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<channel>
	<title>Neurosurgery Blog &#187; Oncology</title>
	<atom:link href="http://www.neurosurgery-blog.com/archives/category/oncology/feed" rel="self" type="application/rss+xml" />
	<link>http://www.neurosurgery-blog.com</link>
	<description>Daily bibliographic and video review of the Neurosurgery Department. La Fe University Hospital. Valencia, Spain</description>
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		<title>Percutaneous biopsy of lesions in the cavernous sinus region through the foramen ovale: diagnostic accuracy and limits in 50 patients</title>
		<link>http://www.neurosurgery-blog.com/archives/3808</link>
		<comments>http://www.neurosurgery-blog.com/archives/3808#comments</comments>
		<pubDate>Wed, 08 Feb 2012 23:00:07 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Clinical Trial]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[skull base surgery]]></category>
		<category><![CDATA[cavernous sinus]]></category>
		<category><![CDATA[diagnostic accuracy]]></category>
		<category><![CDATA[histopathological examination]]></category>
		<category><![CDATA[Meckel cave]]></category>
		<category><![CDATA[parasellar lodge]]></category>
		<category><![CDATA[percutaneous biopsy]]></category>
		<category><![CDATA[petroclival region]]></category>
		<category><![CDATA[skull base]]></category>
		<category><![CDATA[tumors]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3808</guid>
		<description><![CDATA[J Neurosurg 116:390–398, 2012.DOI: 10.3171/2011.10.JNS11783
The cavernous sinus and surrounding regions—specifically the Meckel cave, posterior sector of the cavernous sinus itself, and the upper part of the petroclival region—are the location of a large variety of lesions that require individual consideration regarding treatment strategy. These regions may be reached for biopsy by a percutaneous needle inserted [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/Percutaneous-biopsy-of-lesions-in-the-cavernous-sinus-region-through-the-foramen-ovale-diagnostic-accuracy-and-limits-in-50-patients.jpg"><img class="alignleft size-thumbnail wp-image-3809" title="Percutaneous biopsy of lesions in the cavernous sinus region through the foramen ovale- diagnostic accuracy and limits in 50 patients" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/Percutaneous-biopsy-of-lesions-in-the-cavernous-sinus-region-through-the-foramen-ovale-diagnostic-accuracy-and-limits-in-50-patients-150x150.jpg" alt="" width="150" height="150" /></a>J Neurosurg 116:390–398, 2012.DOI: 10.3171/2011.10.JNS11783</strong></p>
<p style="text-align: justify;">The cavernous sinus and surrounding regions—specifically the Meckel cave, posterior sector of the cavernous sinus itself, and the upper part of the petroclival region—are the location of a large variety of lesions that require individual consideration regarding treatment strategy. These regions may be reached for biopsy by a percutaneous needle inserted through the foramen ovale. The aim of this retrospective study was to evaluate the diagnostic accuracy of percutaneous biopsy in a consecutive series of 50 patients referred for surgery between 1991 and 2010.</p>
<p style="text-align: justify;">Methods. Seven biopsies (14%) were unproductive and 43 (86%) were productive, among which 28 lesions subsequently underwent histopathological examination during a second (open) surgery. To evaluate the diagnostic accuracy of the procedure, results from surgery were compared with those from the biopsy.</p>
<p style="text-align: justify;">Results. Sensitivity of the percutaneous biopsy was 0.83 (95% CI 0.52–0.98), specificity was 1 (95% CI 0.79–1), and k coefficient was 0.81.</p>
<p style="text-align: justify;">Conclusions. Because of its valuable diagnostic accuracy, percutaneous biopsy of the cavernous sinus and surrounding regions should be performed in patients with parasellar masses when neuroimaging does not provide sufficient information of a histopathological nature. This procedure would enable patients to obtain the most appropriate therapy, such as resective surgery, corticosteroids, chemotherapy, radiotherapy, or radiosurgery.</p>
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		<item>
		<title>A clinical trial of bevacizumab, temozolomide, and radiation for newly diagnosed glioblastoma</title>
		<link>http://www.neurosurgery-blog.com/archives/3802</link>
		<comments>http://www.neurosurgery-blog.com/archives/3802#comments</comments>
		<pubDate>Tue, 07 Feb 2012 23:00:33 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Clinical Trial]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Outcome]]></category>
		<category><![CDATA[bevacizumab]]></category>
		<category><![CDATA[Glioblastoma]]></category>
		<category><![CDATA[radiation therapy]]></category>
		<category><![CDATA[Temozolomide]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3802</guid>
		<description><![CDATA[J Neurosurg 116:341–345, 2012.DOI: 10.3171/2011.9.JNS11656
The presence of angiogenesis is a hallmark of glioblastoma (GBM). Vascular endothelial growth factor (VEGF), which drives angiogenesis, provides an additional target for conventional therapy. The authors conducted a prospective clinical trial to test the effectiveness of bevacizumab, an inhibitor of VEGF, in newly diagnosed GBM.
Methods. From 2006 through 2010, 51 [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/A-clinical-trial-of-bevacizumab-temozolomide-and-radiation-for-newly-diagnosed-glioblastoma.jpg"><img class="alignleft size-thumbnail wp-image-3804" title="A clinical trial of bevacizumab, temozolomide, and radiation for newly diagnosed glioblastoma" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/A-clinical-trial-of-bevacizumab-temozolomide-and-radiation-for-newly-diagnosed-glioblastoma-150x150.jpg" alt="" width="150" height="150" /></a>J Neurosurg 116:341–345, 2012.DOI: 10.3171/2011.9.JNS11656</strong></p>
<p style="text-align: justify;">The presence of angiogenesis is a hallmark of glioblastoma (GBM). Vascular endothelial growth factor (VEGF), which drives angiogenesis, provides an additional target for conventional therapy. The authors conducted a prospective clinical trial to test the effectiveness of bevacizumab, an inhibitor of VEGF, in newly diagnosed GBM.</p>
<p style="text-align: justify;">Methods. From 2006 through 2010, 51 eligible patients with newly diagnosed GBM were treated with involvedfield radiation therapy and concomitant temozolomide (75 mg/m2 daily for 42 days) along with bevacizumab (10 mg/ kg every 2 weeks), starting 29 days after surgery. This was followed by 6 cycles of adjuvant temozolomide therapy (150 mg/m2 on Days 1–7 of a 28-day cycle) with bevacizumab administered at 10 mg/kg on Days 8 and 22 of each 28-day cycle.</p>
<p style="text-align: justify;">Results. The 6- and 12-month progression-free survival (PFS) rates were 85.1% and 51%, respectively. The 12- and 24-month overall survival (OS) rates were 85.1% and 42.5%, respectively. Grade III/IV toxicities were noted in 10 patients (19.6%). No treatment-related deaths were observed. Asymptomatic intracranial bleeding was noted in 5 patients.</p>
<p style="text-align: justify;">Conclusions. The addition of bevacizumab to conventional therapy in newly diagnosed GBM appears to improve both PFS and OS in patients with newly diagnosed GBM, with acceptable morbidity. A shift toward diffuse relapse was noted in a significant number of patients. Ongoing Phase III clinical trials will show the true benefit of this antiangiogenic approach.</p>
]]></content:encoded>
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		<item>
		<title>Accuracy of Diffusion Tensor Magnetic Resonance Imaging-Based Tractography for Surgery of Gliomas Near the Pyramidal Tract</title>
		<link>http://www.neurosurgery-blog.com/archives/3776</link>
		<comments>http://www.neurosurgery-blog.com/archives/3776#comments</comments>
		<pubDate>Thu, 02 Feb 2012 23:00:26 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[diffusion tensor imaging]]></category>
		<category><![CDATA[Glioma]]></category>
		<category><![CDATA[magnetic resonance imaging]]></category>
		<category><![CDATA[Pyramidal tract]]></category>
		<category><![CDATA[tractography]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3776</guid>
		<description><![CDATA[Neurosurgery 70:283–294, 2012 DOI: 10.1227/NEU.0b013e31823020e6
Diffusion tensor (DT) imaging-based fiber tracking is a noninvasive magnetic resonance technique that can delineate the course of white matter fibers.
OBJECTIVE: To evaluate the accuracy and usefulness of this DT imaging-based fiber tracking for surgery in patients with gliomas near the pyramidal tract (PT).
METHODS: Subjects comprised 32 patients with gliomas near [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/Accuracy_of_Diffusion_Tensor_Magnetic_Resonance.jpg"><img class="alignleft size-thumbnail wp-image-3778" title="Accuracy_of_Diffusion_Tensor_Magnetic_Resonance" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/Accuracy_of_Diffusion_Tensor_Magnetic_Resonance-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:283–294, 2012 DOI: 10.1227/NEU.0b013e31823020e6</strong></p>
<p style="text-align: justify;">Diffusion tensor (DT) imaging-based fiber tracking is a noninvasive magnetic resonance technique that can delineate the course of white matter fibers.</p>
<p style="text-align: justify;">OBJECTIVE: To evaluate the accuracy and usefulness of this DT imaging-based fiber tracking for surgery in patients with gliomas near the pyramidal tract (PT).</p>
<p style="text-align: justify;">METHODS: Subjects comprised 32 patients with gliomas near the PT. DT imagingbased fiber tracks of the PT were generated before and within 3 days after surgery in all patients. A tractography-integrated navigation system was used during the operation. Cortical and subcortical motor-evoked potentials (MEPs) were also monitored during resection to maximize the preservation of motor function. The threshold intensity for subcortical MEPs was examined by searching the stimulus points and changing the stimulus intensity. Minimum distance between the resection border and the illustrated PT was measured on postoperative tractography.</p>
<p style="text-align: justify;">RESULTS: In all subjects, DT imaging-based tractography of the PT was successfully performed, preoperatively demonstrating the relationship between tumors and the PT. With the use of the tractography-integrated navigation system and intraoperative MEPs, motor function was preserved postoperatively in all patients. A significant correlation was seen between threshold intensity for subcortical MEPs and the distance between the resection border and PT on postoperative DT imaging.</p>
<p style="text-align: justify;">CONCLUSION: DT imaging-based fiber tracking is a reliable and accurate method for mapping the course of subcortical PTs. Fiber tracking and intraoperative MEPs were useful for preserving motor function in patients with gliomas near the PT.</p>
]]></content:encoded>
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		<item>
		<title>5-Aminolevulinic acid (5-ALA)-induced fluorescence in intracerebral metastases: a retrospective study</title>
		<link>http://www.neurosurgery-blog.com/archives/3770</link>
		<comments>http://www.neurosurgery-blog.com/archives/3770#comments</comments>
		<pubDate>Wed, 01 Feb 2012 23:00:57 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Clinical Trial]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[ALA-derived fluorescence]]></category>
		<category><![CDATA[Cerebral metastasis]]></category>
		<category><![CDATA[Histopathological features]]></category>
		<category><![CDATA[resection]]></category>
		<category><![CDATA[Surgery]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3770</guid>
		<description><![CDATA[Acta Neurochir (2012) 154:223–228. DOI 10.1007/s00701-011-1200-5
Microsurgical, circumferential stripping of intracerebral metastases often proves to be insufficient to prevent local tumor recurrence.
Objective We were interested in the potential impact of 5- aminolevulinic acid (5-ALA)-induced-fluorescence (5-AIF) as a diagnostic tool for the resection of intracerebral metastases.
Methods A retrospective analysis was performed for 52 patients who underwent 5-AIF-guided [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/5-Aminolevulinic-acid-5-ALA-induced-fluorescence-in-intracerebral-metastases-a-retrospective-study.jpg"><img class="alignleft size-thumbnail wp-image-3774" title="5-Aminolevulinic acid (5-ALA)-induced fluorescence in intracerebral metastases- a retrospective study" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/02/5-Aminolevulinic-acid-5-ALA-induced-fluorescence-in-intracerebral-metastases-a-retrospective-study-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2012) 154:223–228. DOI 10.1007/s00701-011-1200-5</strong></p>
<p style="text-align: justify;">Microsurgical, circumferential stripping of intracerebral metastases often proves to be insufficient to prevent local tumor recurrence.</p>
<p style="text-align: justify;">Objective We were interested in the potential impact of 5- aminolevulinic acid (5-ALA)-induced-fluorescence (5-AIF) as a diagnostic tool for the resection of intracerebral metastases.</p>
<p style="text-align: justify;">Methods A retrospective analysis was performed for 52 patients who underwent 5-AIF-guided resection for intracerebral mass lesions that histologically corresponded to metastases from tumors outside the central nervous system. The presence of ALA fluorescence in the tumor was determined in each patient. In 42 patients, fluorescence of the resection cavity after tumor removal was additionally recorded. Data were correlated with neuropathological findings in tissue specimens.</p>
<p style="text-align: justify;">Results A total of 32 of the 52 metastases (62%) exhibited 5-AIF in tumor parts. All 5-AIF-positive metastases exhibited an inhomogeneous fluorescence pattern. 5-AIF was neither associated with the histological type nor with the site of origin of the metastases. Residual fluorescence of the resection cavity was detected after macroscopically complete white light resection in 24 patients with 5-AIF positive metastases. Residual tumor tissue was histologically confirmed in 6 of 18 patients with available tissue specimens from such 5-AIF positive areas (33%).</p>
<p style="text-align: justify;">Conclusions The majority of metastases (62%) were 5-AIF positive, suggesting a potential impact of 5-AIF for improved visualization of metastatic tumor tissue within the brain. However, residual 5-AIF after macroscopically complete resection of a metastasis needs to be interpreted with caution because of the limited specificity for detection of residual tumor tissue.</p>
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		</item>
		<item>
		<title>Dual-room 1.5-T intraoperative magnetic resonance imaging suite with a movable magnet: implementation and preliminary experience</title>
		<link>http://www.neurosurgery-blog.com/archives/3727</link>
		<comments>http://www.neurosurgery-blog.com/archives/3727#comments</comments>
		<pubDate>Tue, 24 Jan 2012 23:00:45 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[Dual-room magnetic resonance imaging suite]]></category>
		<category><![CDATA[Intraoperative magnetic resonance imaging]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3727</guid>
		<description><![CDATA[Neurosurg Rev (2012) 35:95–110. DOI 10.1007/s10143-011-0336-3
We hereby report our initial clinical experience of a dual-room intraoperative magnetic resonance imaging (iMRI) suite with a movable 1.5-T magnet for both neurosurgical and independent diagnostic uses. The findings from the first 45 patients who underwent scheduled neurosurgical procedures with iMRI in this suite (mean age, 41.3±12.0 years; intracranial [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Dual-room-1.jpg"><img class="alignleft size-thumbnail wp-image-3731" title="Dual-room 1" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Dual-room-1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurg Rev (2012) 35:95–110. DOI 10.1007/s10143-011-0336-3</strong></p>
<p style="text-align: justify;">We hereby report our initial clinical experience of a dual-room intraoperative magnetic resonance imaging (iMRI) suite with a movable 1.5-T magnet for both neurosurgical and independent diagnostic uses. The findings from the first 45 patients who underwent scheduled neurosurgical procedures with iMRI in this suite (mean age, 41.3±12.0 years; intracranial tumors, 39 patients; cerebral vascular lesions, 5 patients; epilepsy surgery, 1 patient) were reported. The extent of resection depicted at intraoperative imaging, the surgical consequences of iMRI, and the clinical practicability of the suite were analyzed.</p>
<p style="text-align: justify;">Fourteen resections with a trans-sphenoidal/transoral approach and 31 craniotomies were performed. Eighty-two iMRI examinations were performed in the operating room, while during the same period of time, 430 diagnostic scans were finished in the diagnostic room. In 22 (48.9%) of 45 patients, iMRI revealed accessible residual tumors leading to further resection. No iMRI-related adverse event occurred. Complete lesion removal was achieved in 36 (80%) of all 45 cases.</p>
<p style="text-align: justify;">It is concluded that the dual-room 1.5-T iMRI suite can be successfully integrated into standard neurosurgical workflow. The layout of the dual-room suite can enable the maximum use of the system and save costs by sharing use of the 1.5-T magnet between neurosurgical and diagnostic use. Intraoperative MR imaging may provide valuable information that allows intraoperative modification of the surgical strategy.</p>
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		<item>
		<title>Localization of Primary Language Areas by Arcuate Fascicle Fiber Tracking</title>
		<link>http://www.neurosurgery-blog.com/archives/3721</link>
		<comments>http://www.neurosurgery-blog.com/archives/3721#comments</comments>
		<pubDate>Mon, 23 Jan 2012 23:00:07 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[Arcuate fascicle]]></category>
		<category><![CDATA[Broca]]></category>
		<category><![CDATA[Fiber tracking]]></category>
		<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Wernicke]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3721</guid>
		<description><![CDATA[Neurosurgery 70:56–65, 2012 DOI: 10.1227/NEU.0b013e31822cb882
To reduce the risk of disabling postoperative functional deficit in patients with lesions in the dominant hemisphere, information about the localization of eloquent language areas is mandatory.
OBJECTIVE: To demonstrate the feasibility of arcuate fascicle (AF) tractography for proper localization of eloquent language areas in the superior temporal (STG) and inferior frontal [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Localization_of_Primary_Language_Areas_by_Arcuate-1.jpg"><img class="alignleft size-thumbnail wp-image-3725" title="Localization_of_Primary_Language_Areas_by_Arcuate-1" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Localization_of_Primary_Language_Areas_by_Arcuate-1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:56–65, 2012 DOI: 10.1227/NEU.0b013e31822cb882</strong></p>
<p style="text-align: justify;">To reduce the risk of disabling postoperative functional deficit in patients with lesions in the dominant hemisphere, information about the localization of eloquent language areas is mandatory.</p>
<p style="text-align: justify;">OBJECTIVE: To demonstrate the feasibility of arcuate fascicle (AF) tractography for proper localization of eloquent language areas in the superior temporal (STG) and inferior frontal gyrus (IFG).</p>
<p style="text-align: justify;">METHODS: Between January and June 2010, we performed surgery in 13 patients with highly eloquent lesions with close spatial relationship to the primary language areas. All of them received preoperative diffusion tensor imaging for AF tractography. The STG and IFG were delineated at the ends of the AF. Five patients underwent functional magnetic resonance imaging of the primary language areas. The results were compared with tractography.</p>
<p style="text-align: justify;">RESULTS: Tractography of the AF without prior knowledge of the localization of the STG and IFG was feasible in all cases. In the cases with functional magnetic resonance imaging, the activation maps matched the tractography results. In all but 1 patient, preservation of the primary language areas was possible, proven by the good neurological outcome. One patient suffered from a language dysfunction caused by a lesion in the medial and inferior temporal gyrus along the surgical pathway.</p>
<p style="text-align: justify;">CONCLUSION: Tractography of the AF is a useful tool for identification of parts of the main primary language areas. Using tractography as a localization procedure to determine the primary language areas aids in the delineation of the STG and IFG and thus may help reduce the risk of postoperative permanent neurological deficit.</p>
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		<item>
		<title>Posterior petrous bone meningiomas: surgical experience in 53 patients and literature review</title>
		<link>http://www.neurosurgery-blog.com/archives/3686</link>
		<comments>http://www.neurosurgery-blog.com/archives/3686#comments</comments>
		<pubDate>Mon, 16 Jan 2012 23:00:47 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Outcome]]></category>
		<category><![CDATA[skull base surgery]]></category>
		<category><![CDATA[cerebellopontine angle]]></category>
		<category><![CDATA[Internal auditory canal]]></category>
		<category><![CDATA[meningioma]]></category>
		<category><![CDATA[Petroclival]]></category>
		<category><![CDATA[Petrous bone]]></category>
		<category><![CDATA[skull base]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3686</guid>
		<description><![CDATA[Neurosurg Rev (2012) 35:53–66. DOI 10.1007/s10143-011-0333-6
Meningiomas of the posterior fossa represent a heterogeneous group of tumors regarding difficulty of resection and functional outcome.
The aim of this review was to focus on tumors located mainly on the posterior surface of the petrous bone and threatening hearing and facial functions.
An anatomical classification was used to evaluate surgical [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Posterior-petrous-bone-meningiomas.jpg"><img class="alignleft size-thumbnail wp-image-3690" title="Posterior petrous bone meningiomas" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Posterior-petrous-bone-meningiomas-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurg Rev (2012) 35:53–66. DOI 10.1007/s10143-011-0333-6</strong></p>
<p style="text-align: justify;">Meningiomas of the posterior fossa represent a heterogeneous group of tumors regarding difficulty of resection and functional outcome.</p>
<p style="text-align: justify;">The aim of this review was to focus on tumors located mainly on the posterior surface of the petrous bone and threatening hearing and facial functions.</p>
<p style="text-align: justify;">An anatomical classification was used to evaluate surgical outcome depending on the relationship of the tumor to the internal auditory meatus. The authors performed a retrospective chart review of 53 consecutive patients operated on for a posterior petrous bone meningioma in a tertiary referral center and a literature review. Tumors were classified in four groups according to the modified Desgeorges and Sterkers classification: posterior petrous (P; 17 tumors), meatus and internal auditory canal (M; 12 tumors), petrous apex without invasion of the internal auditory canal (A; 9 tumors), and cerebellopontine angle with invasion of the internal auditory canal (AMP; 15 tumors).</p>
<p style="text-align: justify;">The facial function was preserved in 100% of P and A tumors, 75% of group M tumors, and 53% of AMP tumors. Hearing preservation was attempted only in P, A, and M groups where rates of serviceable hearing preservation were 82%, 80%, and 66%, respectively. The cumulative rate of hearing preservation for AMP tumors was 45% in our literature review. The increased facial morbidity associated with AMP tumors compared with other groups was also confirmed by the review of the literature.</p>
<p style="text-align: justify;">In conclusion, this study shows that among posterior petrous bone meningiomas, tumors invading the internal auditory canal present with increased postoperative functional morbidity in spite of a tailored approach regarding dural insertion.</p>
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		<item>
		<title>Primary Vertebral Tumors: A Review of Epidemiologic, Histological and Imaging Findings, Part II: Locally Aggressive and Malignant Tumors</title>
		<link>http://www.neurosurgery-blog.com/archives/3674</link>
		<comments>http://www.neurosurgery-blog.com/archives/3674#comments</comments>
		<pubDate>Thu, 12 Jan 2012 23:00:04 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Spine]]></category>
		<category><![CDATA[Bone tumors]]></category>
		<category><![CDATA[Chondrosarcoma]]></category>
		<category><![CDATA[Chordoma]]></category>
		<category><![CDATA[Multiple myeloma]]></category>
		<category><![CDATA[Osteosarcoma]]></category>
		<category><![CDATA[Primary vertebral tumor]]></category>
		<category><![CDATA[Spinal malignancies]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3674</guid>
		<description><![CDATA[Neurosurgery 70:211–219, 2012 DOI: 10.1227/NEU.0b013e31822d5f17
This second part of a comprehensive review of primary vertebral tumors focuses on locally aggressive and malignant tumors. As discussed in the earlier part of the review, both benign and malignant types of these tumors affect the adult and the pediatric population, and an understanding of their subtleties may increase their [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Chordoma-sacrum.jpg"><img class="alignleft size-thumbnail wp-image-3677" title="Chordoma sacrum" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Chordoma-sacrum-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:211–219, 2012 DOI: 10.1227/NEU.0b013e31822d5f17</strong></p>
<p style="text-align: justify;">This second part of a comprehensive review of primary vertebral tumors focuses on locally aggressive and malignant tumors. As discussed in the earlier part of the review, both benign and malignant types of these tumors affect the adult and the pediatric population, and an understanding of their subtleties may increase their effective resection. In this review, we discuss the epidemiologic, histological, and imaging features of the most common locally aggressive primary vertebral tumors (chordoma and giantcell tumor) and malignant tumors (chondrosarcoma, Ewing sarcoma, multiple myeloma or plasmacytoma, and osteosarcoma). The figures used for illustration are from operative patients of the senior authors (Z.L.G. and J.H.C.). Taken together, parts 1 and 2 of this article provide a thorough and illustrative review of primary vertebral tumors.</p>
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		<title>Application of Novel Response/Progression Measures for Surgically Delivered Therapies for Gliomas: Response Assessment in Neuro-Oncology (RANO) Working Group</title>
		<link>http://www.neurosurgery-blog.com/archives/3645</link>
		<comments>http://www.neurosurgery-blog.com/archives/3645#comments</comments>
		<pubDate>Mon, 09 Jan 2012 23:00:28 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Outcome]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[Brain surgery]]></category>
		<category><![CDATA[Clinical trials]]></category>
		<category><![CDATA[End points]]></category>
		<category><![CDATA[Macdonald criteria]]></category>
		<category><![CDATA[Response evaluation]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3645</guid>
		<description><![CDATA[Neurosurgery 70:234–244, 2012 DOI: 10.1227/NEU.0b013e318223f5
The Response Assessment in Neuro-Oncology (RANO) Working Group is an international, multidisciplinary effort to develop new standardized response criteria for clinical trials in brain tumors. The RANO group identified knowledge gaps relating to the definitions of tumor response and progression after the use of surgical or surgically based treatments.
OBJECTIVE: To outline [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;"><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Application_of_Novel_Response_Progression_Measures.jpg"><img class="alignleft size-thumbnail wp-image-3647" title="Application_of_Novel_Response_Progression_Measures" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Application_of_Novel_Response_Progression_Measures-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:234–244, 2012 DOI: 10.1227/NEU.0b013e318223f5</strong></p>
<p style="text-align: justify;">The Response Assessment in Neuro-Oncology (RANO) Working Group is an international, multidisciplinary effort to develop new standardized response criteria for clinical trials in brain tumors. The RANO group identified knowledge gaps relating to the definitions of tumor response and progression after the use of surgical or surgically based treatments.</p>
<p style="text-align: justify;">OBJECTIVE: To outline a proposal for new response and progression criteria for the assessment of the effects of surgery and surgically delivered therapies for patients with gliomas.</p>
<p style="text-align: justify;">METHODS: The Surgery Working Group of RANO identified surgically related end-point evaluation problems that were not addressed in the original Macdonald criteria, performed an extensive literature review, and used a consensus-building process to develop recommendations for how to address these issues in the setting of clinical trials.</p>
<p style="text-align: justify;">RESULTS: Recommendations were formulated for surgically related issues, including imaging changes associated with surgical resection or surgically mediated adjuvant local therapies, the determination of progression in the setting where all enhancing tumor has been removed, and how new enhancement should be interpreted in the setting where local therapies that are known to produce nonspecific enhancement have been used. Additionally, the terminology used to describe the completeness of surgical resections has been recognized to be inconsistently applied to enhancing vs nonenhancing tumors, and a new set of descriptors is proposed.</p>
<p style="text-align: justify;">CONCLUSION: The RANO process is intended to produce end-point criteria for clinical trials that take into account the effects of prior and ongoing therapies. The RANO criteria will continue to evolve as new therapies and technologies are introduced into clinical trial and/or practice.</p>
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		<title>Long-term Follow-up of Pediatric Benign Cerebellar Astrocytomas</title>
		<link>http://www.neurosurgery-blog.com/archives/3635</link>
		<comments>http://www.neurosurgery-blog.com/archives/3635#comments</comments>
		<pubDate>Thu, 05 Jan 2012 23:00:19 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Pediatrics]]></category>
		<category><![CDATA[astrocytoma]]></category>
		<category><![CDATA[Cerebellum]]></category>
		<category><![CDATA[prognostic factors]]></category>
		<category><![CDATA[Recurrence]]></category>
		<category><![CDATA[Spontaneous regression]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3635</guid>
		<description><![CDATA[Neurosurgery 70:40–48, 2012 DOI: 10.1227/NEU.0b013e31822ff0ed
The long-term prognosis of cerebellar astrocytomas needs to be reviewed.
OBJECTIVE: To elucidate the factors influencing tumor recurrence or progression and to determine how long these patient with cerebellar astrocytomas require surveillance with neuroimaging.
METHODS: A retrospective review of 101 children surgically treated for a cerebellar astrocytoma and followed up for &#62;10 years [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Long_term_Follow_up_of_Pediatric_Benign_Cerebellar.jpg"><img class="alignleft size-thumbnail wp-image-3638" title="Long_term_Follow_up_of_Pediatric_Benign_Cerebellar" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Long_term_Follow_up_of_Pediatric_Benign_Cerebellar-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:40–48, 2012 DOI: 10.1227/NEU.0b013e31822ff0ed</strong></p>
<p style="text-align: justify;">The long-term prognosis of cerebellar astrocytomas needs to be reviewed.</p>
<p style="text-align: justify;">OBJECTIVE: To elucidate the factors influencing tumor recurrence or progression and to determine how long these patient with cerebellar astrocytomas require surveillance with neuroimaging.</p>
<p style="text-align: justify;">METHODS: A retrospective review of 101 children surgically treated for a cerebellar astrocytoma and followed up for &gt;10 years was performed.</p>
<p style="text-align: justify;">RESULTS: Mean follow-up was 18.4 years. Total resection confirmed by postoperative imaging was performed in 51 patients (50.5%; group A). Twenty-three patients (22.8%) had surgical total resection; however, equivocal residual tumor was found on postoperative imaging (group B). Subtotal resection leaving a portion of brainstem or cerebellar peduncle was performed in 27 patients (26.7; group C). Of these 50 residual tumors, 16 (32%) showed spontaneous regression and 8 (16%) showed arrested growth. Radiographic recurrence or progression was noted in 29 patients (28.7%). Only 3 of 51 patients (5.9%) of group A with total resection had recurrence, whereas 26 of 50 residual tumors (52%; groups B and C) progressed. The only factor affecting recurrence or progression by multivariate analysis was the extent of surgical resection. All tumor recurrence or progression except for 1 (96.6%) occurred within 8 years from the original surgery (range, 2-132 months).</p>
<p style="text-align: justify;">CONCLUSIONS: Overall prognosis of cerebellar astrocytomas is good; the 10-year survival rate was 100% and recurrence- or progression-free rate was 71.3% in our cohort. Almost half of residual tumors showed spontaneous regression or arrested growth in the long term. Eight to 10 years is considered to be a reasonable follow-up period by neuroimaging.</p>
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