpinar B, Martinez-Alvarez R, Martinez-Moreno N, et al. Gamma knife radiosurgery for hemangioma of the cavernous sinus. J Neurosurg. (2017) 126:1498–505. doi: 10.3171/2016.4.JNS152097

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Yin YH, Yu XG, Xu BN, Zhou DB, Bu B, Chen XL. Surgical management of large and giant cavernous sinus hemangiomas. J Clin Neurosci. (2013) 20:128–33. doi: 10.1016/j.jocn.2012.01.050

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Escudeiro GP, Leal RTM, Leal da Silveira R, Landeiro JA. Cavernous sinus hemangioma: surgical aspects. World Neurosurg. (2019) 123:156. doi: 10.1016/j.wneu.2018.11.162

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Khattar NK, Adams SW, Schaber AS, White AC, Al Ghamdi M, Hruska RT, et al. Endoscopic endonasal surgery for the resection of a cavernous hemangioma with a sellar extension. Cureus. (2018) 10:e3663. doi: 10.7759/cureus.3663

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Iwai Y, Yamanaka K, Nakajima H, Yasui T. Stereotactic radiosurgery for cavernous sinus cavernous hemangioma–case report. Neurol Med chir (Tokya). (1999) 39:288–90. doi: 10.2176/nmc.39.288

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Anqi X, Zhang S, Jiahe X, Chao Y. Cavernous sinus cavernous hemangioma: imaging features and therapeutic effect of Gamma knife radiosurgery. Clin Neurol Neurosurg. (2014) 127:59–64. doi: 10.1016/j.clineuro.2014.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Tripathi M, Batish A, Kumar N, Ahuja CK, Oinam AS, Kaur R, et al. Safety and efficacy of single-fraction gamma knife radiosurgery for benign confined cavernous sinus tumors: our experience and literature review. Neurosurg Rev. (2018) 43:27–40. doi: 10.1007/s10143-018-0975-8

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Yamamoto M, Kida Y, Fukuoka S, Iwai Y, Jokura H, Akabane A, et al. Gamma knife radiosurgery for hemangiomas of the cavernous sinus: a seven-institute study in Japan. J Neurosurg. (2010) 112:772–9. doi: 10.3171/2009.6.JNS08271

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Haghighi N, Seely A, Paul E, Dally M. Hypofractionated stereotactic radiotherapy for benign intracranial tumours of the cavernous sinus. J Clin Neurosci. (2015) 22:1450–5. doi: 10.1016/j.jocn.2015.03.026

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Wang X, Liu X, Mei G, Dai J, Pan L, Wang E. Phase II study to assess the efficacy of hypofractionated stereotactic radiotherapy in patients with large cavernous sinus hemangiomas. Int J Radiat Oncol Biol Phys. (2012) 83:e223–30. doi: 10.1016/j.ijrobp.2011.12.051

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Park S, Yoon SM, Lee S, Park JH, Song SY, Lee SW, et al. Role of fractionated radiotherapy in patients with hemangioma of the cavernous sinus. Radiat Oncol J. (2017) 35:268–73. doi: 10.3857/roj.2017.00199

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Meincke J, Lutzen N, Doostkam S, Urbach H. Teaching neuroimages: “Filling out” in cavernous hemangioma of the cavernous sinus. Clin Neuroradiol. (2018) 28:137–8. doi: 10.1007/s00062-017-0607-7

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Zhou LF, Mao Y, Chen L. Diagnosis and surgical treatment of cavernous sinus hemangiomas: an experience of 20 cases. Surg Neurol. (2003) 60:31–6 discussion 6–7. doi: 10.1016/S0090-3019(03)00190-3

PubMed Abstract | CrossRef Full Text | Google Scholar

18. McDowell LJ, Ringash J, Xu W, Chan B, Lu L, Waldron J, et al. A cross sectional study in cognitive and neurobehavioral impairment in long-term nasopharyngeal cancer survivors treated with intensity-modulated radiotherapy. Radiother Oncol. (2019) 131:179–85. doi: 10.1016/j.radonc.2018.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Hsiao KY, Yeh SA, Chang CC, Tsai PC, Wu JM, Gau JS. Cognitive function before and after intensity-modulated radiation therapy in patients with nasopharyngeal carcinoma: a prospective study. Int J Radiat Oncol Biol Phys. (2010) 77:722–6. doi: 10.1016/j.ijrobp.2009.06.080

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Shibata S, Mori K. Effect of radiation therapy on extracerebral cavernous hemangioma in the middle fossa. Report of three cases. J Neurosurg. (1987) 67:919–22. doi: 10.3171/jns.1987.67.6.0919

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Chou CW, Wu HM, Huang CI, Chung WY, Guo WY, Shih YH, et al. Gamma knife surgery for cavernous hemangiomas in the cavernous sinus. Neurosurgery. (2010) 67:611–6 discussion 6. doi: 10.1227/01.NEU.0000378026.23116.E6

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Wang X, Mei G, Liu X, Pan L, Wang E. The role of stereotactic radiosurgery in cavernous sinus hemangiomas: a systematic review and meta-analysis. J Neurooncol. (2012) 107:239–45. doi: 10.1007/s11060-011-0753-8

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Kuo JS, Chen JC, Yu C, Zelman V, Giannotta SL, Petrovich Z, et al. Gamma knife radiosurgery for benign cavernous sinus tumors: quantitative analysis of treatment outcomes. Neurosurgery. (2004) 54:1385–93 discussion 93–4. doi: 10.1227/01.NEU.0000124750.13721.94

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Levegrun S, Hof H, Essig M, Schlegel W, Debus J. Radiation-induced changes of brain tissue after radiosurgery in patients with arteriovenous malformations: dose/volume-response relations. Strahlenther Onkol. (2004) 180:758–67. doi: 10.1007/s00066-004-1266-6

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Jacob J, Durand T, Feuvret L, Mazeron JJ, Delattre JY, Hoang-Xuan K, et al. Cognitive impairment and morphological changes after radiation therapy in brain tumors: a review. Radiother Oncol. (2018) 128:221–8. doi: 10.1016/j.radonc.2018.05.027

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Meyers CA, Brown PD. Role and relevance of neurocognitive assessment in clinical trials of patients with CNS tumors. J Clin Oncol. (2006) 24:1305–9. doi: 10.1200/JCO.2005.04.6086

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Ali FS, Hussain MR, Gutierrez C, Demireva P, Ballester LY, Zhu JJ, et al. Cognitive disability in adult patients with brain tumors. Cancer Treat Rev. (2018) 65:33–40. doi: 10.1016/j.ctrv.2018.02.007

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Valk PE, Dillon WP. Radiation injury of the brain. AJNR Am J Neuroradiol. (1991) 12:45–62.

PubMed Abstract | Google Scholar

29. Rola R, Raber J, Rizk A, Otsuka S, VandenBerg SR, Morhardt DR, et al. Radiation-induced impairment of hippocampal neurogenesis is associated with cognitive deficits in young mice. Exp Neurol. (2004) 188:316–30. doi: 10.1016/j.expneurol.2004.05.005

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Mizumatsu S, Monje ML, Morhardt DR, Rola R, Palmer TD, Fike JR. Extreme sensitivity of adult neurogenesis to low doses of X-irradiation. Cancer Res. (2003) 63:4021–7.

PubMed Abstract | Google Scholar

31. Grosu AL, Nieder C. Stereotactic fractionated radiotherapy for recurrent capillary hemangioma of the cavernous sinus. Strahlenther Onkol. (2006) 182:179–82. doi: 10.1007/s00066-006-1473-4

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Mayo C, Martel MK, Marks LB, Flickinger J, Nam J, Kirkpatrick J. Radiation dose-volume effects of optic nerves and chiasm. Int J Radiat Oncol Biol Phys. (2010) 76(3 Suppl):S28–35. doi: 10.1016/j.ijrobp.2009.07.1753

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Leavitt JA, Stafford SL, Link MJ, Pollock BE. Long-term evaluation of radiation-induced optic neuropathy after single-fraction stereotactic radiosurgery. Int J Radiat Oncol Biol Phys. (2013) 87:524–7. doi: 10.1016/j.ijrobp.2013.06.2047

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: hemangioma, cavernous sinus, central nervous system, radiotherapy, cognitive function

Citation: Xin Z, Yao Y, Chen G, Wang L, Shu M, Lv Q, Yu H and Zhang T (2020) Fractionated Radiation Therapy for Large and Giant Cavernous Sinus Hemangioma: A Retrospective Study. Front. Neurol. 11:355. doi: 10.3389/fneur.2020.00355

Received: 29 November 2019; Accepted: 09 April 2020;
Published: 13 May 2020.

Edited by:

Maciej Harat, Franciszek Lukaszczyk Oncology Centre, Poland

Reviewed by:

Eric Marvin, Virginia Tech Carilion, United States
Brad E. Zacharia, Penn State Milton S. Hershey Medical Center, United States

Copyright © 2020 Xin, Yao, Chen, Wang, Shu, Lv, Yu and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ting Zhang, zezht@zju.edu.cn

These authors have contributed equally to this work