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. 2020 Sep 22;149(3):403–411. doi: 10.1007/s11060-020-03609-2

The ability to return to work: a patient-centered outcome parameter following glioma surgery

Christian Senft 1,5,✉,#, Marion Behrens 2,#, Irina Lortz 1, Katharina Wenger 3,5, Katharina Filipski 4,5,6,7, Volker Seifert 1,5, Marie-Thérèse Forster 1,5
PMCID: PMC7609423  PMID: 32960402

Abstract

Background

With refinements in diagnosis and therapy of gliomas, the importance of survival time as the sole outcome parameter has decreased, and patient-centered outcome parameters have gained interest. Pursuing a profession is an indispensable component of human happiness. The aim of this study was to analyze the professional outcomes besides their neuro-oncological and functional evaluation after surgery for gliomas in eloquent areas.

Methods

We assessed neuro-oncological and functional outcomes of patients with gliomas WHO grades II and III undergoing surgery between 2012 and 2018. All patients underwent routine follow-up and adjuvant treatment. Treatment and survival parameters were collected prospectively. Repercussions of the disease on the patients’ professional status, socio-economic situation, and neurocognitive function were evaluated retrospectively with questionnaires.

Results

We analyzed data of 58 patients with gliomas (WHO II: 9; III: 49). Median patient age was 35.8 years (range 21–63 years). Awake surgery techniques were applied in 32 patients (55.2%). Gross total and subtotal tumor resections were achieved in 33 (56.9%) and 17 (29.3%) patients, respectively, whereas in 8 patients (13.8%) resection had to remain partial. Most patients (n = 46; 79.3%) received adjuvant treatment. Median follow up was 43.8 months (range 11–82 months). After treatment 41 patients (70.7%) were able to resume a working life. Median time until returning to work was 8.0 months (range 0.2–22.0 months). To be younger than 40 at the time of the surgery was associated with a higher probability to return to work (p < .001). Multivariable regression analysis showed that patient age < 40 years as well as occupational group and self-reported fatigue were factors independently associated with the ability to return to work.

Conclusion

The ability to resume professional activities following brain tumor surgery is an important patient-oriented outcome parameter. We found that the majority of patients with gliomas were able to return to work following surgical and adjuvant treatment. Preservation of neurological function is of utmost relevance for individual patients´ quality of life.

Electronic supplementary material

The online version of this article (10.1007/s11060-020-03609-2) contains supplementary material, which is available to authorized users.

Keywords: Return to work, Glioma, Brain tumor surgery, Quality of life

Introduction

For decades, overall and progression-free survival have been the main outcome parameters for patients with gliomas. Gliomas are classified in Grades I–IV, according to morphological and genetic features that are laid out in the revised WHO classification of brain tumors [1]. Prognosis is dismal especially for patients with Grade IV tumors, even when administering multimodal treatment.

Today, personalized medicine approaches according to molecular and epigenetic tumor data tailor adjuvant treatment for patients with lower grade gliomas [2, 3]. With refinements in therapy and improvements in life expectancy, [46] the perception of glioma gradually shifts from a lethal to a chronic disease, with median survival times ranging between 5 and 15 years [69]. Therefore, effects of therapeutic interventions on patients’ quality of life have gained interest in recent years [10, 11].

Surgery plays a major role in the first-line treatment of gliomas [1214]. Preserving neurological function is of upmost importance when it comes to surgical approaches and extent of tumor removal. Many studies have addressed surgical complications as well as sequelae of surgery on neurological outcome [1517]. In contrast to brain tumor patients, more attention has been paid to the long-term health and well-being of people living longer with or having survived cancer [18, 19]. An emphasis has recently been placed to uphold also capabilities for social life, especially in lower-grade gliomas [11]. Latest reports also accentuate the importance of patient-reported outcome parameters [20].

Of particular concern in other cancers, but often overlooked in brain tumor patients due to traditionally poor survival, is the effect of the disease on productivity and work ability. For example, in breast cancer patients, the disruption of working life reportedly threatens not only their economic well-being, but also negatively affects their social relationships and personal satisfaction with life [21, 22].

Pursuing a professional career is an integral part of life and a major source of self-satisfaction and self-fulfillment. Diagnosis of a brain tumor severely disrupts also the professional lives of affected patients. Surgery and recovery from it, as well as any adjuvant treatment, may withhold patients from employment and thus their ability to continue normal lives. Side-effects of treatment or clinical deterioration from tumor progression might cause permanent inability to work. Few studies so far have specifically addressed return-to-work quota in brain tumor patients. Earlier studies focused on cognitive limitations in brain tumor patients, including patients suffering from benign tumors who returned to work, and found tasks requiring working memory highly challenging for these patients [23, 24].

So far, no clinical factors have been clearly established to answer a patient’s question, if and when they may return to work following surgery for glioma. Ng et al. recently presented details on 74 patients with WHO grade II gliomas only [25]. In their series, mean patient age was 35.7 years, and 66 patients (89.2%) were able to return to work. However, they did not find any factor associated with the ability to return to work.

With this report, we aimed to assess the impact of brain tumor surgery and adjuvant treatment on our patients’ occupational status as well as on their social and economic situation, and to identify clinical factors associated with their capability to return to work.

Materials and methods

Patients

We prospectively collected clinical data of patients with newly diagnosed gliomas between 8/2012 and 6/2018 who were scheduled to undergo surgery. All patients gave written consent prior to data collection. Patients who had biopsy only or were found to have WHO grade I or IV tumors were not included in this analysis. Detailed information on the occupational status and the time until patients resumed their professional careers, on their familial and economic situation and on quality-of-life-related aspects were obtained retrospectively by a one-time, detailed questionnaire well after adjuvant treatment.

For this analysis, we included only patients who were professionally active before tumor diagnosis. Patients were considered professionally active when they were employed, self-employed or unemployed but actively seeking for a job. If they were on permanent sick leave or retired, we considered them not professionally active, and these patients were not included. Our patients’ occupational status was assessed and grouped according to the International Standard Classification of Occupation, ISCO-08 [26]. This study was conducted with approval from our local ethics committee (SNO 04/09 and SNO 8/16).

Postsurgical treatment and outcome measures

We looked at factors potentially influencing the ability of patients to resume their working lives, including age, WHO grade and histological subtypes of their respective tumor. Tumors were classified according to the WHO Classification of Tumours of the Central Nervous System 4th edition (2007) or revised 4th edition (2016), respectively, depending on disease onset. IDH mutational status was determined by immunohistochemistry as previously described [27]. Particularly, we assessed treatment interventions and their effect on the patients’ ability to return to work, such as the type or extent of surgery or the type of adjuvant treatment such as radiation and/or chemotherapy. At our institution, patients with tumors near speech-eloquent brain areas undergo awake surgery, whereas preservation of motor function during surgery is routinely assessed by transcortical monitoring and direct cortical or subcortical stimulation techniques in addition to measuring sensory evoked potentials as described previously [28, 29]. The extent of tumor resection was assessed by independent review of pre- and postoperative MRI and determined to be radiologically complete, subtotal (when there was less than 10% of the original volume as residual tumor), or partial, if less than 90% of the original tumor volume were removed. Pre- and postoperatively, an interdisciplinary tumor board gave treatment recommendations based on WHO grades and histological subtypes. All patients were followed up with clinical and radiological examinations in regular, usually three-monthly, intervals. Disease progression was defined according to the RANO criteria [30].

Statistics

All analyses were performed with SPSS version 26 (IBM Inc., Armonk, New York). The association between dichotomized clinical and/or patient specific variables with the ability to return to work was assessed with chi-square or Fisher’s exact test, when appropriate. We performed a logistic regression analysis account for multivariable testing. The time until a professional life was resumed was analyzed with Kaplan–Meier estimates, for multivariate testing we used a cox regression analysis (backward stepwise). P-values < 0.05 were considered to be statistically significant.

Results

For this analysis, 58 patients were included. Due to tumor location, 32 patients (55.2%) underwent tumor resection employing awake mapping and monitoring techniques to allow for intraoperative testing and preservation of speech function, in addition to motor or sensory evoked potential monitoring. All other patients underwent surgery under general anesthesia, employing motor or sensory evoked potential monitoring if deemed necessary according to tumor location. Early postoperative MRI revealed that complete or subtotal tumor removal could be achieved in 33 and 17 patients, respectively (56.9% and 29.3%, resp.), while a partial removal could only be achieved in 8 patients (13.8%). Baseline characteristics are provided in Table 1.

Table 1.

Baseline characteristics

N (%) or median [range]
Gender
 Female 27 (46.6)
 Male 31 (53.4)
Age (years) 35.8 [21.8–63.6]
Preoperative KPS 100 [80–100]
Preoperative seizures
 Yes 41 (70.7)
 No 17 (29.3)
Tumor localization
 Frontal 35 (60.3)
 Temporal 15 (25.9)
 Parietal 7 (12.1)
 Occipital 1 (1.7)
Histopathological diagnosis
 Grade II
  Astrocytoma 4 (6.9)
  Oligodendroglioma 4 (6.9)
  Xanthoastrocytoma 1 (1.7)
 Grade III
  Astrocytoma 31 (53.4)
  Oligodendroglioma 17 (29.3)
  Xanthoastrocytoma 1 (1.7)
IDH mutation
  Yes 47 (81)
  No 11 (19)
Extent of resection
  Gross total resection 33 (56.9)
  Subtotal resection 17 (29.3)
  Partial resection 8 (13.8)
Marital status
  Married/cohabiting 47 (81.0)
  Single/divorced 12 (20.7)

KPS Karnofsky Performance Score, IDH isocitrate dehydrogenase

Following tumor board recommendation and patients’ personal preference, most patients (n = 46, 79.3%) received adjuvant treatment. Chemotherapy or radiation therapy only were administered in 3 patients (5.2%). 43 patients (74.1%) received both, chemotherapy and radiation therapy. 12 patients (20.7%) were treated only surgically, without adjuvant treatment. Before treatment, 41 (70.7%) patients had seizures, whereas 17 (29.3%) did not.

Median follow-up time of all patients was 44.3 months (range 11–82 months). During follow-up, 10 patients (17.2%) showed disease progression and 3 patients have died. Figure 1 depicts Kaplan–Meier curves stratified by WHO grade. Median survival was not reached.

Fig. 1.

Fig. 1

Kaplan Meier graph showing patient survival stratified by WHO grade. Median survival was not reached

Return to work

Following surgery and adjuvant treatment, if applicable, of the 58 patients, 41 (70.7%) were able to return to work, whereas 17 (29.3%) were not; of the latter, 2 patients retired, and 15 patients were on permanent sick leave, including the 3 patients who had died.

When given the questionnaires, the majority of patients (n = 28, 48.3%) reported that their economic status was unchanged at follow-up. However, a large proportion of patients (n = 16, 27.6%) reported a reduction in income, whereas a minority (n = 6, 10.3%) had an increase in income. 5 patients (8.6%) were not willing to share economic information, and data were not available for the patients who had died.

The most prevailing self-reported symptom was fatigue (31 patients out of 51 reports, 60.8%). Half of the patients (25 out of 50 reports) reported memory disturbances, while a minority described difficulties concentrating (22 patients out of 51 reports, 43.1%) or finding words (18 patients out of 51 reports, 35.3%).

At the time of analysis, 32 (55.2%) patients were on antiepileptic drug treatment, but only 6 (10.3%) patients were still experiencing seizures. To treat epilepsy, 19 (32.8%) patients received a monotherapy with levetiracetam and 12 (20.7%) had a combination therapy that included levetiracetam. Details on clinical and socio-economic data at follow-up are given in Table 2.

Table 2.

Survival, clinical and sociodemographic outcomes at follow-up

Outcomes N (%) or Median [range]
Overall follow-up period, months 43.9 [11.2–82.0]
Overall survival
 Alive at last follow-up 55 (94.8)
Oncological outcomea
 Progressive disease 7 (12.7)
 Stable disease 48 (87.3)
Clinical outcomea
 KPS 100 [60–100]
 Seizures 64 (7.3)
 Anticonvulsive therapy 29 (52.7)
 Levetiracetam 19 (34.5)
 Levetiracetam + 1 other AED 10 (18.2)
Marital statusa
 Married/cohabiting 39 (70.9)
 Single/divorced 16 (29.1)
Economic statusa
 Increased income 6 (10.9)
 Decreased income 16 (29.1)
 Income unchanged 28 (50.9)
 Not available 5 (9.1)

KPS Karnofsky performance scale, AED antiepileptic drug

aExcluding deceased patients

Assessment of factors associated with resumption of professional activities

When stratifying between patients younger than 40 years of age and those 40 years and above, younger patients were more likely to resume professional activities than older patients (94.1% vs. 37.5%, Table 3). Patient age was statistically significantly associated with the ability to return to work (P < 0.001, Fisher’s exact test).

Table 3.

Factors associated with return to work according to monovariable analysis

Factor Return to work Total P
Yes No
Age
 < 40 years 32 (94.1%) 2 (5.9%) 34 0.001#
 ≥ 40 years 9 (37.5%) 15 (62.5%) 24
Extent of resection
 Complete/subtotal 37 (75.5%) 12 (24.5%) 49 0.106#
 Partial 4 (24.4%) 5 (55.6%) 9
ISCO-08
 Groups 1–2 23 (85.2%) 4 (14.8%) 27 0.041#
 Groups 3–9 18 (58.1%) 13 (41.9%) 31
Fatiguea
 Yes 20 (64.5%) 11 (35.5%) 31 0.017#
 No 19 (95.0%) 1 (5.0%) 20
Epilepsya
 Controlled 39 (75.0%) 13 (25.0%) 52 0.055#
 Having seizures 2 (33.3%) 4 (66.7%) 6

P values < 0.05 were considered statistically significant

ISCO-08 international standard classifications of occupations (ref. no [26])

#Fisher’s exact test

aAt follow-up

Also, occupational status as determined according to ISCO-08 was associated with return to work. Patients within groups 1–2 were more likely to return to work than patients in groups 3–9 (proportion returning to work 85% vs. 58%; P = 0.041, Fisher’s exact test; Table 4).

Table 4.

Details on occupational groups and their association with return to work

ISCO-08 Groups At presentation At follow-up
RTW, n (%)
Professionally active patients, n Patients alive and not retired, n Yes, n (%) No, n (%)
Group 1—Managers 4 4 3 (75) 1 (25)
Group 2—Professionals 22 21 20 (95.2) 1 (4.8)
Group 3—Technicians and Associate Professionals 12 10 8 (80) 2 (20)
Group 4—Clerical Support Workers 4 4 4 (100) 0
Group 5—Services and Sales Workers 7 7 2 (28.6) 5 (71.4)
Group 7—Craft and Related Trads Workers 6 6 3 (50) 3 (50)
Group 9—Elementary Occupations 3 1 1 (100) 0
58 53 41 (77.4) 12 (22.6)

3 patients have died, 2 have retired

ISCO-08 International standard classification of occupations (ref. no [26]), RTW return to work

There was a trend for a higher chance of patients returning to work after more extensive resections (removal of 90% or more of the preoperative tumor volume) compared to a less extensive resection (proportion returning to work 76% vs. 44%; P = 0.106, Fisher’s exact test, Table 3).

While the proportion of patients reporting fatigue was higher in the subgroup of patients who did not return to work (95% vs. 64% in the subgroup who did return to work; P = 0.017, Fisher’s exact test; Table 3), there were no significant differences between groups regarding other symptoms (supplementary data).

Interestingly, we found that the proportion of patients still experiencing seizures despite antiepileptic drug treatment tended to be higher in the subgroup of patients who did not return to work compared to those who did (30.8% vs. 5.1%; P = 0.055, Fisher’s exact test).

Contrastingly, gender, WHO grade, KPS score at presentation, tumor histology, IDH mutational status, or administration of adjuvant therapy were not found to be statistically significantly associated with the ability of patients to return to work. Likewise, patients’ marital status or the presence of epilepsy at diagnosis was not associated with the ability to return to work (supplementary data).

Logistic regression analysis

We performed a multinomial logistic regression analysis to account for multivariable testing. We included all factors that showed an association according to monovariable analysis. Accordingly, age (P < 0.02), ISCO groups (P < 0.02), and fatigue (P < 0.03) were independently associated with the ability to return to work, while extent of resection (P = 0.38) and uncontrolled seizures (P = 0.18) were not.

Duration of absence from work

Data could be established for 36 out of 41 patients returning to work. We then performed Kaplan–Meier analyses to identify factors potentially associated with an early return to work. The median duration until return to work was 7.5 months (95%-confidence interval [CI] 5.1–9.9 months; Fig. 2). One patient resumed work as early as 7 days following surgery; the longest interval between surgery and resumption of work was 22.0 months.

Fig. 2.

Fig. 2

Kaplan Meier graphs showing the duration until return to work for the entire cohort (a) and stratified by fatigue (b) as reported at follow-up. There was a statistical trend for the differences between patients with or without fatigue to be significant (P < 0.067, Log-rank test)

There were no statistically significant differences in the time until patients returned to work when stratifying according to gender, age, tumor location, type of surgery, extent of resection, tumor histology, WHO grade, IDH mutation, adjuvant radiotherapy, presence of epilepsy at presentation or during follow-up, marital status, or ISCO groups (data not shown; P > 0.1 for all, Log-rank test).

When looking at self-reported symptoms, there was a trend for fatigue only to be associated with the time until professional activities were resumed: 19 patients reporting fatigue returned to work later than 16 patients who did not (median time until return to work: 8.3 vs. 3.5 months; P = 0.067, Log-rank test; Fig. 2). There were no associations between return to work times and word-finding difficulties, memory disturbances, or difficulties concentrating (P > 0.2 for all, Log-rank test).

Likewise, there was a trend for 26 patients receiving chemotherapy to return to work later than 10 patients who did not (median time until return to work: 8.0 vs. 5.6 months; P = 0.058, Log-rank test). The administration of radiation therapy did not affect the duration until return to work on a statistically significant level (P = 0.11, Log-rank test).

Cox-regression analysis

Following a multivariable Cox-regression analysis, the association between chemotherapy on return to work times did not remain independently significant (P = 0.18), while the trend for fatigue persisted (P = 0.076).

Discussion

We observed that most of our patients were able to resume their working lives following brain tumor surgery.

In contrast to the recent study from Ng et al. [25] we also included patients with WHO grade III gliomas, and the proportion of patients receiving adjuvant treatment was greater in our cohort. Importantly, we could establish younger age and higher occupational status variables to be statistically significantly associated with the ability to return to work following multivariate analyses. We also observed that the proportion of patients experiencing fatigue was significantly higher in the subgroup of patients who did not return to work, and fatigue was associated with a longer interval until professional activities could be resumed.

A multitude of literature suggests that employing awake mapping and monitoring techniques is particularly beneficial for glioma patients [16, 17, 3133]. We frequently use awake surgery for tumor resection, and in our current series, more than half of the patients underwent awake craniotomy. Other groups have argued that awake surgery may facilitate return to work [3335], most likely because of the high chance of preserving neurological function. While in general glioma surgery may result in a survival benefit [36, 37] or relief from tumor symptoms [38], our results did not show an effect of extent of resection on the ability or duration of patients returning to work.

Likewise, compared to general anesthesia with cortical and subcortical stimulation for MEP monitoring and continuous SSEP recording, employing awake techniques in our series did not influence the ability to return to work or the time until resumption of work on a statistically significant level. Tumor location clearly contributes to the decision to perform awake or non-awake surgery, but we did not find tumor location to be associated with return to work.

Radiation therapy is known to negatively influence cognitive function, and this effect may occur as a late sequel of therapy [39]. Interestingly, we did not observe any adverse effect of radiation therapy in terms of the patients´ ability to return to work. In contrast, patients who received chemotherapy tended to suspend professional activities for a longer period of time. Adjuvant therapy, however, did not influence the general capability of patients to return to professional lives.

Our results compare well with previously published literature. Altshuler et al. studied the association of genetic alterations with neurocognitive function and ability to return to work in a series of 34 patients with gliomas WHO grades II and III who did not receive adjuvant treatment following surgery [40]. Here, 42% of the patients returned to work within three months following surgery. In our current series, this proportion was only slightly lower with 4 out of 12 patients (33.3%) without adjuvant treatment having returned to work three months after surgery (data not shown).

The results in patients with lower grade gliomas juxtapose with observations made in patients with higher grade tumors. Starnoni et al. reported that fewer than 20% of patients with glioblastoma were able to return to work [41]. Very recently Yoshida et al. reported on 50 patients undergoing awake surgery for gliomas of WHO grades II–IV [35]. In their series, only 54% of patients were able to return to work. We did not observe an association between WHO grade and the ability to return to work, but the duration of absence from work was longer for patients with WHO grade III tumors compared to WHO grades II, albeit this difference was not significant (8.0 vs. 5.6 months, data not shown).

Median age of patients harboring lower grade gliomas is below 50 years, and a vast majority of patients are employed when being confronted with tumor diagnosis. Aside from receiving life-prolonging treatment, being able to generate income and sustain their lives independently is essential for patients’ well-being and happiness [42, 43]. Of note, we found that patients with higher occupational status, i.e. groups 1 and 2 according to ISCO-08, were more likely to return to work than patients with less elaborate professions which usually are lower paid for. We can only speculate as to how this can be explained, but for these groups their workplaces might provide greater opportunities for self-fulfillment in addition to above-average salaries.

Our study is certainly limited by the fact that we were not able to determine whether patients who did not return to work made that decision due to disease related factors or personal choice. Another limitation is the fact that a structured assessment of working status was not repeatedly performed during the regular follow-up, but only once.

Due to legal or socio-cultural differences [44], the results observed in our study might very well be different from other regions of the world. In a recent study from Japan for example, being the sole breadwinner in contrast to patient age was a predictive factor for returning to work according to multivariate analysis [35]. In our cohort, marital status did not seem to play a role. With our social security system being very supportive, motivating pressures to return to work may be lower in our country compared to others where financial insecurity is higher.

The ability of patients to maintain or return to professional activities after treatment is influenced by multiple intrinsic and extrinsic factors. Thus, variables that affect patients’ capability or motivation to return to work may be identified only in larger cohorts. We did, however, observe that fatigue as a frequently encountered burden of gliomas is of great importance when it comes to patients’ ability to return to work following glioma surgery and adjuvant treatment. Practitioners should emphasize this aspect, as other factors like age or occupational status cannot be therapeutically addressed.

We conclude that the ability to return to work is an important patient-centered outcome parameter in glioma treatment that should be evaluated more systematically.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Acknowledgements

The authors would like to thank M. Heibel for technical support.

Funding

Open Access funding provided by Projekt DEAL.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Christian Senft and Marion Behrens have contributed equally.

References

  • 1.Louis D, Ohgaki H, Wiestler O. World Health Organization histological classification of tumours of the central nervous system. France: International Agency for Research on Cancer; 2016. [Google Scholar]
  • 2.Baumert BG, Hegi ME, van den Bent MJ, von Deimling A, Gorlia T, Hoang-Xuan K, Brandes AA, Kantor G, Taphoorn MJB, Hassel MB, Hartmann C, Ryan G, Capper D, Kros JM, Kurscheid S, Wick W, Enting R, Reni M, Thiessen B, Dhermain F, Bromberg JE, Feuvret L, Reijneveld JC, Chinot O, Gijtenbeek JMM, Rossiter JP, Dif N, Balana C, Bravo-Marques J, Clement PM, Marosi C, Tzuk-Shina T, Nordal RA, Rees J, Lacombe D, Mason WP, Stupp R. Temozolomide chemotherapy versus radiotherapy in high-risk low-grade glioma (EORTC 22033–26033): a randomised, open-label, phase 3 intergroup study. Lancet Oncol. 2016;17:1521–1532. doi: 10.1016/S1470-2045(16)30313-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Buckner JC, Shaw EG, Pugh SL, Chakravarti A, Gilbert MR, Barger GR, Coons S, Ricci P, Bullard D, Brown PD, Stelzer K, Brachman D, Suh JH, Schultz CJ, Bahary JP, Fisher BJ, Kim H, Murtha AD, Bell EH, Won M, Mehta MP, Curran WJ., Jr Radiation plus procarbazine, CCNU, and vincristine in low-grade glioma. N Engl J Med. 2016;374:1344–1355. doi: 10.1056/NEJMoa1500925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Wijnenga MMJ, French PJ, Dubbink HJ, Dinjens WNM, Atmodimedjo PN, Kros JM, Smits M, Gahrmann R, Rutten GJ, Verheul JB, Fleischeuer R, Dirven CMF, Vincent A, van den Bent MJ. The impact of surgery in molecularly defined low-grade glioma: an integrated clinical, radiological, and molecular analysis. Neuro Oncol. 2018;20:103–112. doi: 10.1093/neuonc/nox176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Kinslow CJ, Garton ALA, Rae AI, Marcus LP, Adams CM, McKhann GM, Sisti MB, Connolly ES, Bruce JN, Neugut AI, Sonabend AM, Canoll P, Cheng SK, Wang TJC. Extent of resection and survival for oligodendroglioma: a U.S. population-based study. J Neurooncol. 2019;144:591–601. doi: 10.1007/s11060-019-03261-5. [DOI] [PubMed] [Google Scholar]
  • 6.Choi J, Kim SH, Ahn SS, Choi HJ, Yoon HI, Cho JH, Roh TH, Kang SG, Chang JH, Suh CO. Extent of resection and molecular pathologic subtype are potent prognostic factors of adult WHO grade II glioma. Sci Rep. 2020;10:2086. doi: 10.1038/s41598-020-59089-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Iwadate Y, Matsutani T, Hara A, Hirono S, Ikegami S, Kobayashi M, Ito D, Kawauchi D, Horiguchi K, Tamiya A, Higuchi Y. Eighty percent survival rate at 15 years for 1p/19q co-deleted oligodendroglioma treated with upfront chemotherapy irrespective of tumor grade. J Neurooncol. 2019;141:205–211. doi: 10.1007/s11060-018-03027-5. [DOI] [PubMed] [Google Scholar]
  • 8.Lin AJ, Kane LT, Molitoris JK, Smith DR, Dahiya S, Badiyan SN, Wang TJC, Kruser TJ, Huang J. A multi-institutional analysis of clinical outcomes and patterns of care of 1p/19q codeleted oligodendrogliomas treated with adjuvant or salvage radiation therapy. J Neurooncol. 2020;146:121–130. doi: 10.1007/s11060-019-03344-3. [DOI] [PubMed] [Google Scholar]
  • 9.Pala A, Nadji-Ohl M, Faust K, Ruckriegel S, Roder C, von der Brelie C, Forster MT, Lobel F, Schommer S, Lohr M, Grubel N, Rothenbacher D, Konig R, Engelke J, Schmitz B, Wirtz CR, Senft C, Rohde V, Tatagiba M, Ernestus RI, Vajkoczy P, Ganslandt O, Nagel G, Coburger J. Multicentric registry study on epidemiological and biological disease profile as well as clinical outcome in patients with low-grade gliomas: The LoG-Glio Project. J Neurol Surg A. 2020;81:48–57. doi: 10.1055/s-0039-1693650. [DOI] [PubMed] [Google Scholar]
  • 10.Hickmann AK, Hechtner M, Nadji-Ohl M, Janko M, Reuter AK, Kohlmann K, Haug M, Gruninger S, Deininger M, Ganslandt O, Konig J, Wirtz CR, Coburger J, Renovanz M. Evaluating patients for psychosocial distress and supportive care needs based on health-related quality of life in primary brain tumors: a prospective multicenter analysis of patients with gliomas in an outpatient setting. J Neurooncol. 2017;131:135–151. doi: 10.1007/s11060-016-2280-0. [DOI] [PubMed] [Google Scholar]
  • 11.Nickel K, Renovanz M, Konig J, Stockelmaier L, Hickmann AK, Nadji-Ohl M, Engelke J, Weimann E, Freudenstein D, Ganslandt O, Bullinger L, Wirtz CR, Coburger J. The patients' view: impact of the extent of resection, intraoperative imaging, and awake surgery on health-related quality of life in high-grade glioma patients-results of a multicenter cross-sectional study. Neurosurg Rev. 2018;41:207–219. doi: 10.1007/s10143-017-0836-x. [DOI] [PubMed] [Google Scholar]
  • 12.Mandonnet E, Wager M, Almairac F, Baron MH, Blonski M, Freyschlag CF, Barone F, Fontaine D, Pallud J, Hegi M, Viegas C, Zetterling M, Spena G, Goodden J, Rutten GJ, Taillandier L, Foroglu N, Darlix A, Skrap M, Martino J, von Campe G, Madadaki C, Gayat E, de Witt HP, Gil Robles S, Sarubbo S, Santarius T, Bello L, Forster MT, Duffau H. Survey on current practice within the European Low-Grade Glioma Network: where do we stand and what is the next step? Neurooncol Pract. 2017;4:241–247. doi: 10.1093/nop/npw031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Scherer M, Ahmeti H, Roder C, Gessler F, Jungk C, Pala A, Mayer B, Senft C, Tatagiba M, Synowitz M, Wirtz CR, Unterberg AW, Coburger J. Surgery for diffuse WHO Grade II gliomas: volumetric analysis of a multicenter retrospective cohort from the German Study Group for intraoperative magnetic resonance imaging. Neurosurgery. 2020;86:E64–E74. doi: 10.1093/neuros/nyz397. [DOI] [PubMed] [Google Scholar]
  • 14.Darlix A, Mandonnet E, Freyschlag CF, Pinggera D, Forster MT, Voss M, Steinbach J, Loughrey C, Goodden J, Banna G, Di Blasi C, Foroglou N, Hottinger AF, Baron MH, Pallud J, Duffau H, Rutten GJ, Almairac F, Fontaine D, Taillandier L, Pessanha Viegas C, Albuquerque L, von Campe G, Urbanic-Purkart T, Blonski M. Chemotherapy and diffuse low-grade gliomas: a survey within the European Low-Grade Glioma Network. Neurooncol Pract. 2019;6:264–273. doi: 10.1093/nop/npy051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.De Witt Hamer PC, Robles SG, Zwinderman AH, Duffau H, Berger MS. Impact of intraoperative stimulation brain mapping on glioma surgery outcome: a meta-analysis. J Clin Oncol. 2012;30:2559–2565. doi: 10.1200/JCO.2011.38.4818. [DOI] [PubMed] [Google Scholar]
  • 16.Yordanova YN, Moritz-Gasser S, Duffau H. Awake surgery for WHO Grade II gliomas within "noneloquent" areas in the left dominant hemisphere: toward a "supratotal" resection. J Neurosurg. 2011;115:232–239. doi: 10.3171/2011.3.JNS101333. [DOI] [PubMed] [Google Scholar]
  • 17.Nakajima R, Kinoshita M, Okita H, Yahata T, Nakada M. Glioma surgery under awake condition can lead to good independence and functional outcome excluding deep sensation and visuospatial cognition. Neurooncol Pract. 2019;6:354–363. doi: 10.1093/nop/npy054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Ganz PA. Why and how to study the fate of cancer survivors: observations from the clinic and the research laboratory. Eur J Cancer. 2003;39:2136–2141. doi: 10.1016/s0959-8049(03)00489-1. [DOI] [PubMed] [Google Scholar]
  • 19.Syse A, Tretli S, Kravdal O. Cancer's impact on employment and earnings–a population-based study from Norway. J Cancer Surviv. 2008;2:149–158. doi: 10.1007/s11764-008-0053-2. [DOI] [PubMed] [Google Scholar]
  • 20.Onken J, Goerling U, Heinrich M, Pleissner S, Krex D, Vajkoczy P, Misch M. Patient reported outcome (PRO) among high-grade glioma patients receiving TTFields treatment: a two center observational study. Front Neurol. 2019;10:1026. doi: 10.3389/fneur.2019.01026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Chirikos TN, Russell-Jacobs A, Jacobsen PB. Functional impairment and the economic consequences of female breast cancer. Women Health. 2002;36:1–20. doi: 10.1300/J013v36n01_01. [DOI] [PubMed] [Google Scholar]
  • 22.Maunsell E, Drolet M, Brisson J, Brisson C, Masse B, Deschenes L. Work situation after breast cancer: results from a population-based study. J Natl Cancer Inst. 2004;96:1813–1822. doi: 10.1093/jnci/djh335. [DOI] [PubMed] [Google Scholar]
  • 23.Calvio L, Feuerstein M, Hansen J, Luff GM. Cognitive limitations in occupationally active malignant brain tumour survivors. Occup Med (Lond) 2009;59:406–412. doi: 10.1093/occmed/kqp094. [DOI] [PubMed] [Google Scholar]
  • 24.Collins C, Gehrke A, Feuerstein M. Cognitive tasks challenging brain tumor survivors at work. J Occup Environ Med. 2013;55:1426–1430. doi: 10.1097/JOM.0b013e3182a64206. [DOI] [PubMed] [Google Scholar]
  • 25.Ng S, Herbet G, Moritz-Gasser S, Duffau H. Return to work following surgery for incidental diffuse low-grade glioma: a prospective series with 74 patients. Neurosurgery. 2019 doi: 10.1093/neuros/nyz513. [DOI] [PubMed] [Google Scholar]
  • 26.International Standard Classification of Occupations . Structure, group definitions and correspondence tables. Geneva: ILO Publications, International Labour Office; 2012. p. 420. [Google Scholar]
  • 27.Gessler F, Bernstock JD, Braczynski A, Lescher S, Baumgarten P, Harter PN, Mittelbronn M, Wu T, Seifert V, Senft C. Surgery for glioblastoma in light of molecular markers: impact of resection and MGMT promoter methylation in newly diagnosed IDH-1 wild-type glioblastomas. Neurosurgery. 2019;84:190–197. doi: 10.1093/neuros/nyy049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Szelenyi A, Senft C, Jardan M, Forster MT, Franz K, Seifert V, Vatter H. Intra-operative subcortical electrical stimulation: a comparison of two methods. Clin Neurophysiol. 2011;122:1470–1475. doi: 10.1016/j.clinph.2010.12.055. [DOI] [PubMed] [Google Scholar]
  • 29.Senft C, Forster MT, Bink A, Mittelbronn M, Franz K, Seifert V, Szelenyi A. Optimizing the extent of resection in eloquently located gliomas by combining intraoperative MRI guidance with intraoperative neurophysiological monitoring. J Neurooncol. 2012;109:81–90. doi: 10.1007/s11060-012-0864-x. [DOI] [PubMed] [Google Scholar]
  • 30.Wen PY, Macdonald DR, Reardon DA, Cloughesy TF, Sorensen AG, Galanis E, Degroot J, Wick W, Gilbert MR, Lassman AB, Tsien C, Mikkelsen T, Wong ET, Chamberlain MC, Stupp R, Lamborn KR, Vogelbaum MA, van den Bent MJ, Chang SM. Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol. 2010;28:1963–1972. doi: 10.1200/JCO.2009.26.3541. [DOI] [PubMed] [Google Scholar]
  • 31.Eseonu CI, Rincon-Torroella J, ReFaey K, Lee YM, Nangiana J, Vivas-Buitrago T, Quinones-Hinojosa A. Awake craniotomy vs craniotomy under general anesthesia for perirolandic gliomas: evaluating perioperative complications and extent of resection. Neurosurgery. 2017;81:481–489. doi: 10.1093/neuros/nyx023. [DOI] [PubMed] [Google Scholar]
  • 32.Gerritsen JKW, Vietor CL, Rizopoulos D, Schouten JW, Klimek M, Dirven CMF, Vincent AJE. Awake craniotomy versus craniotomy under general anesthesia without surgery adjuncts for supratentorial glioblastoma in eloquent areas: a retrospective matched case-control study. Acta Neurochir (Wien) 2019;161:307–315. doi: 10.1007/s00701-018-03788-y. [DOI] [PubMed] [Google Scholar]
  • 33.Ng JCH, See AAQ, Ang TY, Tan LYR, Ang BT, King NKK. Effects of surgery on neurocognitive function in patients with glioma: a meta-analysis of immediate post-operative and long-term follow-up neurocognitive outcomes. J Neurooncol. 2019;141:167–182. doi: 10.1007/s11060-018-03023-9. [DOI] [PubMed] [Google Scholar]
  • 34.Mandonnet E, De Witt HP, Poisson I, Whittle I, Bernat AL, Bresson D, Madadaki C, Bouazza S, Ursu R, Carpentier AF, George B, Froelich S. Initial experience using awake surgery for glioma: oncological, functional, and employment outcomes in a consecutive series of 25 cases. Neurosurgery. 2015;76:382–389. doi: 10.1227/NEU.0000000000000644. [DOI] [PubMed] [Google Scholar]
  • 35.Yoshida A, Motomura K, Natsume A, Chalise L, Iijima K, Hara D, Kadono I, Wakai K, Wakabayashi T. Preoperative predictive factors affecting return to work in patients with gliomas undergoing awake brain mapping. J Neurooncol. 2020;146:195–205. doi: 10.1007/s11060-019-03371-0. [DOI] [PubMed] [Google Scholar]
  • 36.Roelz R, Strohmaier D, Jabbarli R, Kraeutle R, Egger K, Coenen VA, Weyerbrock A, Reinacher PC. Residual tumor volume as best outcome predictor in low grade glioma - a nine-years near-randomized survey of surgery vs biopsy. Sci Rep. 2016;6:32286. doi: 10.1038/srep32286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Jakola AS, Skjulsvik AJ, Myrmel KS, Sjavik K, Unsgard G, Torp SH, Aaberg K, Berg T, Dai HY, Johnsen K, Kloster R, Solheim O. Surgical resection versus watchful waiting in low-grade gliomas. Ann Oncol. 2017;28:1942–1948. doi: 10.1093/annonc/mdx230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Still MEH, Roux A, Huberfeld G, Bauchet L, Baron MH, Fontaine D, Blonski M, Mandonnet E, Guillevin R, Guyotat J, Taillandier L, Capelle L, Duffau H, Pallud J. Extent of resection and residual tumor thresholds for postoperative total seizure freedom in epileptic adult patients harboring a supratentorial diffuse low-grade glioma. Neurosurgery. 2019;85:E332–E340. doi: 10.1093/neuros/nyy481. [DOI] [PubMed] [Google Scholar]
  • 39.Jacob J, Durand T, Feuvret L, Mazeron JJ, Delattre JY, Hoang-Xuan K, Psimaras D, Douzane H, Ribeiro M, Capelle L, Carpentier A, Ricard D, Maingon P. Cognitive impairment and morphological changes after radiation therapy in brain tumors: a review. Radiother Oncol. 2018;128:221–228. doi: 10.1016/j.radonc.2018.05.027. [DOI] [PubMed] [Google Scholar]
  • 40.Altshuler DB, Wang L, Zhao L, Miklja Z, Linzey J, Brezzell A, Kakaizada S, Krishna S, Orringer DA, Briceno EM, Gabel N, Hervey-Jumper SL. BDNF, COMT, and DRD2 polymorphisms and ability to return to work in adult patients with low- and high-grade glioma. Neurooncol Pract. 2019;6:375–385. doi: 10.1093/nop/npy059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Starnoni D, Berthiller J, Idriceanu TM, Meyronet D, d'Hombres A, Ducray F, Guyotat J. Returning to work after multimodal treatment in glioblastoma patients. Neurosurg Focus. 2018;44:E17. doi: 10.3171/2018.3.FOCUS1819. [DOI] [PubMed] [Google Scholar]
  • 42.Main DS, Nowels CT, Cavender TA, Etschmaier M, Steiner JF. A qualitative study of work and work return in cancer survivors. Psychooncology. 2005;14:992–1004. doi: 10.1002/pon.913. [DOI] [PubMed] [Google Scholar]
  • 43.Schubart JR, Kinzie MB, Farace E. Caring for the brain tumor patient: family caregiver burden and unmet needs. Neuro Oncol. 2008;10:61–72. doi: 10.1215/15228517-2007-040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Vanacor C, Duffau H. Analysis of legal, cultural, and socioeconomic parameters in low-grade glioma management: variability across countries and implications for awake surgery. World Neurosurg. 2018;120:47–53. doi: 10.1016/j.wneu.2018.08.155. [DOI] [PubMed] [Google Scholar]

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