| Literature DB >> 27446888 |
Jacob Levman1, Emi Takahashi1.
Abstract
Brain cancer and neurological injuries, such as stroke, are life-threatening conditions for which further research is needed to overcome the many challenges associated with providing optimal patient care. Multivariate analysis (MVA) is a class of pattern recognition technique involving the processing of data that contains multiple measurements per sample. MVA can be used to address a wide variety of neuroimaging challenges, including identifying variables associated with patient outcomes; understanding an injury's etiology, development, and progression; creating diagnostic tests; assisting in treatment monitoring; and more. Compared to adults, imaging of the developing brain has attracted less attention from MVA researchers, however, remarkable MVA growth has occurred in recent years. This paper presents the results of a systematic review of the literature focusing on MVA technologies applied to brain injury and cancer in neurological fetal, neonatal, and pediatric magnetic resonance imaging (MRI). With a wide variety of MRI modalities providing physiologically meaningful biomarkers and new biomarker measurements constantly under development, MVA techniques hold enormous potential toward combining available measurements toward improving basic research and the creation of technologies that contribute to improving patient care.Entities:
Keywords: MRI; fetal; machine learning; multivariate analysis; neonatal; pediatric; review
Year: 2016 PMID: 27446888 PMCID: PMC4917540 DOI: 10.3389/fped.2016.00065
Source DB: PubMed Journal: Front Pediatr ISSN: 2296-2360 Impact factor: 3.418
Summary of multivariate analyses applied to pediatric brain tumors.
| Author | Year | Results | Noteworthy comments | |
|---|---|---|---|---|
| Rodriguez Gutierrez et al. ( | 2013 | 40 | Accuracy = 91–97% | Medulloblastoma, pilocytic astrocytoma, ependymoma, and posterior fossa tumor classification |
| Ahmed et al. ( | 2011 | 10 | Jaccard Index: 0.60 | Posterior fossa tumor segmentation |
| Weizman et al. ( | 2012 | 28 | Mean surface distance error: 0.73 mm | Optic pathway gliomas: segmentation, classification, and follow-up |
| Reynolds et al. ( | 2007 | 46 | Error rate = 33% | MR spectroscopy |
| Iftekharuddin et al. ( | 2011 | 10 | True positive = 100% | Combines T1, T2, and fluid-attenuated inversion recovery (FLAIR) |
| False positive = 25% | ||||
| Tantisatirapong et al. ( | 2014 | 74 | Accuracy = 69% | Texture analysis and feature selection |
| Wels et al. ( | 2008 | 6 | Jaccard index: 0.78 | Fully automatic tumor ROIs |
| Jansen et al. ( | 2015 | 316 | AUC = 0.68 | Survival prediction |
| Grech-Sollars et al. ( | 2012 | 61 | Apparent transient coefficient in tumor (ATCT) is significantly associated with poor prognosis | Apparent transient coefficient in tumor (ATCT: change in ADC from edema to tumor core) investigated |
| Felicetti et al. ( | 2015 | 15 | Meningioma is associated with development of a second neoplasm | Childhood cancer survivors treated with cranial radiation therapy were assessed with MRI and computed tomography (CT) |
| Sun et al. ( | 2013 | 33 | Focal growth pattern is associated with better survival | Study focused on clinical outcomes in subjects with pediatric brainstem tumors |
| Youland et al. ( | 2013 | 351 | Improved progression-free survival and overall survival associated with gross total resection informed by MRI | Study looking at prognostic factors and survival patterns in pediatric low-grade gliomas |
| Dorward et al. ( | 2010 | 40 | Nodular enhancement on MRI associated with recurrence | Pilocytic astrocytomas (slow growing tumors) |
| Bucci et al. ( | 2004 | 39 | Multivariate analysis: extent of resection and histologic grade were significant predictors of outcome | Investigating outcomes in pediatric gliomas |
| Fernandez et al. ( | 2003 | 80 | Partial resection: worse prognosis. Optochiasmatic localization and pilomyxoid variant: worse prognosis but not independent of extent of resection | Investigating clinicopathological factors underlying prognosis in pediatric pilocytic astrocytomas |
| Mulhern et al. ( | 1999 | 18/18 | Patients treated for medulloblastoma had significantly less normal white matter and lower IQ | Two groups: medulloblastoma survivors and posterior fossa tumors |
| Liu et al. ( | 1998 | 22 | Radiation dose strategy (hyperfractionation) associated with better outcomes | Prognostic factors and therapeutic options in pediatric brain stem gliomas |
| Arle et al. ( | 1997 | 33 | Accuracy = 58–95% | MR spectroscopy, artificial neural networks for identifying posterior fossa tumors |
| Shrieve et al. ( | 1992 | 41 | Duration of symptoms >2 months prior to treatment was a significant prognostic indicator of favorable outcome | Radiation therapy for gliomas of the brainstem |
Figure 1MRI examinations of two patients with diffuse intrinsic pontine gliomas (see arrows). (A) demonstrates a small nodular enhancement (arrow) and (B) demonstrates a large ring enhancement (arrow). Figure reproduced with permission (38).
Figure 2Two preterm infants born at 29 weeks gestational age, imaged at term with T2 weighted MRI. Subject A exhibited multiple small streak-like hemorrhages in both cerebellar hemispheres (see arrows). Subject B exhibited a single small hemorrhage in the left cerebellar hemisphere (see arrow). Figure was reproduced with permission (61).
Figure 3Patterns of enhancement on T2 weighted MRI classified as severe demonstrating right intraparenchymal hematoma (arrow) with surrounding hyperintensity. Figure is reproduced with permission (76).
Figure 4A preterm neonate MRI examination, including spectroscopy performed at eight different of regions-of-interest (squares), located at the level of (A) the high centrum semi-ovale and (B) the basal ganglia. This includes regions-of-interest corresponding to high white matter [(1) anterior, (2) central, and (3) posterior], (4) caudate, (5) lentiform nuclei, (6) thalamus, (7) optic radiations, and (8) calcarine region. The provided spectrum corresponds to the left frontal white matter. Cho, choline; Cr, creatine; Lac, lactate; NAA, N-acetylaspartate. Figure reproduced with permission (103).