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Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV.

Publication ,  Journal Article
McDuff, SGR; Dietrich, J; Atkins, KM; Oh, KS; Loeffler, JS; Shih, HA
Published in: Cancer Med
January 2020

PURPOSE: The majority of patients with high-risk lower grade gliomas (LGG) are treated with single-agent temozolomide (TMZ) and radiotherapy despite three randomized trials showing a striking overall survival benefit with adjuvant procarbazine, lomustine, and vincristine (PCV) chemotherapy and radiotherapy. This article aims to evaluate the evidence and rationale for the widespread use of TMZ instead of PCV for high-risk LGG. METHODS AND MATERIALS: We conducted a literature search utilizing PubMed for articles investigating the combination of radiotherapy and chemotherapy for high-risk LGG and analyzed the results of these studies. RESULTS: For patients with IDH mutant 1p/19q codeleted LGG tumors, there is limited evidence to support the use of TMZ. In medically fit patients with codeleted disease, existing data demonstrate a large survival benefit for PCV as compared to adjuvant radiation therapy alone. For patients with non-1p/19q codeleted LGG, early data from the CATNON study supports inclusion of adjuvant TMZ for 12 months. Subset analyses of the RTOG 9402 and EORTC 26951 do not demonstrate a survival benefit for adjuvant PCV for non-1p/19q codeleted gliomas, however secondary analyses of RTOG 9802 and RTOG 9402 demonstrated survival benefit in any IDH mutant lower grade gliomas, regardless of 1p/19q codeletion status. CONCLUSIONS: At present, we conclude that current evidence does not support the widespread use of TMZ over PCV for all patients with high-risk LGG, and we instead recommend tailoring chemotherapy recommendation based on IDH status, favoring adjuvant PCV for patients with any IDH mutant tumors, both those that harbor 1p/19q codeletion and those non-1p/19q codeleted. Given the critical role radiation plays in the treatment of LGG, radiation oncologists should be actively involved in discussions regarding chemotherapy choice in order to optimize treatment for their patients.

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Published In

Cancer Med

DOI

EISSN

2045-7634

Publication Date

January 2020

Volume

9

Issue

1

Start / End Page

3 / 11

Location

United States

Related Subject Headings

  • Vincristine
  • Temozolomide
  • Randomized Controlled Trials as Topic
  • Progression-Free Survival
  • Procarbazine
  • Neoplasm Grading
  • Mutation
  • Lomustine
  • Isocitrate Dehydrogenase
  • Humans
 

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McDuff, S. G. R., Dietrich, J., Atkins, K. M., Oh, K. S., Loeffler, J. S., & Shih, H. A. (2020). Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV. Cancer Med, 9(1), 3–11. https://doi.org/10.1002/cam4.2686
McDuff, Susan G. R., Jorg Dietrich, Katelyn M. Atkins, Kevin S. Oh, Jay S. Loeffler, and Helen A. Shih. “Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV.Cancer Med 9, no. 1 (January 2020): 3–11. https://doi.org/10.1002/cam4.2686.
McDuff SGR, Dietrich J, Atkins KM, Oh KS, Loeffler JS, Shih HA. Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV. Cancer Med. 2020 Jan;9(1):3–11.
McDuff, Susan G. R., et al. “Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV.Cancer Med, vol. 9, no. 1, Jan. 2020, pp. 3–11. Pubmed, doi:10.1002/cam4.2686.
McDuff SGR, Dietrich J, Atkins KM, Oh KS, Loeffler JS, Shih HA. Radiation and chemotherapy for high-risk lower grade gliomas: Choosing between temozolomide and PCV. Cancer Med. 2020 Jan;9(1):3–11.
Journal cover image

Published In

Cancer Med

DOI

EISSN

2045-7634

Publication Date

January 2020

Volume

9

Issue

1

Start / End Page

3 / 11

Location

United States

Related Subject Headings

  • Vincristine
  • Temozolomide
  • Randomized Controlled Trials as Topic
  • Progression-Free Survival
  • Procarbazine
  • Neoplasm Grading
  • Mutation
  • Lomustine
  • Isocitrate Dehydrogenase
  • Humans