Gliomas: Predicting Time to Progression or Survival with Cerebral Blood Volume Measurements at Dynamic Susceptibility-weighted Contrast-enhanced Perfusion MR Imaging1
Purpose: To retrospectively determine whether relative cerebral blood volume (CBV) measurements can be used to predict clinical outcome in patients with high-grade gliomas (HGGs) and low-grade gliomas (LGGs) and specifically whether patients who have gliomas with a high initial relative CBV have mor...
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Veröffentlicht in: | Radiology 2008-05, Vol.247 (2), p.490 |
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Sprache: | eng |
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Zusammenfassung: | Purpose: To retrospectively determine whether relative cerebral blood volume (CBV) measurements can be used to predict clinical outcome
in patients with high-grade gliomas (HGGs) and low-grade gliomas (LGGs) and specifically whether patients who have gliomas
with a high initial relative CBV have more rapid progression than those who have gliomas with a low relative CBV.
Materials and Methods: Approval for this retrospective HIPAA-compliant study was obtained from the Institutional Board of Research Associates, with
waiver of informed consent. One hundred eighty-nine patients (122 male and 67 female patients; median age, 43 years; range,
4â80 years) were examined with dynamic susceptibility-weighted contrast materialâenhanced perfusion magnetic resonance (MR)
imaging and were followed up clinically with MR imaging (median follow-up, 334 days). Log-rank tests were used to evaluate
the association between relative CBV and time to progression by using Kaplan-Meier curves. Binary logistic regression was
used to determine whether age, sex, and relative CBV were associated with an adverse event (progressive disease or death).
Results: Values for the mean relative CBV for patients according to each clinical response were as follows: 1.41 ± 0.13 (standard
deviation) for complete response ( n = 4), 2.36 ± 1.78 for stable disease ( n = 41), 4.84 ± 3.32 for progressive disease ( n = 130), and 3.82 ± 1.93 for death ( n = 14). Kaplan-Meier estimates of median time to progression in days indicated that patients with a relative CBV of less than
1.75 had a median time to progression of 3585 days, whereas patients with a relative CBV of more than 1.75 had a time to progression
of 265 days. Age and relative CBV were also independent predictors for clinical outcome.
Conclusion: Dynamic susceptibility-weighted contrast-enhanced perfusion MR imaging can be used to predict median time to progression
in patients with gliomas, independent of pathologic findings. Patients who have HGGs and LGGs with a high relative CBV (>1.75)
have a significantly more rapid time to progression than do patients who have gliomas with a low relative CBV.
© RSNA, 2008 |
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ISSN: | 0033-8419 1527-1315 |
DOI: | 10.1148/radiol.2472070898 |