"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead

Original article

A Retrospective Analysis of the Demographics, Treatment, and Survival Outcomes of Patients with Desmoplastic Nodular Medulloblastoma Using the Surveillance, Epidemiology, and End Results (SEER) Database



Medulloblastoma is the most common malignant brain tumor in children younger than four years of age. Children diagnosed with desmoplastic nodular medulloblastoma (DNMB) have more favorable survival outcomes when compared to other subtypes of this disease and, to date, the demographics of DNMB have only been characterized by a few small clinical case series. Additionally, the current effort is being made at reducing radiotherapeutic modalities in this patient population to avoid the adverse effects associated with radiotherapy in children. Therefore, the goal of this study was to characterize the demographics, treatments, and survival outcomes of patients with DNMB using a large federal database.


The Surveillance, Epidemiology, and End Results database was queried to retrieve demographical, treatment, and survival data for patients diagnosed with DNMB. Statistical testing was performed with the R software stats package (R Foundation for Statistical Computing, Vienna, Austria). Student’s t tests and analysis of variance tests were used to measure differences among survival rates.


Data from 360 patients with DNMB were retrieved from 1975-2016. There was a higher prevalence of DNMB in children younger than four years of age (33% of all cases). Males had a higher prevalence than females (57%). There was a preponderance of diagnoses in white individuals (82% of all cases) and more diagnoses in the Pacific Coast region (49% of all cases). Distant metastases were present at initial diagnosis in 8.7%. Surgery was performed in almost all patients, and gross total resection was achieved in 77%. The overall rate of survival was 77.8% at five years; age, sex, race, and geographical region of diagnosis were not associated with differences in survival outcomes. Patients with no radiotherapy had a lower rate of survival compared to patients with postoperative radiotherapy (mean difference = 19.7%; [95% CI 1.4%-38.0%], p = 0.0314). However, radiotherapy did not improve survival outcomes in patients undergoing chemotherapeutic treatment to a degree with any statistical significance. There was no statistically significant improvement in survival for patients undergoing radiotherapy prior to procedure when compared to patients with no radiotherapy.


In patients undergoing chemotherapeutic treatment for the DNMB subtype of medulloblastoma specifically, additional radiotherapy may offer only minimal benefit to the survival outcome. It is essential continued clinical trials be performed for the purpose of devising alternate treatments to radiotherapy.


Medulloblastoma is the most common malignant brain tumor in children younger than four years of age [1]. The WHO has divided medulloblastoma into four different histological subtypes, of which, desmoplastic nodular medulloblastoma (DNMB) is associated with the most favorable prognosis [2]. The WHO utilizes both histological and molecular profiling methods to identify and differentiate among these medulloblastoma subtypes. DNMBs are found to be hedgehog activated and TP53 wild-type [2].

Traditional approaches to treatment for medulloblastoma involve resection, chemotherapy, and craniospinal radiation for optimal survival outcomes [3]. Unfortunately, radiotherapy has been found to cause many long-term and detrimental side effects in children, including cognitive damage, central endocrinopathies, vasculopathies, as well as having been associated with the induction of secondary malignancies post-therapy [4-6]. Therefore, current effort is being made in identifying and investigating alternative treatment options to radiotherapy that also offer equal survival outcomes. To date, the use of post-operative chemotherapy comprising methotrexate and autologous hematopoietic cell rescue has been found to offer promising rates of survival without radiotherapy [7-10]. Investigating alternative treatment options for the purpose of minimizing the side effects of radiotherapy is crucial for DNMB since these patients already have more favorable rates of survival when compared to other medulloblastoma subtypes.

One goal of this study was to further characterize outcomes associated with radiotherapy use in this patient population. Additionally, there are only a few clinical case series describing patients with the DNMB subtype of medulloblastoma specifically [11-13]. Therefore, another goal of this study was to characterize the demographics of this patient population using a large patient size from a longitudinal database. To accomplish these goals, the Surveillance, Epidemiology, and End Results (SEER) database was queried during the time frame of 1975-2016 for all patients diagnosed with DNMB. All data of this patient population’s demographics, treatments, and rates of survival were extracted and statistically analysed.

Materials & Methods

Database information

The SEER database is a federally funded cancer data repository made available by the United States Centers for Disease Control and Prevention, the United States National Cancer Institute, and several other regional and state cancer registries [14]. It is a well-validated system for providing individual patient data for the purpose of measuring the incidence, prevalence, mortality rates, and treatment modalities of cancer in the United States [15].

Database search parameters

The SEER database was queried for all patient data of individuals diagnosed with DNMB using guidelines previously suggested for analysing large-volume databases [16]. Data for demographic characterization was retrieved from the most recent dataset: Incidence - SEER 18 Regs Research Data + Hurricane Katrina Impacted Louisiana Cases, Nov 2018 Sub (1975-2016 varying). For the purpose of retrieving data on survival outcomes, the following database was used: Incidence - SEER 18 Regs Research Data + Hurricane Katrina Impacted Louisiana Cases, Nov 2018 Sub (2000-2016) <Katrina/Rita Population Adjustment>. For the purpose of retrieving chemotherapeutic and radiotherapeutic data, the following dataset was used: Incidence - SEER 9 Regs Custom Data (with additional treatment fields), Nov 2018 Sub (1975-2016) <Katrina/Rita Population Adjustment>. The data were extracted and survival rates were calculated with the SEER*STAT v 8.3.6 software (National Cancer Institute, Bethesda, MD). All patients with the International Classification of Diseases for Oncology, Third Edition (ICD-O-3) diagnosis code of 9471/3 for DNMB were included.

Collected data included sex, race, geographical region, age at diagnosis, metastasis at diagnosis, extent of surgical resection, treatment with chemotherapy, treatment with radiotherapy, and sequence of radiotherapy as it related to the surgical resection of the tumor. Survival outcomes were also calculated at one, two, three, four, and five years post diagnosis.

The extent of surgical resection was divided into gross total resection (GTR) and subtotal resection (STR). The GTR group had patients identified with surgical codes 55 (GTR of the lobe of brain), 40 (partial resection of the lobe of brain), and 30 (radical, total, gross resection of tumor, lesion mass, or mass in brain). The STR group was identified with patients who were listed with surgical codes 27 (excisional biopsy), 22 (partial resection of tumor, lesion, or mass), 21 (STR of tumor, lesion, or mass, not otherwise specified [NOS]), and 20 (local excision of tumor, lesion, or mass, excisional biopsy, or stereotactic biopsy of the brain).

Metastases at diagnosis data included the diagnosis codes of 50 (distant metastasis in addition to a distant metastasis at a lymph node), 20 (distant metastasis at a lymph node plus a metastasis at an inferior vena cava lymph node), 10 (metastasis present at distant lymph nodes, NOS), and 0 (no metastases present at diagnosis).

Statistical analysis

Analysis and visualization were performed with the R software (R Foundation for Statistical Computing, Vienna, Austria) using the stats package. The analysis was performed according to guidelines established for describing large observational datasets.Student’s t tests were used to calculate mean differences and 95% confidence intervals when comparing two separate means. Analysis of variance (ANOVA) testing was used to compare means across multiple groups. Subsequent post hoc analysis was performed with Tukey’s test. In this statistical testing, p < 0.05 was considered significant.



There were 360 patients with DNMB diagnosed from 1975 to 2016. Males had a higher prevalence than female patients (57%). There were 33% of the total DNMB diagnoses in children younger than four years of age. There was a preponderance of diagnoses in white individuals (82% of all cases) and individuals in the Pacific Coast geographical region (49% of all cases). Surgery was performed in 96.7% of patients, and GTR was achieved in 77%. Patient demographics including sex, race, geographic region, age, and extent of resection are displayed in Table 1.

Characteristic N % of demographic
Overall   360 -
Sex Male 206 57
  Female 154 43
Race White 295 82
  African American 28 8
  Other* 37 10
Region Alaska 0 0
  East 110 31
  Northern Plains 34 9
  Pacific Coast 176 49
  Southwest 40 11
Age <1 20 6
  1-4 100 28
  5-9 56 16
  10-14 26 7
  15-19 29 8
  20-24 30 8
  25-29 28 8
  30-34 24 7
  35-39 18 5
  40-44 8 2
  45-49 9 2
  50-54 8 2
  >55 4 1
Resection GTR 216 77
  STR 66 23

Tumor size ranged from 12 to 73 mm. Laterality was largely equal with most tumors labeled as “not a paired site.” Of the tumors where laterality was specified, 47% were identified as right-sided origin and 53% were identified as left-sided origin. 

Distant metastases were present at initial diagnosis in 8.7% patients. Locations of metastatic disease at initial diagnosis included the bone (one case), other areas of the brain (four cases), and at unspecified locations (two cases).

Survival analysis

Survival data was available for 270 patients with data ranging from 2000 to 2016. Survival data was not collected before 2000 for this particular SEER database. Overall survival at five years was 77.8%. Rates of survival at five years stratified by demographical subgroups are displayed in Table 2.

Characteristic N Five-year survival rate %
Overall 270 77.8
Sex Male 159 80.5
  Female 111 73.7
Race White 219 78.7
  African American 20 85.1
  Asian or Pacific Islander 28 67.1
  American Indian/Alaska Native 3 66.7
Region East 87 73.4
  Northern Plains 20 79.1
  Pacific Coast 139 80.5
  Southwest 24 77.4
Age <1 15 100
  1-4 83 75.6
  5-9 43 83.9
  10-14 19 78.6
  15-19 25 71.6
  20-24 23 79
  25-29 24 72
  30-34 14 71.4
  35-39 9 84.6
  40-44 4 100
  45-49 5 36
  50-54 5 75
  >55 2 50

Student’s t testing revealed no statistically significant differences in survival between sex categories. ANOVA revealed no statistically significant variances among race, geographical region, or age groups associated with survival outcomes.

Radiotherapy and chemotherapy

The database included data for 169 patients regarding their status of undergoing either treatment with chemotherapy or radiotherapy (Table 3).

  No radiotherapy (%) Radiation prior to surgery (%) Radiation after surgery (%)
No chemotherapy 15 (88.8) 4 (2.4) 34 (20.1)
Chemotherapy 39 (23.1) 1 (0.6) 76 (45.0)
Total 54 (32.0) 5 (3.0) 110 (65.1)

Chemotherapy was reported using binary values only: either with or without chemotherapy. Patients who underwent chemotherapy had a higher rate of survival at five years than patients who did not undergo chemotherapy (mean difference = 20.4%; [95% CI 5.2%-35.6%], p < 0.01).

Radiotherapy was reported as binary variables: with beam radiotherapy or without beam therapy. Entries involving radioactive implants (two), refused radiotherapy (two), and unknown if administered (one) were excluded from the analysis. Radiotherapy sequence was reported as eight different potential variables: no radiation delivered, radiation prior to surgery, radiation after surgery, radiation both before and after surgery, intraoperative radiation, intraoperative radiation with either additional radiotherapy before or after surgery, surgery both before and after radiation, and unknown sequence of radiotherapy with surgery. Only the treatment categories of no radiation, radiation prior to surgery, and radiation after surgery had entries of patient data.

Patients undergoing beam radiation had a statistically significant improved survival rate when compared to patients not undergoing radiotherapy (mean difference = 16.4%; [95% CI 0.54%-32.34%], p = 0.043). Of patients undergoing chemotherapeutic treatment (N = 116), radiotherapy did not have a statistically significant improvement in survival outcome at five years (Figure 1).

ANOVA revealed variances among radiotherapy sequence and survival (p < 0.035). Post hoc Tukey’s testing revealed that patients undergoing no radiotherapy had a lower rate of survival at five years when compared to patients with radiotherapy after surgery (mean difference = 19.7; [95% CI 1.4%-38.0%], p = 0.031). There was no statistical difference between patients undergoing no radiotherapy and radiotherapy prior to surgery. Survival plot of radiotherapy sequence as it relates to surgery is displayed in Figure 2.


The SEER database includes approximately 28% of the US population, and this retrospective analysis retrieved data on 360 patients diagnosed with DNMB in the database. Therefore, it is reasonable to assume that the total incidence of DNMB was approximately 1286 diagnoses spanning the time frame of 1975-2016 in the United States. It is also important to consider that the database included a “medulloblastoma not otherwise specified” classification, which could have potentially contained additional diagnoses of DNMB. Thus, this calculation could underestimate the total incidence during this time frame.

In terms of demographics, when comparing this study to a recent retrospective analysis of all medulloblastoma diagnoses in the SEER database by Khanna et al., DNMBs appear to be diagnosed in patients in younger age ranges [17]. In the age group ranges of younger than one year to one through four, the percentage increased significantly (3.08% to 21.37%) for all medulloblastomas, and it likewise did in this study (5.56% to 27.78%). However, in all medulloblastomas, the prevalence again increased from the one- to four-year to the five to nine age groups (21.37% to 25.68%), and in this study the prevalence decreased between these age groups (27.78% to 15.56%). Demographical percentages of sex and race were similar between both database reviews. Of note, there was original evidence to suggest that DNMBs were predominantly found in younger patients by a case series of 12 patients, which is supported by this study [18]. However, this same case series also suggested a female predominant distribution of DNMB, which was not supported by this present database review (males 57%; females 43%).

In the study by Khanna et al., overall survival was much lower for all medulloblastomas when comparing to the data for the DNMB subtype specifically. In all medulloblastomas, the survival rate for the age group of younger than one year was 48.4%. For DNMBs, this review found 100% survival rates, providing further evidence that this subtype offers better prognoses for patients in terms of survival. In the one- to four-year age group, survival in medulloblastomas was 61.9% compared to 75.6% in DNMBs [17]. It is thought that patients younger than three years of age had poorer prognoses for all medulloblastomas; however, this may not be true for the DNMB subtype [19,20]. When considering differences in sex, it was found that survival outcomes were better in females by a previous study when analysing all medulloblastomas, but for DNMB, the survival outcome appears slightly better in males (males 80.5%; females 73.7%) [21].

Before this database review, one of the largest studies measuring survival rates for the DNMB subtype specifically was a multicenter retrospective review including 108 patients. All individuals underwent chemotherapies, radiotherapies, and autologous hematopoietic stem-cell transplantations according to their prospective clinical trials for which they were enrolled. In patients with early-childhood DNMB, a survival rate of 72% was found at eight years in 87 patients [7]. The rates provided by this study are similar to the survival rates found in this database review when measuring survival at five years (100% survival, age less than one; 75.6% survival, age one to four years).

When considering eliminating radiotherapy for medulloblastomas, Rutkowski et al. found that patients undergoing chemotherapy with persistent post-chemotherapeutic surveillance had comparable survival to patients undergoing both chemotherapy and radiotherapy when looking at early childhood medulloblastomas (10-year survival = 63.6% and 55.2%, respectively, p = 0.274) by comparing results from the HIT-SKK’87 (Therapieprotokoll für Säuglinge und Kleinkinder mit Hirntumoren [Brain Tumor Radiotherapy for Infants and Toddlers with Medulloblastoma] 1987) and HIT-SKK’92 trials [22]. This overall survival rate is lower than the rates in this analysis, which is to be expected as these trials included all subtypes of medulloblastomas. Many other reviews have found that avoiding radiotherapy is a viable option for young children without metastatic disease and for children with complete resection [8,23,24]. Apart from these data, there are several other clinical trials that have been performed measuring the impact of avoidance of radiotherapy on survival outcome for other tumors of the central nervous system [25,26]. These trials have shown promising results and are pioneering the future in avoiding the long-term cognitive deficits associated with radiotherapy. Avoiding the need for radiotherapy is also beneficial to patients in resource-limited areas that are unable to offer these types of advanced treatment modalities [27].

For the DMNB subtype of medulloblastoma tumors specifically, there are even more promising outcomes. In the HIT-SKK protocol trials, the authors used intravenous and intraventricular methotrexate in place of radiotherapy except for patients with metastatic disease or residual disease after chemotherapy. In their long-term data of eight years, overall survival was reported to be 91% in 115 patients [28]. Another previous review of HIT protocol trials also supports this good prognosis in DNMB patients [29]. Despite this, there were concerns of poor neurocognitive outcomes with the intraventricular methotrexate. After these concerns, a new clinical trial with 26 participants diagnosed with DNMB was developed by the Children’s Oncology Group eliminating this intraventricular methotrexate (clinical trial #NCT02017964), but it was aborted early in 2018 when the progression-free survival dropped lower than 90%.

Recently in 2020, Dhall et al. reported excellent survival rates in 92 DNMB patients enrolled in the prospective multicenter “Head Start” III trial using myeloablative chemotherapy and autologous hematopoietic cell rescue. They reported preservation of mean intelligence quotient scores and quality of life scores with an overall survival rate of 89% at five years [30]. Interestingly, this database review found that patients undergoing chemotherapeutic treatment did not have improvement in five-year survival outcomes to any statistical significance (81.3% vs 72.1%, p = 0.298) among 116 patients. Therefore, this review provides further evidence that adding radiotherapeutic treatment to patients undergoing chemotherapy for the DNMB subtype of medulloblastoma may have only minimal benefit to survival outcomes.


This database offered no metrics to measure intelligence scores or quality of life scores in patients who underwent these regimens of surgeries, chemotherapies, and radiotherapies. Neither did this database measure cognitive changes in children undergoing long-term radiotherapy, measure rates of seizure control, or measure rates of cranial neuropathies associated with these diseases. All of these outcomes should be characterized with future clinical case series.

This database is currently unable to monitor the molecular profiles of these tumors. Therefore, correlations of specific molecular profiles to outcomes post-intervention were unable to be made. Future updates should further optimize and adapt the database to store such molecular profiling for cancer data in future.

Some patient age ranges included a small number of individual cases (40-45, 45-49, 50-54 had five patients; 60-64, 65-69 had one patient). This limited the statistical power of this analysis when looking at the data of DNMB, especially in adult diagnoses.

It is also important to consider that the database included a “medulloblastoma not otherwise specified” classification, which could have potentially contained additional diagnoses of DNMB that went unreviewed in this study and were not included in the final data or conclusions.


With this retrospective review of 360 patients diagnosed with DNMBs, the authors find that DNMBs follow trends similar to all medulloblastomas except for having an increased percentage of diagnoses in the younger than four age range. From 1975 to 2016, a majority of the patients underwent resection of the tumor, and received chemotherapy, as well as post-operative radiotherapy. In patients undergoing chemotherapeutic treatment for DNMB, additional radiotherapy was found to offer only minimal benefit to the survival outcome that did not achieve statistical significance. This subtype of medulloblastoma has a favorable survival outcome, but patients still experience significant long-term morbidity as a result of these lifesaving treatments. Devising therapeutic modalities toward the reduction of these long-term adverse effects related to treatment is an important goal for the neurosurgical community.


  1. Ostrom QT, De Blank PM, Kruchko C, et al.: Alex’s Lemonade Stand Foundation infant and childhood primary brain and central nervous system tumors diagnosed in the United States in 2007-2011. Neuro Oncol. 2014, 16:x1-x36. 10.1093/neuonc/nou327
  2. Louis DN, Perry A, Reifenberger G, et al.: The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary. Acta Neuropathol. 2016, 131:803-820. 10.1007/s00401-016-1545-1
  3. Gottardo NG, Gajjar A: Current therapy for medulloblastoma. Curr Treat Options Neurol. 2006, 8:319-334. 10.1007/s11940-006-0022-x
  4. Jenkin D, Danjoux C, Greenberg M: Subsequent quality of life for children irradiated for a brain tumor before age four years. Med Pediatr Oncol. 1998, 31:506-511. 10.1002/(SICI)1096-911X(199812)31:6<506::AID-MPO7>3.0.CO;2-X
  5. Mulhern RK, Horowitz ME, Kovnar EH, Langston J, Sanford RA, Kun LE: Neurodevelopmental status of infants and young children treated for brain tumors with preirradiation chemotherapy. J Clin Oncol. 1989, 7:1660-1666. 10.1200/JCO.1989.7.11.1660
  6. Packer RJ, Zhou T, Holmes E, Vezina G, Gajjar A: Survival and secondary tumors in children with medulloblastoma receiving radiotherapy and adjuvant chemotherapy: Results of Children’s Oncology Group trial A9961. Neuro Oncol. 2013, 15:97-103. 10.1093/neuonc/nos267
  7. Rutkowski S, Von Hoff K, Emser A, et al.: Survival and prognostic factors of early childhood medulloblastoma: an international meta-analysis. J Clin Oncol. 2010, 28:4961-4968. 10.1200/JCO.2010.30.2299
  8. Dhall G, Grodman H, Ji L, et al.: Outcome of children less than three years old at diagnosis with non-metastatic medulloblastoma treated with chemotherapy on the “Head Start” I and II protocols. Pediatr Blood Cancer. 2008, 50:1169-1175. 10.1002/pbc.21525
  9. Dhall G, Ji L, Haley K, Gilles F, Gardner S, Sposto R, Finlay JL: P11.02 Long-term outcome of infants and young children with newly diagnosed non-nodular/desmoplastic medulloblastoma treated on “Head Start” III protocol. Neuro Oncol. 2017, 19:iii91-iii92. 10.1093/neuonc/nox036.347
  10. Dhall G, Ji L, Haley K, et al.: Outcome of infants and young children with newly diagnosed medulloblastoma treated on Head Start III protocol. J Clin Oncol. 2011, 29:2011. 10.1200/jco.2011.29.15_suppl.2011
  11. Siegfried A, Bertozzi AI, Bourdeaut F, et al.: Clinical, pathological, and molecular data on desmoplastic/nodular medulloblastoma: case studies and a review of the literature. Clin Neuropathol. 2016, 35:106-113. 10.5414/NP300205
  12. Yamasaki F, Takayasu T, Nosaka R, Kawaguchi H, Sugiyama K, Kobayashi M, Kurisu K: Cavernous angioma after chemotherapy for desmoplastic/nodular medulloblastoma associated with anhidrotic ectodermal dysplasia. Childs Nerv Syst. 2016, 32:395-398. 10.1007/s00381-015-2848-6
  13. Pramanik P, Sharma MC, Mukhopadhyay P, Singh VP, Sarkar C: A comparative study of classical vs. desmoplastic medulloblastomas. Neurol India. 2003, 51:27-34.
  14. Overview of the SEER Program. Accessed: June 8, 2020: https://seer.cancer.gov/about/overview.html.
  15. Doll KM, Rademaker A, Sosa JA: Practical guide to surgical data sets: Surveillance, Epidemiology, and End Results (SEER) database. JAMA Surg. 2018, 153:588-589. 10.1001/jamasurg.2018.0501
  16. Kaji AH, Rademaker AW, Hyslop T: Tips for analyzing large data sets from the JAMA Surgery statistical editors. JAMA Surg. 2018, 153:508-509. 10.1001/jamasurg.2018.0647
  17. Khanna V, Achey RL, Ostrom QT, Block-Beach H, Kruchko C, Barnholtz-Sloan JS, de Blank PM: Incidence and survival trends for medulloblastomas in the United States from 2001 to 2013. J Neurooncol. 2017, 135:433-441. 10.1007/s11060-017-2594-6
  18. Fruehwald-Pallamar J, Puchner SB, Rossi A, et al.: Magnetic resonance imaging spectrum of medulloblastoma. Neuroradiology. 2011, 53:387-396. 10.1007/s00234-010-0829-8
  19. Gilbertson RJ: Medulloblastoma: signalling a change in treatment. Lancet Oncol. 2004, 5:209-218. 10.1016/S1470-2045(04)01424-X
  20. Zeltzer PM, Boyett JM, Finlay JL, et al.: Metastasis stage, adjuvant treatment, and residual tumor are prognostic factors for medulloblastoma in children: conclusions from the Children’s Cancer Group 921 randomized phase III study. J Clin Oncol. 1999, 17:832. 10.1200/jco.1999.17.3.832
  21. Weil MD, Lamborn K, Edwards MSB, Wara WM: Influence of a child’s sex on medulloblastoma outcome. J Am Med Assoc. 1998, 279:1474-1476. 10.1001/jama.279.18.1474
  22. Rutkowski S, Gerber NU, von Hoff K, et al.: Treatment of early childhood medulloblastoma by postoperative chemotherapy and deferred radiotherapy. Neuro Oncol. 2009, 11:201-210. 10.1215/15228517-2008-084
  23. Rutkowski S, Bode U, Deinlein F, et al.: Treatment of early childhood medulloblastoma by postoperative chemotherapy alone. N Engl J Med. 2005, 352:978-986. 10.1056/NEJMoa042176
  24. Grill J, Sainte-Rose C, Jouvet A, et al.: Treatment of medulloblastoma with postoperative chemotherapy alone: an SFOP prospective trial in young children. Lancet Oncol. 2005, 6:573-580. 10.1016/S1470-2045(05)70252-7
  25. Grundy RG, Wilne SH, Robinson KJ, et al.: Primary postoperative chemotherapy without radiotherapy for treatment of brain tumours other than ependymoma in children under 3 years: results of the first UKCCSG/SIOP CNS 9204 trial. Eur J Cancer. 2010, 46:120-133. 10.1016/j.ejca.2009.09.013
  26. Duffner PK, Horowitz ME, Krischer JP, et al.: Postoperative chemotherapy and delayed radiation in children less than three years of age with malignant brain tumors. N Engl J Med. 1993, 328:1725-1731. 10.1056/NEJM199306173282401
  27. Aristizabal P, Burns L, Rivera-Gomez R, Levy ML, Roberts W, Crawford JR: Medulloblastoma with extensive nodularity: tailored therapy in a low-resource setting. J Pediatr Hematol Oncol. 2017, 39:299-301. 10.1097/MPH.0000000000000798
  28. Gerber, Nicolas Ulrich, Juhnke BO, et al.: MB-89 Treatment failure in young children with desmoplastic medulloblastoma (DMB)/medulloblastoma with extensive nodularity (MBEN) treated according to the HIT protocols. Neuro Oncol. 2016, 18:iii117. 10.1093/neuonc/now076.85
  29. Von Bueren AO, Von Hoff K, Pietsch T, et al.: Treatment of young children with localized medulloblastoma by chemotherapy alone: results of the prospective, multicenter trial HIT 2000 confirming the prognostic impact of histology. Neuro Oncol. 2011, 13:669-679. 10.1093/neuonc/nor025
  30. Dhall G, O’Neil SH, Ji L, et al.: Excellent outcome of young children with nodular desmoplastic medulloblastoma treated on “Head Start” III: a multi-institutional, prospective clinical trial [Epub ahead of print]. Neuro Oncol. 2020, noaa102. 10.1093/neuonc/noaa102
Original article

A Retrospective Analysis of the Demographics, Treatment, and Survival Outcomes of Patients with Desmoplastic Nodular Medulloblastoma Using the Surveillance, Epidemiology, and End Results (SEER) Database

Author Information

Julian L. Gendreau Corresponding Author

Medicine, Eisenhower Army Medical Center, Fort Gordon, Augusta, USA

Shishir Gupta

Medicine, Rollins School of Public Health, Emory University School of Medicine, Atlanta, USA

Tyler X. Giles

Medicine, Mercer University School of Medicine, Macon, USA

Courtney E. Stone

Medicine, Mercer University School of Medicine, Savannah, USA

Mickey E. Abraham

Neurological Surgery, University of California, San Diego, USA

James G. Lindley

Neurosurgery, Neurological & Spine Institute, Savannah, USA

Ethics Statement and Conflict of Interest Disclosures

Human subjects: All authors have confirmed that this study did not involve human participants or tissue. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


The authors would like to thank the United States Centers for Disease Control and Prevention, the United States National Cancer Institute, and any regional cancer registries involved for providing these data for analysis.

Original article

A Retrospective Analysis of the Demographics, Treatment, and Survival Outcomes of Patients with Desmoplastic Nodular Medulloblastoma Using the Surveillance, Epidemiology, and End Results (SEER) Database

Figures etc.


Scholary Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.