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Population-Based Study of Pseudoprogression after Chemoradiotherapy in GBM

  • Gloria B. Roldán (a1) (a2), James N. Scott (a3), John B. McIntyre (a1) (a4), Marisa Dharmawardene (a1), Paula A. de Robles (a1) (a2), Anthony M. Magliocco (a1) (a4), Elizabeth S. Y. Yan (a5), Ian F. Parney (a6), Peter A. Forsyth (a1) (a2) (a7), J. Gregory Cairncross (a2) (a7), Mark G. Hamilton (a2) (a7) and Jacob C. Easaw (a1) (a7)...

Abstract

Introduction:

Chemoradiotherapy followed by monthly temozolomide (TMZ) is the standard of care for patients with glioblastoma multiforme (GBM). Case reports have identified GBM patients who experienced transient radiological deterioration after concurrent chemoradiotherapy which stabilized or resolved after additional cycles of adjuvant TMZ, a phenomenon known as radiographic pseudoprogression. Little is known about the natural history of radiographic pseudoprogression.

Methods:

We retrospectively evaluated the incidence of radiographic pseudoprogression in a population-based cohort of GBM patients and determined its relationship with outcome and MGMT promoter methylation status.

Results:

Out of 43 evaluable patients, 25 (58%) exhibited radiographic progression on the first MRI after concurrent treatment. Twenty of these went on to receive adjuvant TMZ, and subsequent investigation demonstrated radiographic pseudoprogression in 10 cases (50%). Median survival (MS) was better in patients with pseudoprogression (MS 14.5 months) compared to those with true radiologic progression (MS 9.1 months, p=0.025). The MS of patients with pseudoprogression was similar to those who stabilized/responded during concurrent treatment (p=0.31). Neither the extent of the initial resection nor dexamethasone dosing was associated with pseudoprogression.

Conclusions:

These data suggest that physicians should continue adjuvant TMZ in GBM patients when early MRI scans show evidence of progression following concurrent chemoradiotherapy, as up to 50% of these patients will experience radiologic stability or improvement in subsequent treatment cycles.

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Copyright

Corresponding author

Room 111G, Tom Baker Cancer Centre, 1331 29th Street NW, Calgary, Alberta, T2N 4N2, Canada

References

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