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Surgical
resection and permanent brachytherapy for recurrent atypical and malignant
meningioma
Ware ML, Larson DA, Sneed PK, Wara WW, McDermott MW
Departments of Neurological Surgery and Radiation Oncology,
University of California, San Francisco, San Francisco, California.
Objective. Recurrent atypical and malignant meningiomas are difficult to treat
successfully.
Chemotherapy to date has been unsuccessful, and radiosurgery is
limited to smaller tumors.
Reoperation alone provides limited tumor control and
limited prolonged survival.
The addition of brachytherapy at the time of
operation is an option.
Here, we report the results of our series of patients
with recurrent malignant meningioma treated with resection and brachytherapy
with permanent low-dose
(125)I.
Methods. The charts of patients in our database
with recurrent atypical and malignant meningiomas treated by surgical resection
and permanent (125)I brachytherapy at the University of California, San
Francisco, between 1988 and 2002 were selected for this study.
Calculations of
disease-free survival and overall survival curves were made by the Kaplan-Meier
actuarial method.
Univariate analysis between Kaplan-Meier curves was based on
the log-rank statistic, with a significance level set at a value of P </=
0.05.
Results. Seventeen patients had recurrent malignant meningioma, and four
had recurrent atypical meningioma.
The median number of sources implanted after
surgical resection was 30 (range, 4-112 sources), with a median total activity
of 20 mCi (range, 3.3-85.9 mCi).
The median time to progression after
brachytherapy was 11.6 months for patients with malignant meningioma and 10.4
months for the combined group.
There was a trend toward longer disease-free
survival time in patients after gross total resection versus subtotal resection
and in patients with tumors located at the convexity and parasagittally versus
at the cranial base.
These differences did not reach statistical significance.
The median overall survival after diagnosis was 9.4 years for patients with
atypical meningioma, 6.6 years for those with malignant meningioma, and 8.0
years for all patients combined.
Survival from the time of resection and
implantation of (125)I was 1.6 years for patients with atypical meningioma, 2.4
years for patients with malignant meningioma, and 2.4 years for the combined
group.
Thirty-three percent of patients had complications requiring surgical
intervention.
Radiation necrosis occurred in 27% of patients; 13% underwent
surgery for radiation necrosis.
In addition, 27% had a wound breakdown and
required surgical intervention.
Conclusion. The options for patients with
recurrent atypical or malignant meningiomas are limited.
Our results suggest
that for tumors not suitable for radiosurgery, resection followed by permanent
brachytherapy should be considered as a potential salvage treatment.
However,
this approach results in a relatively high complication rate in these heavily
treated patients and requires meticulous surgical technique and medical
therapies to assist with wound healing after surgery.
PMID: 14683541 [PubMed - in process]
Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=14683541&dopt=Abstract |