Abstract
Purpose
Our aim was to determine the main risk factors related to the occurrence of permanent alopecia in childhood medulloblastoma (MB) survivors.
Methods
We retrospectively analyzed the clinical features of all consecutive MB survivors treated at our institute. We divided the patients into 3 groups depending on the craniospinal irradiation (CSI) dose received and defined permanent alopecia first in terms of the skin region affected (whole scalp and nape region), then on the basis of the toxicity degree (G). Any relationship between permanent alopecia and other characteristics was investigated by a univariate and multivariate analysis and Odds ratio (OR) with confidence interval (CI) was reported.
Results
We included 41 patients with a mean10-year follow-up. High dose CSI resulted as an independent factor leading to permanent hair loss in both groups: alopecia of the whole scalp (G1 p-value 0.030, G2 p-value 0.003) and of the nape region (G1 p-value 0.038, G2 p-value 0.006). The posterior cranial fossa (PCF) boost volume and dose were not significant factors at multivariate analysis neither in permanent hair loss of the whole scalp nor only in the nuchal region.
Conclusion
In pediatric patients with MB, the development of permanent alopecia seems to depend only on the CSI dose ≥ 36 Gy. Acute damage to the hair follicle is dose dependent, but in terms of late side effects, constant and homogeneous daily irradiation of a large volume may have a stronger effect than a higher but focal dose of radiotherapy.
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Introduction
Medulloblastoma (MB) is the most common Central Nervous System (CNS) embryonal tumor in children [1], accounting for approximately 20% of all pediatric CNS tumors. It typically arises in the posterior cranial fossa and metastasizes along the neuroaxis [2].
Although MB is a malignant brain tumor, survival rates at 5-years from diagnosis can reach up to 80% for the standard-risk patients and close to 100% for WNT-activated biomolecular subgroup [2, 3].
Standard treatment involves surgery and adjuvant therapy, which includes radiotherapy (RT) and/or chemotherapy (CT), that are tailored to the clinical case according to age, extent of post-surgery residual disease, metastatic status, and molecular and cellular markers[4]. Radiation therapy consists of risk-adapted craniospinal irradiation (CSI) followed by a boost to the whole posterior cranial fossa (WPCF) or to the primary tumor bed (PCF tb-boost) [5]. MB is divided into low, standard and high risk, according to clinical, histological and molecular features [3, 6]. The last European trial SIOP PNET5 MB (already closed for recruitment, although the observation is still ongoing) included reduction of craniospinal irradiation intensity from 23.40 to 18 Gy for low-risk patients and randomization to RT alone or RT concomitant with Carboplatin in standard-risk patients with a classic CSI dose of 23.40 G; in both risk groups a volumetric boost reduction in PCF, from WPCF boost to tumor bed boost, with RT dose up to 54 Gy was provided [6]. These improvements aim to spare the organs at risk minimizing doses to hippocampi, temporal lobes, hypothalamic-pituitary axis, and cochleae, increasing long-term survivors’ clinical outcomes and quality of life.
Radiotherapy planning based on the fusion of pre- and post-surgery brain MRIs and the use of intensity-modulated radiation therapy (IMRT) techniques or proton beam therapy are mandatory in the Protocol [6].
High risk MB treatment consists of high dose CSI up to 39 Gy and often high dose chemotherapy with a stem cell rescue [7]. The MB survivors are at high risk to develop long term late effects, such as neurocognitive and psychosocial impairments, neuroendocrine damage, and alopecia [6, 8].
Permanent alopecia in childhood cancer survivors is a late effect that negatively impacts vitality and social function [9].
The risk of permanent hair loss after radiotherapy has been studied more extensively in adults [9] and increases with radiation therapy and high dose chemotherapy [10, 11]. Due to the large volume involved, the craniospinal irradiation seems to be associated with a higher risk of permanent alopecia [10, 12]. High dose chemotherapy after RT increases the risk of radio-necrosis and other toxicities. However, in long-term childhood cancer survivors its role is still unclear [10, 12,13,14,15].
In this study, we analyzed a cohort of MB long-term survivors treated with standard, intermediate and high radiotherapy dose intensity regimes, to assess dose-associated factors that can be predictive of permanent hair loss. Our secondary aim was to assess the possible effect of high dose chemotherapy on the development of alopecia in pediatric patients.
Materials and methods
Study criteria
We retrospectively analyzed the clinical records of all consecutive survivors of MB who underwent chemotherapy at Gaslini Children’s Hospital in Genoa, Italy, and radiotherapy at IRCCS Policlinico San Martino Hospital in Genoa, from January 1999 to September 2019. Inclusion criteria were histological diagnosis of MB, completed radiotherapy treatment plan and at least 1-year-long-follow-up after the end of treatment. We excluded patients younger than 3 years of age because they do not receive radiotherapy.
All patients (or their parents if minors) gave written informed consent to undergo RT and accepted that their anonymous data could be used in scientific studies. This study was approved by the local Ethics Committee of IRCCS Policlinico San Martino Hospital of Genoa (n°717/2021).
We collected and retrospectively reviewed clinical and instrumental data of all eligible patients including demographic data, age at time of treatments and at the last follow up, endocrinological screening, oncological treatments and the resulting hair-bearing areas of the head toxicities.
Oncological treatments
All patients received chemotherapy and radiotherapy according to the oncological protocol in use at the start of the treatment.
Patients were treated with three-dimensional conformal radiation therapy (3D CRT) technique (Varian CLINAC 2100, Treatment Planning System (TPS) Eclipse 13.0 and previous) before 2010, Intensity-Modulated Radiation Therapy (IMRT) has been used for the PCF boost from 2010 and volumetric technique by Helical Tomotherapy (HiArtAccuray TPS) has become the standard treatment from 2015. The radiotherapy plan consisted of CSI (Phase 1) and, according to the protocol in use, PCF boost or WPCF boost (Phase 2). In this second phase, patients received a radiation boost only of tumor bed or of the whole PCF or of both in case of residual disease after surgery. For each radiotherapy plan we retrospectively analyzed prescription data: total dose, number of fractions (dose/die, fraction/die, daily dose) and radiotherapy technique (3D-CRT or IMRT). The Planning Target Volume (PTV) -boost in milliliters (mL) was calculated to assess if higher treatment boost volume was associated with a higher incidence of alopecia.
The photon beam energy used for 3D CRT was mainly 6MV (except for oversize patients) and 6MV in helical tomotherapy. Typical brain beam arrangements in patients treated by 3D-CRT included two fields with 90° and 270° gantry conformed with 1 cm Multileaf collimator (MLC), whereas HiArtTomotheraphy, with 0.287 pitch, included a 2.5 cm field and modulation factor ranging from 2–3.
Patients were all treated supine, with immobilization masks on both face and body, and positioning tattoos on the trunk and abdomen-pelvis region.
We classified the patients in 3 groups, according to the class of risk, based on CSI dose: standard risk dose, adapted dose, and high risk dose. Supplementary table 1 shows the radiotherapy dose adopted.
Alopecia
Alopecia was assessed in the scalp and nape region, based on irradiated volume (Supplementary Fig. 1), according to the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 rating scale [14]: G1 (less than 50% hair loss and/or possibility of camouflage with other hair) and G2 (greater than 50% loss, no possibility of camouflage, use of wigs/other aids necessary). It was determined by physical examination performed by the oncologist (A.V.) and defined as permanent if persistent longer than 1 year [15]. For each patient, we examined the other hair-bearing areas of the head: the eyebrows and the eyelashes.
Statistical analysis
Data analysis was conducted by using SPSS® software version 26 (IBM Corp. Released 2019. IBM SPSS Statistics for Windows, Version 26.0. Armonk, NY: IBM Corp). Dichotomous and continuous variables were compared with the chi squared test and by using a one way analysis of variance (ANOVA), respectively.
Univariate and multivariate binary logistic regression analysis with a stepwise backward procedure was performed. In the multivariate model were included all the variables with a p-value < 0.10 at the univariate analysis. The occurrence of permanent alopecia of the whole scalp and the one of the nape region were set as dependent variables. The same analysis was conducted considering separately and jointly (sum group) the grade of severity (grade 1 and grade 2) of alopecia in both two groups. In the alopecia whole scalp group, the PCF dosimetry data were not considered.
Odds ratio (OR) were reported with the respective 95% confidence interval (CI).
Statistical significance was set at p < 0.05.
Results
We analyzed a total of 41 patients with MB with a median follow-up of 116 months (range: 15—250). Twenty-three (56%) were males and 18 (44%) were females. The mean age at diagnosis was 7.09 years (range: 2- 16). The mean age at last follow up was 17 years (range: 6–30). The demographic and clinical features of the patients, including endocrinological results, related to the grade of alopecia, are reported in Table 1.
Whole scalp alopecia was observed in 22 patients (54%), equally divided between G1 and G2 (11 each); among the 11 with G1, 7 presented a G2 alopecia in the nape region too.
Nape region alopecia was observed in 22 patients (54%). 19 patients (46%) had no signs of permanent hair loss (G0) neither in the whole scalp nor in the nape region.
There were no cases of permanent hair loss of eyebrows or eyelashes.
All patients received chemotherapy. Furthermore, patients (n = 22) with high risk MB received two courses of high dose chemotherapy: 14/22 patients (64%) received Thiotepa [8 patients (57%) after the end of radiotherapy and 6 (43%) before the start], 8/22 patients (36%) received other chemotherapies such as Etoposide, Carboplatin, Methotrexate.
Craniospinal irradiation with a median dose of 25.20 Gy and PCF boost with a dose up to 69 Gy were administered to all patients.
Every clinical and dosimetric variable was included in the univariate analysis, in order to assess their association with the risk of permanent hair loss of the whole scalp (Table 2) or of the nape region (Table 3).
Alopecia of the whole scalp
Considering the alopecia sum group, at the univariate analysis, high dose chemotherapy (OR 3.000, 95% CI 0.839–10.727), high dose of CSI (OR 25.667, 95% CI 2.680–245.842), CSI daily dose per fraction (OR 0.976, 95% CI 0.955–0.999), and total dose at the tumor bed (OR 1.002, 95% CI 1.000–1.003) resulted eligible for multivariate analysis (p-value < 0.1 for all the variables). The multivariate model confirmed only the high dose of CSI as an independent predictor of the development of the whole skin alopecia (p-value 0.005).
Considering the alopecia G1 group, the univariate analysis identified high dose of CSI (OR 14.000, 95% CI 1.299–150.889) and total dose at the tumor bed (OR 1.002, 95% CI 1.000–1.003) as possible predictors (for both, p-value < 0.1). Again, at the multivariate analysis only high dose of CSI resulted an independent prognostic factor (p-value 0.030). Similarly, the univariate analysis detected high dose chemotherapy (OR 13.500, 95% CI 1.421–128.258), high dose of CSI (OR 84.000, 95% CI 4.476–1576.519), CSI daily dose per fraction (OR 0.961, 95% CI 0.929–0.993), CSI daily dose (OR 1.035, 95% CI 1.011–1.060), and total dose at the tumor bed (OR 1.002, 95% CI 1.000–1.004) as possible predictors of the development of G2 alopecia (p-value < 0.1 for all the variables), but only high dose of CSI reached significance at the multivariate model (p-value 0.008).
Alopecia of the nape region
The univariate analysis showed high dose of CSI (OR 25.667, 95% CI 2.680–245.842), CSI daily dose per fraction (OR 0.972, 95% CI 0.949–0.996), CSI daily dose (OR 1.020, 95% CI 1.000–1.040), PCF daily dose per fraction (OR 0.973, 95% CI 0.944–1.001) and total dose at the tumor bed (OR 1.002, 95% CI 1.000–1.003) as possible predictors of the development of PCF alopecia (p-value < 0.1 for all the variables). At the multivariate analysis, only the high dose of CSI resulted an independent prognosticator (p-value 0.005).
In patients with G1 PCF alopecia, high dose of CSI (OR 28.000, 95% CI 1.208–648.809) and PCF dose (OR 0.997, 95% CI 0.993–1.000) resulted possible predictors at the univariate analysis (for both, p-value < 0.1). The multivariate model confirmed only high dose of CSI as an independent prognostic factor (p-value 0.038). Analogously, the univariate analysis identified high dose chemotherapy (OR 3.300, 95% CI 0.826–13.181), high dose of CSI (OR 25.200, 95% CI 2.515–252.497), CSI daily dose per fraction (OR 0.969, 95% CI 0.944–0.994), CSI daily dose (OR 1.023, 95% CI 1.002–1.044), and total dose at the tumor bed (OR 1.002, 95% CI 1.000–1.003) as possible predictors of the development of G2 alopecia of the PCF (p-value < 0.1 for all the variables), but the only independent prognosticator at the multivariate analysis was high dose of CSI (p-value 0.006).
Discussion
In our study, we have analyzed a cohort of MB survivors treated with radiotherapy to define the prevalence of permanent alopecia and the risk factors for its onset.
Permanent hair loss was observed in 54% patients. Among several clinical parameters assessed, only the high dose CSI (36 to 39 Gy) emerged as significant predictor of the development of alopecia G1 and G2, independently from the boost dose delivered to the tumor bed above CSI dose, the daily dose administered, the radiotherapy technique applied (3D-CRT vs IMRT-helicoidally), the boost volume and the use of high doses chemotherapy pre- or post-radiotherapy. Exceeding these doses of radiotherapy, the other risk factors lose their significance.
Previous reports showed a dose–response relationship describing the possibility of alopecia onset after radiation therapy [16]. In 2004, Lawanda et al. retrospectively examined 26 brain tumor patients and concluded that a cranial field radiotherapy dose of 43 Gy was associated with onset of permanent alopecia in 50% of patients [17].
Min et al. in 2014 reported on 12 pediatric patients with MB the occurrence of permanent alopecia after craniospinal proton therapy and chemotherapy. Based on their results, the mean dose of ~ 21 Gy (RBE-Relative Biological Effectiveness) could be considered the threshold for permanent alopecia in patients treated with high dose chemotherapy, while the threshold dose for alopecia could be 30 Gy (RBE) with conventional chemotherapy [10].
Scoccianti et al. in 2020, in a large prospective observational study including 101 brain tumor patients (adults and children), identified V40Gy < 5.4 cc as the threshold dose for permanent hair loss. They also hypothesized that Volumetric Modulated Arc Therapy (VMAT), a technique allowing highly conformal dose, is the most appropriate for reducing the dose to the scalp [18].
Based on our results, high dose CSI of ≥ 36 Gy is the only risk factor for development of G1 and G2 permanent alopecia in the whole-scalp as well as in the PCF region, independent of other clinical and therapeutic variables. The higher dose of the PCF boost was not found to be a significant risk factor for developing alopecia, even in the subgroup of patients with alopecia limited to the posterior cranial fossa. These results confirm that the homogeneous dose distribution for a large scalp volume increases the sensitivity of the hair follicles to the dose and thus decreases the tolerated dose level [10, 17, 19]. Oncological treatment-induced alopecia has multifactorial etiopathogenesis, as shown in Fig. 1 the causes of permanent alopecia are unclear [20].
Our results support the assumption that the high dose chemotherapy does not influence the occurrence of permanent alopecia in patients treated with high dose radiotherapy, the presence of eyelashes and eyebrows in our cohort could be a clinical indicator of this result [20]; it is however conceivable that in patients treated by low or standard dose CSI, the high dose chemotherapy could play a role in the permanent hair tinning onset.
Therefore, in order to confirm the data identified by Min et al. and from Scoccianti et al. as relevant factors in development of permanent alopecia, it is necessary to carry out a further study in a larger cohort of patients with a CSI dose lower than 36 Gy, in order to statistically assess whether other parameters may also influence the onset of permanent alopecia. In these patients, a specific scalp contouring as shown in Fig. 2 could allow dose scalp sparing without uncovering the tumor target.
The strengths of our study are represented by the fact that our cohort consisted of a homogeneous sample of MB survivors (especially by histology, therapy, and age group), treated with CSI and PCF boost with a median very long-term follow-up (9.6 years), subjected to statistical analysis.
On the other hand, this work presents two main limitations: retrospective and monocentric design and the limited number of subjects, due to the fact that MB is a rare disease.
However, despite these limitations, we identified a statistically significant CSI dose as the single permanent alopecia determinant.
Conclusion
Our study identifies high doses radiotherapy as an independent risk factor for the development of permanent alopecia G1 and G2. Parents and patients undergoing MB high risk treatment, with high doses radiotherapy, should be always informed of this unavoidable risk.
Future studies are necessary to identify the main risk factors for the development of permanent alopecia G1-G2 for patients undergoing standard dose and low dose CSI. For this purpose, whole scalp and PCF contouring is a useful tool which allows conforming the dose to the scalp without discovering the target.
Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- CNS:
-
Central Nervous System
- CP:
-
Cyclophosphamide
- CSI:
-
Craniospinal Irradiation
- CT:
-
Chemotherapy
- CTCAE:
-
Common Terminology Criteria for Adverse Events
- CTV:
-
Clinical Target Volume
- D:
-
Dose
- fr:
-
fraction
- G:
-
Grade
- Gy:
-
Gray
- HD-CT:
-
High dose chemotherapy
- IMRT:
-
Intensity Modulated Radiation Therapy
- MB:
-
Medulloblastoma
- MLC:
-
Multileaf collimator
- MV:
-
Megavolt
- PCF:
-
Posterior Cranial Fossa
- PTV:
-
Planning Target Volume
- QoL:
-
Quality of Life
- RT:
-
Radiotherapy
- TPS:
-
Treatment Planning System
- VMAT:
-
Volumetric Modulated Arc Therapy
- V40:
-
The percentage volume that received at least 40 Gy
- WPCF:
-
Whole Posterior Cranial Fossa
- 3D-CRT:
-
Three-dimensional conformal radiation therapy
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Camilla Satragno and Antonio Verrico designed the study, collected the data and drafted the manuscript. Flavio Giannelli, Alfonso Ferrero, Sucheeta Campora and Marianna Turazzi contributed to the collection of radiotherapy patient data. Francesca Cavagnetto revised the physical part. Irene Schiavetti carried out and revised the statistical part. Federica Garibotto, Gianluca Piccolo and Marco Crocco contributed to the collection of pediatric oncology patient data. Maria Luisa Garrè, Claudia Milanaccio, Antonia Ramaglia, Sonia Di Profio reviewed the study as subject specialists. Salvina Barra coordinated the clinical part of the work. Liliana Belgioia coordinated the research part of the work, reviewed the study and revised the manuscript.
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All patients (or their parents if minors) gave written informed consent to undergo RT and accepted that their anonymous data could be used in scientific studies.
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Satragno, C., Verrico, A., Giannelli, F. et al. High dose craniospinal irradiation as independent risk factor of permanent alopecia in childhood medulloblastoma survivors: cohort study and literature review. J Neurooncol 160, 659–668 (2022). https://doi.org/10.1007/s11060-022-04186-2
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DOI: https://doi.org/10.1007/s11060-022-04186-2