Literature DB >> 12057096

Adults with newly diagnosed high-grade gliomas.

D Croteau1, T Mikkelsen.   

Abstract

Despite tremendous advances in brain tumor molecular biology and several emerging novel therapies, multimodality therapy that includes surgery, radiation therapy (RT), and chemotherapy is still the cornerstone of high-grade glioma treatment. The first step in high-grade glioma therapy is surgery and a maximal resection should be attempted to reduce the tumor burden before initiation of other adjuvant therapies. External beam radiation therapy (EBRT) generally follows surgery, using conventional dosage, and fractionation, and ideally a three-dimensional conformal technique. Stereotactic radiosurgery (SRS) to maximize cytoreduction may be used in selected cases. Because no curative chemotherapy exists for high-grade glioma, we always consider an investigational agent either before or concurrently with RT. However, the use of a standard cytotoxic agent, such as temozolomide alone or combined with 13-cis-retinoic acid also is a rational choice particularly for patients with relatively good prognostic factors for whom an investigational agent would not be available. The management of anaplastic oligodendroglioma does not differ significantly from other high-grade gliomas in terms of surgery, RT, or investigational or protocol agent; however, these tumors appear to respond to chemotherapy that includes a combination of procarbazine, CCNU, and vincristine (PCV) [1**]. The vincristine provides more toxicity than benefit and it is our practice to only use a combination of procarbazine and CCNU (PC). A single agent, such as temozolomide is an increasingly used and rational choice for anaplastic oligodendroglioma. It is our belief that early, aggressive multimodality treatment still provides the best chance for long-term control of high-grade gliomas, particularly in patients with good prognostic factors. However, despite best therapy and state-of-the-art technology, most patients with high-grade glioma will experience progression or recurrence and will require either a change in the ongoing therapeutic strategy or additional treatment. Better therapies are necessary and progress will only be made through investigation of promising agents in well-designed clinical trials.

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Year:  2001        PMID: 12057096     DOI: 10.1007/s11864-001-0072-y

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  18 in total

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Review 3.  Environmental risk factors for primary malignant brain tumors: a review.

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Journal:  Ann Neurol       Date:  1999-08       Impact factor: 10.422

5.  Procarbazine, lomustine, and vincristine (PCV) chemotherapy for anaplastic astrocytoma: A retrospective review of radiation therapy oncology group protocols comparing survival with carmustine or PCV adjuvant chemotherapy.

Authors:  M D Prados; C Scott; W J Curran; D F Nelson; S Leibel; S Kramer
Journal:  J Clin Oncol       Date:  1999-11       Impact factor: 44.544

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Journal:  J Clin Oncol       Date:  1999-09       Impact factor: 44.544

7.  Patterns of failure following high-dose 3-D conformal radiotherapy for high-grade astrocytomas: a quantitative dosimetric study.

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Journal:  Cancer Chemother Pharmacol       Date:  1998       Impact factor: 3.333

9.  Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas.

Authors:  J G Cairncross; K Ueki; M C Zlatescu; D K Lisle; D M Finkelstein; R R Hammond; J S Silver; P C Stark; D R Macdonald; Y Ino; D A Ramsay; D N Louis
Journal:  J Natl Cancer Inst       Date:  1998-10-07       Impact factor: 13.506

10.  Treatment of recurrent malignant gliomas with high-dose 13-cis-retinoic acid.

Authors:  W K Yung; A P Kyritsis; M J Gleason; V A Levin
Journal:  Clin Cancer Res       Date:  1996-12       Impact factor: 12.531

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  4 in total

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3.  Retinoids in the treatment of glioma: a new perspective.

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4.  The role of radiotherapy and chemotherapy in the treatment of primary adult high grade gliomas: assessment of patients for these treatment approaches and the common immediate side effects.

Authors:  E E Philip-Ephraim; K I Eyong; U E Williams; R P Ephraim
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