Central nervous system tumors in children under 5 years of age: a report on treatment burden, survival and long-term outcomes

Purpose The challenges of treating central nervous system (CNS) tumors in young children are many. These include age-specific tumor characteristics, limited treatment options, and susceptibility of the developing CNS to cytotoxic therapy. The aim of this study was to analyze the long-term survival, health-related, and educational/occupational outcomes of this vulnerable patient population. Methods Retrospective study of 128 children diagnosed with a CNS tumor under 5 years of age at a single center in Switzerland between 1990 and 2019. Results Median age at diagnosis was 1.81 years [IQR, 0.98–3.17]. Median follow-up time of surviving patients was 8.39 years [range, 0.74–23.65]. The main tumor subtypes were pediatric low-grade glioma (36%), pediatric high-grade glioma (11%), ependymoma (16%), medulloblastoma (11%), other embryonal tumors (7%), germ cell tumors (3%), choroid plexus tumors (6%), and others (9%). The 5-year overall survival (OS) was 78.8% (95% CI, 71.8–86.4%) for the whole cohort. Eighty-seven percent of survivors > 5 years had any tumor- or treatment-related sequelae with 61% neurological complications, 30% endocrine sequelae, 17% hearing impairment, and 56% visual impairment at last follow-up. Most patients (72%) attended regular school or worked in a skilled job at last follow-up. Conclusion Young children diagnosed with a CNS tumor experience a range of complications after treatment, many of which are long-lasting and potentially debilitating. Our findings highlight the vulnerabilities of this population, the need for long-term support and strategies for rehabilitation, specifically tailored for young children. Supplementary Information The online version contains supplementary material available at 10.1007/s11060-022-03963-3.


Introduction
CNS tumors are the most common pediatric solid cancers. The average annual incidence rate is 6.18 per 100,000 in 0-4-year-olds in the U.S. [1]. This is higher than what is reported in age groups 5-9 years (5.49 per 100,000) and 10-14 years (5.83 per 100,000) [1]. In recent years, molecular profiling studies led to major advances in the understanding and classification of pediatric CNS tumors [2][3][4]. Development of new therapies is ongoing and expected to increase further patient survival, mitigate long-term treatment toxicities, and improve the quality of life of survivors. Notwithstanding, CNS tumors remain the most common cause of cancer-related death in children and adolescents.
Young children (< 5 years of age) are particularly prone to long-term sequelae of cytotoxic therapies [5]. Radiotherapy (RT) is associated with neurocognitive and psychological impairment, increased risk of stroke, secondary malignancies, hearing loss, and neuroendocrine deficiencies [6]. Due to its impact on the developing CNS, RT is often entirely omitted or delayed in the management of brain tumors in young children, risking suboptimal disease control. Radiation-sparing regimens used as an alternative in this population often comprise high-dose chemotherapy with stem cell rescue as a consolidation therapy or intensified intrathecal chemotherapy. Increasing the intensity of chemotherapy has led to improved disease control, however several studies report serious events including toxic deaths, mostly due to myelosuppression, sepsis and/or organ dysfunction [7][8][9][10][11].
Health care professionals often face the dilemma between augmenting treatment intensity for optimal disease control and minimizing acute toxicity as well as the risk of longterm sequelae [12]. Clinical outcome and quality of life of CNS tumor survivors pose a serious concern to treating physicians as well as parents, but literature focusing on young children is scarce. Here, we describe the long-term survival, health, and academic outcomes of young children at the time of CNS tumor diagnosis and treated at our institution over the last 3 decades.

Patient population
In this retrospective study, young children aged 0-5 years with a newly diagnosed primary CNS tumor and treated at the University Children's Hospital of Zurich between January 1990 and December 2019 were identified. Date of diagnosis was defined as either date of histological confirmation of tissue sample or, if not available, date of diagnostic imaging.
The design of the study was approved by the Ethics Committee of the Canton of Zurich. A general research consent was implemented at our institution in 2015. The need for informed consent was waived for deceased patients, patients diagnosed prior to 2015 and lost to follow-up. Patients with documented refusal to participate in research were excluded.

Clinical characteristics and long-term outcome measures
The baseline clinical characteristics included age at diagnosis, sex, tumor characteristics (histology, location, dissemination status), hydrocephalus at diagnosis, underlying genetic predisposition and treatment details. Extent of resection was determined based on neurosurgical reports and postsurgical MRI when available; if a residual tumor was described in the neurosurgical report and/or postsurgical MRI, the tumor was considered partially resected. Progression-free survival (PFS) was calculated from date of diagnosis to disease progression leading to change in treatment or death in patients without such a progression, and overall survival (OS) from date of diagnosis to death. In the absence of progression and for patients alive at last follow-up, PFS and OS were censored at the last documented date that the patient was seen by a physician (last follow-up).
The long-term health-related outcome information was extracted from the medical charts of all patients and included neurologic status, endocrine function, hearing loss, visual acuity, secondary malignancies, and cerebral vasculopathy. Ototoxicity was graded according to Chang after review of available audiograms [13]. Neurologic status was assessed during exams at regular physician's visits and changes present in the most recent neurological examination were summarized. Neurologic deficits collected included cranial nerve deficit, motor and sensory deficits, coordination, gait, reflexes, and tonus. At our pediatric institution, patients are followed up until 20 years of age and information on schooling and employment is regularly documented at long-term follow-up clinic visits. Academic achievement was categorized into two groups. The first group contains patients who attend regular school or work in a skilled job and the second group includes patients who attend an assisted or modified school program e.g. with smaller student numbers per class and additional assistance or who work in an unskilled or assisted job. A skilled job was defined as student with graduation after vocational training with a Federal Diploma (Fig. S3). An unskilled job includes only training on-site without graduation. Preschool-aged children were excluded from this analysis.

Statistical analysis
Descriptive analyses were used to summarize the study population. Kaplan-Meier survival curves were generated to estimate OS probability and progression-free survival probability. Log-rank test was performed for comparison between different subgroups.
To quantify the association between different treatment modalities and long-term outcomes fisher's exact test was used.

Patient cohort characteristics
We identified 164 children under 5 years of age and diagnosed with a primary CNS tumor between 1990 and 2019 at the University Children's Hospital of Zurich, the largest pediatric oncology center in Switzerland. Thirty-six patients were excluded: 28 patients due to lack of sufficient information and 8 patients due to refusal to participate in research. Thus, 128 patients were included in the final analysis (Table S1).
Sixty-three percent of patients received chemotherapy, most of them enrolled on or treated as per tumor-specific protocols ( Fig. S2; Table S2) [14,15].
Most of the deceased patients died within the first 5 years after diagnosis. Of those patients who died, the majority (25 of 28, 92.8%) died of tumor progression/relapse. One patient initially diagnosed with medulloblastoma died after diagnosis of radiation-induced high-grade glioma. The cause of death was undocumented or unclear for two patients.
Fourteen patients were over 18 years of age at last followup. As far as documented none of them conceived a child. Four patients (4 of 8 females) had ovarian insufficiency and two required estradiol replacement. For the male patients (n = 6), spermiograms were not available.

Visual outcomes
Visual impairment is multifactorial and prevalent also in the general population. Focusing on the subset of patients with optic pathway glioma and tumor-associated visual impairment, all patients (n = 13; 2/13 patients with NF1) with optic pathway glioma showed some degree of visual impairment at last follow-up and four patients were blind in at least one eye.

Secondary malignancies
Three patients were diagnosed with a secondary malignancy during follow-up ( Table 2). All of them had been irradiated by either proton or photon radiation, received chemotherapy, and underwent surgery. None of them had a known underlying genetic predisposition, including NF1. Importantly, the patient with ATRT and later MPNST had no evidence of germline alterations in SMARCB1, SMARCA4, NF1 or TP53. One patient succumbed to his secondary malignancy.

Cerebrovascular disease
Two out of 51 irradiated patients (3.9%) presented with a moyamoya vasculopathy during follow-up. Both had been diagnosed with posterior fossa ependymoma and had received focal proton radiation at below 4 years of  In summary, among survivors followed for more than 5 years (n = 77), 87% present with any tumor-or treatmentrelated sequelae, 61% had any neurological deficit, 30% presented with endocrine sequelae and 81% of them with need for hormone replacement, 17% with hearing impairment, and 56% with visual impairment at last follow-up.

Education and occupational outcomes
Thirty-seven patients had not yet reached school age at time of last follow-up. Information on schooling was not available for 6 patients. Of the remaining 85 patients, 71.8% were able to attend regular school and/or work in a skilled job, whereas 28.2% were schooled in a modified program or working in an unskilled or assisted job (Fig. 3). Of the patients over 18 years of age at last follow-up (n = 14), one patient attended university. Fifteen of 68 (22%) patients 1 year or older at diagnosis were schooled in a special school environment or working in an unskilled job, compared to 9 out of 17 (53%) patients under 1 year of age at diagnosis. Despite limited patient numbers, this trend suggests lower academic achievement in children diagnosed in the first year of life.

Discussion
Among survivors of childhood cancer, the cumulative burden of chronic health conditions is highest in patients diagnosed with CNS malignancies [16]. Providing treatments which are both efficient and of acceptable toxicity is thus a great challenge in pediatric neuro-oncology, especially when treating young children. A report from the Childhood Cancer Survivor Study (CCSS) suggested that treatment transformation over the past decades has already decreased the overall treatment burden [17]. Nevertheless, the long-term impact of therapy in the immature CNS and in the developing child remains a major concern. In addition, CNS tumors in young children often display distinct clinical and biological features when compared to those in older children and adolescents [18][19][20][21]. In this study we report the survival, health-related and educational outcomes of young children with CNS tumors treated at a tertiary pediatric oncology center over a period of three decades. Importantly, our study provides long follow-up and comprehensive clinical outcome data on a large cohort of sequentially diagnosed, unselected patients in this age group. We found that mortality was largely due to tumor progression/relapse and predominantly within the first 5 years after diagnosis. The high prevalence of tumorand treatment-related sequelae (87%) highlights the need for close monitoring and long-term, multidisciplinary support strategies. With a 5-year OS of 78.8%, the survival outcome of our cohort is comparable to previous studies, albeit differences regarding patient characteristics and therapy between studies [1,[22][23][24]. One study including 35 children under 1 year of age at diagnosis reported a considerably lower 5-year OS of 57% [25]. The OS of pLGG in our cohort seems to be better than reported in previous studies [20,21], which were multi-institutional and thus more heterogenous in treatment approach. PFS was defined in our study as time from diagnosis to a progression leading to change in treatment. This may overestimate PFS compared to other studies with other definitions and should be considered when interpreting our results, especially for patients with pLGG.
Other studies reported a higher mortality rate in children diagnosed under 1 year of age when compared to older children [20,26,27]. Despite a trend in literature towards worse outcome in children diagnosed in the first year of life, we could not confirm this finding in our cohort, noting however a trend towards worse OS in children diagnosed in the first 6 months of life (Fig. S1) [28]. This may be explained by differences in patient characteristics (age at diagnosis limited to 5 years or younger in this study) and tumor distribution (e.g. lower numbers of patients with ATRT in our cohort).
Survival rates of children diagnosed with a CNS tumor seem to have increased over the last years [23,24], while the prognosis for high grade subtypes remains poor. Similarly, despite encouraging survival rates of the whole cohort, patients with pHGG and medulloblastoma had an unfavorable outcome, with a 5-year OS of 35.7% and 55.4%, respectively. A study summarizing the outcomes of a cohort of 20 survivors, previously diagnosed with a brain tumor in the first year of life, reported 70% with neurological dysfunction, 25% with endocrine dysfunction, 15% with hearing impairment, and 45% with visual impairment [25]. These numbers are comparable to our findings, despite differences in age of inclusion. A report from the CCSS showed that patients diagnosed with a CNS malignancy had a significantly higher risk of developing a chronic health condition 5 years after diagnosis when compared to their siblings, including endocrine, neurologic, or sensory deficits [29]. Hearing impairment was associated with radiation therapy and platinum chemotherapy, both known risk factors for sensorineural hearing loss [30,31]. A previous study from the CCSS reported hearing impairment in 12% of childhood CNS tumors survivors [30]. A study conducted at St. Jude Children's Hospital compared survivors of CNS tumors to survivors of non-CNS tumors exposed to high-risk ototoxic cancer therapy and reported a prevalence of 36% of severe hearing loss in CNS tumor survivors. There was no association between age at diagnosis and hearing loss [32].
Hypopituitarism was associated with radiotherapy, as previously described [33][34][35]. A recent study identified younger age, tumor location, and radiotherapy as relevant risk factors for developing hypothalamic-pituitary disease [36]. Due to lack of sufficient information, an analysis on radiation dose-dependent outcomes was not possible in our cohort. A report from the CCSS could not find a dose-dependent risk elevation in radiotherapy for endocrine deficits [37]. The important issue of fertility could not be addressed in a uniform manner in our cohort and should be addressed in future studies.
We found that most (71.8%) of our school-aged patients or older at the time of analysis attended regular school or were employed in a skilled job. This is higher than what a previous study reported including children diagnosed with a CNS tumor in the first year of life [25]. A recent study with children aged 4 years or younger at diagnosis and treated with proton radiotherapy described a rate of 90% of children functioning in regular schools, 46% of them followed a specialized educational plan, whereas 23% and 36% had a classroom aid or outside tutor, respectively [38]. Interestingly, recent analyses of childhood cancer survivors showed that especially CNS malignancy, younger age at diagnosis, and radiotherapy increased the risk of unemployment and lower educational attainment [39][40][41]. Another analysis showed that childhood survivors of CNS tumors were less likely to complete high school than their siblings but could lower that risk by using special education support [42]. These findings further highlight the need to develop toxicity-sparing treatments and provide long-term support for these patients.
The size and heterogeneity of our study population, as well as limitations associated with the retrospective nature of the study, need to be considered when interpreting our findings. Assessment of long-term outcome has not followed a standard procedure in terms of frequency and tools used, limiting interpatient comparisons. The classification of CNS tumors has undergone several important revisions over the decades covered in this study. The main tumor entities have been reclassified and subdivided into new subgroups, reflecting the heterogeneity in tumor biology, especially in pediatric brain tumors in young children [3,43]. Though molecular profiling was beyond the scope of this study, future studies dissecting correlation between tumor biology and healthrelated outcome will be critical to understand the impact of tumor biology on long term functional outcomes. A further limitation of our study is lack of comparison cohort of older pediatric and adolescent patients diagnosed with CNS tumors. Nevertheless, our findings provide a comprehensive overview of an unselected large cohort of patients, diagnosed and followed by a multidisciplinary team in a tertiary center over a period spanning 3 decades.

Conclusions
Young children are at a high risk for long-term morbidity after diagnosis of a CNS tumor. Encouragingly, though a vast proportion of survivors experience health-related sequelae, most were integrated in regular schools. Our study highlights the importance of long-term support strategies, tailored to young children. These include early screening for visual and hearing impairment, as well as endocrinopathy and neuropsychology assessments, to offer appropriate support. Advances in treatment modalities, including targeted anti-tumor therapies and improvement in high-precision radiation techniques, will hopefully lead to a further reduction in treatment burden and better long-term outcomes in these children.

Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

Conflict of interest
The authors have no relevant financial or non-financial interests to disclose.
Ethical approval The design of the study was approved by the Ethics Committee of the Canton of Zurich, Switzerland (Nr. 2020-00801).
Consent to participate A general research consent was implemented at our institution in 2015. The need for informed consent was waived for deceased patients, patients diagnosed prior to 2015 and lost to followup. Patients who refused general consent were excluded from the study.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.