Physical Address
304 North Cardinal St.
Dorchester Center, MA 02124
Treatment-related increase in contrast enhancement mimics tumor progression
Classically described after treatment with chemoradiation (temozolomide with radiation therapy)
Typically occurs within 3-6 months after conclusion of radiation therapy (XRT)
New enhancing lesion + ↑ FLAIR hyperintensity in treated malignant glioma at 3-4 months after XRT completion
T2/FLAIR: Increased hyperintensity with mass effect
DWI: Higher ADC values in PsP compared with tumor
DSC MR
Lower mean rCBV values in PsP compared with tumor
DCE MR
Mean K trans (volume transfer constant) is lower in PsP compared with true progression
MRS: No significant elevation of choline in PsP
Best imaging: Contrast-enhanced MR, DWI, ± MRS, MRP
Follow-up studies may be necessary to make accurate diagnosis of PsP
Knowing clinical history and timing of therapy is key to accurate brain tumor imaging
Recurrent malignant glioma
Radiation necrosis
Current standard of care for malignant gliomas is surgical resection followed by concurrent XRT and chemotherapy with temozolomide (Temodar)
PsP occurs in ~ 35-50% of patients
PsP is self-limited, enhancing lesions resolve without new treatment
PsP has been associated with improved survival
Important to recognize that not all new enhancement in patient with treated glioblastoma is progressive tumor
Pseudoprogression (PsP)
Treatment-related enhancement
Treatment-related changes
Treatment-related increase in contrast enhancement mimicking tumor progression
Classically described after treatment with chemoradiation (temozolomide with radiation therapy)
Typically occurs within 3-6 months after conclusion of radiotherapy (XRT)
Self-limited, enhancing lesions resolve without new treatment
Become a Clinical Tree membership for Full access and enjoy Unlimited articles
If you are a member. Log in here