Figures
Abstract
Background
Meningioma surgery has evolved over the last 20 years with increased use of minimally invasive approaches including the endoscopic endonasal route and endoscope-assisted and gravity-assisted transcranial approaches. As the “keyhole” concept remains controversial, we present detailed outcomes in a cohort series.
Methods
Retrospective analysis was done for all patients undergoing meningioma removal at a tertiary brain tumor referral center from 2008–2021. Keyhole approaches were defined as: use of a minimally invasive “retractorless” approach for a given meningioma in which a traditional larger approach is often used instead. The surgical goal was maximal safe removal including conservative (subtotal) removal for some invasive locations. Primary outcomes were resection rates, complications, length of stay and Karnofsky Performance Scale (KPS). Secondary outcomes were endoscopy use, perioperative treatments, tumor control and acute MRI FLAIR/T2 changes to assess for brain manipulation and retraction injury.
Results
Of 329 patients, keyhole approaches were utilized in 193(59%) patients (mean age 59±13; 30 (15.5%) had prior surgery) who underwent 213 operations; 205(96%) were skull base location. Approaches included: endoscopic endonasal (n = 74,35%), supraorbital (n = 73,34%), retromastoid (n = 38,18%), mini-pterional (n = 20,9%), suboccipital (n = 4,2%), and contralateral transfalcine (n = 4,2%). Primary outcomes: Gross total/near total (>90%) resection was achieved in 125(59%) (5% for petroclival, cavernous sinus/Meckel’s cave, spheno-cavernous locations vs 77% for all other locations). Major complications included: permanent neurological worsening 12(6%), CSF leak 2(1%) meningitis 2(1%). There were no DVTs, PEs, MIs or 30-day mortality. Median LOS decreased from 3 to 2 days in the last 2 years; 94% were discharged to home with favorable 90-day KPS in 176(96%) patients. Secondary outcomes: Increased FLAIR/T2 changes were noted on POD#1/2 MRI in 36/213(17%) cases, resolving in all but 11 (5.2%). Endoscopy was used in 87/139(63%) craniotomies, facilitating additional tumor removal in 55%. Tumor progression occurred in 26(13%) patients, mean follow-up 42±36 months.
Conclusions & relevance
Our experience suggests minimally invasive keyhole transcranial and endoscopic endonasal meningioma removal is associated with comparable resection rates and low complication rates, short hospitalizations and high 90-day performance scores in comparison to prior reports using traditional skull base approaches. Subtotal removal may be appropriate for invasive/adherent meningiomas to avoid neurological deficits and other post-operative complications, although longer follow-up is needed. With careful patient selection and requisite experience, these approaches may be considered reasonable alternatives to traditional transcranial approaches.
Citation: Thakur JD, Mallari RJ, Corlin A, Yawitz S, Eisenberg A, Rhee J, et al. (2022) Critical appraisal of minimally invasive keyhole surgery for intracranial meningioma in a large case series. PLoS ONE 17(7): e0264053. https://doi.org/10.1371/journal.pone.0264053
Editor: Panagiotis Kerezoudis, Mayo Clinic, UNITED STATES
Received: February 1, 2022; Accepted: July 1, 2022; Published: July 28, 2022
Copyright: © 2022 Thakur et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The author(s) received no specific funding for this work.
Competing interests: The authors have read the journal’s policy and have the following competing interests: DFK receives royalties from Mizuho Inc. GB is a consultant for Vascular Technologies Inc. and Cerevasc Inc. outside of the current study. WS is a consultant for Stryker Corporation outside of the current study. This does not alter our adherence to PLOS ONE policies on sharing data and materials. There are no patents, products in development or marketed products associated with this research to declare.
Introduction
Meningiomas are the most common primary brain tumor with almost 35,000 patients being diagnosed annually in the US [1], and although 85–90% are benign (WHO Grade 1), they frequently encase or become adherent to arteries, veins and cranial nerves, and have a propensity to invade multiple skull base compartments. While surgery remains first-line treatment for meningiomas, the approach used and aggressiveness of removal is highly location-dependent and influenced by other factors such as tumor invasiveness, tumor consistency, prior treatments and surgeons’ philosophy. Innovative skull base surgery approaches developed in the early 1990s generally employed large incisions, extensive bone removal and promoted maximal tumor removal as the primary goal. However, results from multiple series using these approaches indicate that overly aggressive tumor removal can be associated with relatively high rates of permanent cranial nerve deficits and other neurological complications [2–5]. Furthermore, stereotactic radiosurgery and radiotherapy (SRS or SRT) have long-term control rates of 90% or higher for most recurrent or progressive WHO grade I meningiomas, and some primarily treated cavernous sinus (CS) meningiomas [6, 7]. Thus, over time, restoring or maintaining neurological function and quality of life have gained greater priority and the dictum of maximal safe tumor removal has gained wider acceptance [2, 8–11].
Minimally invasive surgical (MIS) techniques have been increasingly applied across multiple surgical subspecialties often with the aid of endoscopy [12–15]. Although the concept of minimally invasive brain tumor removal has been promoted for decades, it has remained controversial and not widely practiced. The term “keyhole surgery” was introduced 50 years ago by Donald Wilson in his 1971 technical note, “Limited exposure in cerebral surgery” [16]. Since the 1990s, the keyhole concept has been refined by application of modern micro-neurosurgical techniques and technology including low profile instrumentation, neuro-navigation and high-definition endoscopy. The keyhole concept emphasizes use of tailored and targeted approaches that limit brain exposure through strategically placed craniotomies, minimizing brain manipulation without static brain retractors, facilitated by gravity-assistance, and with the ultimate goal of achieving maximal safe tumor removal [17–22]. Notably, in the last 20 years, the endoscopic endonasal approach has evolved into an accepted and commonly used minimally invasive route for many midline skull base pathologies including meningiomas, given its ability to facilitate tumor removal without brain retraction. As such, the endonasal craniotomy route to the ventral skull base should arguably be included in the keyhole definition and armamentarium, and by so doing provides a more comprehensive 360-degree keyhole paradigm for meningioma management [23–28].
For over a decade, we have used several minimally invasive approaches for brain tumors, particularly for skull base and parafalcine meningiomas that eliminate the need for fixed brain retraction by relying on gravity assistance and endoscopic visualization [27–35]. Except for our recent report on elderly meningioma patients and that by Burks et al, to our knowledge, there are no prior studies with over 40 patients treated with a minimally invasive keyhole paradigm for all intracranial meningiomas [26, 33]. Herein we report detailed outcomes of our experience with these approaches to intracranial meningiomas including extent of resection, complications, length of stay (LOS), performance status, readmissions, and resection and recurrence rates. We also quantify the degree of parenchymal brain injury from retraction and manipulation injury by measuring acute MRI changes, and to what extent was endoscopy helpful in transcranial approaches for achieving additional tumor removal. We then assess our outcomes in aggregate compared to those reported in prior publications in meningioma patients operated through traditional skull base approaches. With this comprehensive analysis we attempt to answer one overarching question: ‘What is the benefit of keyhole surgery on neurological and overall surgical recovery and can such minimally invasive approaches be considered reasonable alternatives to traditional approaches? Six illustrative case examples are provided in two videos (S1 and S2 Videos).
Methods
Patient population & data collection
After institutional review board approval (IRB# JWCI-19-1101), all patients at Saint John’s Health Center, Santa Monica, CA, between January 2008 and January 2021 who underwent surgical removal of an intracranial meningioma were identified. Patient consent was not necessary as data was deidentified. All operations were performed by one of two neurosurgeons (DK, GB) and endonasal operations were performed with otolaryngology collaboration (CG). Data collection included prior treatments, tumor histopathology, size and location on MRI, endoscope usage, extent of resection, complications, length of stay, disposition, readmissions and long-term tumor control.
MIS “keyhole” definition and approach selection
Keyhole approaches were defined as: the use of a minimally invasive approach for a given tumor in which a traditional larger approach may be used instead. These six approaches included the endoscopic endonasal, supraorbital, mini-pterional, retromastoid, suboccipital tentorial and transfalcine routes. This definition follows that detailed by Lan et al in their 2019 consensus paper on keyhole microneurosurgery and aligns with our definition from prior publications on keyhole surgery [21, 27, 28] (Fig 1A & 1B, S1 Fig, S1 Table). Non-keyhole approaches include convexity craniotomies, pterional, bifrontal and far-lateral approaches. Table 1 describes the strategy for applying these 6 keyhole approaches and two videos provide 6 case examples. During the study period, traditional open skull base craniotomies including orbito-zygomatic, transpetrosal, translabyrinthine, transcondylar craniotomies were not used. Four patients who underwent a staged operation using one or more keyhole approaches are identified and each keyhole approach was considered as a separate outcome.
(1A) Drawing depicting 6 keyhole approaches for meningioma removal: endonasal, supraorbital, minipterional, retromastoid, suboccipital sitting gravity-assisted and transfalcine gravity-assisted, along with the total number of surgeries for each approach. (1B) A composite of the 6 keyhole approaches.
Surgical goals, preparation and technique
A goal of maximal safe tumor removal was applied across all tumor locations. However, subtotal removal was typically the goal for three meningioma subtypes given their invasive nature and tendency to encase neurovascular structures: petroclival, CS/Meckel’s cave, and spheno-cavernous locations, as well as some meningiomas with prior surgery and/or radiotherapy [32]. Residual meningioma was deliberately left along neurovascular structures if too adherent or left in the skull base bone if deemed too infiltrative. Four patients had planned staged approaches for large meningiomas (maximal diameter >6 cm: endonasal debulking combined with a pterional, mini-pterional or retromastoid approach.
Total intravenous anesthesia (TIVA) was used to promote rapid emergence from anesthesia [34]. Preoperative tumor embolization was not used. Lumbar drains for CSF diversion were used infrequently and only early in the series. As recently described, all endonasal cases were performed fully endoscopically using a 0° 4-mm rigid endoscope initially; 30° and 45° endoscopes (Karl Storz-America, El Segundo, CA), are used at various stages of the procedure [27, 32]. A pedicled nasoseptal flap (or middle turbinate flap) is harvested in cases of tuberculum and planum meningiomas but not for all CS/Meckel cave meningiomas, depending upon CSF leak grade [27, 32, 33].
Except for the fully endoscopic sitting suboccipital approach, all transcranial keyhole craniotomies are performed initially with the microscope and then with endoscopy as needed for illuminating areas poorly seen with the microscope, and for endoscopic tumor resection. Endoscopy is typically performed with an assistant driving the endoscope. Patient positioning is critical to optimize gravity-assisted exposure and for endoscopy. Our use of the supraorbital and mini-pterional approaches have been well-described [27, 34, 36]. The retromastoid approach is performed with the patient supine or lateral position, utilizing a short linear or curvilinear incision with approximately 2x3cm craniotomy [19]. The suboccipital approach is performed in the sitting or lateral position typically using an approximate 2x2cm craniotomy for tentorial meningiomas. The gravity-assisted transfalcine approach is performed specifically for parafalcine meningiomas that have a rind of edematous overlying eloquent cortex at risk from an ipsilateral approach. The patient is placed in lateral position with tumor side up and inclined in reverse Trendelenburg position with the vertex at 30–45 degrees [29], allowing for gravity-retraction and access from the unaffected contralateral side.
Outcome and statistical analysis
The primary and secondary outcomes analyses detailed below attempt to answer the question of benefit of keyhole surgery approaches in terms of neurological and overall surgical recovery. Primary outcomes included extent of tumor resection, complications, hospital LOS, reoperations and readmissions within 90 days, 30-day mortality, KPS, and cranial (CN) outcomes. A favorable KPS at ≥90 days follow-up was defined as improved or unchanged from preoperative KPS. As previously published, resection rates were categorized as: gross total resection (GTR), near total resection (NTR ≥ 90% tumor resection), or subtotal resection (< 90%) [27, 28]. Simpson resection classification was not assessed given that most patients had invasive skull base meningiomas in which complete tumor resection and removal of involved bone and dura is typically not feasible [27, 28, 37].
Three secondary outcomes were included: 1) To quantify approach-related trauma of tumor removal, post-operative day #1 or 2 MRIs were independently assessed by a neuroradiologist (JR) for new FLAIR/T2 signal changes in the peritumoral and surgical approach areas [27]. New FLAIR/T2 change in the axial plane around the resection area or approach trajectory was quantified by maximal diameters. Persistence or resolution was documented on 3-month postoperative MRI. 2) To assess the utility of endoscopic visualization for transcranial operations, as previously published, it was determined if endoscopy facilitated additional tumor removal [27, 34] 3) To assess tumor progression or recurrence, sequential postoperative MRIs and need for additional treatment (repeat surgery and/or radiotherapy) were quantified for each patient.
The statistical comparison of the mean in the data amongst different groups was performed using ANOVA and independent Student’s t-test. Univariate analysis was done using Chi-square or Fisher’s exact test when applicable. Binomial multivariate analysis was done using logistic regression analysis and p-values less than 0.05 were considered statistically significant. Tumor control data for testing binomial variables were plotted using Cox Regression and Kaplan-Meier analysis.
Results
Demographics
Of 329 patients, keyhole approaches were used in 193 (59%) (74% female, mean age 59±13, mean follow up 42±36 months; WHO Grade I: 173/193(89.6%), Grade II: 19/193(9.8%), Grade III: 1/193(0.6%)); 32(9.7%) had prior radiation. The 213 keyhole operations included 205 (96%) for skull base location and 47(22%) were in patients with prior surgery. Operative approaches used included: endonasal (n = 74), supraorbital (n = 73), retromastoid (n = 38), mini-pterional (n = 20), sitting suboccipital (n = 4), and contralateral gravity-assisted transfalcine (n = 4) (Table 2). Four patients had planned staged operations using two approaches for large meningiomas (endonasal combined with a pterional n = 1, supraorbital n = 1, mini-pterional n = 1 or retromastoid approach n = 1). Lumbar drains were used in 5/74(7%) endonasal operations all prior to 2013, and 1/139 (0.7%) transcranial operation in 2017.
Primary outcomes
Resection rates by approach and tumor location.
As shown in Tables 2 and 3, GTR was achieved in 85(40%) operations while GTR/NTR (>90% resection) was achieved in 125(59%) operations. By meningioma location, GTR/NTR rates were highest for frontal fossa, parafalcine tentorial, olfactory groove and planum meningiomas (N = 158, range 84–100%), and lowest for invasive spheno-cavernous, CS/Meckel’s cave and petroclival locations (N = 55, range 5–6%) (Table 3). Excluding these invasive subgroups (petroclival, CS/MC and spheno-cavernous), GTR/NTR was achieved in 114/136 (84%) first-time operations. Dense adherence to neurovascular structures was associated with 36% GTR/NTR versus 100%, without dense adhesions (p<0.001) (S2 Table). All patients with STR/NTR had at least one risk factor (prior surgery, radiotherapy, invasion cavernous sinus/Meckel’s cave/infratemporal fossa/orbit).
Clinical outcomes and complications.
Major complications occurred in 23/193 (11.9%) patients (Table 4). Permanent neurological worsening occurred in 12(6%) patients including 4 with strokes and 8 with cranial nerve injuries (S3 Table). Reoperations were needed in 10(5%) patients, (two for CSF leaks); 2(1%) patients had meningitis No patients developed perioperative DVT, PE or MI. Three patients all with multiple prior surgeries, died of disease progression at 80, 229, and 3508 days after their last operation.
Discharge to home, functional outcomes and readmissions.
Of 213 operations, 201(94%) resulted in patients being discharged to home and 12(6%) to skilled nursing facility or rehabilitation (Table 4). Median LOS was higher for patients discharged to rehabilitation or skilled nursing facility versus home (5 vs 2, p = 0.012). Over 11 years, median LOS decreased: 3 days (first 71 cases), 3 days (middle 71 cases) and 2 days (last 71 cases), p = 0.013. Longer LOS (LOS≥ 4) was associated with major complications (22% vs 7%, p = 0.005), discharge to rehabilitation or nursing facility (67% vs. 28%, p = 0.008). Ninety-day readmissions occurred in 6 (2.8%) cases, including 4 who required surgery.
Of 184/193 (95%) patients with available follow-up, favorable 90-day KPS was noted in 176(96%): improved in 126/176(72%) and stable in 50/176 (28%). Mean KPS for the entire cohort improved postoperatively from 72.3 to 82.4 (p<0.001).
Secondary outcomes
Acute MRI changes in region of approach.
Of 213 operations, POD 1 or 2 MRIs showed regional increase in FLAIR/T2 signal in 36(16.9%), highest in the retromastoid cohort (37.5%) (Table 2). FLAIR/T2 averaged 8±5 mm in maximal diameter and completely resolved in all but 11(5.2%) cases on follow-up MRI. No patients with increased FLAIR had attributable neurological deficits to their FLAIR changes.
Utility of endoscopy.
Endoscopy was used in 161(76%) keyhole operations, including all 74 endonasal cases and 87/139(63%) transcranial cases (Table 2). Of 87 endoscope-assisted transcranial cases, in 48(55%) it facilitated additional tumor removal.
Long-term tumor progression or recurrence.
Mean follow-up for the 193 patients was 41±36 months. Recurrence after GTR was seen in 1(1.2%) patient, while progression of residual tumor occurred in 26(24.1%) patients, for an overall recurrence/progression rate of 13.9% (27/193). As per Kaplan-Meier analysis, mean time to recurrence or progression was 23.7 ± 27.3 months (range 3–94 months). Of these 27 patients, 4 had repeat surgery only, 11 SRT only, 2 SRS followed by another surgery and 10 were observed or medically managed.
Discussion
MIS philosophy applied to meningiomas
MIS techniques aim to minimize collateral damage to normal tissues while achieving the surgical goal, be it tumor resection, valve replacement or disc replacement [12, 13, 15, 38, 39]. Striking that balance while being cost-effective and maximizing patients’ quality of life is the ultimate “sweet spot” of any surgical procedure [38, 40]. We propose that the present series of MIS approaches and prior series from our group and others for intracranial meningioma are a step forward for neurosurgery and endoscopic skull base surgery, demonstrating the potential effectiveness of this keyhole paradigm [19–21, 28, 34]. In attempting to answer our central question, we suggest these results show a potential benefit of keyhole meningioma surgery on neurological and overall patient recovery, and thus offer a reasonable and in some instances, a preferred alternative to traditional approaches.
This evolution of keyhole surgery is in part a result of cross-specialty collaboration. The adoption of the endoscope into transsphenoidal surgery that began in the 1990s with our colleagues in otorhinolaryngology, has transformed not only pituitary surgery but also the entire field of skull base surgery. Most pituitary adenomas are now removed through an endoscopic endonasal approach, and as we show here, many midline skull base meningiomas can be removed via the endonasal route [27, 41, 42]. Furthermore, the endoscope was used in almost two thirds of transcranial keyhole approaches and helped facilitate additional tumor removal in 55% of these operations.
Keyhole meningioma surgery aims to limit brain exposure and manipulation, accessing tumors through smaller strategically placed craniotomies, including ventral skull base craniotomies via the endoscopic endonasal approach, without static brain retractors, facilitated by gravity-assistance, low profile instrumentation and endoscopy, with the goal of achieving maximal safe tumor removal [17–21]. Despite the benefits of visualization, there is ample evidence that fixed brain retractors can cause acute and lasting brain injury [17, 43]. Recent reports highlight the potential for retraction injury and associated complications with traditional craniotomies for tuberculum and planum meningiomas [44–46]. A major benefit of keyhole retractorless and gravity-assisted endoscopic approaches and the endoscopic endonasal approach may be in less brain exposure and parenchymal manipulation [17, 18, 20, 21, 27, 46, 47]. This advantage was evidenced by the absence of early postoperative FLAIR/T2 changes along the surgical corridor in 82% of patients in this series including 100% of endonasal approaches; for 36 patients with FLAIR/T2 increases, these were small and resolved in all but 5% of patients.
For a neoplasm as diverse in location and invasiveness as meningioma, the surgical team should be facile working through multiple surgical corridors with both microscope and endoscope (see Table 1). Using TIVA anesthesia, smaller scalp and muscle incisions, minimal monopolar cautery, and focused craniotomies to minimize brain exposure, appears to promote rapid healing, less post-operative pain and a greater willingness and ability for patients to mobilize and leave the hospital [34, 35]. Adoption of MIS techniques have been a key component of success in enhanced recovery protocols in other surgical subspecialties which we are adopting as well in all of our brain tumor patients [34, 48]. Having reliable skull base closure techniques especially for endonasal, supraorbital and retromastoid routes where bony sinus and mastoid air cell entry frequently occurs is also essential to avoid CSF leaks and meningitis. This preventative strategy includes liberal use of abdominal fat grafts to obliterate sinus or air cell entry after craniotomy and a graded repair approach for skull base reconstruction including fat grafts and nasoseptal flaps in endonasal surgery without lumbar CSF drainage [33, 36, 49].
Complication rates, functional recovery and LOS compared to prior reports
To be valid and to show benefit in terms of neurological and overall surgical recovery, the MIS keyhole concept should yield low rates of new neurological deficits, CSF leaks and high rates of functional outcomes. Our results in terms of infrequent complications, short LOS and improved post-operative KPS scores support this approach. New cranial neuropathy was observed in only 4% of patients. Lumbar drains were used in only 3% of operations, while post-operative CSF leak rate and meningitis rates were only 1%. There were no cases of perioperative DVT, PE, MI or 30-day mortality. The absence of thromboembolic events is likely due in part to our high patient functionality with few neurovascular complication, early ambulation and limited perioperative narcotic use, and compares favorably to the 2.7–4.1% incidence of PE/DVT recently published [50, 51].
Prior studies and our experience demonstrate that complications impact quality of life, lengthen hospital stay, increase costs and often require reoperations and readmissions [29, 36, 38–40]. Compared to our outcomes of 3-day median LOS, 94% discharged to home, and 7% 90-day readmission rate, and no 30-day mortality, recent reports encompassing all intracranial meningiomas have documented LOS for skull base and other meningioma patients ranging from 4–11 days, discharge to home ranging from 70–83.4%, 90-day readmission rates of 9.2–17.9%, and 30-day mortality ranging from 0–5.4% [52–56]. This comparison is notable, given our series is comprised predominantly (96%) of skull base meningiomas (which are generally considered to be of higher complexity and risk profile than convexity meningiomas), while these 5 series include all intracranial meningiomas. A rapid complication-free recovery also benefits those patients who may have more aggressive (WHO Graded 2 or 3) or previously-treated meningiomas who may need to begin adjuvant therapy shortly after surgery [37].
In our recent publication on streamlining brain tumor care during the COVID-19 pandemic, we highlighted the importance and utility of an all-encompassing minimally invasive 360-degree approach to brain tumor surgery (for all tumor types), as a foundation for being able to not monitor many patients in the ICU and allowing for early hospital discharge, typically on POD#1 or #2 [35]. In this case control series of 293 patients, from pre-pandemic to pandemic, ICU utilization decreased from 54% to 29% of operations (p<0.001) and hospital LOS≤1 day increased from 12.2% to 41.4%, p<0.001, respectively. We believe that more routine and rigorous patient education on early discharge, recovery room assessment for non-ICU admission and earlier mobilization, layered upon a foundation of MIS, TIVA anesthesia and early post-operative imaging contributed to these significant and favorable trends (including our median LOS of 2 days in the last tertile of patients in this meningioma cohort).
Balancing goals of maximal tumor removal and complication avoidance
Perhaps the most serious critique of keyhole meningioma surgery is that ultimately the patient is not well-served because overly conservative tumor removal leads to the eventual need for repeat surgery, radiosurgery, or possibly both. This issue is the essence of the second part of our central question: ‘can keyhole approaches be considered reasonable alternatives to traditional approaches?’ Our overall meningioma resection rates for all locations except petroclival meningiomas are comparable to prior reports [8, 9, 44–46, 56], and our progression/recurrence rate of 14% is similar to prior reports (almost all in patients who underwent NTR or STR), although this rate will undoubtedly increase with longer follow-up [8, 57–62]. First-time resection rates for anterior cranial fossa and suprasellar meningiomas in the literature vary widely, ranging from 63% to 100%, with recurrence/progression rates ranging from 2% to 14% [19, 63, 64]. Considering petroclival meningiomas, we did not achieve GTR in any of 17 operations and had one new CN deficit (6%). In multiple series of petroclival meningiomas approached through traditional skull base approaches including the retromastoid approach, the GTR rate ranged from 21%-76% but permanent CN and other neurovascular complications ranged from 22%-54% [2–5, 65–71]. Collectively, these reports indicate that overly aggressive attempts at GTR, will likely be associated with a relatively high rate of permanent neurovascular morbidity and lower quality of life for many patients; thus we prefer a more conservative surgical approach for such invasive skull base meningiomas as other groups have also recommended [8, 10, 57–61, 72, 73].
A growing collective experience places functional preservation as a higher priority than GTR resection, as highlighted by recent reports [2, 8, 9, 37]. The beneficial impact of this approach for a given patient is a greater likelihood of no new postoperative neurological deficits and preserved or improved QOL while acknowledging that for many patients their meningioma becomes a chronic illness that warrants long-term monitoring with a higher likelihood of tumor progression and need for additional surgery, SRS/SRT or possible medical therapies in the years after non-GTR resection [8, 10, 57–61, 72, 73].
We highlight in Table 3 and S2 Table the factors most commonly responsible for not achieving a GTR which include invasiveness into the skull base and dense adherence to critical neurovascular structures. Heeding such anatomical realities accounts in large part for our low neurovascular complication rate but relatively high residual tumor rate for some locations. Overall, our results and those of other centers, seem to indicate a keyhole paradigm applied to meningiomas is a reasonable alternative to traditional skull base approaches, given our low neurovascular and systemic complication rates and short LOS, although further validation with longer follow-up at multiple centers is needed [19–22, 27, 28, 42].
Study limitations and bias
The major limitation of this study is its retrospective nature, heterogenous meningioma patient population, and our selection bias for using these 6 keyhole approaches without a comparison cohort of patients treated with traditional skull base approaches or other relatively new minimally invasive approaches such as the endoscopic transorbital route [74, 75]. We specifically did not compare clinical outcomes in the keyhole cohort to the 136 (41%) non-keyhole patient cohort. Also, the follow-up in our patients averaged 44 months which is relatively short. Longer follow-up is necessary to assess the efficacy of this approach more fully and determine how many patients who underwent NTR or STR ultimately need radiotherapy or additional surgery.
Conclusions
A minimally invasive keyhole paradigm applied to skull base and other select meningiomas can yield reasonable tumor resection rates with low rates of neurovascular and systemic complications, short LOS and high rates of functional outcomes. While traditional skull base approaches remain useful and effective, we suggest that with increasing experience, transcranial and endonasal keyhole approaches can be considered part of the surgical armamentarium for many intracranial meningiomas.
Supporting information
S1 Fig. Six keyhole approaches animated GIF.
The corresponding GIF animation of the 6 approaches illustrated in Fig 1.
https://doi.org/10.1371/journal.pone.0264053.s001
(GIF)
S1 Table. Keyhole and traditional approaches used for skull base and non-skull base meningiomas.
A breakdown of number of cases in which keyhole and traditional approaches were used for skull base and non-skull base meningiomas.
https://doi.org/10.1371/journal.pone.0264053.s002
(DOCX)
S2 Table. Multivariate regression analysis for tumor resection and progression.
Preoperative factors limiting GTR and factors predicting progression are analyzed using multivariate binomial and cox regression analysis.
https://doi.org/10.1371/journal.pone.0264053.s003
(DOCX)
S3 Table. Cranial nerve outcomes in 193 patients undergoing Keyhole meningioma removal.
A breakdown of the cranial nerve outcomes and recovery for patients undergoing keyhole meningioma surgery.
https://doi.org/10.1371/journal.pone.0264053.s004
(DOCX)
S1 Video. Anterior cranial fossa case examples.
Illustrative case examples of 3 anterior cranial fossa meningiomas: 1) tuberculum sella meningioma approached via endoscopic endonasal route, 2) olfactory groove meningioma approached via supraorbital route; 3) clinoidal meningioma approached via supraorbital route.
https://doi.org/10.1371/journal.pone.0264053.s005
(DOCX)
S2 Video. Three meningioma illustrative case examples.
Illustrative case examples of 3 meningiomas: 1) petroclival meningioma approached via retromastoid route, 2) tentorial meningioma approached via suboccipital sitting position route; 3) falx meningioma approached via transfalcine gravity-assisted route.
https://doi.org/10.1371/journal.pone.0264053.s006
(DOCX)
Acknowledgments
The authors would like to acknowledge the support of Pacific Neuroscience Institute Foundation and Saint John’s Health Center Foundation for their support. We would also like to acknowledge Josh Emerson for providing the artwork for Fig 1.
References
- 1. Ostrom Q. T., Patil N., Cioffi G., Waite K., Kruchko C., and Barnholtz-Sloan J. S., "CBTRUS statistical report: Primary brain and other central nervous system tumors diagnosed in the United States in 2013–2017," Neuro-oncology, vol. 22, no. Supplement_1, pp. iv1–iv96, 2020.
- 2. Nanda A., Javalkar V., and Banerjee A. D., "Petroclival meningiomas: study on outcomes, complications and recurrence rates," Journal of neurosurgery, vol. 114, no. 5, pp. 1268–1277, 2011. pmid:21184632
- 3. Couldwell W. T., Fukushima T., Giannotta S. L., and Weiss M. H., "Petroclival meningiomas: surgical experience in 109 cases," Journal of neurosurgery, vol. 84, no. 1, pp. 20–28, 1996. pmid:8613831
- 4. Little K. M., Friedman A. H., Sampson J. H., Wanibuchi M., and Fukushima T., "Surgical management of petroclival meningiomas: defining resection goals based on risk of neurological morbidity and tumor recurrence rates in 137 patients," Neurosurgery, vol. 56, no. 3, pp. 546–559, 2005. pmid:15730581
- 5. Isolan G. R., Wayhs S. Y., Lepski G. A., Dini L. I., and Lavinsky J., "Petroclival meningiomas: factors determining the choice of approach," Journal of neurological surgery. Part B, Skull base, vol. 79, no. 4, p. 367, 2018.
- 6. Faramand A., Kano H., Niranjan A., Park K.-J., Flickinger J. C., and Lunsford L. D., "Tumor control and cranial nerve outcomes after adjuvant radiosurgery for low-grade skull base meningiomas," World neurosurgery, vol. 127, pp. e221–e229, 2019. pmid:30880202
- 7. Pollock B. E., Stafford S. L., Link M. J., Garces Y. I., and Foote R. L., "Single-fraction radiosurgery of benign cavernous sinus meningiomas," Journal of neurosurgery, vol. 119, no. 3, pp. 675–682, 2013. pmid:23808540
- 8. Gozal Y. M., Alzhrani G., Abou-Al-Shaar H., Azab M. A., Walsh M. T., and Couldwell W. T., "Outcomes of decompressive surgery for cavernous sinus meningiomas: long-term follow-up in 50 patients," Journal of neurosurgery, vol. 132, no. 2, pp. 380–387, 2019. pmid:30771770
- 9. Beer-Furlan A. et al., "Improving Function in Cavernous Sinus Meningiomas: A Modern Treatment Algorithm," Frontiers in Neurology, vol. 11, 2020.
- 10. Gousias K., Schramm J., and Simon M., "The Simpson grading revisited: aggressive surgery and its place in modern meningioma management," Journal of neurosurgery, vol. 125, no. 3, pp. 551–560, 2016. pmid:26824369
- 11. Sughrue M. E. et al., "The relevance of Simpson Grade I and II resection in modern neurosurgical treatment of World Health Organization Grade I meningiomas," Journal of neurosurgery, vol. 113, no. 5, pp. 1029–1035, 2010. pmid:20380529
- 12. Tsui C., Klein R., and Garabrant M., "Minimally invasive surgery: national trends in adoption and future directions for hospital strategy," Surgical endoscopy, vol. 27, no. 7, pp. 2253–2257, 2013. pmid:23660720
- 13. Goh H. K. C., Ng Y. H., and Teo D. T. W., "Minimally invasive surgery for head and neck cancer," The lancet oncology, vol. 11, no. 3, pp. 281–286, 2010. pmid:20202612
- 14. Hamed O. H., Gusani N. J., Kimchi E. T., and Kavic S. M., "Minimally invasive surgery in gastrointestinal cancer: benefits, challenges, and solutions for underutilization," JSLS: Journal of the Society of Laparoendoscopic Surgeons, vol. 18, no. 4, 2014.
- 15. Smith Z. A. and Fessler R. G., "Paradigm changes in spine surgery—evolution of minimally invasive techniques," Nature Reviews Neurology, vol. 8, no. 8, pp. 443–450, 2012. pmid:22710631
- 16. Wilson D. H., "Limited exposure in cerebral surgery," Journal of neurosurgery, vol. 34, no. 1, pp. 102–106, 1971. pmid:4924207
- 17. Spetzler R. F. and Sanai N., "The quiet revolution: retractorless surgery for complex vascular and skull base lesions," Journal of neurosurgery, vol. 116, no. 2, pp. 291–300, 2012. pmid:21981642
- 18. Kalani M. Y. S., "Prospective Evaluation of the Need for Fixed Brain Retractors During Complex Cranial Surgery," World neurosurgery, vol. 139, pp. e61–e69, 2020. pmid:32289512
- 19. Burks J. D. et al., "Management of intracranial meningiomas using keyhole techniques," Cureus, vol. 8, no. 4, 2016.
- 20. Reisch R., Stadie A., Kockro R. A., and Hopf N., "The keyhole concept in neurosurgery," World neurosurgery, vol. 79, no. 2, pp. S17. e9–S17. e13, 2013.
- 21. Lan Q. et al., "International expert consensus statement about methods and indications for keyhole microneurosurgery from International Society on Minimally Invasive Neurosurgery," Neurosurgical review, pp. 1–17, 2019.
- 22. Reisch R. and Perneczky A., "Ten-year experience with the supraorbital subfrontal approach through an eyebrow skin incision," Operative Neurosurgery, vol. 57, no. suppl_4, pp. ONS-242-ONS-255, 2005.
- 23. Gardner P. A. et al., "Endoscopic endonasal resection of anterior cranial base meningiomas," Neurosurgery, vol. 63, no. 1, pp. 36–54, 2008. pmid:18728567
- 24. Cavallo L. M. et al., "Endoscopic endonasal surgery of the midline skull base: anatomical study and clinical considerations," Neurosurgical focus, vol. 19, no. 1, pp. 1–14, 2005.
- 25. Dusick J. R. et al., "The extended direct endonasal transsphenoidal approach for nonadenomatous suprasellar tumors," Journal of neurosurgery, vol. 102, no. 5, pp. 832–841, 2005. pmid:15926706
- 26. Laws E. R., Kanter A. S., Jane J. A., and Dumont A. S., "Extended transsphenoidal approach," Journal of neurosurgery, vol. 102, no. 5, pp. 825–828, 2005. pmid:15926704
- 27. Mallari R. J. et al., "Endoscopic Endonasal and Supraorbital Removal of Tuberculum Sellae Meningiomas: Anatomic Guides and Operative Nuances for Keyhole Approach Selection," Operative Neurosurgery, 2021.
- 28. Mallari R. J. et al., "Tuberculum Sellae Meningiomas in Pregnancy: 3 Cases Treated in the Second Trimester and Literature Review," World Neurosurgery, vol. 143, pp. 268–275, 2020. pmid:32758650
- 29. Barkhoudarian G. et al., "Microsurgical endoscope-assisted gravity-aided transfalcine approach for contralateral metastatic deep medial cortical tumors," Operative Neurosurgery, vol. 13, no. 6, pp. 724–731, 2017. pmid:29186601
- 30. Villanueva P. et al., "Endoscopic and gravity-assisted resection of medial temporo-occipital lesions through a supracerebellar transtentorial approach: technical notes with case illustrations," Operative Neurosurgery, vol. 11, no. 4, pp. 475–483, 2015. pmid:29506159
- 31. Fatemi N., Dusick J. R., de Paiva Neto M. A., Malkasian D., and Kelly D. F., "Endonasal versus supraorbital keyhole removal of craniopharyngiomas and tuberculum sellae meningiomas," Operative Neurosurgery, vol. 64, no. suppl_5, pp. ons269-ons287, 2009.
- 32. Sivakumar W. et al., "Strategy and Technique of Endonasal Endoscopic Bony Decompression and Selective Tumor Removal in Symptomatic Skull Base Meningiomas of the Cavernous Sinus and Meckel’s Cave," World neurosurgery, vol. 131, pp. e12–e22, 2019. pmid:31226453
- 33. Conger A. et al., "Evolution of the graded repair of CSF leaks and skull base defects in endonasal endoscopic tumor surgery: trends in repair failure and meningitis rates in 509 patients," Journal of neurosurgery, vol. 130, no. 3, pp. 861–875, 2018. pmid:29749920
- 34. Avery M. B., Mallari R. J., Barkhoudarian G., and Kelly D. F., "Supraorbital and mini-pterional keyhole craniotomies for brain tumors: a clinical and anatomical comparison of indications and outcomes in 204 cases," Journal of neurosurgery, 2021 2021.
- 35. Mallari R. J. et al., "Streamlining brain tumor surgery care during the COVID-19 pandemic: A case-control study," Plos one, vol. 16, no. 7, p. e0254958, 2021. pmid:34324519
- 36. Ansari S. F., Eisenberg A., Rodriguez A., Barkhoudarian G., and Kelly D. F., "The supraorbital eyebrow craniotomy for intra-and extra-axial brain tumors: a single-center series and technique modification," Operative Neurosurgery, vol. 19, no. 6, pp. 667–677, 2020. pmid:32745195
- 37. Schwartz T. H. and McDermott M. W., "The Simpson grade: abandon the scale but preserve the message," Journal of Neurosurgery, vol. 1, no. aop, pp. 1–8, 2020.
- 38. Schmitto J. D., Mokashi S. A., and Cohn L. H., "Minimally-invasive valve surgery," Journal of the American College of Cardiology, vol. 56, no. 6, pp. 455–462, 2010. pmid:20670754
- 39. Yeo H. L., Isaacs A. J., Abelson J. S., Milsom J. W., and Sedrakyan A., "Comparison of open, laparoscopic, and robotic colectomies using a large national database: outcomes and trends related to surgery center volume," Diseases of the Colon & Rectum, vol. 59, no. 6, pp. 535–542, 2016.
- 40. Robinson T. and Stiegmann G., "Minimally invasive surgery," Endoscopy, vol. 36, no. 01, pp. 48–51, 2004.
- 41. Asemota A. O., Ishii M., Brem H., and Gallia G. L., "Comparison of complications, trends, and costs in endoscopic vs microscopic pituitary surgery: analysis from a US health claims database," Neurosurgery, vol. 81, no. 3, pp. 458–472, 2017. pmid:28859453
- 42. Koutourousiou M., Fernandez-Miranda J. C., Stefko S. T., Wang E. W., Snyderman C. H., and Gardner P. A., "Endoscopic endonasal surgery for suprasellar meningiomas: experience with 75 patients," Journal of neurosurgery, vol. 120, no. 6, pp. 1326–1339, 2014. pmid:24678782
- 43. Rosenørn J. and Diemer N., "The risk of cerebral damage during graded brain retractor pressure in the rat," Journal of neurosurgery, vol. 63, no. 4, pp. 608–611, 1985. pmid:4032025
- 44. Makarenko S., Carreras E. M., and Akagami R., "Craniotomy for perisellar meningiomas: comparison of simple (appropriate for endoscopic approach) versus complex anatomy and surgical outcomes," Journal of neurosurgery, vol. 126, no. 4, pp. 1191–1200, 2017. pmid:27285536
- 45. Kong D.-S. et al., "Selection of endoscopic or transcranial surgery for tuberculum sellae meningiomas according to specific anatomical features: a retrospective multicenter analysis (KOSEN-002)," Journal of neurosurgery, vol. 130, no. 3, pp. 838–847, 2018. pmid:29775151
- 46. Bander E. D. et al., "Endoscopic endonasal versus transcranial approach to tuberculum sellae and planum sphenoidale meningiomas in a similar cohort of patients," Journal of Neurosurgery, vol. 128, no. 1, pp. 40–48, 2017. pmid:28128693
- 47. Teo C., "The concept of minimally invasive neurosurgery," Neurosurgery Clinics of North America, vol. 21, no. 4, pp. 583–4, v, 2010. pmid:20947027
- 48. Ljungqvist O., Scott M., and Fearon K. C., "Enhanced recovery after surgery: a review," JAMA surgery, vol. 152, no. 3, pp. 292–298, 2017. pmid:28097305
- 49. Taha A. N. M., Almefty R., Pravdenkova S., and Al-Mefty O., "Sequelae of autologous fat graft used for reconstruction in skull base surgery," World neurosurgery, vol. 75, no. 5–6, pp. 692–695, 2011. pmid:21704937
- 50. Karhade A. V. et al., "Impact of operative length on post-operative complications in meningioma surgery: a NSQIP analysis," Journal of neuro-oncology, vol. 131, no. 1, pp. 59–67, 2017. pmid:27864707
- 51. Fluss R. et al., "The incidence of venous thromboembolism following surgical resection of intracranial and intraspinal meningioma. A systematic review and retrospective study," Clinical Neurology and Neurosurgery, p. 106460, 2021. pmid:33444944
- 52. Sharma M., Ugiliweneza B., Boakye M., Andaluz N., and Williams B. J., "Feasibility of bundled payments in anterior, middle, and posterior cranial fossa skull base meningioma surgery: MarketScan analysis of health care utilization and outcomes," World neurosurgery, vol. 131, pp. e116–e127, 2019. pmid:31323403
- 53. James Z., Leach P. A., and Hayhurst C., "Is 30-day readmission an accurate measure of morbidity in cranial meningioma surgery?," British journal of neurosurgery, vol. 33, no. 4, pp. 379–382, 2019. pmid:30968699
- 54. Abou-Al-Shaar H., Azab M. A., Karsy M., Guan J., Couldwell W. T., and Jensen R. L., "Assessment of costs in open microsurgery and stereotactic radiosurgery for intracranial meningiomas," World neurosurgery, vol. 119, pp. e357–e365, 2018. pmid:30064026
- 55. McKee S. P. et al., "Intracranial meningioma surgery: value-based care determinants in New York state, 1995–2015," World neurosurgery, vol. 118, pp. e731–e744, 2018. pmid:30010072
- 56. Ehresman J. S. et al., "Risk of developing postoperative deficits based on tumor location after surgical resection of an intracranial meningioma," Journal of neurological surgery. Part B, Skull base, vol. 80, no. 1, p. 59, 2019.
- 57. Goldsmith B. J., Wara W. M., Wilson C. B., and Larson D. A., "Postoperative irradiation for subtotally resected meningiomas: A retrospective analysis of 140 patients treated from 1967 to 1990," Journal of neurosurgery, vol. 80, no. 2, pp. 195–201, 1994. pmid:8283256
- 58. De Jesús O., Sekhar L. N., Parikh H. K., Wright D. C., and Wagner D. P., "Long-term follow-up of patients with meningiomas involving the cavernous sinus: recurrence, progression, and quality of life," Neurosurgery, vol. 39, no. 5, pp. 915–920, 1996. pmid:8905745
- 59. Heald J. B., Carroll T. A., and Mair R. J., "Simpson grade: an opportunity to reassess the need for complete resection of meningiomas," Acta neurochirurgica, vol. 156, no. 2, pp. 383–388, 2014. pmid:24193889
- 60. Savardekar A. R. et al., "Differential Tumor Progression Patterns in Skull Base Versus Non–Skull Base Meningiomas: A Critical Analysis from a Long-Term Follow-Up Study and Review of Literature," World neurosurgery, vol. 112, pp. e74–e83, 2018. pmid:29258946
- 61. Oya S. et al., "Effect of adjuvant radiotherapy after subtotal resection for WHO grade I meningioma: a propensity score matching analysis of the Brain Tumor Registry of Japan," Journal of Neuro-Oncology, vol. 153, no. 2, pp. 351–360, 2021. pmid:34002302
- 62. Lagman C. et al., "Adjuvant radiosurgery versus serial surveillance following subtotal resection of atypical meningioma: a systematic analysis," World neurosurgery, vol. 98, pp. 339–346, 2017. pmid:27856384
- 63. Yang C., Fan Y., Shen Z., Wang R., and Bao X., "transsphenoidal versus transcranial Approach for treatment of tuberculum sellae Meningiomas: A systematic Review and Meta-analysis of Comparative studies," Scientific reports, vol. 9, no. 1, pp. 1–10, 2019.
- 64. Komotar R. J., Starke R. M., Raper D. M., Anand V. K., and Schwartz T. H., "Endoscopic endonasal versus open transcranial resection of anterior midline skull base meningiomas," World neurosurgery, vol. 77, no. 5–6, pp. 713–724, 2012. pmid:22120296
- 65. Kawase T., Shiobara R., and Toya S., "Middle fossa transpetrosal-transtentorial approaches for petroclival meningiomas selective pyramid resection and radicality," Acta neurochirurgica, vol. 129, no. 3, pp. 113–120, 1994.
- 66. Aziz K. M. A., Sanan A., van Loveren H. R., Tew J. M. Jr, Keller J. T., and Pensak M. L., "Petroclival meningiomas: predictive parameters for transpetrosal approaches," Neurosurgery, vol. 47, no. 1, pp. 139–152, 2000. pmid:10917357
- 67. Natarajan S. K., Sekhar L. N., Schessel D., and Morita A., "Petroclival meningiomas: multimodality treatment and outcomes at long-term follow-up," Neurosurgery, vol. 60, no. 6, pp. 965–981, 2007. pmid:17538370
- 68. Almefty R., Dunn I. F., Pravdenkova S., Abolfotoh M., and Al-Mefty O., "True petroclival meningiomas: results of surgical management," Journal of neurosurgery, vol. 120, no. 1, pp. 40–51, 2014. pmid:24160473
- 69. Li D. et al., "Surgical management and outcomes of petroclival meningiomas: a single-center case series of 259 patients," Acta neurochirurgica, vol. 155, no. 8, pp. 1367–1383, 2013. pmid:23801089
- 70. Mathiesen T., Gerlich Å., Kihlström L., Svensson M., and Bagger-Sjöbäck D., "Effects of using combined transpetrosal surgical approaches to treat petroclival meningiomas," Neurosurgery, vol. 60, no. 6, pp. 982–992, 2007. pmid:17538371
- 71. Giammattei L. et al., "Petroclival meningiomas: update of current treatment and consensus by the EANS skull base section," Acta Neurochirurgica, vol. 163, no. 6, pp. 1639–1663, 2021. pmid:33740134
- 72. Brokinkel B., Stummer W., and Sporns P., "Simpson grade IV resections of skull base meningiomas: does the postoperative tumor volume impact progression?," Journal of neuro-oncology, vol. 137, no. 1, pp. 219–221, 2018. pmid:29243010
- 73. Nanda A., Bir S. C., Maiti T. K., Konar S. K., Missios S., and Guthikonda B., "Relevance of Simpson grading system and recurrence-free survival after surgery for World Health Organization Grade I meningioma," Journal of neurosurgery, vol. 126, no. 1, pp. 201–211, 2017. pmid:27058201
- 74. Dallan I. et al., "Endoscopic transorbital superior eyelid approach for the management of selected spheno-orbital meningiomas: preliminary experience," Operative Neurosurgery, vol. 14, no. 3, pp. 243–251, 2018. pmid:29462449
- 75. Kong D.-S., Kim Y. H., and Hong C.-K., "Optimal indications and limitations of endoscopic transorbital superior eyelid surgery for spheno-orbital meningiomas," Journal of Neurosurgery, vol. 134, no. 5, pp. 1472–1479, 2020. pmid:32502989