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Staging and Prognosis | Treatment > Radiotherapy


Japanese Journal of Clinical Oncology, June 2001, 31:240-245. (Clinical Study)


Abstract

Supratentorial Astrocytomas and Oligodendrogliomas Treated in the MRI Era

Koh-ichi Sakata, Masato Hareyama, Takashi Komae, Hiroki Shirato, Osamu Watanabe, Jiroh Watarai, Kenji Takai, Shogo Yamada, Emiko Tsuchida and Kunio Sakai

Department of Radiology, Sapporo Medical University, School of Medicine, Sapporo [Ko.S., M.H.], Department of Radiology, Hokkaido University, School of Medicine, Sapporo [T.K., H.S.], Department of Radiology, Akita University, School of Medicine, Akita [O.W., J.W.], Department of Radiology, Tohoku University, School of Medicine, Sendai [K.T., S.Y.] and Department of Radiology, Niigata University, School of Medicine, Niigata, Japan [E.T., Ku.S.]. 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.

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.

© 2001 Foundation for Promotion of Cancer Research


Source: http://jjco.oupjournals.org/cgi/content/abstract/31/6/240?maxtoshow=&HITS=&hits=&RESULTFORMAT=&fulltext=%22Low+Grade+Gliomas%
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DOI: http://dx.doi.org/10.1093/jjco/hye052


 

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