Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study

Standard

Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study. / Friedrich, Carsten; von Bueren, André O; von Hoff, Katja; Kwiecien, Robert; Pietsch, Torsten; Warmuth-Metz, Monika; Hau, Peter; Deinlein, Frank; Kuehl, Joachim; Kortmann, Rolf D; Rutkowski, Stefan.

in: EUR J CANCER, Jahrgang 49, Nr. 4, 4, 2013, S. 893-903.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Friedrich, C, von Bueren, AO, von Hoff, K, Kwiecien, R, Pietsch, T, Warmuth-Metz, M, Hau, P, Deinlein, F, Kuehl, J, Kortmann, RD & Rutkowski, S 2013, 'Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study', EUR J CANCER, Jg. 49, Nr. 4, 4, S. 893-903. https://doi.org/10.1016/j.ejca.2012.10.006

APA

Friedrich, C., von Bueren, A. O., von Hoff, K., Kwiecien, R., Pietsch, T., Warmuth-Metz, M., Hau, P., Deinlein, F., Kuehl, J., Kortmann, R. D., & Rutkowski, S. (2013). Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study. EUR J CANCER, 49(4), 893-903. [4]. https://doi.org/10.1016/j.ejca.2012.10.006

Vancouver

Bibtex

@article{874cb0c4af964ee6ab03fb26e5b578f0,
title = "Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study",
abstract = "BACKGROUND: Medulloblastoma in adulthood is rare. Knowledge is limited, and the efficacy and toxicity of chemotherapy--especially in nonmetastatic disease--is still elusive.METHODS: Seventy adults aged ≥21 years (median age: 28.5 years) with nonmetastatic medulloblastoma were followed as observational patients within the prospective paediatric multicentre trial HIT 2000. Treatment consisted of radiotherapy (35.2 Gy to the craniospinal axis and a boost to 55.2 Gy to the posterior fossa) followed in most patients by maintenance chemotherapy (lomustine (CCNU), vincristine and cisplatin, n=49).RESULTS: The implementation of maintenance chemotherapy was feasible. Peripheral neuropathy (74%) and haematotoxicity (55%) during maintenance chemotherapy appear to be more common in adults than in children. At a median follow-up of 3.7 years, the 4-year event-free survival (EFS) and overall survival (OS) rates±standard error (SE) were 68%±7% and 89%±5%. Patients with desmoplastic medulloblastoma and lateral tumour location (n=19) had a lower EFS compared to patients with centrally located desmoplastic tumours (n=10) (p=0.011). Absence of residual postoperative tumour (n=40) was associated to a lower rate of progression/relapse compared to present (n=11) or unknown (n=12) residual tumour status (p=0.006). Lateral tumour location and unknown residual tumour status were independent negative prognostic factors.CONCLUSIONS: Maintenance chemotherapy is applicable in adults with nonmetastatic medulloblastoma. Histological subtype and tumour location were newly identified risk factors in this age-group, and should be further analysed in prospective trials.",
keywords = "Adult, Humans, Male, Aged, Female, Middle Aged, Prospective Studies, Prognosis, Survival Rate, Follow-Up Studies, Combined Modality Therapy, Neoplasm Staging, Chemotherapy, Adjuvant, Radiotherapy, Adjuvant, Antineoplastic Combined Chemotherapy Protocols/*therapeutic use, Vincristine/administration & dosage, Cisplatin/administration & dosage, *Cranial Irradiation, Cerebellar Neoplasms/mortality/pathology/*therapy, Lomustine/administration & dosage, Medulloblastoma/mortality/pathology/*therapy, Neoplasm Recurrence, Local/mortality/pathology/*therapy, Adult, Humans, Male, Aged, Female, Middle Aged, Prospective Studies, Prognosis, Survival Rate, Follow-Up Studies, Combined Modality Therapy, Neoplasm Staging, Chemotherapy, Adjuvant, Radiotherapy, Adjuvant, Antineoplastic Combined Chemotherapy Protocols/*therapeutic use, Vincristine/administration & dosage, Cisplatin/administration & dosage, *Cranial Irradiation, Cerebellar Neoplasms/mortality/pathology/*therapy, Lomustine/administration & dosage, Medulloblastoma/mortality/pathology/*therapy, Neoplasm Recurrence, Local/mortality/pathology/*therapy",
author = "Carsten Friedrich and {von Bueren}, {Andr{\'e} O} and {von Hoff}, Katja and Robert Kwiecien and Torsten Pietsch and Monika Warmuth-Metz and Peter Hau and Frank Deinlein and Joachim Kuehl and Kortmann, {Rolf D} and Stefan Rutkowski",
note = "Copyright {\textcopyright} 2012 Elsevier Ltd. All rights reserved.",
year = "2013",
doi = "10.1016/j.ejca.2012.10.006",
language = "English",
volume = "49",
pages = "893--903",
journal = "EUR J CANCER",
issn = "0959-8049",
publisher = "Elsevier Limited",
number = "4",

}

RIS

TY - JOUR

T1 - Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study

AU - Friedrich, Carsten

AU - von Bueren, André O

AU - von Hoff, Katja

AU - Kwiecien, Robert

AU - Pietsch, Torsten

AU - Warmuth-Metz, Monika

AU - Hau, Peter

AU - Deinlein, Frank

AU - Kuehl, Joachim

AU - Kortmann, Rolf D

AU - Rutkowski, Stefan

N1 - Copyright © 2012 Elsevier Ltd. All rights reserved.

PY - 2013

Y1 - 2013

N2 - BACKGROUND: Medulloblastoma in adulthood is rare. Knowledge is limited, and the efficacy and toxicity of chemotherapy--especially in nonmetastatic disease--is still elusive.METHODS: Seventy adults aged ≥21 years (median age: 28.5 years) with nonmetastatic medulloblastoma were followed as observational patients within the prospective paediatric multicentre trial HIT 2000. Treatment consisted of radiotherapy (35.2 Gy to the craniospinal axis and a boost to 55.2 Gy to the posterior fossa) followed in most patients by maintenance chemotherapy (lomustine (CCNU), vincristine and cisplatin, n=49).RESULTS: The implementation of maintenance chemotherapy was feasible. Peripheral neuropathy (74%) and haematotoxicity (55%) during maintenance chemotherapy appear to be more common in adults than in children. At a median follow-up of 3.7 years, the 4-year event-free survival (EFS) and overall survival (OS) rates±standard error (SE) were 68%±7% and 89%±5%. Patients with desmoplastic medulloblastoma and lateral tumour location (n=19) had a lower EFS compared to patients with centrally located desmoplastic tumours (n=10) (p=0.011). Absence of residual postoperative tumour (n=40) was associated to a lower rate of progression/relapse compared to present (n=11) or unknown (n=12) residual tumour status (p=0.006). Lateral tumour location and unknown residual tumour status were independent negative prognostic factors.CONCLUSIONS: Maintenance chemotherapy is applicable in adults with nonmetastatic medulloblastoma. Histological subtype and tumour location were newly identified risk factors in this age-group, and should be further analysed in prospective trials.

AB - BACKGROUND: Medulloblastoma in adulthood is rare. Knowledge is limited, and the efficacy and toxicity of chemotherapy--especially in nonmetastatic disease--is still elusive.METHODS: Seventy adults aged ≥21 years (median age: 28.5 years) with nonmetastatic medulloblastoma were followed as observational patients within the prospective paediatric multicentre trial HIT 2000. Treatment consisted of radiotherapy (35.2 Gy to the craniospinal axis and a boost to 55.2 Gy to the posterior fossa) followed in most patients by maintenance chemotherapy (lomustine (CCNU), vincristine and cisplatin, n=49).RESULTS: The implementation of maintenance chemotherapy was feasible. Peripheral neuropathy (74%) and haematotoxicity (55%) during maintenance chemotherapy appear to be more common in adults than in children. At a median follow-up of 3.7 years, the 4-year event-free survival (EFS) and overall survival (OS) rates±standard error (SE) were 68%±7% and 89%±5%. Patients with desmoplastic medulloblastoma and lateral tumour location (n=19) had a lower EFS compared to patients with centrally located desmoplastic tumours (n=10) (p=0.011). Absence of residual postoperative tumour (n=40) was associated to a lower rate of progression/relapse compared to present (n=11) or unknown (n=12) residual tumour status (p=0.006). Lateral tumour location and unknown residual tumour status were independent negative prognostic factors.CONCLUSIONS: Maintenance chemotherapy is applicable in adults with nonmetastatic medulloblastoma. Histological subtype and tumour location were newly identified risk factors in this age-group, and should be further analysed in prospective trials.

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Prospective Studies

KW - Prognosis

KW - Survival Rate

KW - Follow-Up Studies

KW - Combined Modality Therapy

KW - Neoplasm Staging

KW - Chemotherapy, Adjuvant

KW - Radiotherapy, Adjuvant

KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use

KW - Vincristine/administration & dosage

KW - Cisplatin/administration & dosage

KW - Cranial Irradiation

KW - Cerebellar Neoplasms/mortality/pathology/therapy

KW - Lomustine/administration & dosage

KW - Medulloblastoma/mortality/pathology/therapy

KW - Neoplasm Recurrence, Local/mortality/pathology/therapy

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Prospective Studies

KW - Prognosis

KW - Survival Rate

KW - Follow-Up Studies

KW - Combined Modality Therapy

KW - Neoplasm Staging

KW - Chemotherapy, Adjuvant

KW - Radiotherapy, Adjuvant

KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use

KW - Vincristine/administration & dosage

KW - Cisplatin/administration & dosage

KW - Cranial Irradiation

KW - Cerebellar Neoplasms/mortality/pathology/therapy

KW - Lomustine/administration & dosage

KW - Medulloblastoma/mortality/pathology/therapy

KW - Neoplasm Recurrence, Local/mortality/pathology/therapy

U2 - 10.1016/j.ejca.2012.10.006

DO - 10.1016/j.ejca.2012.10.006

M3 - SCORING: Journal article

C2 - 23182688

VL - 49

SP - 893

EP - 903

JO - EUR J CANCER

JF - EUR J CANCER

SN - 0959-8049

IS - 4

M1 - 4

ER -