David Gorodezki, Felix Tonagel, Julian Zipfel, Markus Mezger, Karin Haas-Lude, Ursula Holzer, Thomas Nägele, Martin Ulrich Schuhmann, Martin Ebinger
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VA was assessed as minimal angle of resolution (logMAR) with age-appropriate measures during regular ophthalmology visits.</p><p><strong>Results: </strong>During observation, therapeutic intervention was initiated in 64% of individuals due to VA deterioration or radiological progress. Impaired VA occurred in 55 vs 80% of NF1-associated vs sporadic OPG patients, respectively, while blindness of at least one eye occurred in 36% of individuals. Tumor burden showed significant correlation with VA impairment at diagnosis and individual logMAR change during follow-up (R<sup>2</sup> = .22, p = .011), while individual tumor growth velocity during follow-up showed correlation with VA deterioration in non-NF1 OPG (R<sup>2</sup> = .35, p = .04). ROC analyses identified a threshold tumor burden (> 11.1 cm<sup>3</sup>, AU ROC 0.76) and growth velocity (> 0.1 cm<sup>3</sup>/month, AU ROC 0.81) to predict loss of VA with modest sensitivity and specificity.</p><p><strong>Conclusion: </strong>These data indicate a predictive value of three-dimensionally assessed tumor burden and growth velocity for VA outcomes in OPG. Prospective evaluation within future trials may facilitate further implementation for advanced stratification, potentially identifying patients who may benefit from early therapeutic intervention.</p>","PeriodicalId":520587,"journal":{"name":"Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery","volume":"41 1","pages":"230"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12254072/pdf/","citationCount":"0","resultStr":"{\"title\":\"MRI-based, three-dimensionally assessed tumor burden and growth velocity to predict visual acuity deterioration in optic pathway glioma - results of a retrospective longitudinal analysis.\",\"authors\":\"David Gorodezki, Felix Tonagel, Julian Zipfel, Markus Mezger, Karin Haas-Lude, Ursula Holzer, Thomas Nägele, Martin Ulrich Schuhmann, Martin Ebinger\",\"doi\":\"10.1007/s00381-025-06890-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Optic pathway gliomas (OPGs) bear a high risk of visual acuity (VA) impairment, while balancing disease-related morbidity and potential therapy-related sequelae remains challenging. We assess the predictive value of MRI-based, three-dimensionally assessed tumor burden and growth velocity for VA outcomes in NF1-associated and sporadic OPGs.</p><p><strong>Methods: </strong>Thirty-three OPG patients were longitudinally observed over a median follow-up period of 10.3 years, while sequential tumor volumetry was performed to assess tumor burden and tumor growth velocity. VA was assessed as minimal angle of resolution (logMAR) with age-appropriate measures during regular ophthalmology visits.</p><p><strong>Results: </strong>During observation, therapeutic intervention was initiated in 64% of individuals due to VA deterioration or radiological progress. Impaired VA occurred in 55 vs 80% of NF1-associated vs sporadic OPG patients, respectively, while blindness of at least one eye occurred in 36% of individuals. Tumor burden showed significant correlation with VA impairment at diagnosis and individual logMAR change during follow-up (R<sup>2</sup> = .22, p = .011), while individual tumor growth velocity during follow-up showed correlation with VA deterioration in non-NF1 OPG (R<sup>2</sup> = .35, p = .04). ROC analyses identified a threshold tumor burden (> 11.1 cm<sup>3</sup>, AU ROC 0.76) and growth velocity (> 0.1 cm<sup>3</sup>/month, AU ROC 0.81) to predict loss of VA with modest sensitivity and specificity.</p><p><strong>Conclusion: </strong>These data indicate a predictive value of three-dimensionally assessed tumor burden and growth velocity for VA outcomes in OPG. Prospective evaluation within future trials may facilitate further implementation for advanced stratification, potentially identifying patients who may benefit from early therapeutic intervention.</p>\",\"PeriodicalId\":520587,\"journal\":{\"name\":\"Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery\",\"volume\":\"41 1\",\"pages\":\"230\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12254072/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s00381-025-06890-6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s00381-025-06890-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:视神经胶质瘤(OPGs)具有很高的视力损害风险,而平衡疾病相关的发病率和潜在的治疗相关的后遗症仍然是一个挑战。我们评估了基于mri的、三维评估的肿瘤负荷和生长速度对nf1相关和散发性OPGs的VA结果的预测价值。方法:纵向观察33例OPG患者,中位随访时间为10.3年,同时采用序贯肿瘤体积法评估肿瘤负荷和肿瘤生长速度。在定期眼科就诊期间,以最小分辨角(logMAR)与年龄相适应的方法评估VA。结果:在观察期间,有64%的个体由于VA恶化或放射学进展而开始了治疗干预。在nf1相关和散发性OPG患者中,分别有55%和80%的患者发生了VA受损,而至少有一只眼睛失明的患者占36%。肿瘤负荷与诊断时VA损害及随访期间个体logMAR变化有显著相关性(R2 =。22, p = .011),而随访期间个体肿瘤生长速度与非nf1 OPG的VA恶化相关(R2 = .011)。35, p = .04)。ROC分析确定了阈值肿瘤负荷(> 11.1 cm3, AU ROC 0.76)和生长速度(> 0.1 cm3/月,AU ROC 0.81)预测VA的损失具有中等的敏感性和特异性。结论:这些数据表明三维评估的肿瘤负荷和生长速度对OPG的VA结果具有预测价值。未来试验中的前瞻性评估可能有助于进一步实施高级分层,潜在地确定可能从早期治疗干预中受益的患者。
MRI-based, three-dimensionally assessed tumor burden and growth velocity to predict visual acuity deterioration in optic pathway glioma - results of a retrospective longitudinal analysis.
Purpose: Optic pathway gliomas (OPGs) bear a high risk of visual acuity (VA) impairment, while balancing disease-related morbidity and potential therapy-related sequelae remains challenging. We assess the predictive value of MRI-based, three-dimensionally assessed tumor burden and growth velocity for VA outcomes in NF1-associated and sporadic OPGs.
Methods: Thirty-three OPG patients were longitudinally observed over a median follow-up period of 10.3 years, while sequential tumor volumetry was performed to assess tumor burden and tumor growth velocity. VA was assessed as minimal angle of resolution (logMAR) with age-appropriate measures during regular ophthalmology visits.
Results: During observation, therapeutic intervention was initiated in 64% of individuals due to VA deterioration or radiological progress. Impaired VA occurred in 55 vs 80% of NF1-associated vs sporadic OPG patients, respectively, while blindness of at least one eye occurred in 36% of individuals. Tumor burden showed significant correlation with VA impairment at diagnosis and individual logMAR change during follow-up (R2 = .22, p = .011), while individual tumor growth velocity during follow-up showed correlation with VA deterioration in non-NF1 OPG (R2 = .35, p = .04). ROC analyses identified a threshold tumor burden (> 11.1 cm3, AU ROC 0.76) and growth velocity (> 0.1 cm3/month, AU ROC 0.81) to predict loss of VA with modest sensitivity and specificity.
Conclusion: These data indicate a predictive value of three-dimensionally assessed tumor burden and growth velocity for VA outcomes in OPG. Prospective evaluation within future trials may facilitate further implementation for advanced stratification, potentially identifying patients who may benefit from early therapeutic intervention.