Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Sakata, K.-i.
Right arrow Articles by Sakai, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sakata, K.-i.
Right arrow Articles by Sakai, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Japanese Journal of Clinical Oncology 31:240-245 (2001)
© 2001 Foundation for Promotion of Cancer Research

Supratentorial Astrocytomas and Oligodendrogliomas Treated in the MRI Era

Koh-ichi Sakata1, Masato Hareyama1, Takashi Komae2, Hiroki Shirato2, Osamu Watanabe3, Jiroh Watarai3, Kenji Takai4, Shogo Yamada4, Emiko Tsuchida5 and Kunio Sakai5,+

1Department of Radiology, Sapporo Medical University, School of Medicine, Sapporo, 2Department of Radiology, Hokkaido University, School of Medicine, Sapporo, 3Department of Radiology, Akita University, School of Medicine, Akita, 4Department of Radiology, Tohoku University, School of Medicine, Sendai and 5Department of Radiology, Niigata University, School of Medicine, Niigata, Japan

Background: There is at present no consensus on the policy for the treatment of patients with low-grade gliomas (LGGs).

Methods: This report is a retrospective multi-institutional study of 100 patients (ages 16–65 years) with astrocytoma (grade II), oligodendroglioma, anaplastic oligodendroglioma and anaplastic oligoastrocytoma of the supratentorial areas which were treated with surgery and postoperative radiotherapy at five university hospitals in northern Japan between 1990 and 1997 when MRI was routinely used to determine the target volume. Most patients were irradiated with 50–60 Gy. The target volume usually covered the areas with T2 prolongation of MRI with a margin of 2 cm.

Results: The disease-specific 5-year survival rate was 87.4% for patients with oligodendroglioma and 75.3% for patients with astrocytoma. Survival for patients with astrocytoma in the MRI era appears to be improved compared with historical controls in the literature. Patients with astrocytoma aged 40 years and under had a significantly better disease-specific survival rate than those over 40 years (P < 0.05) and patients with oligodendroglioma and oligoastrocytoma showed a similar tendency. Patients with astrocytoma who had over 50% of their tumor removed had a significantly better survival rate than those who had less than 50% removed (P < 0.05). Chemotherapy appeared to improve the disease-specific survival rate of patients with oligodendroglioma but not that of patients with astrocytoma.

Conclusion: Oligodendroglioma has a more protracted course of disease progression than astrocytoma. This particular feature and the sensitivity of LGGs to chemotherapy as well as their relevant prognostic factors, such as age, histopathology and amount of tumor removal, should be taken into account before any decision on treatment methods for LGGs is made.

+ For reprints and all correspondence: Koh-ichi Sakata, Department of Radiology, Sapporo Medical University, School of Medicine, S1W16, Chuo-ku, Sapporo 060-8543, Japan. E-mail: sakatako@sapmed.ac.jp


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.