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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">MI</journal-id>
<journal-title-group>
<journal-title>Medicine International</journal-title>
</journal-title-group>
<issn pub-type="ppub">2754-3242</issn>
<issn pub-type="epub">2754-1304</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">MI-6-3-00315</article-id>
<article-id pub-id-type="doi">10.3892/mi.2026.315</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Use of neuroendoscopy in metastatic brain tumours: A systematic review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Fouda</surname><given-names>Basem</given-names></name>
<xref rid="af1-MI-6-3-00315" ref-type="aff">1</xref>
<xref rid="fn1-MI-6-3-00315" ref-type="author-notes">&#x002A;</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Laffey</surname><given-names>Matthew</given-names></name>
<xref rid="af1-MI-6-3-00315" ref-type="aff">1</xref>
<xref rid="fn1-MI-6-3-00315" ref-type="author-notes">&#x002A;</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Al-Abri</surname><given-names>Usama</given-names></name>
<xref rid="af1-MI-6-3-00315" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Dovhan</surname><given-names>Yuriy</given-names></name>
<xref rid="af1-MI-6-3-00315" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Al-Saadi</surname><given-names>Tariq</given-names></name>
<xref rid="af2-MI-6-3-00315" ref-type="aff">2</xref>
<xref rid="c1-MI-6-3-00315" ref-type="corresp"/>
</contrib>
</contrib-group>
<aff id="af1-MI-6-3-00315"><label>1</label>School of Medicine, Trinity College Dublin, The University of Dublin, Dublin, D02 PN40, Ireland</aff>
<aff id="af2-MI-6-3-00315"><label>2</label>Department of Neurosurgery - Cedars-Sinai Medical Centre, Los Angeles, CA 90048, USA</aff>
<author-notes>
<corresp id="c1-MI-6-3-00315"><italic>Correspondence to:</italic> Dr Tariq Al-Saadi, Department of Neurosurgery - Cedars-Sinai Medical Centre, 8700 Beverly Blvd, Los Angeles, CA 90048, USA <email>tariq.al-saadi@mail.mcgill.ca</email></corresp>
<fn id="fn1-MI-6-3-00315"><p><sup>&#x002A;</sup>Contributed equally</p></fn>
<fn><p><italic>Abbreviations:</italic> CSF, cerebrospinal fluid; CT, computed tomography; GTR, gross total resection; LOS, length of hospital stay; MRI, magnetic resonance imaging; NBI, narrow band imaging; NTR, near total resection; PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses; SRS, stereotactic radiosurgery; STR, subtotal resection; WBRT, whole brain radiation therapy</p></fn>
</author-notes>
<pub-date pub-type="collection"><season>May-Jun</season><year>2026</year></pub-date>
<pub-date pub-type="epub"><day>14</day><month>04</month><year>2026</year></pub-date>
<volume>6</volume>
<issue>3</issue>
<elocation-id>31</elocation-id>
<history>
<date date-type="received">
<day>05</day>
<month>11</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>02</month>
<year>2026</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2026 Fouda et al.</copyright-statement>
<copyright-year>2026</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.</license-p></license>
</permissions>
<abstract>
<p>Neuroendoscopy allows the performance of biopsy and the resection of metastatic brain lesions using a minimally invasive approach. The present systematic review aimed to survey the existing evidence surrounding the use of neuroendoscopic techniques in the setting of metastatic brain lesions. A systematic search of the available literature was performed using the approach outlined by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) method. The search identified 34 studies that enrolled 150 participants. The average age of the patients was 57 years (range, 37-80 years), and the female-to-male ratio was 51 to 54. The most common primary sites were the lung (42/113), breast (18/113) and melanoma (16/113). Supratentorial tumours represented 93 of the 115 cases. Of the 34 included studies, the goal of the procedure was resection in 23 studies, biopsy in six studies (with ventriculostomy in 3), and both in five studies. The degree of resection was reported for 93 participants, in which a gross, near and subtotal resection was achieved in 60, 13 and 20 cases, respectively. Overall, 13 studies encompassing 34 participants reported that 28 (82&#x0025;) patients demonstrated post-operative symptomatic improvement following resection. The overall survival was reported for 50 patients following resection across four studies, yielding a weighted average of 12.8 months. To the best of our knowledge, the present study represents the first comprehensive systematic assessment of the existing evidence surrounding the role of neuroendoscopy for brain metastases. The findings presented herein demonstrate promise for the role of neuroendoscopy in this setting; however, the quality and quantity of evidence limit the drawing of strong conclusions.</p>
</abstract>
<kwd-group>
<kwd>neuroendoscopy</kwd>
<kwd>metastatic brain tumours</kwd>
<kwd>brain metastases</kwd>
<kwd>minimally invasive neurosurgery</kwd>
<kwd>surgical outcomes</kwd>
<kwd>intracranial metastasis</kwd>
</kwd-group>
<funding-group>
<funding-statement><bold>Funding:</bold> No funding was received.</funding-statement>
</funding-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Brain metastasis is considered a major complication of the later stages of cancer. This is associated with various signs and symptoms, including headaches, seizures, weakness in the arms or legs, loss of balance, memory loss and speech disruptions (<xref rid="b1-MI-6-3-00315" ref-type="bibr">1</xref>). The management of these metastatic lesions has always been a challenge. There are different approaches employed in treating metastatic brain tumours, including the following:</p>
<p>Radiation therapy uses X-rays, protons and other high-energy electron beams to eliminate cancer cells. The two most known techniques are stereotactic radiosurgery (SRS) and whole-brain radiation therapy (WBRT). SRS provides precise radiation towards the cancerous cells and is performed in a few sessions, whereas the radiation in WBRT is applied to the whole brain and requires 10-15 sessions (<xref rid="b2-MI-6-3-00315" ref-type="bibr">2</xref>). Traditionally, SRS was limited to patients with up to four brain metastases. However, it is increasingly being considered a viable treatment option for those with more numerous metastases, with a recent study demonstrating a promising safety and efficacy profile in patients with &#x2265;15 brain metastases (<xref rid="b3-MI-6-3-00315" ref-type="bibr">3</xref>).</p>
<p>Chemotherapy is limited as the majority of chemotherapeutic agents cannot cross the blood-brain barrier. However, it is still considered a viable option. Extensive research has been performed in an aim to improve drug delivery to the brain (<xref rid="b2-MI-6-3-00315" ref-type="bibr">2</xref>).</p>
<p>Targeted therapy is one of the newest methods in the treatment of cancer. The agents used in this type of therapy can cross the blood-brain barrier and can identify cancerous cells with minimal harm to normal cells. It is usually co-administered with radiation therapy or administered following surgery to eliminate the remaining cancerous cells (<xref rid="b1-MI-6-3-00315" ref-type="bibr">1</xref>).</p>
<p>Recently, neuroendoscopy has gained increasing attention in the field of neurosurgery, being used for the treatment of a wide range of conditions including hydrocephalus, intracranial cysts, craniosynostosis, intraventricular tumours, and skull base tumours (<xref rid="b4-MI-6-3-00315" ref-type="bibr">4</xref>,<xref rid="b5-MI-6-3-00315" ref-type="bibr">5</xref>). Due to its minimally invasive technique, while maintaining effectiveness and comparative safety, it has become the preferred surgical approach for the management of many intracranial diseases (<xref rid="b5-MI-6-3-00315" ref-type="bibr">5</xref>). A recent single-centre retrospective study surveying 318 neuroendoscopic procedures for intracranial pathologies reported that only 5.4&#x0025; of cases were affected by an early surgical adverse event while 3.1&#x0025; were affected by a non-surgical adverse event (<xref rid="b5-MI-6-3-00315" ref-type="bibr">5</xref>).</p>
<p>The present systematic review aimed to summarise the available literature surrounding neuroendoscopic procedures in patients diagnosed with metastatic brain tumours. In particular, the authors were interested in summarising the available evidence regarding the characteristics of patients selected for this technique, technical details regarding the procedure in this patient population, and evaluating the evidence regarding the outcomes of these neuroendoscopic procedures.</p>
</sec>
<sec sec-type="Data|methods">
<title>Data and methods</title>
<p>The present systematic review was undertaken using the approach outlined by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) method (<xref rid="b6-MI-6-3-00315" ref-type="bibr">6</xref>). Articles assessed as part of the present systematic review were identified from a search of the PubMed library electronic database performed on June 1, 2022. The search string utilised was: &#x2018;(Endoscop&#x002A;&#x005B;Title/Abstract&#x005D; OR Neuroendoscop&#x002A;&#x005B;Title/Abstract&#x005D;) AND (Metast&#x002A;&#x005B;Title/Abstract&#x005D;) AND (Brain&#x005B;Title/Abstract&#x005D;)&#x2019;. Asterisks (&#x2018;&#x002A;&#x2019;) and Boolean operators &#x2018;AND&#x2019; and &#x2018;OR&#x2019; are established tools used to search the PubMed library and were used to enhance search yield.</p>
<p>Studies were included or excluded from analysis in the present systematic review in accordance with predefined inclusion and exclusion criteria. Following a review of the existing literature and discussions with an expert in this field, the present systematic review decided to focus its search on the use of endoscopic techniques in the management of metastatic brain tumours.</p>
<p>The inclusion criteria were the following: i) Studies involving only adult (&#x2265;18 years) participants; ii) studies in which an endoscopic procedure was conducted on a metastatic brain lesion; iii) studies that reported specific demographic, procedural, or outcome parameters for those with metastatic brain lesions who received endoscopic intervention(s).</p>
<p>The exclusion criteria were as follows: i) Studies involving non-human participants; ii) studies not available in the English language; iii) studies that did not report demographic, procedural, or outcome parameters for those with metastatic brain lesions who received an endoscopic intervention. Duplicate studies were removed, and for instances in which multiple papers were written on the same trial, the study with the largest sample size was selected.</p>
<p>Data recorded and discussed as part of the present systematic review arose from distinct article selection and data extraction steps. All articles were assessed against the previously described inclusion and exclusion criteria at both title and abstract and full-text screening stages by two independent reviewers. Conflicts were resolved by a third-party reviewer. Following study selection, the following data were extracted from the included studies: i) Citation data; ii) study design characteristics; iii) study population characteristics (number, disease, intervention, age, sex, presenting symptoms, primary cancer histology, lesion location and lesion size); iv) intervention characteristics (aim/indication, preoperative assessment, operative route, operative technique, adjunctive tools and therapies, post-operative assessment; and v) outcome measures (procedure success, duration, adverse events, length of hospital stay (LOS), mean follow-up, and clinical outcomes). Details surrounding the number of articles screened at each stage and the extracted data are presented in the Results section.</p>
</sec>
<sec sec-type="Results">
<title>Results</title>
<sec>
<title/>
<sec>
<title>Study selection</title>
<p>Findings from the electronic database search and article screening stages are outlined in accordance with the most recent PRISMA guidelines published by Page <italic>et al</italic> (<xref rid="b6-MI-6-3-00315" ref-type="bibr">6</xref>) in <xref rid="f1-MI-6-3-00315" ref-type="fig">Fig. 1</xref>. The literature search identified 242 articles. Covidence software identified none of these as duplicates. Title and abstract screening identified 62 articles meeting the inclusion and exclusion criteria for full-text review. Upon full-text review, studies that could not be retrieved, duplicate studies, and those that did not meet the inclusion and exclusion criteria were identified and removed, as illustrated in <xref rid="f1-MI-6-3-00315" ref-type="fig">Fig. 1</xref>. Ultimately, 34 studies were selected for data extraction and subsequent analysis as part of the present systematic review. These are listed in <xref rid="tI-MI-6-3-00315" ref-type="table">Table I</xref> (<xref rid="b7-MI-6-3-00315 b8-MI-6-3-00315 b9-MI-6-3-00315 b10-MI-6-3-00315 b11-MI-6-3-00315 b12-MI-6-3-00315 b13-MI-6-3-00315 b14-MI-6-3-00315 b15-MI-6-3-00315 b16-MI-6-3-00315 b17-MI-6-3-00315 b18-MI-6-3-00315 b19-MI-6-3-00315 b20-MI-6-3-00315 b21-MI-6-3-00315 b22-MI-6-3-00315 b23-MI-6-3-00315 b24-MI-6-3-00315 b25-MI-6-3-00315 b26-MI-6-3-00315 b27-MI-6-3-00315 b28-MI-6-3-00315 b29-MI-6-3-00315 b30-MI-6-3-00315 b31-MI-6-3-00315 b32-MI-6-3-00315 b33-MI-6-3-00315 b34-MI-6-3-00315 b35-MI-6-3-00315 b36-MI-6-3-00315 b37-MI-6-3-00315 b38-MI-6-3-00315 b39-MI-6-3-00315 b40-MI-6-3-00315" ref-type="bibr">7-40</xref>).</p>
</sec>
<sec>
<title>Patient demographics</title>
<p>Demographic data for the included studies are outlined in <xref rid="SD1-MI-6-3-00315" ref-type="supplementary-material">Table SI</xref>. In total, the included studies reported data on 686 participants, 150 of whom received an endoscopic intervention on a non-primary brain tumour. Within this cohort, the average age of the patients was 57 years (range, 37-80 years), and the female-to-male ratio was 51 to 54. Patient presenting symptoms were reported in 18 studies and are outlined below. Tumour histology was reported by 27 of the included 34 studies for a total of 113 patients. Metastases from the lung (42/113), breast (18/113) and melanoma (16/113) represented the most common diagnoses. The remaining tumours were either unclassified adenocarcinomas (10/113) or small numbers of other tumour types, including renal (5/113), GIT (5/113) and bladder (4/113).</p>
<p>Lesion location was reported in 29 studies for a total of 115 patients and was subclassified with relation to the tentorium cerebelli for the purposes of the present systematic review. Supratentorial tumours represented 93 of the 115 cases and primarily comprised tumours located in the cortex (38/115), sella (14/115), and ventricles (10/115). Alternative locations included subcortical (9/115), sinuses (4/115) and other/not otherwise specified (18/115). Infratentorial tumours comprised 22 of the 115 described lesions and primarily comprised those located in the cerebellum (10/115). Lesion size was reported in 13 of the included 34 studies. Maximum dimension was the most commonly reported metric, with measurements ranging from 10 to 41 mm across 8 studies.</p>
</sec>
<sec>
<title>Procedures performed</title>
<p>Details on the operative procedure undertaken are summarised in <xref rid="SD2-MI-6-3-00315" ref-type="supplementary-material">Table SII</xref>. Of the 34 included studies, the goal of the procedure was resection in 23, biopsy in six studies (with ventriculostomy in 3), and both in 5 studies. The procedure was undertaken using a fully endoscopic approach in 26 studies and in combination with microsurgery in eight studies. The majority of procedures were undertaken using a transcranial route via a corticotomy (20/32). Alternative routes included extended endonasal (8/32), transorbital (3/32) and a combined transorbital and extended endonasal approach utilised in one study. Procedures were undertaken using rigid endoscopes in 18 of the 21 studies that reported this. Furthermore, intraoperative fluorescence was utilized in procedures undertaken in 7 of the included studies.</p>
<p><xref rid="SD2-MI-6-3-00315" ref-type="supplementary-material">Table SII</xref> also includes a summary of the pre- and post-operative assessments undertaken alongside the use of adjuvant therapy. Magnetic Resonance Imaging (MRI) was utilised in pre-operative assessment in all 32 studies that reported on this. Computed Tomography (CT) imaging was also performed in the preoperative assessment, utilised in nine studies. Similarly, MRI and CT scan were used in the post-operative assessment of patients in 26 and 11 of the 27 studies reporting this variable, respectively. The use of adjunctive chemotherapy and radiotherapy was poorly reported (10 and 13 studies, respectively), with 5 and 11 studies reporting their use, respectively.</p>
</sec>
<sec>
<title>Outcomes of procedures</title>
<p>Periprocedural outcomes reported by the studies included in this analysis are presented in <xref rid="SD3-MI-6-3-00315" ref-type="supplementary-material">Table SIII</xref>. Procedural time was reported in two studies, yielding an average of 122 min (range, 83-160 min). Procedural success was measured in terms of the extent of resection &#x005B;gross total resection (GTR), near total resection (NTR) and subtotal resection (STR)&#x005D; for resections and obtaining sufficient tissue for histological assessment for biopsies. Of the 28 studies reporting resection as a goal, 23 studies recorded the degree of resection in terms of the definitions of GTR, NTR and STR utilised by the present systematic review for a cohort of 93 patients. Within this cohort, GTR was achieved in 60 patients, NTR was achieved in 13, and STR was achieved in 20 patients. Furthermore, of the six studies that performed biopsies alone, the procedure was successful in all 7 patients.</p>
<p>Overall, 13 studies encompassing 34 patients reported that 28 (82&#x0025;) patients demonstrated post-operative symptomatic improvement. The overall survival was reported for 50 patients across four studies, yielding a weighted average of 12.8 months.</p>
<p>Adverse events were classed as intraoperative and post-operative, and LOS was reported in days. Overall, a total of 22 participants experienced adverse events from a total of 124 participants across 15 studies. Intraoperatively, there were seven CSF leaks and one bleed requiring 400 ml transfusion, resulting in a total of eight intraoperative complications. Post-operatively, there was a total of 14 individuals who experienced post-operative adverse events, which included 3 cases of wound infection; 3 cases of panhypopituitarism, 2 cases of transient arm paresis; one post-operative CSF leak; one patient who suffered both a brain abscess and pulmonary embolism; one instance of re-cannulation where a second cannulation was required to adequately access the target lesion; one proximal optic radiation infarct; and two deaths in the 30 days following the procedure arising from multiorgan failure and pulmonary embolism, respectively. Post-operative LOS was reported for the metastatic cohort in one study in which the patient remained in hospital for 14 days after his surgery, before being discharged with outpatient follow-up.</p>
</sec>
</sec>
</sec>
<sec sec-type="Discussion">
<title>Discussion</title>
<p>Neuroendoscopy represents a promising avenue to facilitate the diagnosis and treatment of metastatic brain lesions both in isolation and in conjunction with microsurgical techniques. The present systematic review aimed to assess and summarise the existing evidence surrounding the role of neuroendoscopy in this setting. In undertaking the present systematic review, the authors assessed the existing evidence and have provided aggregate measures of the demographic factors of the study population, details of the operative procedures undertaken, and relevant outcome measures, including procedural success and complication rates. Throughout this section, the relevance of the findings concerning the existing literature in this space and the strengths and limitations of the study are discussed, and these are applied to yield recommendations for future research.</p>
<p>The initial literature search yielded 242 articles. Following the abstract and full-text screening, 34 studies were included for data extraction and subsequent analysis; these are listed in <xref rid="tI-MI-6-3-00315" ref-type="table">Table I</xref>. Across the 34 studies, there were 686 patients, of whom 150 patients had neuroendoscopic procedures performed for the resection or biopsy of metastatic brain tumours.</p>
<p>The number of patients relevant to the present systematic review in each study was low, with an average of 4.41 patients per study. The largest number of patients in one study was 26, while 15 of the included papers only had 1 patient who had undergone neuroendoscopy for the biopsy or resection of a metastatic brain tumour.</p>
<p>The extraction sheets were designed to contain the most critical characteristics and outcomes that the authors were interested in summarising. However, surprisingly, a number of the studies did not provide information on these outcomes that is specific to metastatic patients who had undergone neuroendoscopy (<xref rid="b8-MI-6-3-00315" ref-type="bibr">8</xref>,<xref rid="b11-MI-6-3-00315 b12-MI-6-3-00315 b13-MI-6-3-00315 b14-MI-6-3-00315" ref-type="bibr">11-14</xref>,<xref rid="b16-MI-6-3-00315" ref-type="bibr">16</xref>,<xref rid="b20-MI-6-3-00315 b21-MI-6-3-00315 b22-MI-6-3-00315 b23-MI-6-3-00315 b24-MI-6-3-00315 b25-MI-6-3-00315" ref-type="bibr">20-25</xref>,<xref rid="b28-MI-6-3-00315" ref-type="bibr">28</xref>,<xref rid="b29-MI-6-3-00315" ref-type="bibr">29</xref>,<xref rid="b31-MI-6-3-00315 b32-MI-6-3-00315 b33-MI-6-3-00315" ref-type="bibr">31-33</xref>,<xref rid="b35-MI-6-3-00315" ref-type="bibr">35</xref>). Most strikingly, only two studies, conducted by the same group, reported the total duration of surgery (<xref rid="b24-MI-6-3-00315" ref-type="bibr">24</xref>,<xref rid="b25-MI-6-3-00315" ref-type="bibr">25</xref>), while only one study reported LOS (<xref rid="b7-MI-6-3-00315" ref-type="bibr">7</xref>). Furthermore, data were limited for the total length of follow-up and detailed reports of clinical outcomes post-procedure. Likewise, the number of studies that reported on the lesion size, the use of fluorescence, adjuvant chemotherapy, or adjuvant radiotherapy was limited.</p>
<p>The average age of patients with metastatic brain disease who had undergone neuroendoscopy was 57.46 years (range, 37 to 80 years). This is consistent with data available demonstrating that the most common age for the incidence of brain metastases is the 6th decade of life (<xref rid="b41-MI-6-3-00315" ref-type="bibr">41</xref>). Furthermore, this is similar to that reported by other groups, such as Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>) who reported a median age of 63 years (range, 18-89 years) in their retrospective assessment of 373 patients who underwent conventional craniotomy and resection of single brain metastases.</p>
<p>A total of 28 of the 34 included studies utilised neuroendoscopy for the resection of tumours, while the remaining percentage only carried out biopsies. The procedural time in this series was reported in two studies, yielding an average of 122 min (range, 83-160 min). This is comparable to that reported in the study by Gupta <italic>et al</italic> (<xref rid="b43-MI-6-3-00315" ref-type="bibr">43</xref>); they reported a median operative time of 139 min (interquartile range, 98-193 min) following their assessment of 3,500 cases of craniotomy for resection of brain metastasis.</p>
<p>GTR was achieved in 64.51&#x0025; of the cases, whereas in 13.98 and 21.50&#x0025; of cases, NTR and STR were achieved, respectively. A recent retrospective study by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>) examining patients with brain metastases, reported improved survival with GTR compared to STR, highlighting the importance of the extent of resection. The extent of resection rates reported in the present analysis is similar to those reported in the study by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>), where they found that out of 373 patients, 64&#x0025; achieved GTR, and 36&#x0025; achieved STR. This indicates that with neuroendoscopic procedures, it is possible to achieve similar extents of resection to other techniques (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>).</p>
<p>As regards clinical outcomes, it was found that 82.35&#x0025; of patients were reported to have at least some level of symptomatic improvement. There was overall very poor reporting of overall survival for the included patients with metastatic brain tumours. The average of overall survival reported in four studies (50 patients) was 14.99 months (<xref rid="b10-MI-6-3-00315" ref-type="bibr">10</xref>,<xref rid="b18-MI-6-3-00315" ref-type="bibr">18</xref>,<xref rid="b26-MI-6-3-00315" ref-type="bibr">26</xref>,<xref rid="b38-MI-6-3-00315" ref-type="bibr">38</xref>). When weighted by the number of patients in each study, the average overall survival is 12.82 months. This is again in line with the study by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>), which reported that the median overall survival was 11.0 months.</p>
<p>Adverse events were poorly reported in this series, with only 15 of the 34 included studies reporting adverse event outcomes on a subpopulation of 124 participants (<xref rid="b8-MI-6-3-00315 b9-MI-6-3-00315 b10-MI-6-3-00315" ref-type="bibr">8-10</xref>,<xref rid="b15-MI-6-3-00315" ref-type="bibr">15</xref>,<xref rid="b17-MI-6-3-00315" ref-type="bibr">17</xref>,<xref rid="b21-MI-6-3-00315" ref-type="bibr">21</xref>,<xref rid="b24-MI-6-3-00315 b25-MI-6-3-00315 b26-MI-6-3-00315" ref-type="bibr">24-26</xref>,<xref rid="b31-MI-6-3-00315" ref-type="bibr">31</xref>,<xref rid="b32-MI-6-3-00315" ref-type="bibr">32</xref>,<xref rid="b37-MI-6-3-00315 b38-MI-6-3-00315 b39-MI-6-3-00315 b40-MI-6-3-00315" ref-type="bibr">37-40</xref>). Overall, a total of 22 patients suffered adverse events across intra-operative and post-operative time periods. Intra-operatively, there was one major haemorrhage requiring transfusion (0.8&#x0025;) reported in this series, which is infrequent compared to that of 3.65&#x0025; reported by Aziz <italic>et al</italic> (<xref rid="b44-MI-6-3-00315" ref-type="bibr">44</xref>) following their assessment of 40,883 patients who underwent craniotomy for brain tumour resection. There were seven intra-operative CSF leaks, however, only 1 participant (0.8&#x0025;) went on to experience a post-operative CSF leak which is similar to that of 1&#x0025; reported by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>). With regards to post operative adverse events, the aggregate figure of 11.3&#x0025; observed in the present study cohort is comparable to the 7&#x0025; reported by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>). Notably, 2 patients in the series examined in the present study died within 30 days of surgery (1.6&#x0025;) due to pulmonary embolism and multiorgan failure respectively, which is less than the 3.7&#x0025; of those who died in the 6 weeks following intervention in the series published by Winther <italic>et al</italic> (<xref rid="b42-MI-6-3-00315" ref-type="bibr">42</xref>)..</p>
<p>Neuroendoscopy provides several unique advantages compared to conventional microsurgical approaches, particularly in the setting of minimally invasive surgery and applications for label-free imaging techniques.</p>
<p>Minimally invasive surgery aims to limit unnecessary damage to intracranial and extracranial tissues by minimising the size of the access site, surgical corridor, and the degree of intraoperative tissue retraction utilised in neurosurgical procedures (<xref rid="b45-MI-6-3-00315" ref-type="bibr">45</xref>). In pursuit of this aim, neuroendoscopy demonstrates several clear advantages over microscopic and unassisted approaches through allowing a wide field of view, slim and flexible instrumentation, and improved illumination, which allow the use of longer, narrower, and tortuous surgical routes (<xref rid="b45-MI-6-3-00315" ref-type="bibr">45</xref>). While the use of minimally invasive surgical techniques requires careful patient selection and a significant learning curve, these approaches demonstrate clear advantages over open transcranial techniques in terms of decreased procedural morbidity and complication rate, quicker recovery time and improved cosmesis (<xref rid="b45-MI-6-3-00315" ref-type="bibr">45</xref>).</p>
<p>Furthermore, the use of neuro-endoscopes capable of label-free imaging techniques such as narrow band imaging (NBI) may allow intra-operative histopathological diagnosis and improve resection margins. NBI describes the use of optical filters that transmit only light of 540 nm (green) and 415 nm (blue) wavelengths, which are absorbed by haemoglobin, which provides coloration to tissues based on capillary density and architecture (<xref rid="b46-MI-6-3-00315" ref-type="bibr">46</xref>). Endoscopic narrow band imaging has demonstrated utility in the detection of a wide range of early cancers, including cancers of the head and neck, upper and lower gastrointestinal tract, urological and gynaecological tracts, and lungs and bronchus (<xref rid="b46-MI-6-3-00315" ref-type="bibr">46</xref>). NBI has also demonstrated applications in the setting of cerebral malignancy, such as that reported by Sasagawa <italic>et al</italic> (<xref rid="b47-MI-6-3-00315" ref-type="bibr">47</xref>), who found that neuroendoscopic NBI allowed for the intraoperative identification and biopsy of tumour surfaces which were not perceptible on white light imaging. Additionally, the development of endoscopes capable of other label-free imaging techniques, such as confocal laser endomicroscopy, coherent anti-stokes Raman scattering, two-photon excitation fluorescence and second harmonic generation also represents promising avenues to allow intraoperative diagnosis and improve tumour resection margins (<xref rid="b48-MI-6-3-00315 b49-MI-6-3-00315 b50-MI-6-3-00315 b51-MI-6-3-00315" ref-type="bibr">48-51</xref>).</p>
<p>The present study is subject to several limitations. First, the majority of studies included in the present systematic review were retrospective in nature and involved small numbers of participants that meet the inclusion criteria. These factors should be taken into account when assessing the aggregate data and limit the strength by which recommendations can be made based on this evidence. Second, the present systematic review undertook data collection through the analysis of the published manuscripts. As a result, in some cases, heterogeneity with regard to the type and specificity of data reported limited the amount of data specific to our cohort of interest that could be extracted and contributed to data loss. Lastly, the present systematic review was limited to published manuscripts in the English language. As such, evidence, including ongoing trials, pre-prints or other grey literature, or those not available in the English language, have not been included in this review.</p>
<p>Despite these limitations, the produced work demonstrates several key strengths. First, present systematic review represents the most recent summary of the literature regarding the use of neuroendoscopy in the setting of metastatic brain lesions, providing an update as to the recent evidence in this space. Second, the authors utilised a broad search strategy and inclusion criteria, which allowed the inclusion and assessment of all relevant studies regardless of study design or size. Lastly, the present study assessed the existing evidence across numerous domains, including participant demographics, procedural factors and outcome measures, including procedural success and adverse events, which are relevant to clinical decision-making and service planning.</p>
<p>Following the completion of the present study, the following future directions for research in this field are proposed arising from limitations of this work. First, it is recommended that future work should stratify reported data by disease histology and procedures undertaken to allow assessment of differential treatment efficacy across these different patient cohorts. Second, it is recommended that the performance of more prospective studies with greater numbers of participants is required in order to increase the generalizability of the study findings and provide a stronger evidence base to inform clinical practice. Third, it is recommended that future work should incorporate greater comparisons and incorporate alternative methods, such as microsurgery, to allow comparisons of efficacy and inform clinical decision-making.</p>
<p>In conclusion, the analysis of the aggregated data revealed that neuroendoscopy provides a similar resection rate and overall survival to microsurgical techniques. However, the strength of the analysis is limited by the quality of the included studies, the majority of which were small in scale and retrospective in nature, and data loss arising from heterogeneity in reported data. From the findings of the present study, several priorities have been identified for future research, including the stratification of outcome measure reporting by disease histology, the performance of large-scale prospective studies, and comparisons to alternative diagnostic and treatment modalities. Overall, the present study demonstrates the value of neuroendoscopy as a tool to facilitate the diagnosis and treatment of metastatic brain lesions, and we look forward to further research in this space.</p>
</sec>
<sec sec-type="supplementary-material">
<title>Supplementary Material</title>
<supplementary-material id="SD1-MI-6-3-00315" content-type="local-data">
<caption>
<title>Patient demographics.</title>
</caption>
<media mimetype="application" mime-subtype="pdf" xlink:href="Supplementary_Data.pdf"/>
</supplementary-material>
<supplementary-material id="SD2-MI-6-3-00315" content-type="local-data">
<caption>
<title>Summary of the procedures performed in the included studies.</title>
</caption>
<media mimetype="application" mime-subtype="pdf" xlink:href="Supplementary_Data.pdf"/>
</supplementary-material>
<supplementary-material id="SD3-MI-6-3-00315" content-type="local-data">
<caption>
<title>Summary of outcomes of procedures.</title>
</caption>
<media mimetype="application" mime-subtype="pdf" xlink:href="Supplementary_Data.pdf"/>
</supplementary-material>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>Not applicable.</p>
</ack>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>The data generated in the present study may be requested from the corresponding author.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>BF and ML contributed equally to the study. BF and ML contributed to the conception and design of the study, to the literature search, data extraction, analysis, drafting, and the revision of the manuscript. UAA contributed to the conception and design of the study, to the literature search, data extraction, and the drafting of the manuscript. YD contributed to the conception and design of the study, to the literature search and data extraction. TAS supervised the study and contributed to the conception and design of the study, and to the editing of the final manuscript. All authors have read and approved the final version of the manuscript. BF and ML confirm the authenticity of all the raw data.</p>
</sec>
<sec>
<title>Ethics approval and consent to participate</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
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</back>
<floats-group>
<fig id="f1-MI-6-3-00315" position="float">
<label>Figure 1</label>
<caption><p>PRISMA diagram detailing identification and screening processes used to select studies. Format based on that outlined in the most recent PRISMA statement provided by Page <italic>et al</italic> (<xref rid="b6-MI-6-3-00315" ref-type="bibr">6</xref>).</p></caption>
<graphic xlink:href="mi-06-03-00315-g00.tif"/>
</fig>
<table-wrap id="tI-MI-6-3-00315" position="float">
<label>Table I</label>
<caption><p>List of the studies included in the present systematic review.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">First author, year of publication</th>
<th align="center" valign="middle">Title of study</th>
<th align="center" valign="middle">(Refs.)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Andreev, 2020</td>
<td align="left" valign="middle">Breast cancer metastasis into a giant hormone-inactive pituitary adenoma (clinical case and literature review).</td>
<td align="center" valign="middle">(<xref rid="b7-MI-6-3-00315" ref-type="bibr">7</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Ansari, 2020</td>
<td align="left" valign="middle">The Supraorbital Eyebrow Craniotomy for Intra- and Extra-Axial Brain Tumors: A Single-Center Series and Technique Modification.</td>
<td align="center" valign="middle">(<xref rid="b8-MI-6-3-00315" ref-type="bibr">8</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Barkhoudarian, 2017</td>
<td align="left" valign="middle">Microsurgical Endoscope-Assisted Gravity-Aided Transfalcine Approach for Contralateral Metastatic Deep Medial Cortical Tumors.</td>
<td align="center" valign="middle">(<xref rid="b9-MI-6-3-00315" ref-type="bibr">9</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Bettag, 2022</td>
<td align="left" valign="middle">Endoscope-assisted visualization of 5-aminolevulinic acid fluorescence in surgery for brain metastases.</td>
<td align="center" valign="middle">(<xref rid="b10-MI-6-3-00315" ref-type="bibr">10</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Cathel, 2019</td>
<td align="left" valign="middle">Metastatic Disease to Clivus: Biopsy or Not?</td>
<td align="center" valign="middle">(<xref rid="b11-MI-6-3-00315" ref-type="bibr">11</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Ceylan, 2009</td>
<td align="left" valign="middle">Extended endoscopic approaches for midline skull-base lesions.</td>
<td align="center" valign="middle">(<xref rid="b12-MI-6-3-00315" ref-type="bibr">12</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Choo, 2018</td>
<td align="left" valign="middle">Neuroendoscopic Cylinder Surgery and 5-Aminolevulinic Acid Photodynamic Diagnosis of Deep-Seated Intracranial Lesions.</td>
<td align="center" valign="middle">(<xref rid="b13-MI-6-3-00315" ref-type="bibr">13</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Gazzeri, 2014</td>
<td align="left" valign="middle">Endoscopic supraorbital eyebrow approach for the surgical treatment of extraaxialand intraaxial tumors.</td>
<td align="center" valign="middle">(<xref rid="b14-MI-6-3-00315" ref-type="bibr">14</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Hanada, 2010</td>
<td align="left" valign="middle">Metastatic pineal tumors treated by neuroendoscopic surgery-two case reports.</td>
<td align="center" valign="middle">(<xref rid="b15-MI-6-3-00315" ref-type="bibr">15</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Hong, 2016</td>
<td align="left" valign="middle">Comparison of endoscope- vs. microscope-assisted resection of deep-seated intracranial lesions using a minimally invasive port retractor system.</td>
<td align="center" valign="middle">(<xref rid="b16-MI-6-3-00315" ref-type="bibr">16</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Hu, 2020</td>
<td align="left" valign="middle">Pituitary Metastasis of Pulmonary Large Cell Neuroendocrine Carcinoma: A Case Report.</td>
<td align="center" valign="middle">(<xref rid="b17-MI-6-3-00315" ref-type="bibr">17</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Iacoangeli, 2012</td>
<td align="left" valign="middle">Endoscopy-verified occult subependymal dissemination of glioblastoma and brain metastasis undetected by MRI: prognostic significance.</td>
<td align="center" valign="middle">(<xref rid="b18-MI-6-3-00315" ref-type="bibr">18</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Jeon, 2018</td>
<td align="left" valign="middle">Endoscopic transorbital surgery for Meckel&#x0027;s cave and middle cranial fossa tumors: surgical technique and early results.</td>
<td align="center" valign="middle">(<xref rid="b19-MI-6-3-00315" ref-type="bibr">19</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Jimenez-Vazquez, 2017</td>
<td align="left" valign="middle">Neuroendoscopic and histopathological correlation in 13 cases of cystic fluid filled brain tumours.</td>
<td align="center" valign="middle">(<xref rid="b20-MI-6-3-00315" ref-type="bibr">20</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kassam, 2009</td>
<td align="left" valign="middle">Completely endoscopic resection of intraparenchymal brain tumors.</td>
<td align="center" valign="middle">(<xref rid="b21-MI-6-3-00315" ref-type="bibr">21</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kruljac, 2010</td>
<td align="left" valign="middle">Hypopituitarism caused by pituitary metastasis of supraglottic laryngeal carcinoma: case report.</td>
<td align="center" valign="middle">(<xref rid="b22-MI-6-3-00315" ref-type="bibr">22</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kutlay, 2016</td>
<td align="left" valign="middle">Fully Endoscopic Resection of Intra-Axial Brain Lesions Using Neuronavigated Pediatric Anoscope.</td>
<td align="center" valign="middle">(<xref rid="b23-MI-6-3-00315" ref-type="bibr">23</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kutlay, 2021</td>
<td align="left" valign="middle">Fluorescein Sodium-Guided Neuroendoscopic Resection of Deep-Seated Malignant Brain Tumors: Preliminary Results of 18 Patients.</td>
<td align="center" valign="middle">(<xref rid="b24-MI-6-3-00315" ref-type="bibr">24</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Kutlay, 2021</td>
<td align="left" valign="middle">Resection of intra- and paraventricular malignant brain tumors using fluorescein sodium-guided neuroendoscopic transtubular approach.</td>
<td align="center" valign="middle">(<xref rid="b25-MI-6-3-00315" ref-type="bibr">25</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Ma, 2018</td>
<td align="left" valign="middle">Endoscopy in Temporal Lobe Glioma and Metastasis Resection: Is There a Role?</td>
<td align="center" valign="middle">(<xref rid="b26-MI-6-3-00315" ref-type="bibr">26</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Maeshima, 2022</td>
<td align="left" valign="middle">Hemorrhagic brain metastasis from small-cell carcinoma of the urinary bladder.</td>
<td align="center" valign="middle">(<xref rid="b27-MI-6-3-00315" ref-type="bibr">27</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">McLaughlin, 2012</td>
<td align="left" valign="middle">Side-Cutting Aspiration Device for Endoscopic and Microscopic Tumor Removal.</td>
<td align="center" valign="middle">(<xref rid="b28-MI-6-3-00315" ref-type="bibr">28</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Mitsumasa, 2020</td>
<td align="left" valign="middle">Diplopia Presenting in a Case of Pineal Metastasis of Pulmonary Sarcomatoid Carcinoma Refractory to Treatment.</td>
<td align="center" valign="middle">(<xref rid="b29-MI-6-3-00315" ref-type="bibr">29</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Nemoto, 2013</td>
<td align="left" valign="middle">Isolated pineal region metastasis from lung adenocarcinoma with obstructive hydrocephalus: a case report.</td>
<td align="center" valign="middle">(<xref rid="b30-MI-6-3-00315" ref-type="bibr">30</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Newman, 2019</td>
<td align="left" valign="middle">Stereotactic-Guided Dilatable Endoscopic Port Surgery for Deep-Seated Brain Tumors: Technical Report with Comparative Case Series Analysis.</td>
<td align="center" valign="middle">(<xref rid="b31-MI-6-3-00315" ref-type="bibr">31</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Plaha, 2014</td>
<td align="left" valign="middle">Minimally invasive endoscopic resection of intraparenchymal brain tumors.</td>
<td align="center" valign="middle">(<xref rid="b32-MI-6-3-00315" ref-type="bibr">32</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Serra, 2020</td>
<td align="left" valign="middle">Microneurosurgical removal of thalamic lesions: surgical results and considerations from a large, single-surgeon consecutive series.</td>
<td align="center" valign="middle">(<xref rid="b33-MI-6-3-00315" ref-type="bibr">33</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Shirane, 2001</td>
<td align="left" valign="middle">Surgical treatment of posterior fossa tumors via the occipital transtentorial approach: evaluation of operative safety and results in 14 patients with anterosuperior cerebellar tumors.</td>
<td align="center" valign="middle">(<xref rid="b34-MI-6-3-00315" ref-type="bibr">34</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Souweidane, 2000</td>
<td align="left" valign="middle">Endoscopic Biopsy for Tumors of the Third Ventricle.</td>
<td align="center" valign="middle">(<xref rid="b35-MI-6-3-00315" ref-type="bibr">35</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Stamates, 2018</td>
<td align="left" valign="middle">Combined Open and Endoscopic Endonasal Skull Base Resection of a Rare Endometrial Carcinoma Metastasis.</td>
<td align="center" valign="middle">(<xref rid="b36-MI-6-3-00315" ref-type="bibr">36</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Villanueva, 2015</td>
<td align="left" valign="middle">Endoscopic and Gravity-Assisted Resection of Medial Temporo-occipital Lesions Through a Supracerebellar Transtentorial Approach: Technical Notes With Case Illustrations.</td>
<td align="center" valign="middle">(<xref rid="b37-MI-6-3-00315" ref-type="bibr">37</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Zacharia, 2015</td>
<td align="left" valign="middle">Endoscopic Endonasal Management of Metastatic Lesions of the Anterior Skull Base: Case Series and Literature Review.</td>
<td align="center" valign="middle">(<xref rid="b38-MI-6-3-00315" ref-type="bibr">38</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Zagzoog, 2017</td>
<td align="left" valign="middle">Metastatic Liposarcoma of the Skull Base: A Case Report and Review of Literature.</td>
<td align="center" valign="middle">(<xref rid="b39-MI-6-3-00315" ref-type="bibr">39</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Zhang, 2018</td>
<td align="left" valign="middle">Clival metastasis of renal clear cell carcinoma: Case report and literature review.</td>
<td align="center" valign="middle">(<xref rid="b40-MI-6-3-00315" ref-type="bibr">40</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</article>
