Clinical investigation
Brain
Fractionated stereotactic radiotherapy in patients with benign or atypical intracranial meningioma: Long-term experience and prognostic factors

https://doi.org/10.1016/j.ijrobp.2004.07.669Get rights and content

Purpose

To analyze our long-term experience and prognostic factors after fractionated stereotactic radiotherapy (FSRT) in patients with benign or atypical intracranial meningioma.

Methods and materials

Between January 1985 and December 2001, 317 patients with a median age of 55.7 years were treated with FSRT for intracranial meningioma. The tumor distribution was World Health Organization (WHO) Grade 1 in 48.3%, WHO Grade 2 in 8.2%, and unknown in 43.5%. Of the 317 patients, 97 underwent RT as their primary treatment, 79 underwent postoperative RT (subtotal resection in 38 and biopsy only in 41), and 141 were treated for recurrent disease. The median target volume was 33.6 cm3 (range, 1.0–412.6 cm3). The median total dose was 57.6 Gy at 1.8 Gy/fraction five times weekly.

Results

The median follow-up was 5.7 years (range, 1.2–14.3 years). The overall local tumor control rate was 93.1% (295 of 317). Of the 317 patients, 72 had a partial response on CT/MRI and 223 (70.4%) remained stable. At a median of 4.5 years after FSRT, 22 patients (6.9%) had local tumor progression on MRI. Local tumor failure was significantly greater in patients with WHO Grade 2 meningioma (p <0.002) than in patients with WHO Grade 1 or unknown histologic features. Patients treated for recurrent meningioma showed a trend toward decreased progression-free survival compared with patients treated with primary therapy, after biopsy, or after subtotal resection (p <0.06). Patients with a tumor volume >60 cm3 had a recurrence rate of 15.5% vs. 4.3% for those with a tumor volume of ≤60 cm3 (p <0.001). In 42.9% of the patients, preexisting neurologic deficits improved. Worsening of preexisting neurologic symptoms occurred in 8.2%. Eight patients developed new clinical symptoms, such as reduced vision, trigeminal neuralgia, and intermittent tinnitus located at the side of the irradiated meningioma after FSRT.

Conclusion

These data have demonstrated that FSRT is an effective and safe treatment modality for local control of meningioma with a low risk of significant late toxicity. We identified the tumor volume, indication for FSRT, and histologic features of the meningioma as statistically significant prognostic factors.

Introduction

Meningiomas are the most common non–glial primary brain tumors, accounting for approximately 14–20% of all brain tumors (1, 2). Most meningiomas are histologically benign and typically slow-growing lesions arising from the arachnoidal cap cells (3). In the literature, the 5-year survival rates for patients with benign meningioma range from 90% to 100% in the era of modern imaging and treatment modalities (4). Patients with malignant meningioma have had 5-year survival rates of 50–60% (5). The treatment of choice for benign meningioma is radical surgical resection (6). Long-term local control rates of 33–60% after surgical resection of benign meningiomas have been reported. High local control rates can be achieved by more radical tumor resection (7, 8). Most meningiomas can be completely resected, but they have a high tendency for local recurrence, especially after subtotal surgical intervention. Postoperative radiotherapy (RT) has prolonged the time to recurrence and prevented tumor regrowth in several cases. Whether postoperative RT is also capable of improving the survival of patients with incompletely resected meningiomas is still controversial. After complete resection, long-term disease-free survival has been achieved in 81% of patients, with a local tumor control rate of 96%. Relapses occurred 4–17 years after the initial surgical intervention. In patients with inoperable or incompletely resected meningioma, postoperative RT may improve local tumor control comparable to that after complete resection (8, 9, 10). The aim of RT is to shrink the existing tumor burden and prevent regrowth (3, 4).

In this article, we report our analysis of our own long-term experience with fractionated stereotactic RT (FSRT) in the treatment of benign intracranial meningiomas with respect to local tumor control, radiation-induced side effects, and overall survival. We also analyzed our results with respects to prognostic factors after FSRT.

Section snippets

Methods and materials

Between January 1985 and December 2001, 317 patients with a median age of 55.7 years (range, 11–86 years) were treated with FSRT for benign or atypical intracranial meningioma at the German Cancer Research Center, Heidelberg, Germany. Our institutional review board approved this study. The male/female ratio was 1:2.7 (86 men and 231 women). The median Karnofsky performance score was 90%. Of the 317 patients, 179 (56.5%) had a histologically proven diagnosis of meningioma and 138 had clinical

Results

The median follow-up was 5.7 years (range, 1.2–14.3 years), and all patients were followed for >12 months; 264 patients (83.2%) were followed for >36 months. The median target volume was 33.6 cm3 (range, 1–412.6 cm3).

Discussion

These data indicate that FSRT is safe and feasible in the treatment of intracranial meningiomas with a low risk of significant chronic late toxicity. The indications for RT have included residual tumors after subtotal resection, disease recurrence, and inoperable tumors because of the proximity to critical structures or comorbid patient conditions.

In our analysis, the overall survival rate of patients with benign or atypical intracranial meningiomas was 94.7% at 5 years and 90% at 10 years. The

Conclusion

These data demonstrate that FSRT is an effective and safe treatment modality for local control of intracranial meningiomas with low risk of significant late toxicity. We identified tumor volume, the indication for FSRT, and the histologic type of meningioma as statistically significant prognostic factors.

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