Evaluation of treatment-associated eye toxicity after irradiation in childhood and adolescence—results from the Registry of the Evaluation of Side Effects after Radiotherapy in Childhood and Adolescence (RiSK)

Approximately one third of pediatric oncology patients need radiation therapy during the treatment of their malignant disease [1, 2]. The survival rates have significantly improved during the past years, with the 5‑year-survival rate nowadays being over 80% [3]. Therefore, evaluation of treatment-related acute or late adverse effects is of major importance [4]. The acute (defined from start until 90 days after radiation therapy) and late (occurring after more than 90 days after radiation therapy) effects can be documented organ specifically by the RTOG/EORTC criteria [5, 6].

The eye, specifically the lens, is a sensitive structure and may develop relevant acute and late disorders, including cataract and retinopathy, after radiation therapy in children and adolescents [7‐10].

To standardize the documentation of acute and late effects after radiation therapy in pediatric patients the Registry of the Evaluation of Side Effects after Radiotherapy in Childhood and Adolescence (RiSK) was founded in 2001 by the German Working Group of Paediatric Radio-Oncology (APRO) chaired by N. Willich, Münster. Financial support was provided by the Deutsche Kinderkrebsstiftung. In addition to the basic data of the radiation therapy, the acute and late effects to relevant organs at risk were documented according EORTC/RTOG [6] for each patient. Evidence of a correlation between radiation dose, radiation volume, and occurrence of acute and late effects in several organs, such as liver, lung, and thyroid gland has already been published using the RiSK database [11‐13].

The aim of this study was to evaluate treatment-associated acute and late effects in the eye after radiation therapy in childhood and adolescence under consideration of the radiation dose–response relationship and further influencing factors.

The Registry of the Evaluation of Side Effects after Radiotherapy in Childhood and Adolescence includes altogether 1725 children and adolescents in 62 German centers, who underwent radiation therapy between 2001 and 2016. A standardized documentation of the applied radiotherapy including doses to organs at risk and adverse events based on RTOG/EORTC criteria of the patients was carried out and recorded in the database [1, 2, 6]. The classification of acute and late effects of the eye is displayed in Table 1. The Ethics Committee of the University Hospital Münster approved this project before starting documentation.

In the registry, the radiation doses to the right eye and left eye were documented separately. For evaluation, we used the maximum dose (right or left eye), determined as Dmax, for the further statistical analysis (Table 2). To better analyze the influence of the irradiation dose on ocular toxicity, a classification based on the Dmax value was performed (referring to Whelan et al.), as listed in Table 2; [7]. Late toxicity had been documented in most patients at each follow-up (median 2.5 follow-ups [range 1–11]) and the maximum level of late toxicity reported was used for the analysis. Also included in the analysis were the three most common diagnoses ALL, medulloblastoma, and rhabdomyosarcoma (Table 2).

From 2001 to 2016, 593 patients were included in this study who received a radiation dose to the eye (34.4%) and who were documented within the RiSK database. The basic characteristics of the patients, diagnosis, and treatment are shown in Table 2. 145 forms regarding pre-existing eye impairment were available. These include, for example, loss of vision, ptosis, eye muscle paresis, and strabismus. The median age of the patients was 8.48 years and the majority of patients received a radiation dose of more than 50 Gy to the eye (n = 270).

The eye, mainly the lens, is a particularly radiation-sensitive organ and even low doses of radiation increase the risk for subsequent ocular disorders [7, 9]. Especially the effect of radiation on the lens with regard to development of cataract has been investigated in numerous studies [7‐9, 14‐16]. Whelan et al. indicated in their large cohort study of the Childhood Cancer Survivor Study (CCSS) that survivors have a significantly higher risk for all ocular damages [7]. Acute toxicity reactions predominantly affect the ocular anterior segment and can cause reactions such as conjunctivitis, keratitis, or blepharitis [17]. Acute toxicities (≥ grade 1) did occur in our study in 11.5% of the patients. When analyzing the irradiation dose, the univariate analysis shows that a maximum radiation dose > 50 Gy significantly increased the risk of developing acute toxicity. In other studies the risk was already increased at appreciably lower irradiation doses. According to the ICRP (International Commission on Radiological Protection), ocular pathologies other than lens opacity after acute or fractional exposures already occurred at radiation doses of 5–20 Gy [15]. It can be assumed that the risk of an acute toxicity reaction is also increased by radiation doses lower than 50 Gy. Considering that in our case, only very few patients with documented toxicity were documented in Dmax 0–2.0 Gy, > 2.0–5.0 Gy, > 5.0–12.0 Gy, > 12.0–20.0 Gy, and > 20.0–40.0 Gy, statistical evaluation is not feasible. Acute toxicity reactions are usually reversible. For example, Gordan et al. described the self-limitation of acute complications after irradiation with 2–2.5 Gy to about 37 Gy in the treatment of orbital or conjunctival lymphomas [14]. Despite the frequent regression of acute reactions, the occurrence of toxicities and particularly severe chronic toxicities should not be underestimated—as our study impressively shows. As already demonstrated in another RiSK-based study, high-grade acute toxicities are a risk factor for developing chronic toxicity reactions [18]. In our study, the presence of acute toxicity was also significantly associated with late sequelae (p-value < 0.001). Thus, it is an important conclusion that an acute toxicity reaction should be avoided if possible, in order to consequently minimize the risk of severe late sequelae.

In our study, late toxicity (grade 1–4) was determined in 7.08% of patients, of whom five showed grade 4 toxicity according to the RTOG criteria (Table 1). According to Barabino et al., late reactions are mainly due to permanent vascular damage and the resulting ischemia of ocular structures, which can lead to retinopathies, cataracts, or neuropathies (these sequelae have also been observed in other studies [19]) [17]. In their study, they summarized the effects of radiation on the individual orbital structures based on other studies and evaluated them according to a radiation dose relationship. The pathophysiology of irradiation-induced cataracts is additionally based on DNA damage of lens epithelial cells and the development of posterior subcapsular opacification by migration of abnormal cells [8, 14]. The publication of Whelan et al. from the CCSS examined six different kinds of ocular sequelae originating from an irradiation dose relationship [7]. The development of dry eyes, double vision, legal blindness, cataract, retinal conditions, and glaucoma was evaluated. The occurrence of eye sequelae was compared between survivors and a sibling control group. Patients answered specific questions about the occurrence of the six diagnoses in a self-questionnaire, repeated at 5 and 10 years after diagnosis. The analysis revealed an increased risk for survivors of developing a cataract, glaucoma, legal blindness, double vision, and dry eyes compared to siblings. The relationship between the irradiation dose to the eye and the risk of late complications also showed a defined correlation: a dose of 2–5 Gy significantly increased the risk of double vision and cataract. With a radiation dose of 5–12 Gy, a significant influence on the development of dry eyes and blindness was found. Retinal conditions were more frequent at doses of 20–40 Gy or more. It should be noted that the risk of all diseases increased with higher radiation doses (also observed specifically for cataract in Tinkle et al. [16]). Unfortunately, an exact evaluation of the influence of the irradiation dose to the eye on development of late toxicity was not possible in our study, as the number of patients in the different dose groups was insufficient. However, in the multivariate analysis of the single variable Dmax > 50 Gy, the survival analysis showed significance with a p-value 0.038. Of the 42 patients with documented late toxicity ≥ grade 1, 25 received a radiation dose of > 50 Gy to the eye. We conclude that the risk of toxicity is lower for radiation doses below 50 Gy than above 50 Gy. An irradiation dose of 50 Gy to the eye can be observed as a critical threshold [17]. Although the context of the study by Jazmati et al. is different due to the palliative situation of the irradiated children, no late toxicities were documented in this study with a median irradiation dose of 36 Gy [20]. Another limitation of our study when compared to other studies was the inability to examine the individual specific secondary disorder. The RiSK uses the graduation of consequential damage according to RTOG/EORTC; therefore, a differentiation of specific diseases is not available [6]. The same degree can be assigned by different ocular diseases and their severity (see Table 1). An advantage of this approach can be observed. Radiation-induced damage to one structure can additionally negatively affect other surrounding ocular structures [14]. The indicated degree of toxicity is able to offer an overall impression of the acute and late sequelae, in addition to an overall assessment of the eye and vision.

The influence of chemotherapy as a risk factor for toxicity after RT has been investigated in several studies [7, 9, 11‐13]. Cytostatic drugs such as platinum, vinca alkaloids, taxane, methotrexate, or even 5‑flourouracil can come with ocular toxic side effects [21, 22]. For example, vincristine, frequently used in chemotherapy of various malignant diseases, can cause diplopia, ptosis, optic atrophy, or transient cortical blindness [21, 22]. Our study also showed a significant relationship between chemotherapy and toxicities. In acute toxicity, chemotherapy prior to radiation showed notably significant effects, as did simultaneous chemotherapy for late secondary damage. The relationship between simultaneous chemotherapy and high-grade toxicities has already been suggested by Pixberg et al. [18].

Rhabdomyosarcoma was the most common diagnosis of the included patients in this study and represented a statistically significant risk factor for the development of acute (in uni- and multivariate analysis) and late toxicity (in univariate analysis). In the publication of Eade et al., rhabdomyosarcoma is mentioned as the most frequent primary tumor of the orbit in childhood [23]. Main late complications after treatment are cataract and keratopathy. Other studies also proved ocular late effects after rhabdomyosarcoma therapy in childhood and adolescence [23, 24]. The relevant pre-existing eye impairment also increased the risk for toxicity—in case of acute toxicity even significantly in uni- and multivariate analysis. It cannot be derived from the RiSK data whether previous damage to the eye was caused by the tumor, although it can be assumed. An ophthalmological examination ahead of commencing irradiation can indicate an existing damage, which can be prone to exacerbation [17]. This may help to predict or even prevent a possible risk of secondary late effects and aggravation of existing ocular restrictions.

Children aged 0–4 years had a significantly higher risk of developing acute or late toxicity in univariate analyses. Most ocular structures develop in early childhood [25]. For example, lens thickness decreases and the individual compartments change their depth and length. Due to this early childhood development, it can be assumed that irradiation at this age has an influence on development and the eye is particularly susceptible to secondary damage. The significance in our statistical evaluation can be attributed to this influence. The analysis of the influence of proton irradiation must be viewed critically with regard to any possible impact on toxicity. Even when the univariate analysis of acute toxicity and late toxicity suggests a significant influence, this finding could not be confirmed in multivariate analysis. Most probably, the observed effect was caused by a selection bias. With proton therapy, particularly very young patients diagnosed with rhabdomyosarcoma receiving relatively high radiation doses were treated. Accordingly, our descriptive evaluations show a significantly higher median irradiation dose to the eye with protons when compared to photons. A high median radiation dose for proton irradiation can also be observed in other studies such as Doyen et al. (median total prescribed dose 55.8 Gy) [26]. Therefore, the use of protons cannot be associated with any increased risk for toxicity within this study.

In radiotherapy, the technical possibilities are constantly being developed with the aim of minimizing acute and late sequelae. Techniques such as IMRT or tomotherapy make it possible to irradiate pathological tissue in a more conformal manner while sparing healthy surrounding tissue [27, 28]. It is well known that in addition to the radiation dose used, the volume irradiated has a major impact on organs at risk (OARs) and this is minimized by new radiation methods [29]. Maximum doses are often determined for OARs to minimize sequelae (for example, < 55 Gy at the base of the skull, optic chiasm, optic nerve) [26]. Nevertheless, studies show that late effects occur even with these techniques [28]. In 2020, Bishr et al. show that radiation therapy is used very commonly in pediatric cancer treatment—both curatively and palliatively [30]. Children with radiation-related late effects are forced to live with these effects for significantly more years, and this can have a significant impact on quality of life [28]. This is why, in our view, it is so important to minimize and ideally prevent radiation damage in childhood.

There are limitations of our study. Unfortunately, we did not have all information on late toxicity for our cohort and FU time was still limited. Moreover, information on specific ocular disorders following radiotherapy was not given. Finally, when considering all subgroups and techniques used, the number of patients was still restricted. Data were not analyzed in a matched-pair analysis. Furthermore, we did not investigate consecutive interventions or therapies for eye disorders, which would be of interest to understand the impact of any specific disorder and to better define the role of RT in the future. To conclude, an irradiation dose of > 50 Gy to the eye represented a significantly increased risk for toxicity of the eye. However, young age and RMS diagnosis showed a significant influence as well. To our knowledge, RiSK was the only prospective registry for recording acute and late effects of radiotherapy in childhood and adolescence. The documentation was carried out by qualified radio-oncologists and based on standardized medical follow-up examinations, which is crucial for the aftercare of specific side effects [31]. Therefore, the data from the RiSK must be considered objective with regard to eye damage. Other studies dealing with the same problem are analyzed on the basis of information from patient self-interviews, which are subjective views of the patients [7, 9].

The eye is very sensitive to radiation and, especially in early childhood, any exposure to radiation can have an effect on the development of the eye and the occurrence of secondary damage. Our study indicates that different factors have an influence on the development of eye toxicity after irradiation. Acute and late toxicity seem to be correlated with a high radiation dose to the eye (> 50 Gy). Also, patients having treatment for a rhabdomyosarcoma diagnosis seem to be particularly prone to developing eye disorders. However, even below a dose of 50 Gy is there a certain risk for severe acute and especially chronic toxicities. Therefore, radiation doses to the eye should generally be kept as low as possible to reduce the risk of toxicity. Any radiation therapy in a child and in the craniofacial area has to be carefully balanced against the risk for life-long sequelae.