{"id":9397,"date":"2026-04-08T07:54:28","date_gmt":"2026-04-08T07:54:28","guid":{"rendered":"https:\/\/www.proefschriftmaken.nl\/portfolio\/melissa-kerkhof\/"},"modified":"2026-04-23T08:11:40","modified_gmt":"2026-04-23T08:11:40","slug":"melissa-kerkhof","status":"publish","type":"us_portfolio","link":"https:\/\/www.proefschriftmaken.nl\/en\/portfolio\/melissa-kerkhof\/","title":{"rendered":"Melissa Kerkhof"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":8,"featured_media":13303,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"us_portfolio_category":[45],"class_list":["post-9397","us_portfolio","type-us_portfolio","status-publish","has-post-thumbnail","hentry","us_portfolio_category-new-template"],"acf":{"naam_van_het_proefschift":"ANTIEPILEPTIC AND ANTITUMOR TREATMENT IN BRAIN TUMOR PATIENTS: IMPACT ON CLINICAL AND RADIOLOGICAL OUTCOME","samenvatting":"Met dit proefschrift heb ik geprobeerd een leidraad te geven voor de dagelijkse neuro-oncologische praktijk. Enerzijds heb ik mij gericht op behandeling van epilepsie bij pati\u00ebnten met een glioom, anderzijds op de beoordeling van de beeldvorming na behandeling van pati\u00ebnten met een glioom of hersenmetastase(n).\n\nDeel I van dit proefschrift richtte zich op de rol van de epilepsie behandeling bij glioom pati\u00ebnten in relatie tot klinische uitkomstmaten zoals overleving en de gevolgen van het stoppen van anti-epileptica op recidief epileptische aanvallen in relatie tot de radiologische uitkomst.\n\nDeel II van dit proefschrift richtte zich op de impact van de hersentumor behandeling op klinische en radiologische uitkomsten, in het bijzonder op het vaststellen van (pseudo) progressie.\n\nDeel I: De rol van de epilepsie behandeling in relatie tot klinische en radiologische uitkomsten\n\nEpileptische aanvallen komen frequent voor bij pati\u00ebnten met een hersentumor en kunnen grote invloed hebben op functioneren en kwaliteit van leven. Epileptische aanvallen komen voor bij 60-90% van de pati\u00ebnten met een laaggradige glioom en bij 25-60% van de pati\u00ebnten met een hooggradige glioom. In hoofdstuk 2 bestudeerden we het effect van valproaat (VPA) en levetiracetam (LEV) op de aanvalscontrole in pati\u00ebnten met een glioblastoom. Er werd gestart met VPA- of LEV- monotherapie, wat in 40% van de pati\u00ebnten heeft geleid tot aanvalsvrijheid. In de loop van de ziekte werd aanvalsvrijheid bereikt in 78% van de pati\u00ebnten op VPA-monotherapie, in 70% op LEV-monotherapie en in 60% op de combinatie van VPA en LEV indien \u00e9\u00e9n van beiden niet effectief was. Er werd, gezien het potenti\u00eble antitumor effect van VPA, een aanvullende analyse verricht naar het effect van VPA op de overleving. We vonden dat pati\u00ebnten met een glioblastoom die VPA in combinatie met temozolomide (TMZ) gebruikten, een langere mediane overleving hadden van 69 weken in vergelijking met 61 weken in de groep zonder VPA (hazard ratio 0.63; 95% CI: 0.43\u20130.92), na correctie voor leeftijd, mate van resectie en O6-DNA methylguanine-methyltransferase (MGMT) promotor methylatie.\n\nGlioom pati\u00ebnten kunnen met anti-epileptica aanvalsvrijheid bereiken. De hersentumor behandeling kan daarnaast ook bijdragen aan afname van de aanvalsfrequentie. Na resectie en radiotherapie wordt respectievelijk 53-87% en 32-75% van de laaggradig glioom pati\u00ebnten aanvalsvrij. Chemotherapie resulteert in een \u226550% aanvalsreductie in 48-78% van de laaggradig glioom pati\u00ebnten. In hoofdstuk 3 onderzochten we de noodzaak om anti-epileptica voort te zetten in klinisch en radiologisch stabiele laaggradige en anaplastische glioom pati\u00ebnten die ten minste \u00e9\u00e9n jaar aanvalsvrij waren, gerekend vanaf het einde van de laatste hersentumor behandeling. We bestudeerden zowel het proces van \u2018shared decision making\u2019 tussen pati\u00ebnt en arts ten aanzien van het stoppen van anti-epileptica, als het effect van stoppen van anti-epileptica op recidief epileptische aanvallen. Na overeenstemming tussen zowel pati\u00ebnt als behandelend neuro-oncoloog tot participatie in de studie, werd een gezamenlijk besluit genomen ten aanzien van het al dan niet stoppen van de anti-epileptica. Bij 65% van de in totaal 71 pati\u00ebnten werd besloten de anti-epileptica te stoppen en bij 35% van de pati\u00ebnten om de anti-epileptica te continueren. In de groep die de anti-epileptica stopte, kreeg 26% een recidief epileptische aanval na een mediane follow-up van 2.2 jaar. Van deze pati\u00ebnten bleek 58% tumorprogressie te hebben, waarvan 3 pati\u00ebnten al binnen 3 maanden na het stoppen van de anti-epileptica. Slechts 8% van de pati\u00ebnten in de groep die anti-epileptica continueerde had een recidief epileptische aanval, waarvan \u00e9\u00e9n pati\u00ebnt ook tumorprogressie had.\n\nDeel II: De impact van de hersentumor behandeling op klinische en radiologische uitkomsten\n\nE\u00e9n van de grootste uitdagingen in de neuro-oncologische praktijk is de interpretatie van de beeldvorming na hersentumor behandeling. De behandeling kan namelijk behandelingsgerelateerde effecten op de beeldvorming induceren, lijkend op tumorprogressie, wat ook wel pseudoprogressie wordt genoemd. De conventionele MRI met contrastmiddel is helaas onvoldoende geschikt om het onderscheid te maken tussen tumorprogressie en pseudoprogressie. Geavanceerde MRI-technieken zijn mogelijk meer geschikt om accuraat de status van de hersentumor na behandeling vast te stellen. We bestudeerden om die reden de waarde van de veelgebruikte kwalitatieve beoordeling van de dynamische susceptibiliteits contrast (DSC) perfusie MRI bij hersentumorpati\u00ebnten. De DSC-perfusie MRI maakt het mogelijk het cerebraal bloedvolume zichtbaar te maken door beoordeling van het relatieve cerebraal bloedvolume (rCBV), wat een maat is voor microvasculaire proliferatie in tumorweefsel. De kwalitatieve DSC-perfusie MRI kan gebruikt worden om tumorprogressie van pseudoprogressie te onderscheiden. Dit onderscheid heeft belangrijke klinische en therapeutische consequenties, aangezien in geval van tumorprogressie vaak een aanpassing van de hersentumor behandeling moet worden gedaan. Om de waarde en de reproduceerbaarheid van de kwalitatieve beoordeling van de DSC-perfusie MRI te bestuderen stelden we eerst de interobserver variabiliteit van DSC-perfusie MRI-parameters vast in glioblastoom pati\u00ebnten behandeld met TMZ-chemoradiatie (hoofdstuk 4). Er werd een goede interobserver overeenkomst gevonden bij de kwalitatieve beoordeling van de rCBV overzichten (kappa waarde = 0.63). De interobserver overeenkomst van de interpretatie van de DSC-perfusie MRI daarentegen was veel slechter (kappa waarde = 0.23). De uiteindelijke radiologische beoordeling van de status van de tumor (volledige tumor respons, partiele tumor respons, progressieve ziekte of stabiele ziekte) waarbij zowel de standaard MRI als de DSC-perfusie MRI-beelden","summary":"REFERENCES\n\n1. Sperduto PW, Kased N, Roberge D, et al. Report on the Graded Prognostic Assessment: An Accurate and Facile Diagnosis-Specific Tool to Estimate Survival for Patients With Brain Metastases. J Clin Oncol. 2012;30(4):419-425.\n2. Sneed PK, Mendez J, Vemer-van den Hoek JG, et al. Adverse radiation effect after stereotactic radiosurgery for brain metastases: incidence, time course, and risk factors. J Neurosurg. 2015;123(2):373-386.\n3. Chao ST, Ahluwalia MS, Barnett GH, et al. Challenges with the diagnosis and treatment of cerebral radiation necrosis. Int J Radiat Oncol Biol Phys. 2013;87(3):449-457.\n4. Romagna A, Unterrainer M, Schmid-Tannwald C, et al. Suspected recurrence of brain metastases after focused high dose radiotherapy: can [ 18 FZFET-PET overcome diagnostic uncertainties? Radiat Oncol. 2016;11.\n5. Menoux I, Armspach J-P, No\u00ebl G, Antoni D. Imaging methods used in the differential diagnosis between brain tumour relapse and radiation necrosis after stereotactic radiosurgery of brain metastases: Literature review. Cancer\/Radiotherapie. 2016;20(8).\n6. Menoux I, No\u00ebl G, Namer I, Antoni D. PET scan and NMR spectroscopy for the differential diagnosis between brain radiation necrosis and tumour recurrence after stereotactic irradiation of brain metastases: Place in the decision tree. Cancer\/Radiotherapie. 2017;21(5).\n7. Zach L, Guez D, Last D, et al. Delayed contrast extravasation MRI: A new paradigm in neuro-oncology. Neuro Oncol. 2015;17(3):457-465.\n8. Raimbault A, Cazals X, Lauvin MA, Destrieux C, Chapet S, Cottier JP. Radionecrosis of malignant glioma and cerebral metastasis: A diagnostic challenge in MRI. Diagn Interv Imaging. 2014;95(10):985-1000.\n9. Hoefnagels FWA, Lagerwaard FJ, Sanchez E, et al. Radiological progression of cerebral metastases after radiosurgery: Assessment of perfusion MRI for differentiating between necrosis and recurrence. J Neurol. 2009;256(6):878-887.\n10. Barajas RF, Chang JS, Sneed PK, Segal MR, McDermott MW, Cha S. Distinguishing recurrent intra-axial metastatic tumor from radiation necrosis following gamma knife radiosurgery using dynamic susceptibility-weighted contrast-enhanced perfusion MR imaging. Am J Neuroradiol. 2009;30(2):367-372.\n11. Essig M, Waschkies M, Wenz F, Debus J, Hentrich HR, Knopp M V. Assessment of Brain Metastases with Dynamic Susceptibility-weighted Contrast-enhanced MR Imaging: Initial Results. Radiology. 2003;228(1):193-199.\n12. Jakubovic R, Sahgal A, Soliman H, et al. Magnetic resonance imaging-based tumour perfusion parameters are biomarkers predicting response after radiation to brain metastases. Clin Oncol. 2014;26(11):704-712.\n13. Kerkhof M, Hagenbeek RE, van der Kallen BFW, et al. Interobserver variability in the radiological assessment of magnetic resonance imaging (MRI) including perfusion MRI in glioblastoma multiforme. Eur J Neurol. 2016;23(10):1528-1533.\n14. Hygino Da Cruz LC, Rodriguez I, Domingues RC, Gasparetto EL, Sorensen AG. Pseudoprogression and pseudoresponse: Imaging challenges in the assessment of posttreatment glioma. Am J Neuroradiol. 2011;32(11):1978-1985.\n15. Minniti G, Clarke E, Lanzetta G, et al. Stereotactic radiosurgery for brain metastases: analysis of outcome and risk of brain radionecrosis. Radiat Oncol. 2011;6(1):48.\n16. Huang J, Wang AM, Shetty A, et al. Differentiation between intra-axial metastatic tumor progression and radiation injury following fractionated radiation therapy or stereotactic radiosurgery using MR spectroscopy, perfusion MR imaging or volume progression modeling. Magn Reson Imaging. 2011;29(7):993-1001.\n17. Lev M, Hochberg F. Perfusion Magnetic Resonance Imaging to Assess Brain Tumor Responses to New Therapies. Cancer Control. 1998;5(2):115-123.\n18. Faro SH, Mohamed FB, Law M, Ulmer JL. Functional Neuroradiology: Principles and Clinical Applications.; 2012.\n\nThe goal of this thesis was to provide guidance for the neuro-oncologist\u2019s daily clinical practice with respect to tailoring antiepileptic drug (AED) treatment and improving the radiological assessment of tumor response and progression in patients with gliomas and brain metastases. Part I of this thesis focused on the impact of AEDs on clinical outcome, such as survival, and the consequence of AED withdrawal on seizure recurrence and radiological outcome. Part II focused on the impact of antitumor treatment on clinical and radiological outcome, especially regarding the assessment of (pseudo)progression.\n\nPART I: The role of antiepileptic treatment in relation to clinical and radiological outcome\n\nSeizures are common in brain tumor patients and can significantly impact their functioning and quality of life. A seizure frequency of up to 60-90% is seen in low-grade glioma and 25-60% in high-grade glioma patients. 1\u20133 In chapter 2, we investigated the efficacy of valproic acid (VPA) and levetiracetam (LEV) on seizure control in glioblastoma patients during treatment and follow-up. Monotherapy with either VPA or LEV was initially instituted, resulting in seizure freedom in about 40% of patients on either VPA or LEV monotherapy. During follow-up seizure freedom was achieved in 78% of patients on VPA monotherapy, 70% on LEV monotherapy and 60% on combined VPA\/LEV treatment if either one was not effective enough. As evidence exists on a potential antitumor effect of VPA, an additional analysis on the effect of VPA on survival was performed. We found that glioblastoma patients using VPA in combination with temozolomide (TMZ) showed a longer median survival of 69 weeks as compared to 61 weeks in the group without VPA 6 (hazard ratio 0.63; 95% CI: 0.43\u20130.92) when adjusting for age, extent of resection, and O6-DNA methylguanine-methyltransferase (MGMT) promoter methylation status.\n\nGlioma patients may achieve sustained seizure freedom on AED. Antitumor treatment for glioma can further contribute to a reduction in seizure frequency. After surgical resection or radiotherapy, 53-87% and 32-75% of patients with low grade glioma, respectively, 7 becomes seizure free. Chemotherapy treatment results in a \u226550% reduction in seizure frequency in 48-78% of low-grade glioma patients. 4\u20139 10,11 In chapter 3 we evaluated the need for continuation of AEDs in clinically and radiologically stable low-grade and anaplastic glioma patients with seizure freedom for at least one year after antitumor treatment. We studied the decision-making process on AED withdrawal in patients and physicians as well as seizure recurrence rate. After approval for inclusion by both the patient and their treating neuro-oncologist, they made a shared decision about withdrawal or further continuation of AED treatment. We studied 71 patients, in whom it was decided to withdraw AED treatment in 65% of patients and to continue AED treatment in 35%. Of the patients in the withdrawal group, 26% experienced seizure recurrence during a mean follow-up of 2.2 years. Of these patients, 58% appeared to have tumor progression, of which 3 patients within 3 months after withdrawal. Only 8% of the patients in the AED continuation group experienced seizure recurrence, of which one patient showed tumor progression.\n\nPART II: The impact of antitumor treatment on clinical and radiological outcome\n\nOne of the major challenges in clinical practice is the interpretation of follow-up imaging in brain tumor patients treated with antitumor therapy. Antitumor treatment can induce treatment related effects on imaging which mimic tumor progression. Neuro-oncologists are frequently confronted with the diagnostic dilemma of differentiating progressive disease (PD) from treatment related effects like pseudoprogressive disease (PsPD). Conventional MRI with contrast is insufficient to make the distinction between PD and PsPD. To overcome limitations of conventional MR imaging, advanced MR imaging techniques could offer an alternative for accurate assessment of tumor response. We examined the value of the widely used qualitative assessment of the dynamic susceptibility-contrast (DSC) perfusion MRI in glioma and brain metastases patients in the differentiation of PD from PsPD. DSC perfusion MRI is capable of quantifying vessel blood volume by assessment of the relative cerebral blood volume (rCBV), reflecting the degree of microvascular proliferation in tumor tissue, and might be valuable in the differentiation of PD from PsPD. Discerning PD from PsPD has important clinical and therapeutic consequences in brain tumor patients, as in case of tumor progression a switch of therapy should be considered. To study the value and reproducibility of the widely used qualitative (i.e. visual) method of the DSC perfusion MRI we first assessed the interobserver variability of DSC perfusion MRI in glioblastoma patients treated with TMZ chemoradiotherapy (Chapter 4). The interobserver agreement on qualitative interpretation of rCBV maps was labelled as good (kappa = 0.63). The interobserver agreement on the interpretability of DSC perfusion MR images was poor (kappa = 0.23), however, and only moderate (kappa = 0.48) on the overall conclusion of radiological tumor response, taking conventional MRI and DSC perfusion MRI into account (complete response, partial response, PD or stable disease).\n\nSecond, in chapter 5 we examined whether the qualitative assessment of the DSC perfusion MRI can reliably distinguish PD from PsPD in glioblastoma patients during TMZ chemoradiotherapy. The detection of a nodular high perfusion area on the rCBV map (i.e. \u201chigh rCBV\u201d) within the contrast-enhanced lesion did not reliably indicate PD in patients with glioblastoma (sensitivity and specificity of 72% and 23%, respectively). Furthermore, the qualitative rCBV based DSC perfusion MRI appeared not to be prognostic for survival in glioblastoma patients during TMZ chemoradiotherapy. The median overall survival was similar for the subgroup with high rCBV versus low rCBV.\n\nSubsequently, in chapter 6 the applicability of the qualitative method of the DSC perfusion MRI was assessed in 26 patients with 42 brain metastases. The changes in DSC perfusion MR images before and after stereotactic radiotherapy (SRT) were evaluated. Almost half of all perfusion images could not be evaluated due to localization near large vessels or the scalp, the presence of hemorrhage artefacts, or due to unmeasurable residual metastases. In most brain metastases (52%) a high rCBV at baseline and low rCBV during follow-up were found. Although non-PD and PsPD could be distinguished from PD after SRT on DSC perfusion MRI, the large proportion of images that could not be assessed due to artefacts and small lesion size severely hampered the practical use of DSC perfusion MRI in predicting tumor response after SRT in brain metastases patients.\n\nGENERAL DISCUSSION\n\nPART I: The role of antiepileptic treatment in relation to clinical and radiological outcome\n\nAchieving sustained seizure control is the main goal of treatment in patients with brain tumor related epilepsy, as a higher epilepsy burden has been shown to negatively affect morbidity, cognition and health-related quality of life (HRQOL). 12,13 The AED treatment of seizures in patients with brain tumors is not different from other types of localization-related epilepsy of adult onset, provided that enzyme-inducing AEDs are generally avoided because of possible interactions with systemic therapy. Prospective studies on the efficacy of AEDs in the general epilepsy population have indicated that 29%\u201340% of patients continue to have seizures despite successive treatment attempts. 14\u201317 As described in chapter 2, to achieve adequate seizure control LEV and VPA are most commonly prescribed in brain tumor patients. 18 The choice for either LEV or VPA as initial treatment mainly depends on the physicians\u2019 preference, as evidence from randomized controlled trials supporting the use of one specific AED is lacking. The relatively high percentage of seizure freedom in our study population compares favorably to patients with non-brain tumor related epilepsy. 19 This may be caused by antitumor treatment which is known to contribute strongly to seizure control in studies in low-grade gliomas. 4\u20139\n\nIn general, 20-40% of glioma patients experience AED side effects, which is considerably more than in patients with non-brain tumor related epilepsy. 19 This higher frequency of side effects may be caused by interactions with other drugs such as corticosteroids and chemotherapy, but those symptoms can also be attributed to the tumor itself and its treatment. Mood- and behavioral problems, fatigue and cognitive problems are frequently reported side effect of AEDs, commonly misattributed to the underlying disease. 21 In general, VPA is well-tolerated but it may cause severe side effects. In our study on glioblastoma patients, VPA was discontinued in about 10% due to adverse effects such as depression, weight gain, tremor, psychosis, rash, thrombocytopenia, hepatic test abnormalities or pancreatitis. There are several advantages of LEV in brain tumor patients, including good tolerability and lack of drug-drug interactions. However, approximately 5% of patients on LEV develop behavioral or psychiatric symptoms, such as irritability, aggression or psychosis for which dose adjustment or withdrawal is usually indicated. 22 Regardless of epilepsy burden, glioma patients experience lower levels of cognitive functioning due to the tumor itself, medication, depression, fatigue and tumor-directed therapy. AEDs unfortunately have an additional negative impact on the already compromised cognitive functioning of brain tumor patients. 12 It is found that patients using AEDs performed worse in almost all cognitive domains than those not using AEDs. In the study on glioblastoma patients (chapter 2) we intentionally administered early polytherapy in case of ongoing seizures rather than escalation of the dose of the initial AED. 23 One advantage of this synergistic co-therapy is that a lower total dosage of AEDs may be sufficient for a similar or better antiepileptic effect, as toxicity of AEDs may be related to serum AED concentration rather than the number of drugs administered. 12\n\nPotential antitumor properties of VPA in glioblastoma patients has raised attention from several studies. 24\u201327 VPA has histone deacetylase\u2013inhibiting properties which may lead to a stronger acetylation of histone proteins together with less methylation activity on promoter sites of many individual genes, including tumor-suppressor genes with ensuing apoptosis and autophagy of cancer cells, particularly if given together with chemotherapeutic agents. Several uncontrolled studies including the study described in chapter 2, have noted an improved outcome in glioblastoma patients treated with TMZ chemoradiotherapy who used VPA for seizure treatment. 26,28 However, a meta-analysis could not confirm a survival benefit for glioblastoma patients using VPA. 29 In this analysis, the effect of AED use at the start of TMZ chemoradiotherapy was studied in more than 1800 newly diagnosed glioblastoma patients. Multivariate analyses did not reveal VPA or LEV use at start of chemoradiotherapy to be associated with improved survival. The lack of confirmation of a survival benefit in this meta-analysis could be caused by several reasons. Previous studies, including our study, had a retrospective design with small patient populations in which few data were available on VPA dosage and duration of use. The lack of data on dosage as well as the length of exposure for the presumed mode of action of VPA to achieve a potential antitumor effect also hamper the meta-analysis. As it stands now, VPA is one of the most effective AEDs to achieve seizure control in glioma patients with epilepsy, but unequivocal evidence for its antitumor properties is lacking. In our search to optimize AED treatment for brain tumor patients we critically evaluated the need of continuation of AEDs in glioma patients with stable disease and long-term seizure freedom (Chapter 3). The lack of evidence regarding withdrawal of antiepileptic drugs and the fear for renewed seizures often results in cautiousness and mostly a \u201clifelong policy\u201d. Although our study was based on a relatively small group of patients, we think that patients and neuro-oncologists are now better informed about the risk of seizure recurrence in patients with lower grade gliomas.\n\nIn our opinion withdrawal should only be considered in carefully selected patients with a presumed low risk of tumor progression. Nevertheless, overtreatment in glioma patients with epilepsy should not be overlooked. Patients should not suffer more heavily from the adverse effects of AED treatment than from the seizures that AED treatment is intended to prevent. 30 It is important to note that considerably more patients had tumor progression in the withdrawal group compared to the continuation group. This finding may have influenced the risk of seizure recurrence in the withdrawal group. It is possible that the study groups were not well-balanced with respect to the risk of progression, although no significant differences were found in the baseline patient and tumor-related characteristics. Another explanation for the higher rate of tumor progression in the withdrawal group is that AED withdrawal may facilitate early diagnosis of tumor recurrence, as one might assume that AED treatment is likely to obscure a seizure as an early sign of disease progression. There is evidence that seizures may serve as a surrogate marker of tumor response; i.e. seizure control, as well as loss of seizure control, can be an early indicator of favorable tumor response, respectively tumor progression. 31\u201335 Aside from neuroimaging and survival, seizure control could therefore be used as one of the main outcome measures. 36\n\nPART II: The impact of antitumor treatment on clinical and radiological outcome\n\nThe second part of this thesis addressed the impact of antitumor treatment on clinical and radiological outcomes in patients with glioma and brain metastases. We focused on the value of the qualitative method of DSC perfusion MRI in differentiating PD from PsPD in brain tumor patients treated with (chemo)radiation (chapter 4, 5, 6). As a reliable diagnostic test requires acceptable test reproducibility, we first assessed the interobserver variability of the qualitative assessment of DSC perfusion MRI and conventional imaging. Although reproducibility of qualitative interpretation of perfusion MR images by neuroradiologists was labeled as good, we found that the interobserver agreement on the overall interpretation of MR imaging (using both conventional and perfusion images) was rather disappointing (Chapter 4). The main problem of the relatively low interobserver agreement on overall interpretation of MR imaging is the low interobserver agreement on perfusion imaging interpretability, i.e. that the neuroradiologists disagreed on whether perfusion images should have been selected for the interpretation. There are several causes for the observed interobserver disagreement. First, the visual score was based on a crude yes\/no rating, labelling the presence or absence (\u201cblack hole\u201d) of highly vascularized areas within the contrast-enhanced lesion relative to the contralateral hemisphere as high rCBV versus low rCBV. The choice of the particular slice and location of labelling within the area with contrast leakage depended on the individual neuroradiologist. Second, lesions are likely to contain a mixture of tumor and treatment related effects, resulting in different rCBV within a single contrast-enhancing lesion. Third, rCBV maps had a lower resolution than the conventional MR images. This makes the interpretation of contrast enhancement in close proximity to structures of the brain with higher rCBV values (cortex, blood vessels, focal hemorrhages) challenging.\n\nA reliable radiological assessment of PD and PsPD is of major importance as the clinical distinction between PD and PsPD can be difficult, although, glioma patients with PsPD tend to be younger and are less often symptomatic than patients with PD. 37 Furthermore, tumors of patients with PsPD are more often MGMT promotor methylated and isocitrate dehydrogenase (IDH) mutated. 37\u201341 In our patient group, additional qualitative DSC perfusion MRI could not more reliably distinguish PD from PsPD, nor did it provide prognostic information regarding survival in glioblastoma patients during TMZ chemoradiation (Chapter 5). We also applied the qualitative DSC perfusion MRI in patients with brain metastases treated with SRT, to potentially better differentiate PD from PsPD (Chapter 6). The applicability of DSC perfusion MR imaging in patients with brain metastases was assessed and the changes of perfusion imaging before and after stereotactic radiotherapy (SRT) were evaluated and correlated to tumor response on conventional MRI. We have found that a large proportion of perfusion images could not be assessed due to artefacts and small tumor size, which severely hampered the ability to differentiate PD from PsPD. Advanced quantitative MRI including DSC perfusion imaging showed high diagnostic performance in treatment response assessment in glioma patients demonstrating sensitivity of 71\u201392 % and specificity of 85\u201395 % using diffusion-weighted imaging (DWI), DSC, dynamic contrast-enhanced imaging (DCE) or MR spectroscopy (MRS). 42 DSC perfusion MRI had the second-best sensitivity of 87% (95% CI 82\u201391) and a specificity of 86% (95% CI 77\u201391). The findings in literature on quantitative DSC perfusion imaging with high diagnostic accuracies, are discrepant with the results from our studies. It is important to note that the qualitative technique studied is a derivative of the quantitative method and is a more simple, visual interpretation of the rCBV maps and is therefore far more used in the clinical setting.\n\nThe interpretation of both qualitative as well as quantitative DSC perfusion imaging to discern PD from PsPD remains challenging. First, the clinical definition of PsPD varies considerably with no clear distinction with other treatment related effects. 43 PsPD is mostly used related to early delayed and reversible radiation injury. However, also radiation necrosis, an irreversible and late complication of radiation to the brain, may be regarded as a (late) expression of PsPD. In literature these terms are used interchangeably. 44,43 Second, there is lack of standardization how to perform and interpret DSC perfusion MRI. Differences include for instance the time of scanning after contrast-injection, identifying regions of interest (ROIs), pre- and post-processing, reference tests and in case of the quantitative studies, the cut-off values and calculations of rCBV. 43,45 These methodological differences preclude a fair comparison between different studies. The strength of the study described in chapter 6, is that specifically the applicability of the DSC perfusion was studied, which included the pitfalls of producing the perfusion MRI in a clinical setting. All patients, independent of their tumor response and of the quality of perfusion images were included, whereas most other studies on perfusion imaging included only patients with radiological progression and a technically well performed perfusion MRI. 45\u201348 There is, in contrast to PsPD in glioma patients, a lack of evidence in","auteur":"Melissa Kerkhof","auteur_slug":"melissa-kerkhof","publicatiedatum":"15 december 2020","taal":"NL","url_flipbook":"https:\/\/ebook.proefschriftmaken.nl\/ebook\/melissakerkhof?iframe=true","url_download_pdf":"","url_epub":"","ordernummer":"FTP-202604080750","isbn":"978-94-6423-016-1","doi_nummer":"","naam_universiteit":"Universiteit Leiden","afbeeldingen":13303,"naam_student:":"","binnenwerk":"","universiteit":"Universiteit Leiden","cover":"","afwerking":"","cover_afwerking":"","design":""},"_links":{"self":[{"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/us_portfolio\/9397","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/us_portfolio"}],"about":[{"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/types\/us_portfolio"}],"author":[{"embeddable":true,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/comments?post=9397"}],"version-history":[{"count":1,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/us_portfolio\/9397\/revisions"}],"predecessor-version":[{"id":9400,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/us_portfolio\/9397\/revisions\/9400"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/media\/13303"}],"wp:attachment":[{"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/media?parent=9397"}],"wp:term":[{"taxonomy":"us_portfolio_category","embeddable":true,"href":"https:\/\/www.proefschriftmaken.nl\/en\/wp-json\/wp\/v2\/us_portfolio_category?post=9397"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}