Glioblastoma in childhood – Treatment and outcome of 7 patients

Standard

Glioblastoma in childhood – Treatment and outcome of 7 patients. / Burkhardt, Till; Emami, Pedram; Kordes, Uwe; Matschke, Jakob; Regelsberger, Jan; Westphal, Manfred; Kammler, Gertrud.

62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH). 2011.

Research output: SCORING: Contribution to book/anthologyConference contribution - Article for conferenceResearch

Harvard

Burkhardt, T, Emami, P, Kordes, U, Matschke, J, Regelsberger, J, Westphal, M & Kammler, G 2011, Glioblastoma in childhood – Treatment and outcome of 7 patients. in 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH). https://doi.org/10.3205/11dgnc148

APA

Burkhardt, T., Emami, P., Kordes, U., Matschke, J., Regelsberger, J., Westphal, M., & Kammler, G. (2011). Glioblastoma in childhood – Treatment and outcome of 7 patients. In 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH) https://doi.org/10.3205/11dgnc148

Vancouver

Burkhardt T, Emami P, Kordes U, Matschke J, Regelsberger J, Westphal M et al. Glioblastoma in childhood – Treatment and outcome of 7 patients. In 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH). 2011 https://doi.org/10.3205/11dgnc148

Bibtex

@inbook{f59642df840845d9ad144e3a9a6d6da6,
title = "Glioblastoma in childhood – Treatment and outcome of 7 patients",
abstract = "Objective: While glioblastoma is very common in adults and is the most common primary malignant brain tumour in this age group, it remains a rare diagnosis in children. Postoperative treatment of glioblastoma in adults is well standardized, but in children the treatment is under constant discussion and follows different types of study protocols (HIT-GBM A-D). Methods: Treatment and outcome of 7 consecutive paediatric patients were retrospectively evaluated in order to determine the clinical course, median progression-free survival and overall survival. Results: 7 patients were diagnosed and treated between 2000 and 2010. The median age was 9 years, all patients were under 16. All but one of the patients underwent open surgery; complete resection was performed in 2 cases, subtotal resection in 4 cases. One patient underwent stereotactic biopsy due to the depth of the lesion. Combined radio-chemotherapy was performed in all cases, using the HIT-GBM-C and -D and the HIT 2000 protocols as first-line therapy as well as Topotecan and Temozolomide as second-line chemotherapy for recurrent disease. Median survival in this cohort was 16 months. The progression-free survival was 3 months. Local tumour-recurrences were apparent in all cases. Median survival and progression-free survival in this small cohort did not correlate with extent of resection, depth of the lesion or the adjuvant regimen. Conclusions: Survival of children with glioblastoma is being described as far better than in adults. Although we followed the common study protocols, we cannot confirm these results in this cohort, most probably due to the low case number.",
author = "Till Burkhardt and Pedram Emami and Uwe Kordes and Jakob Matschke and Jan Regelsberger and Manfred Westphal and Gertrud Kammler",
year = "2011",
month = apr,
day = "1",
doi = "10.3205/11dgnc148",
language = "English",
booktitle = "62. Jahrestagung der Deutschen Gesellschaft f{\"u}r Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft f{\"u}r Neurochirurgen (PNCH)",

}

RIS

TY - CHAP

T1 - Glioblastoma in childhood – Treatment and outcome of 7 patients

AU - Burkhardt, Till

AU - Emami, Pedram

AU - Kordes, Uwe

AU - Matschke, Jakob

AU - Regelsberger, Jan

AU - Westphal, Manfred

AU - Kammler, Gertrud

PY - 2011/4/1

Y1 - 2011/4/1

N2 - Objective: While glioblastoma is very common in adults and is the most common primary malignant brain tumour in this age group, it remains a rare diagnosis in children. Postoperative treatment of glioblastoma in adults is well standardized, but in children the treatment is under constant discussion and follows different types of study protocols (HIT-GBM A-D). Methods: Treatment and outcome of 7 consecutive paediatric patients were retrospectively evaluated in order to determine the clinical course, median progression-free survival and overall survival. Results: 7 patients were diagnosed and treated between 2000 and 2010. The median age was 9 years, all patients were under 16. All but one of the patients underwent open surgery; complete resection was performed in 2 cases, subtotal resection in 4 cases. One patient underwent stereotactic biopsy due to the depth of the lesion. Combined radio-chemotherapy was performed in all cases, using the HIT-GBM-C and -D and the HIT 2000 protocols as first-line therapy as well as Topotecan and Temozolomide as second-line chemotherapy for recurrent disease. Median survival in this cohort was 16 months. The progression-free survival was 3 months. Local tumour-recurrences were apparent in all cases. Median survival and progression-free survival in this small cohort did not correlate with extent of resection, depth of the lesion or the adjuvant regimen. Conclusions: Survival of children with glioblastoma is being described as far better than in adults. Although we followed the common study protocols, we cannot confirm these results in this cohort, most probably due to the low case number.

AB - Objective: While glioblastoma is very common in adults and is the most common primary malignant brain tumour in this age group, it remains a rare diagnosis in children. Postoperative treatment of glioblastoma in adults is well standardized, but in children the treatment is under constant discussion and follows different types of study protocols (HIT-GBM A-D). Methods: Treatment and outcome of 7 consecutive paediatric patients were retrospectively evaluated in order to determine the clinical course, median progression-free survival and overall survival. Results: 7 patients were diagnosed and treated between 2000 and 2010. The median age was 9 years, all patients were under 16. All but one of the patients underwent open surgery; complete resection was performed in 2 cases, subtotal resection in 4 cases. One patient underwent stereotactic biopsy due to the depth of the lesion. Combined radio-chemotherapy was performed in all cases, using the HIT-GBM-C and -D and the HIT 2000 protocols as first-line therapy as well as Topotecan and Temozolomide as second-line chemotherapy for recurrent disease. Median survival in this cohort was 16 months. The progression-free survival was 3 months. Local tumour-recurrences were apparent in all cases. Median survival and progression-free survival in this small cohort did not correlate with extent of resection, depth of the lesion or the adjuvant regimen. Conclusions: Survival of children with glioblastoma is being described as far better than in adults. Although we followed the common study protocols, we cannot confirm these results in this cohort, most probably due to the low case number.

U2 - 10.3205/11dgnc148

DO - 10.3205/11dgnc148

M3 - Conference contribution - Article for conference

BT - 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH)

ER -