Treatment strategies for initially disseminated intracranial germinomas: Experiences at a single institute

Yi Wei Chen, Pin I. Huang, Yu Wen Hu, Donald Ming Tak Ho, Kai Ping Chang, Wan Yuo Guo, Feng Chi Chang, Yi Yen Lee, Cheng Ying Shiau, Tai-Tong Wong, Sang Hue Yen

Research output: Contribution to journalArticle

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Abstract

Purpose: Initially disseminated intracranial germinomas (IDIGs) can be observed in pre-adult and adolescent brain tumor patients. However, the disease prognosis is undetermined, and the method of optimal treatment remains controversial. Methods: From January 1990 to January 2011, data on 91 intracranial germinoma patients (≤20 years old) were gathered from the Pediatric Brain Tumor database at Taipei Veterans General Hospital. A total of seven patients with a median age of 17.0 years had IDIGs (lesion sites >2), including IDIGs in the ventricular system or the spinal column. Craniospinal irradiation (CSI) plus a primary or metastatic boost was the mainstay strategy for radiotherapy. Six out of a total of seven patients (85.7%) also received systemic chemotherapy (CHT) after radiotherapy. Survivals rates between IDIGs and patients without dissemination were estimated using the Kaplan-Meier method. Results: The median follow-up time for all seven patients was 67.5 months (range, 10.3-142.3 months). None of the IDIG patients experienced a recurrence or mortality after the completion of treatment. The 5- and 10-year disease-free survival (DFS) between IDIG and non-dissemination patients were 100%, 100%, 93.0% and 78.6%, respectively (p=0.339). The 5- and 10-year overall survival (OS) between IDIGs and non-dissemination cases were 100%, 100%, 93.7% and 89.4%, respectively (p=0.473). Conclusions: IDIG patients did not show reduced survival compared to non-dissemination patients if optimal radiotherapy and chemotherapy were used together.

Original languageEnglish
Pages (from-to)557-563
Number of pages7
JournalChild's Nervous System
Volume28
Issue number4
DOIs
Publication statusPublished - Apr 1 2012
Externally publishedYes

Fingerprint

Germinoma
Therapeutics
Radiotherapy
Brain Neoplasms
Craniospinal Irradiation
Veterans Hospitals
Drug Therapy
Survival
General Hospitals
Disease-Free Survival
Spine
Survival Rate
Databases

Keywords

  • Chemotherapy
  • Craniospinal irradiation
  • Dissemination
  • Germinoma
  • Radiotherapy

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

Cite this

Chen, Y. W., Huang, P. I., Hu, Y. W., Ho, D. M. T., Chang, K. P., Guo, W. Y., ... Yen, S. H. (2012). Treatment strategies for initially disseminated intracranial germinomas: Experiences at a single institute. Child's Nervous System, 28(4), 557-563. https://doi.org/10.1007/s00381-012-1683-2

Treatment strategies for initially disseminated intracranial germinomas : Experiences at a single institute. / Chen, Yi Wei; Huang, Pin I.; Hu, Yu Wen; Ho, Donald Ming Tak; Chang, Kai Ping; Guo, Wan Yuo; Chang, Feng Chi; Lee, Yi Yen; Shiau, Cheng Ying; Wong, Tai-Tong; Yen, Sang Hue.

In: Child's Nervous System, Vol. 28, No. 4, 01.04.2012, p. 557-563.

Research output: Contribution to journalArticle

Chen, YW, Huang, PI, Hu, YW, Ho, DMT, Chang, KP, Guo, WY, Chang, FC, Lee, YY, Shiau, CY, Wong, T-T & Yen, SH 2012, 'Treatment strategies for initially disseminated intracranial germinomas: Experiences at a single institute', Child's Nervous System, vol. 28, no. 4, pp. 557-563. https://doi.org/10.1007/s00381-012-1683-2
Chen, Yi Wei ; Huang, Pin I. ; Hu, Yu Wen ; Ho, Donald Ming Tak ; Chang, Kai Ping ; Guo, Wan Yuo ; Chang, Feng Chi ; Lee, Yi Yen ; Shiau, Cheng Ying ; Wong, Tai-Tong ; Yen, Sang Hue. / Treatment strategies for initially disseminated intracranial germinomas : Experiences at a single institute. In: Child's Nervous System. 2012 ; Vol. 28, No. 4. pp. 557-563.
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abstract = "Purpose: Initially disseminated intracranial germinomas (IDIGs) can be observed in pre-adult and adolescent brain tumor patients. However, the disease prognosis is undetermined, and the method of optimal treatment remains controversial. Methods: From January 1990 to January 2011, data on 91 intracranial germinoma patients (≤20 years old) were gathered from the Pediatric Brain Tumor database at Taipei Veterans General Hospital. A total of seven patients with a median age of 17.0 years had IDIGs (lesion sites >2), including IDIGs in the ventricular system or the spinal column. Craniospinal irradiation (CSI) plus a primary or metastatic boost was the mainstay strategy for radiotherapy. Six out of a total of seven patients (85.7{\%}) also received systemic chemotherapy (CHT) after radiotherapy. Survivals rates between IDIGs and patients without dissemination were estimated using the Kaplan-Meier method. Results: The median follow-up time for all seven patients was 67.5 months (range, 10.3-142.3 months). None of the IDIG patients experienced a recurrence or mortality after the completion of treatment. The 5- and 10-year disease-free survival (DFS) between IDIG and non-dissemination patients were 100{\%}, 100{\%}, 93.0{\%} and 78.6{\%}, respectively (p=0.339). The 5- and 10-year overall survival (OS) between IDIGs and non-dissemination cases were 100{\%}, 100{\%}, 93.7{\%} and 89.4{\%}, respectively (p=0.473). Conclusions: IDIG patients did not show reduced survival compared to non-dissemination patients if optimal radiotherapy and chemotherapy were used together.",
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AU - Chen, Yi Wei

AU - Huang, Pin I.

AU - Hu, Yu Wen

AU - Ho, Donald Ming Tak

AU - Chang, Kai Ping

AU - Guo, Wan Yuo

AU - Chang, Feng Chi

AU - Lee, Yi Yen

AU - Shiau, Cheng Ying

AU - Wong, Tai-Tong

AU - Yen, Sang Hue

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N2 - Purpose: Initially disseminated intracranial germinomas (IDIGs) can be observed in pre-adult and adolescent brain tumor patients. However, the disease prognosis is undetermined, and the method of optimal treatment remains controversial. Methods: From January 1990 to January 2011, data on 91 intracranial germinoma patients (≤20 years old) were gathered from the Pediatric Brain Tumor database at Taipei Veterans General Hospital. A total of seven patients with a median age of 17.0 years had IDIGs (lesion sites >2), including IDIGs in the ventricular system or the spinal column. Craniospinal irradiation (CSI) plus a primary or metastatic boost was the mainstay strategy for radiotherapy. Six out of a total of seven patients (85.7%) also received systemic chemotherapy (CHT) after radiotherapy. Survivals rates between IDIGs and patients without dissemination were estimated using the Kaplan-Meier method. Results: The median follow-up time for all seven patients was 67.5 months (range, 10.3-142.3 months). None of the IDIG patients experienced a recurrence or mortality after the completion of treatment. The 5- and 10-year disease-free survival (DFS) between IDIG and non-dissemination patients were 100%, 100%, 93.0% and 78.6%, respectively (p=0.339). The 5- and 10-year overall survival (OS) between IDIGs and non-dissemination cases were 100%, 100%, 93.7% and 89.4%, respectively (p=0.473). Conclusions: IDIG patients did not show reduced survival compared to non-dissemination patients if optimal radiotherapy and chemotherapy were used together.

AB - Purpose: Initially disseminated intracranial germinomas (IDIGs) can be observed in pre-adult and adolescent brain tumor patients. However, the disease prognosis is undetermined, and the method of optimal treatment remains controversial. Methods: From January 1990 to January 2011, data on 91 intracranial germinoma patients (≤20 years old) were gathered from the Pediatric Brain Tumor database at Taipei Veterans General Hospital. A total of seven patients with a median age of 17.0 years had IDIGs (lesion sites >2), including IDIGs in the ventricular system or the spinal column. Craniospinal irradiation (CSI) plus a primary or metastatic boost was the mainstay strategy for radiotherapy. Six out of a total of seven patients (85.7%) also received systemic chemotherapy (CHT) after radiotherapy. Survivals rates between IDIGs and patients without dissemination were estimated using the Kaplan-Meier method. Results: The median follow-up time for all seven patients was 67.5 months (range, 10.3-142.3 months). None of the IDIG patients experienced a recurrence or mortality after the completion of treatment. The 5- and 10-year disease-free survival (DFS) between IDIG and non-dissemination patients were 100%, 100%, 93.0% and 78.6%, respectively (p=0.339). The 5- and 10-year overall survival (OS) between IDIGs and non-dissemination cases were 100%, 100%, 93.7% and 89.4%, respectively (p=0.473). Conclusions: IDIG patients did not show reduced survival compared to non-dissemination patients if optimal radiotherapy and chemotherapy were used together.

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KW - Dissemination

KW - Germinoma

KW - Radiotherapy

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