Stereotactic Radiosurgery for Facial Nerve
Schwannomas: Meta-analysis and Clinical Review
Theodore R. McRackan, Eric P. Wilkinson, Derald E. Brackmann,
and William H. Slattery
House Clinic, Los Angeles, California, U.S.A.
Objective:
Although several small individual series on stereo-
tactic radiosurgery (SRS) for facial nerve schwannomas (FNSs)
have been published, we aim to systematically aggregate data from
the literature as well as from our institution to better understand the
safety and efficacy of SRS for FNS.
Data Sources:
PubMed English language search for keywords
‘‘facial nerve schwannoma’’ AND ‘‘radiation therapy’’ pub-
lished from January 1995 to 2014. Data from our institution were
also included in the analysis.
Study Selection:
Minimum study inclusion criteria included
tumor treatment outcomes yielding 10 studies in the literature. In
addition, our institution’s data on six patients were included.
Data Extraction:
Data included radiation treatment type, radi-
ation dose, tumor size, tumor control, tumor control definition,
FN function, hearing outcome, and duration of follow-up.
Data Synthesis:
In total, there were 45 patients with at least 2-year
follow-up. Forty-two patients (93.3%) had tumor control. Of those
patients with described growth/shrinkage definitions, 50.0% had
no growth, 43.3% had shrinkage, and 6.7% had growth. Of those
articles that included FN functional outcomes, 26 patients (66.6%)
had stable FN function, 8 (20.5%) had improved function, and
5 (12.8%) had worsened FN function after treatment. In total,
there were 30 patients whose hearing outcomes were discussed
in the literature. Of those with serviceable hearing before SRS
(n = 14), nine (64.3%) had stable hearing and five (36.7%) had
worsened function after SRS. The mean posttreatment follow-up
period was 42.1 months.
Conclusion:
SRS seems to be effective at either stabilizing or
shrinking FNS. However, significant morbidities of FN paral-
ysis hearing loss do exist.
Key Words:
Cyberknife
V
Facial
nerve neuroma
V
Facial nerve schwannoma
V
Fractionated
radiation
V
Gamma knife
V
Radiation therapy
V
Stereotactic
radiosurgery.
Otol Neurotol
36:
393
Y
398, 2015.
Although they represent the most common primary tumor
of the facial nerve (FN), FN schwannomas (FNSs) are rare.
Like acoustic neuromas, FNSs are benign tumors made of
Schwann cells that are slow growing and may be present
for years before symptoms arise (1). The decision of when
and how to intervene has attempted to be established (2),
but there is no clear consensus.
FNSs pose a significant dilemma to the treating physician.
First, they can arise anywhere along the FN (3,4) and may
be mistaken for acoustic neuromas when isolated to the
cerebellopontine angle (CPA) and internal auditory canal
(IAC) (4,5). Second, given that FN fascicles have been shown
to run through the schwannoma (6), operative intervention is
limited to FN decompression or debulking versus resecting
the involved FN segment with direct anastomosis or graft
when necessary. Third, data on stereotactic radiosurgery
(SRS) are limited to small single-institution case series that
often provide inconsistent information with regard to FN
and hearing outcomes.
If SRSs were able to stop or reverse the growth of FNS,
it may be a reasonable initial treatment option if FN
function and hearing did not appreciably suffer. Simi-
larly, SRS may also be used as adjuvant therapy in pa-
tients whose FNSs continue to grow after undergoing FN
decompression. Unfortunately, SRS data on FNS have
yet to clarify these questions. Our study attempts to
systematically pool the literature on this topic in the hope
of better understanding the control rates and side effect
profile of SRS for FNS.
METHODS
Data Sources/Study Selection
PubMed English language search was conducted for articles
on radiation treatment of FNS published from January 1995 to
August 2014. This time frame was used because SRS practices
during this period reflect modern dosing strategies. Key word
Address correspondence and reprint requests to William H.
Slattery, M.D., 2100 West 3rd Street, Los Angeles, CA, U.S.A.;
E-mail:
wslattery@houseclinic.comThe authors disclose no conflicts of interest.
This article will be presented at the 2015 American Neurotology
Society meeting in Boston, MA, U.S.A.
Otology & Neurotology
36:
393
Y
398 2015, Otology & Neurotology, Inc.
Reprinted by permission of Otol Neurotol. 2015; 36(3):393-398.
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