Detection and characterization of neurotoxicity in cancer patients using proton MR spectroscopy
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- Steffen-Smith, E.A., Wolters, P.L., Albert, P.S. et al. Childs Nerv Syst (2008) 24: 807. doi:10.1007/s00381-007-0576-2
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The study objective was to detect abnormalities and identify relationships between brain metabolic ratios determined by proton magnetic resonance spectroscopic imaging (1H-MRSI) and neuropsychological (NP) function in cancer patients at risk for neurotoxicity.
Thirty-two patients received 1H-MRSI using a multi-slice, multi-voxel technique on a 1.5T magnet. Cho/NAA, NAA/Cr, and Cho/Cr ratios were identified in seven pre-determined sites without tumor involvement. A battery of age-appropriate NP tests was administered within 7 days of imaging. Relationships were examined between test scores and metabolite ratios.
This study identifies relationships between brain metabolite ratios and cognitive functioning in cancer patients. 1H-MRSI may be useful in early detection of neurotoxic effects, but prospective longitudinal studies in a homogeneous population are recommended to determine the prognostic value.
KeywordsMRIMRSPrimary brain tumorPediatricNeuropsychological assessment
Neurotoxicity (NT) is a significant treatment complication for many cancer patients but little is known about its etiology, and early objective detection is difficult. Cognitive deficits documented by neuropsychological (NP) testing involve attention and concentration, processing speed, memory, general intelligence, language, and academic achievement [13, 26, 29]. Risk factors identified from studies of patients with acute lymphoblastic leukemia and brain tumors include young age at treatment [1, 3, 13, 23], dose and type of treatment particularly cranial irradiation and high-dose chemotherapy [13, 15, 25], increased time since treatment [23, 26], and female gender . Structural changes, including subacute leukoencephalopathy, mineralizing microangiopathy, and cortical atrophy, have been observed on computed tomography or magnetic resonance imaging (MRI) during and after treatment , but associations between NP deficits and structural abnormalities are inconsistent and yield mixed results [18, 28]. Early detection and improved objective characterization of NT would be useful in the clinical management of these patients.
Eligible patients had a brain tumor, received high-dose systemic chemotherapy, intrathecal chemotherapy or cranial radiation, or had documented or suspected clinical neurotoxicity related to cancer or its treatment. The study was approved by our institution’s review board, and informed consent was obtained from all patients or their legal guardians.
MRI and 1H-MRSI
Patients received 1H-MRSI on a 1.5T whole-body imager (Signa; GE Medical Systems, Milwaukee, WI, USA) equipped with self-shielded gradients and a standard quadrature head coil. Spectroscopy data for metabolites of interest was acquired using a multi-slice, multi-voxel technique using a chemical shift-selective saturation pulse for water suppression and eight outer volume saturation bands for lipid signal suppression. Four 15 mm thick axial slices were acquired (repetition time 2,300 ms, TE 272 ms, 32 × 32 phase encoding steps over 240 mm field of view) . Spectral data were recorded simultaneously for each slice from multiple voxels, each with a nominal volume of 0.84 cm3 (1.5 × .75 × .75 cm). Acquisition time was approximately 20 min. Following 1H-MRSI acquisition, T2-weighted axial fluid attenuated inversion recovery images were obtained using the same field of view and angulations to ensure co-registration with 1H-MRSI.
Spectroscopic data from ROIs were accepted or rejected based on several criteria including Cr and Cho peak separation and signal-to-noise ratio . Additional exclusion criteria included tumor involvement, interference from tissue due to shunt or other surgical intervention, and overlap of other brain structures in ROI voxels. Areas under the peaks were normalized using ratios: Cho/NAA, NAA/Cr, and Cho/Cr. Presence of an abnormal lipid peak (1.6–1.8 ppm) in any brain area as identified in previous analysis  was also recorded.
Neuropsychological tests and results
Verbal IQa [WPPSI-R or WASI]
Performance IQa [WPPSI-R or WASI]
Long delay free recall z-scorec [CVLT]
Trailmaking test part B z-scorec, e 
Processing speed index standard scorea [WISC-III or WAIS-III]
Reading standard scorea [wide range achievement test (WRAT-3) ]
Arithmetic standard scorea [WRAT-3]
Spearman rank correlations were used to estimate the relationships between metabolite ratios in each ROI and NP test scores. Student’s t-tests were used to compare differences in test scores for patients with or without an abnormal lipid peak. Given the exploratory nature of this study, corrections for multiple comparisons were not applied. Two-sided P ≤ 0.05 were considered significant and suggestive of future confirmation.
1H-MRSI and NP testing were performed in 32 patients. One patient was excluded from analysis due to movement during image collection, which interfered with the 1H-MRSI spectra quality. Of the remaining 31 patients, 17 were male and 14 were female. The mean age of subjects was 12.4 years (median 10.4 years, range 2.4–40.5 years). Diagnoses included primary central nervous system tumors (n = 20), acute lymphoblastic leukemia (n = 9), and osteosarcoma (n = 2). Mean age at diagnosis was 7.7 years (median 6.4 years, range 1.3–37.9 years). Due to cross-sectional design, time since diagnosis at enrollment varied greatly across the sample (mean 4.7 years, median 2.9 years, range 0.2–32.9 years).
1H-MRSI data for ROIs
Cho/NAA mean (SD)
NAA/Cr mean (SD)
Cho/Cr mean (SD)
Neuropsychological test results
As listed in Table 1, mean scores for the majority of the tests were within one standard deviation below the normative mean (Average to Low Average Range). The mean score for the time to complete the executive function test was almost two standard deviations slower than the normative mean (Borderline Range). However, these patients demonstrated a wide range of functioning from Deficient to Very Superior on all measures except for the executive function test, which ranged from Deficient to High Average.
Relationships between NP function and 1H-MRSI
Correlations (p < 0.05)
Comparisons of metabolite ratios and NP test scores
Full Scale IQ
NT is a poorly characterized, but frequent consequence, of cancer-related therapy and the pathophysiology remains largely unknown. Most of the previous studies evaluating the neurotoxic effects of treatment on cancer patients have concentrated on structural or functional changes. Studies examining relationships between NP testing and structural changes on MRI have yielded inconsistent results. A noninvasive method for early detection of structural changes that correlates with NP function would be clinically useful in the management of these patients. Proton magnetic resonance imaging is a relatively recent clinical advance that has proven useful in the evaluation of neoplasms  and central nervous system diseases such as white matter disease [4, 16, 34], Alzheimer’s disease , and attention deficit–hyperactive disorder (ADHD) . The relationship between metabolic profiles in proton MRS and NP function has not been well characterized. Previous research on NP function and proton MRS has applied single voxel techniques [8, 9]. This study describes relationships between cognitive function and multi-voxel 1H-MRSI metabolic data in cancer patients.
NAA, an amino acid derivative found predominantly in neurons , is considered a marker of neuronal integrity and implicated in cognitive function . NAA is reduced in pathological states with neuronal loss or injury such as brain tumor , head trauma , and infection . Phosphocholine and glycerophosphocholine are known precursors of cell membrane synthesis and components of membrane breakdown products . Increased Cho is associated with membrane turnover and reflects cellular density . Lactate (Lac) and lipids are also detectable at long TEs but are not seen in normal brain tissue . Lac is a reflection of anaerobic metabolism. Prominent lipid peaks have been reported in MRS studies of multiple sclerosis , Tay–Sachs disease , and Sjögren–Larsson syndrome [24, 42] and are attributed to demyelination or membrane breakdown. Because neuronal loss and demyelination have been associated with NT, we hypothesized that changes in the metabolites that reflect these conditions would be markers of NT.
In this study, metabolite ratios (Cho/Cr, Cho/NAA, and NAA/Cr) were compared to NP test results. We investigated areas of the brain that are known to be involved in selected domains of NP function. Relationships between 1H-MRSI metabolite ratios and lower NP functioning were identified in this study. IQ appears to be the most robust measure for 1H-MRSI comparisons. Comparisons between metabolite ratios in subcortical regions and lower IQ scores yielded significant relationships. Increased levels of choline or lipids, both reflections of membrane turnover or demyelination, are related to lower IQ scores and overall cognitive deficits. This metabolic profile has been observed in other patient groups who present with decreased cognitive function, including patients with head trauma  or white matter disease [4, 16, 34]. Studies using proton MRS techniques to evaluate patients with traumatic brain injury and human immunodeficiency virus disease have also shown that decreased NAA, indicating either neuronal loss or dysfunction, is associated with poor cognitive outcome [17, 19]. In patients with Tay–Sachs disease and Sjögren–Larsson syndrome , populations at risk for impaired cognitive function, memory and executive function , increased levels of choline and prominent lipid peaks have been observed and associated with active demyelination [2, 44] and white matter abnormalities. The relationships identified between poorer NP function and metabolite ratios in our study may reflect changes in myelin metabolism that are not consistently perceptible on MRIs.
The development of NT in cancer patients is variable with regard to clinically detectable onset. When these changes in metabolites and detection of lipid peaks develop in relation to treatment remains to be determined. A prospective, longitudinal study may yield additional information about this unique metabolic profile and its relationship to NP function.
This study shows that 1H-MRSI is a potential tool for early identification of neurological and NP complications in cancer patients. Limitations of this study include cross-sectional design, small sample size, multiple comparisons, and heterogeneous population. Thus, our findings will need to be confirmed in additional studies. Further studies using 1H-MRSI and NP assessment are warranted to determine if this method can be used to noninvasively identify, predict, and better characterize neurotoxicity.
Statistical analysis performed by Dr. Paul Albert, Biometric Research Branch, Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, MD. This research was supported in part by the National Cancer Institute contracts #N01-SC-71102, #N01-SC-07006, and #HHSN261200477004C with the Medical Illness Counseling Center and by the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Center for Cancer Research. The views expressed do not necessarily represent the views of the National Institutes of Health or the United States Government.
The authors report no conflicts of interest.