Literature DB >> 8270446

Radiation therapy of pineal region tumors: 25 new cases and a review of 208 previously reported cases.

B G Fuller1, D S Kapp, R Cox.   

Abstract

PURPOSE: Malignant pineal region tumors are rare neoplasms arising in midline structures of the brain. This report analyzes the influence of histology, tumor location, radiation dose, treatment volume, age and cerebrospinal fluid findings on freedom from relapse, freedom from spinal relapse and survival. METHODS AND MATERIALS: Patient and treatment parameters of 25 cases of pineal region tumors managed at Stanford University are presented, and an additional 208 published cases were reviewed. Univariate and multivariate analysis were performed to delineate parameters predictive of freedom from relapse, freedom from spinal relapse, and survival for all 233 patients.
RESULTS: The 5- and 10-year freedom from relapse for Stanford patients was 63% and 46%, respectively. The 5- and 10-year survival for Stanford patients was 67% and 61%, respectively. The 5- and 10-year freedom from relapse for the total 233 cases was 66% and 61%, respectively. The 5- and 10-year survival for all patients was 74% and 68%, respectively. For the entire group, biopsy confirmed germinoma and non-biopsied tumors had superior freedom from relapse compared to non-germinoma germ cell tumors (p = 0.03, p = 0.005, respectively). Non-biopsied patients had improved survival compared to non-germinoma germ cell tumors (p = 0.004). Pineal parenchymal tumors had worse freedom from relapse compared to non-biopsied patients (p = 0.04). For patients with suprasellar tumors, germinomas were associated with improved freedom from relapse compared to non-germinoma germ cell tumors (p = 0.02). Simultaneous pineal and suprasellar tumors had superior survival compared to solitary tumors of pineal (p = 0.04), suprasellar (p = 0.03), or third ventricle location (p = 0.03). Twenty-two patients (9.4%) developed isolated spinal relapse. Five- and 10-year spinal relapse rates for all patients were 11% and 13%. Survival after spinal relapse was 19%. Pineal parenchymal tumors had lower freedom from spinal relapse compared to non-biopsied patients (p = 0.001). For tumors located in the pineal gland, germinomas and pineal parenchymal tumors had lower freedom from spinal relapse than did non-biopsied patients (p = 0.006, p = 0.004, respectively). Pineal germinomas had lower freedom from spinal relapse than germinomas with suprasellar location (p = 0.04). Univariate and multivariate analysis identified tumor histology as the most significant predictor of freedom from relapse, freedom from spinal relapse and survival.
CONCLUSION: Histologic type had the greatest impact on outcome. Treatment recommendations should be based on assessment of histologic type and extent of disease.

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Year:  1994        PMID: 8270446     DOI: 10.1016/0360-3016(94)90162-7

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  16 in total

1.  Pineal parenchymal tumors. Management with interstitial iodine-125 radiosurgery.

Authors:  Mohammad Maarouf; Faycal El Majdoub; Christian Bührle; Jürgen Voges; Ralph Lehrke; Martin Kocher; Stefan Hunsche; Harald Treuer; Volker Sturm
Journal:  Strahlenther Onkol       Date:  2010-02-22       Impact factor: 3.621

2.  Descriptive epidemiology of central nervous system germ cell tumors: nonpineal analysis.

Authors:  J Lee Villano; Irim Y Virk; Vanessa Ramirez; Jennifer M Propp; Herbert H Engelhard; Bridget J McCarthy
Journal:  Neuro Oncol       Date:  2009-12-21       Impact factor: 12.300

Review 3.  Microsurgical resection of pineal region tumors.

Authors:  Adam M Sonabend; Stephen Bowden; Jeffrey N Bruce
Journal:  J Neurooncol       Date:  2016-05-19       Impact factor: 4.130

4.  Pineal region tumours treated with interstitial brachytherapy with low activity sources (192-iridium).

Authors:  K Matsumoto; H Higashi; S Tomita; T Ohmoto
Journal:  Acta Neurochir (Wien)       Date:  1995       Impact factor: 2.216

5.  Suprasellar/pineal bifocal germ cell tumors.

Authors:  Vicente Cuccia; Daniel Alderete
Journal:  Childs Nerv Syst       Date:  2010-03-11       Impact factor: 1.475

6.  Malignant pineal germ-cell tumors: an analysis of cases from three tumor registries.

Authors:  J Lee Villano; Jennifer M Propp; Kimberly R Porter; Andrew K Stewart; Tibor Valyi-Nagy; Xinyu Li; Herbert H Engelhard; Bridget J McCarthy
Journal:  Neuro Oncol       Date:  2008-02-20       Impact factor: 12.300

7.  Arterial vascularization of the pineal gland.

Authors:  Gokmen Kahilogullari; Hasan Caglar Ugur; Ayhan Comert; Recep Ali Brohi; Onur Ozgural; Mevci Ozdemir; Suleyman Tuna Karahan
Journal:  Childs Nerv Syst       Date:  2013-01-20       Impact factor: 1.475

8.  Treatment strategy for intracranial primary pure germinoma.

Authors:  Kyu-Won Shim; Eun Kyung Park; Yoon-Ho Lee; Chang-Ok Suh; Jaeho Cho; Joong-Uhn Choi; Dong-Seok Kim
Journal:  Childs Nerv Syst       Date:  2012-09-11       Impact factor: 1.475

Review 9.  Primary extramedullary spinal germinoma: case report and review of the literature.

Authors:  Qiang Hu; Wenhua Yu; Quan Du; Qiang Zhu; Zhihao Che
Journal:  Neurosurg Rev       Date:  2016-11-07       Impact factor: 3.042

10.  Primary pineal tumors: outcome and prognostic factors--a study from the Rare Cancer Network (RCN).

Authors:  Salvador Villà; Robert C Miller; Marco Krengli; Huda Abusaris; Brigitta G Baumert; Stephanie Servagi-Vernat; Sefik Igdem; Anna Lucas; Susanna Boluda; René O Mirimanoff
Journal:  Clin Transl Oncol       Date:  2012-08-23       Impact factor: 3.405

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