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European Radiology

, Volume 21, Issue 7, pp 1526–1534 | Cite as

Early postoperative MRI overestimates residual tumour after resection of gliomas with no or minimal enhancement

  • Sinan M. K. Belhawi
  • Friso W. A. Hoefnagels
  • Johannes C. Baaijen
  • Esther Sanchez Aliaga
  • Jaap C. Reijneveld
  • Jan J. Heimans
  • Frederik Barkhof
  • W. Peter Vandertop
  • Philip C. De Witt HamerEmail author
Open Access
Neuro

Abstract

Background

Standards for residual tumour measurement after resection of gliomas with no or minimal enhancement have not yet been established. In this study residual volumes on early and late postoperative T2-/FLAIR-weighted MRI are compared.

Methods

A retrospective cohort included 58 consecutive glioma patients with no or minimal preoperative gadolinium enhancement. Inclusion criteria were first-time resection between 2007 and 2009 with a T2-/FLAIR-based target volume and availability of preoperative, early (<48 h) and late (1–7 months) postoperative MRI. The volumes of non-enhancing T2/FLAIR tissue and diffusion restriction areas were measured.

Results

Residual tumour volumes were 22% smaller on late postoperative compared with early postoperative T2-weighted MRI and 49% smaller for FLAIR-weighted imaging. Postoperative restricted diffusion volume correlated with the difference between early and late postoperative FLAIR volumes and with the difference between T2 and FLAIR volumes on early postoperative MRI.

Conclusion

We observed a systematic and substantial overestimation of residual non-enhancing volume on MRI within 48 h of resection compared with months postoperatively, in particular for FLAIR imaging. Resection-induced ischaemia contributes to this overestimation, as may other operative effects. This indicates that early postoperative MRI is less reliable to determine the extent of non-enhancing residual glioma and restricted diffusion volumes are imperative.

Keywords

Glioma Brain Neurosurgical procedures Magnetic resonance imaging Diagnostic techniques and procedures Diffusion magnetic resonance imaging 

Introduction

Initial treatment for gliomas usually consists of resective surgery in order to obtain a histopathological diagnosis and to accomplish as radical a glioma removal as possible with preservation of brain functions. Important determinants of survival in gliomas are histopathological grading, patient age and clinical condition before treatment [1, 2]. Residual tumour after resection is an independent prognostic factor for survival of low-grade and high-grade gliomas [3, 4, 5, 6]. Therefore, a reliable quantitative measure of residual tumour after resection is important to accurately evaluate the impact of surgery on the course of the disease and to compare the extent of resection between patient series [6, 7].

For high-grade gliomas residual tumour is usually determined by tumour volume calculation on MRI of the elements that enhance after administration of gadolinium on T1-weighted imaging. To avoid artefacts from enhancing gliotic tissue in the resection margins and from adjuvant radiotherapy that can complicate delineation of residual tumour, the postoperative MRI is performed within 48 h of surgery [8]. Gliomas may also present with no or minimal gadolinium enhancement on MRI. A lower grade glioma is then suspected and the target volume for resection is concordantly based on the non-enhancing elements that are hyperintense on T2-weighted sequences. FLAIR-weighted sequences have been particularly useful for this purpose, because the contrast between tumour and normal brain is superior to T2-weighted sequences as the signal from cerebrospinal fluid is suppressed [9]. Standards for the timing of postoperative MRI of gliomas with no or minimal enhancement have however not been established. The effects of the timing of postoperative MRI and of the pulse-sequence on residual tumour measurements have not been determined. We hypothesised that resection-induced ischaemia might contribute to differences in residual tumour volumes.

This study aimed to compare residual tumour volumes measured on early versus late postoperative T2- and FLAIR-weighted MRI after resection of gliomas that show no or minimal gadolinium enhancement on preoperative imaging.

Materials and methods

Inclusion criteria

All adult patients with a histopathological diagnosis of a glioma grade 1 to 4 according to the WHO 2007 criteria [10], who had surgery between January 2007 and December 2009 were retrieved from a consecutive patient series in an electronic database of our institution, which is a tertiary referral centre for brain tumour treatment. Then, patients with first-time resective surgery were selected for analysis, excluding stereotactic or open biopsies. In order to ensure that the target volume for resection was based on T2-/FLAIR-weighted imaging, only gliomas with no or minimal gadolinium enhancement on preoperative T1-weighted imaging were selected. However, focal or faint enhancement arbitrarily up to 15% of the T2/FLAIR volume, as determined volumetrically, was allowed. Furthermore, MR imaging was required to be available (a) preoperatively, (b) within 48 h of surgery, i.e. early postoperatively, and (c) between 2 and 6 months after surgery, i.e. late postoperatively.

The local ethical committee approved the research protocol and waived informed consent of participants.

Resective surgery

The patients in this study were preoperatively considered to have either a low-grade glioma or an anaplastic focus in a previously low-grade glioma. Therefore, the target volume for resection consisted of the T2/FLAIR volume. To minimise the risk of neurological morbidity this target volume was restricted by eloquent brain areas as determined by intraoperative cortical and subcortical electrostimulation mapping. The relation between the tumour and eloquent areas was determined according to the definitions used in the prognostic classification system of Chang et al [2]. Preoperative functional MRI, magnetic source imaging and diffusion tensor imaging tractography were obtained, as required by the location of the tumour. In general, the resection proceeded until eloquent brain areas were reached or volumetric tumour resection was complete. The tumour was subpially resected along sulci and fissures to minimise ischaemia around the resection cavity.

MRI data acquisition

MR imaging was performed on a 1.5T system (Siemens Sonata or Avanto; Siemens Medical Systems, Erlangen, Germany). The imaging protocol included non-enhanced axial T1-weighted spin echo images [repetition time/echo time (TR/TE) 520-600/8-12 ms] with 5-mm section thickness and axial T2-weighted turbo spin echo images (TR/TE 5190-8670/93-101 ms) with 5-mm section thickness. Sagittal 3D turbo fluid-attenuated inversion-recovery (tFLAIR) images [repetition time/echo time/inversion time (TR/TE/TI) 6500/355/2200 ms] with 1.3-mm section thickness plus axial multiplanar reconstructions (MPR) and axial single shot spin echo echo-planar diffusion-weighted (DWI) images (TR/TE 3400/122 ms) with 5-mm section thickness were added to the imaging protocol in 2009. Diffusion gradients were applied along 3 orthogonal directions using b-values of 0, 500 and 1000 s/ mm2. Apparent diffusion coefficient (ADC) maps were calculated from the DWI images. Post-contrast (0.2 mmol/Kg) sagittal 3D T1-weighted gradient-echo (MPRAGE) images (TR/TE/TI 2300-2700/5-4.5/950 ms) with 1- to 1.5-mm section thickness and axial T1-weighted spin echo images with 5-mm section thickness were obtained. In all patients preoperative imaging was repeated at our institution for navigation protocol purposes, even if preoperative imaging was available from a referring hospital.

MRI volumetry

Tumour volumes were measured using image fusion and volumetric software (BrainLab iPlan Cranial 2.6; BrainLab AG, Feldkirchen, Germany). MRI volumetry was based on the Cavalieri principle which provides unbiased volume estimates [11]. For this purpose tumour contours were manually segmented on sequential axial images and verified in the coronal and sagittal reconstruction planes. The sum of tumour contour surfaces of an MRI study was multiplied by slice thickness to obtain the estimated volume in cm3. This method has been demonstrated to be reproducible and accurate [12, 13]. In this way preoperative tumour volumes were determined for T2-, FLAIR- and gadolinium-enhanced T1-weighted images. The residual tumour after resection was also determined on T2- and FLAIR-weighted sequences for early and late postoperative imaging. The postoperative ischaemic volume was measured on an early postoperative diffusion-weighted sequence. Tumour and ischaemia were manually segmented independently by two observers (SB, PW) and disagreement was resolved by consensus with a third observer (ES).

Comparison of volume measurements

Several volume measurements were compared. To determine the effect of MRI timing on tumour volume measurements, early and late postoperative volumes were compared for T2- and FLAIR-weighted MRI. To determine the effect of pulse-sequence on tumour volume assessment, T2 and FLAIR volumes were compared on preoperative, early and late postoperative MRI. To determine the effect of resection-induced ischaemia on differences in residual tumour volumes, tissue volumes with restricted diffusion on early postoperative MRI were compared with the difference between early and late postoperative volumes for T2- and FLAIR-weighted imaging.

Statistical analysis

Tumour volumes for individual patients were plotted for visual inspection. In the case of perfect agreement between two volumes, a linear regression coefficient of 1.0 with an intercept of 0 was expected (plotted as a dashed line) with a correlation coefficient of 1.0. The actual regression coefficients with 95% confidence intervals were calculated by linear regression analysis with a fixed intercept of 0. As the volumes were considered not to be normally distributed, Spearman’s correlation coefficient was calculated. Bland-Altman plots were created to visualise agreement between volume estimates. Absolute volume differences were compared using the Wilcoxon signed rank test for paired samples.

Results

Patient and MRI characteristics and histopathology

The study population was a subset of 58 patients out of 223 with a glioma diagnosis in the inclusion time interval. Table 1 lists the details of the study population, consisting of 25 women and 33 men with a mean age of 44.7 years (range 20 to 70).
Table 1

Patient demographics and MRI characteristics

 

WHO1

WHO2

WHO3

WHO4

total

n (%)

2 (3%)

35 (60%)

14 (24%)

7 (12%)

58

patient demographics

age, mean (SE)

36.0 (0.4)

45.4 (1.7)

45.2 (3.7)

42.8 (7.0)

44.7 (1.6)

female/male

0/2

18/17

5/9

1/6

25/33

No. pts with radiotherapy

0

2

6

2

10

No, pts with chemo-irradiation

0

0

2

5

7

tumour lateralisation and location

L/R

0/2

15/20

5/9

3/4

23/35

nr pts with eloquent tumour location

2

26

7

6

41

frontal

0

8

7

1

16

SMA

0

7

2

2

11

parietal

0

6

3

2

11

temporal

0

2

1

1

4

insula

2

12

1

1

16

MRI characteristics

preoperative T2 hyperintense tumour volume in cm3, mean (SE)

135.0 (58.2)

71.6 (8.7)

129.1 (19.8)

76.6 (12.2)

88.3 (8.0)

preoperative FLAIR hyperintense tumour volume in cm3, mean (SE)

129.9 (52.0)

72.3 (9.9)

138.7 (29.9)

89.8 (16.2)

90.3 (9.7)

days preoperative MRI, mean (SE)

162 (121)

56 (15)

27 (9)

38 (14)

50 (10)

days early postoperative MRI, mean (SE)

1 (0)

1.4 (0.1)

1.8 (0.3)

1.6 (0.4)

1.5 (0.1)

days late postoperative MRI, mean (SE)

189 (10)

104 (7)

117 (21)

96 (15)

109 (7)

Preoperative MRI was performed at a median of 23 days (range: 1 to 282) before resection which showed no T1 gadolinium enhancement in 32 and minimal enhancement in 26 patients. The median preoperative T2 and FLAIR tumour volumes were 80.7 cm3 (range: 0.8 to 288.2) and 77.9 cm3 (range: 1.3 to 344.5), respectively. Histopathological diagnosis established WHO grade 1 in 2 patients (3%), grade 2 in 35 (60%), grade 3 in 14 (24%) and grade 4 in 7 (12%). Histopathological subtypes included 2 pilocytic astrocytomas (WHO grade 1); 14 astrocytomas, 18 oligodendrogliomas and 3 oligoastrocytomas (WHO grade 2); 6 anaplastic astrocytomas, 5 anaplastic oligodendrogliomas, 3 anaplastic oligoastrocytomas (WHO grade 3) and 7 glioblastomas (WHO grade 4).

Early and late postoperative T2 images were available for 52 patients; early and late postoperative FLAIR images for 14 patients. Early postoperative T2 and FLAIR images were available for 23 patients; late postoperative T2 and FLAIR images for 24 patients. Early postoperative diffusion-weighted images were available for 33 patients. Early postoperative MRI was obtained within 48 hours of resection in all patients, 44 on the first postoperative day, 14 on the second day. Late postoperative MRI was performed at a median of 100 days (range: 34 to 192) after resection; 18 within 3 months postoperatively, 31 between four and 6 months and 7 between seven and 9 months.

Residual tumour volumes on early compared with late postoperative MRI

The median early and late T2 residual volumes were 28.7 cm3 and 22.4 cm3, respectively, resulting in a 22% smaller residual volume on late T2 images. Residual T2 tumour volumes on early postoperative MRI demonstrated a systematically larger residual tumour volume (on average 4.3 cm3) compared with late postoperative MRI (Fig. 1a, c) with a regression coefficient of 0.767 (95%CI: 0.665–0.870), a correlation coefficient of 0.81 (p < 0.0001) and a paired Wilcoxon rank sum of V = 746.5 (p = 0.295). Similarly, the median early and late FLAIR residual volumes were 27.3 cm3 and 13.9 cm3, respectively, resulting in a 49% smaller residual volume on late FLAIR images. Systematically larger residual FLAIR tumour volumes (on average 5.7 cm3) were observed based on early postoperative MRI compared with late postoperative MRI (Fig. 1b, d) with a regression coefficient of 0.833 (95%CI: 0.693–0.973), a correlation coefficient of 0.95 (p < 0.0001) and a paired Wilcoxon rank sum of V = 78 (p = 0.119). Data plots confirmed that the differential residual tumour volumes were independent of glioma grading, subtyping and timing of late postoperative MRI.
Fig. 1

Residual tumour volumes in mL comparing early and late postoperative MRI based on T2-weighted imaging and FLAIR-weighted imaging shown as data plots (a and b) and Bland-Altman plots (c and d) respectively depicting systematic overestimation of residual tumour volume by early postoperative MRI. Each data point represents measurements obtained from one patient, tagged by glioma grade according to the legend. The straight diagonal line in a and b represents hypothetical perfect agreement and the dotted lines the actual linear regression fit and corresponding 95% confidence interval. The three dotted horizontal lines in c and d represent the average differential volume and corresponding 95% confidence interval

Tumour volumes on FLAIR- compared with T2-weighted imaging

FLAIR tumour volumes were marginally larger (on average 4.7 cm3) compared with T2 volumes on preoperative MRI (Fig. 2a, d) with a regression coefficient of 1.068 (95%CI: 1.033–1.102), a correlation coefficient of 0.98 (p < 0.0001) and a paired Wilcoxon rank sum of V = 419.5 (p = 0.056). FLAIR residual tumour volumes were substantially larger (on average 7.2 cm3) than T2 tumour volumes on early postoperative MRI (Fig. 2b, e) with a regression coefficient of 1.156 (95%CI: 1.049–1.262), a correlation coefficient of 0.96 (p < 0.0001) and a paired Wilcoxon rank sum of V = 40 (p = 0.009). On the late postoperative MRI, FLAIR and T2 residual tumour volumes were comparable (Fig. 2c, f): T2 tumour volumes on average 1.5 cm3 larger with a regression coefficient of 0.948 (95%CI: 0.880–1.015), a correlation coefficient of 0.94 (p < 0.0001) and a paired Wilcoxon rank sum of V = 194 (p = 0.218). Again, data plots confirmed that the differential residual tumour volumes were independent of glioma grading and timing of late postoperative MRI.
Fig. 2

Residual tumour volumes in mL comparing T2- and FLAIR-weighted imaging respectively based on preoperative, early postoperative and late postoperative MRI shown as data plots (a, b and c) and Bland Altman plots (d, e and f) depicting good agreement in residual tumour volume based on preoperative and late postoperative MRI and systematic overestimation of FLAIR-weighted imaging on early postoperative MRI. Data points, tagging and line styles as in Fig. 1

Postoperative ischaemia

The median restricted diffusion volume was 6.1 cm3. The restricted diffusion volume only weakly correlated with the difference between early and late postoperative volumes on T2-weighted imaging (Fig. 3a) with a correlation coefficient of 0.32 (p = 0.089). The restricted diffusion volume however did correlate more strongly with the difference between early and late postoperative volumes on FLAIR-weighted imaging (Fig. 3b) with a regression coefficient of 0.877 (95%CI: 0.486–1.267) and a correlation coefficient of 0.76 (p = 0.004). In addition, the restricted diffusion volume also correlated with the difference between FLAIR and T2 volumes on early postoperative MRI (Fig. 3c) with a regression coefficient of 0.655 (95%CI: 0.440–0.871) and a correlation coefficient of 0.77 (p = 0.0001).
Fig. 3

Plots of diffusion restriction volume on early postoperative MRI and (a) the difference in T2 residual tumour volumes of early and late postoperative MRI, (b) the difference in FLAIR residual tumour volumes of early and late postoperative MRI and (c) the difference in early postoperative MRI residual tumour volumes of T2- and FLAIR-weighted imaging. Data points, tagging and line styles as in Fig. 1

Discussion

This study population consisted of a consecutive series of patients in whom resective surgery targeted a FLAIR-based tumour volume. Owing to the absence of overt T1 gadolinium enhancement these lesions were deemed low-grade based on preoperative diagnostic neuroimaging. The histopathological diagnosis however established that 21 (36%) of the gliomas were in fact of high grade (WHO grade 3 or 4), reflecting the well-known discordance between MRI and histopathological grading of glioma [14, 15, 16]. Three main observations were made in this study. First, a systematic and substantial overestimation of residual tumour on MRI within 48 h of resection, indicating that late MRI months after surgery is more suitable to determine the extent of resection than an early MRI days after resection. Second, our data do not support a preference for either FLAIR- or T2-weighted imaging for either pre- or late postoperative imaging, although FLAIR-weighted imaging is more sensitive for early postoperative overestimation than T2-weighted imaging. Third, resection-induced diffusion restriction contributes to the residual volume overestimation of early compared with late postoperative MRI. These main findings are illustrated with a patient example in Fig. 4.
Fig. 4

An example of preoperative, early and late postoperative MRI displaying T2-, FLAIR- and diffusion-weighted axial images and volume contours. This 36-year old man with an oligoastrocytoma in the left cingulate gyrus had preoperative T2 and FLAIR tumour volumes of 101 and 94 cm3, respectively, outlined in green, with faint (2%) T1 gadolinium enhancement 3 weeks before resection. The residual T2 and FLAIR volumes 2 days after surgery were 35 and 61 cm3, respectively, outlined in red, with a diffusion restriction volume of 37 cm3. The residual T2 and FLAIR volumes 97 days after resection measured 27 and 21 cm3, respectively, outlined in yellow. Note the involution of the hyperintensity at the lateral margin of the resection cavity with restricted diffusion, interpreted as resection-induced ischaemia, and the stable hyperintensity at the posterior margin of the resection cavity, presumably genuine residual glioma within the corticospinal tract

Several factors likely contribute to the reduction of T2/FLAIR hyperintense regions between early and late postoperative MRI. It is unlikely that residual tumour actually regresses in the months following resection, although in theory involution of tumoural tissue induced by hypoperfusion due to surgical devascularisation can be postulated. The contribution of oedema and contusion of brain tissue surrounding the resection cavity, which subsides in weeks to months after resection, seems to be a more likely explanation. This reversible oedema can be either due to tumour compression that was present before resection, similar to peritumoral oedema as observed in some meningiomas for instance, or due to surgical manipulation of the tissue surrounding the resection cavity. Furthermore, the diffusion restricted areas may evolve in ischaemic (non-tumoral) tissue with volume involution over weeks to months similar to spontaneous infarction [17].

It is not surprising that T2 and FLAIR sequences provide similar tumour volumes on preoperative and late postoperative MRI because these sequences essentially measure the same physical properties of tissue except for the suppression of cerebrospinal fluid signal in the FLAIR sequence. This suppression provides superior contrast among tumour, cerebrospinal fluid and brain, thereby facilitating for instance segmentation algorithms to delineate tumour volume in neuronavigation preplanning [18, 19, 20]. Nevertheless, FLAIR tumour volumes tend to be larger than T2 volumes on early postoperative MRI. This could be explained by differences in sensitivity in detecting ischaemia especially in grey matter [21, 22, 23, 24] rather than by differences in the detection of residual tumour or oedema originating from tumour compression or surgical manipulation.

Recent studies on the extent of resection of non-enhancing gliomas have used various postoperative MRI timings and sequences to determine residual tumour. Examples include using T2 or FLAIR MRI within 48 h postoperatively [25], MRI less than 48 h postoperatively and FLAIR-weighted imaging with subtraction of areas that were likely to contain oedema [3], unspecified postoperative timing of T2- or FLAIR-weighted MRI when available [26], unspecified timing of FLAIR-weighted MRI [4], T1-weighted MRI at three to 6 months postoperatively [27], unspecified postoperative timing of T2- and FLAIR-weighted MRI [28] and T2-weighted MRI at five or six weeks postoperatively [29]. In order to determine the impact of residual tumour on the course of disease and to be able to compare the extent of resection between patient series, it seems reasonable to use standardised objective criteria for measurements of residual tumour. Based on our observations, we recommend avoiding measuring the extent of resection on MRI immediately after resection. We also recommend incorporating diffusion-weighted imaging into the immediate postoperative MRI for distinction between residual tumour and ischaemia in the reporting of results on residual tumour after non-enhancing glioma resections.

Notwithstanding this limitation, early postoperative MRI is clearly useful for a number of other purposes. First, as several of these patients will be diagnosed with high-grade glioma, baseline imaging for response evaluation of adjuvant treatment is assured by early postoperative MRI. Second, incidental tumour progression between resection and late postoperative MRI can be detected only in comparison with an early postoperative MRI. Third, new gadolinium enhancement on late postoperative MRI can be recognised as ischaemia-related luxury perfusion rather than be misinterpreted as anaplastic transformation [30]. Fourth, immediate postoperative deficits can be placed in the context of proximity of the resection cavity to eloquent structures and resection-induced diffusion restriction of these structures. Fifth, it is likely that more educational benefit is obtained for the surgical team from early postoperative MRI with feedback information on the surgical decisions rather than from postoperative MRI months after resection.

One limitation of this study is that the timing of the late postoperative MRI was not standardised and serial late postoperative measurements are lacking. Therefore, the optimal timing for late postoperative MRI remains uncertain. Another limitation is that for only a subset of patients FLAIR-weighted imaging was available both early and late postoperatively. This is due to the fact that the FLAIR and DWI sequences were added to the routine imaging protocol in the last year of patient inclusion. Despite this potential lack of power, a systematic difference was detected between early and late postoperative residual volumes based on FLAIR-weighted imaging in 14 patients. A further limitation is that some patients were adjuvantly treated with radio- or chemotherapy protocolised by trial participation, which could potentially interfere with late residual tumour volumes. This would however result in an underestimation of the observed postoperative reduction of residual tumour volume.

As a consequence of the overestimation of residual tumour on early MRI, we propose that quantitation of extent of resection is preferably based on MRI months after resection. The optimal timing of postoperative MRI for standardized criteria is to be determined in future prospective studies. Furthermore, estimates of residual tumour based on early MRI are to be carefully distinguished from regions with resection-induced diffusion restriction to avoid undue underestimation of surgical treatment effects.

In conclusion, our observation of a systematic and substantial overestimation of residual non-enhancing volume on MRI within 48 h of resection compared with months after resection indicates that early postoperative MRI is less reliable for volumetry of non-enhancing residual glioma. Diffusion-weighted imaging to detect resection-induced ischaemia is imperative in the interpretation of postresection tumour volumes.

Notes

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Copyright information

© The Author(s) 2011

Authors and Affiliations

  • Sinan M. K. Belhawi
    • 1
  • Friso W. A. Hoefnagels
    • 1
  • Johannes C. Baaijen
    • 1
  • Esther Sanchez Aliaga
    • 2
  • Jaap C. Reijneveld
    • 3
  • Jan J. Heimans
    • 3
  • Frederik Barkhof
    • 2
  • W. Peter Vandertop
    • 1
  • Philip C. De Witt Hamer
    • 1
    • 4
    Email author
  1. 1.Neurosurgical Center AmsterdamVU University Medical CenterAmsterdamThe Netherlands
  2. 2.Department of RadiologyVU University Medical CenterAmsterdamThe Netherlands
  3. 3.Department of NeurologyVU University Medical CenterAmsterdamThe Netherlands
  4. 4.Department of Neurosurgery, Room 2F010VU Medical CenterAmsterdamThe Netherlands

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