International Journal of Radiation Oncology * Biology * Physics
Volume 78, Issue 4 , Pages 1147-1155, 15 November 2010

Patterns and Timing of Recurrence After Temozolomide-Based Chemoradiation for Glioblastoma

  • Michael T. Milano, M.D., Ph.D.

      Affiliations

    • Department of Radiation Oncology, University of Rochester Medical Center, Rochester, NY
    • Corresponding Author InformationReprint requests to: Michael T. Milano, M.D., Ph.D., Department of Radiation Oncology, University of Rochester Medical Center, 601 Elmwood Ave, Box 647, Rochester, NY 14642. Tel: (585) 273-4096; Fax: (585) 275-1531
  • ,
  • Paul Okunieff, M.D.

      Affiliations

    • Department of Radiation Oncology, University of Rochester Medical Center, Rochester, NY
  • ,
  • Rosemary S. Donatello, C.M.D.

      Affiliations

    • Department of Radiation Oncology, University of Rochester Medical Center, Rochester, NY
  • ,
  • Nimish A. Mohile, M.D.

      Affiliations

    • Department of Neurology, University of Rochester Medical Center, Rochester, NY
  • ,
  • Joohee Sul, M.D.

      Affiliations

    • Department of Neurology, University of Rochester Medical Center, Rochester, NY
    • National Cancer Institute, Rockville, MD
  • ,
  • Kevin A. Walter, M.D.

      Affiliations

    • Department of Neurosurgery, University of Rochester Medical Center, Rochester, NY
    • Department of Medicine, Division of Oncology, University of Rochester Medical Center, Rochester, NY
  • ,
  • David N. Korones, M.D.

      Affiliations

    • Department of Medicine, Division of Oncology, University of Rochester Medical Center, Rochester, NY
    • Department of Pediatrics, University of Rochester Medical Center, Rochester, NY

Received 1 July 2009; received in revised form 1 September 2009; accepted 2 September 2009. published online 08 March 2010.

Purpose

To determine recurrence patterns of glioblastoma treated with temozolomide-based chemoradiation.

Methods

Pretreatment and serial posttreatment magnetic resonance imaging scans of 54 patients were retrospectively evaluated. Central recurrence (i.e., local progression) and the development of new (i.e., interval appearance of discrete enhancing lesion) in-field, marginal, and distant recurrences were assessed, with the pattern of recurrence of individual lesions defined relative to the 95% isodose line (D95). Distant recurrences were defined as lesions completely outside D95, marginal recurrences crossed D95, and in-field recurrences were completely inside D95.

Results

At a median follow-up of 17 months, 39 of 54 (72%) patients developed recurrent glioblastoma. Among these 39 patients, central recurrence occurred in 80% (at a median of 7 months from diagnosis); new in-field recurrence developed in 33% (at a median of 14 months); marginal recurrences developed in 15% (at a median of 18 months); and distant recurrences developed in 20% (at a median of 11 months). The actuarial rates of central, new in-field, marginal, distant, and any new recurrences at 1-year were 46%, 15%, 3%, 14%, and 25% respectively, whereas at 2 years, the rates were 68%, 60%, 32%, 28%, and 66%, reflecting an increasing probability of new lesions developing at later time points. Ten patients developed subependymal recurrences, of whom 7 developed multiple subependymal lesions.

Conclusions

Whereas central recurrence of glioblastoma treated with radiation and temozolomide predominates and persists over time, new in-field, marginal, and distant recurrences commonly develop, particularly at later time points in patients with longer survival.

Glioblastoma, Radiation therapy, Patterns of recurrence

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 Conflict of interest: none.

PII: S0360-3016(09)03211-8

doi:10.1016/j.ijrobp.2009.09.018

International Journal of Radiation Oncology * Biology * Physics
Volume 78, Issue 4 , Pages 1147-1155, 15 November 2010