Literature DB >> 25749900

Treatment results and prognostic factors for intracranial nongerminomatous germ cell tumors: single institute experience.

I-Chun Lai1, Tai-Tong Wong, Cheng-Ying Shiau, Yu-Wen Hu, Donald Ming-Tak Ho, Kai-Ping Chang, Wan-Yuo Guo, Feng-Chi Chang, Muh-Lii Liang, Yi-Yen Lee, Hsin-Hung Chen, Sang-Hue Yen, Yi-Wei Chen.   

Abstract

PURPOSE: This study aimed to evaluate the treatment of intracranial nongerminomatous germ cell tumors (NGGCT) and to identify the prognostic factors for survival.
METHODS: Thirty-nine patients with nondisseminated NGGCTs, excluding those with pure mature teratomas, were treated between January 1985 and December 2010. Twenty-four patients received gross total or partial removal, 11 had excision biopsies, and 4 had no surgery. Radiotherapy was given postoperatively or definitively with a median tumor bed dose of 54 Gy (range 30-54) with or without craniospinal irradiation. All patients received ten cycles of adjuvant chemotherapy, vinblastine, bleomycin, etoposide, and cisplatin after radiotherapy, except for one with mixed anaplastic astrocytoma component who received oral temozolomide. Survival and prognostic factors were estimated by the Kaplan-Meier method and log-rank tests, respectively.
RESULTS: After a median follow-up of 77.7 months (range 14-336), the 6-year overall survival (OS) and progression-free survival (PFS) were 74.4 and 79.5 %, respectively. Inferior PFS was associated with lesions in the suprasellar region (p = 0.017), poor pathological features (p = 0.048), and with poor image (p < 0.0001) and tumor marker (TM) response (p = 0.003) to irradiation. Decreased OS was associated with lesions in the suprasellar region (p = 0.026) and with poor image (p < 0.0001) and TM response (p = 0.027) to irradiation. Neither the extent of surgery nor the radiation field was found to significantly influence survival.
CONCLUSIONS: By our multimodality approach, patients achieved comparable outcomes. Other than poor pathological features, patients with poor responses to radiotherapy are prone to early recurrence and inferior survival. These patients should be focused for more intensive adjuvant treatment.

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Year:  2015        PMID: 25749900     DOI: 10.1007/s00381-015-2623-8

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


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  2 in total

1.  Global DNA methylation analysis reveals miR-214-3p contributes to cisplatin resistance in pediatric intracranial nongerminomatous malignant germ cell tumors.

Authors:  Tsung-Han Hsieh; Yun-Ru Liu; Ting-Yu Chang; Muh-Lii Liang; Hsin-Hung Chen; Hsei-Wei Wang; Yun Yen; Tai-Tong Wong
Journal:  Neuro Oncol       Date:  2018-03-27       Impact factor: 12.300

Review 2.  Intracranial Germ Cell Tumor in the Molecular Era.

Authors:  Ji Hoon Phi; Kyu-Chang Wang; Seung-Ki Kim
Journal:  J Korean Neurosurg Soc       Date:  2018-05-01
  2 in total

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