Pseudoprogression and pseudoresponse in the treatment of gliomas
被引:257
作者:
Brandsma, Dieta
论文数: 0引用数: 0
h-index: 0
机构:
Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Neurooncol, Amsterdam, NetherlandsErasmusMC Univ Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Neurooncol, NL-3008 AE Rotterdam, Netherlands
Brandsma, Dieta
[2
]
van den Bent, Martin J.
论文数: 0引用数: 0
h-index: 0
机构:
ErasmusMC Univ Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Neurooncol, NL-3008 AE Rotterdam, NetherlandsErasmusMC Univ Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Neurooncol, NL-3008 AE Rotterdam, Netherlands
van den Bent, Martin J.
[1
]
机构:
[1] ErasmusMC Univ Hosp, Dr Daniel Den Hoed Canc Ctr, Dept Neurooncol, NL-3008 AE Rotterdam, Netherlands
[2] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Neurooncol, Amsterdam, Netherlands
Purpose of review Treatment response of brain tumours is typically evaluated with gadolinium-enhanced MRI using the Macdonald criteria. These criteria depend on changes in the area of enhancement. However, gadolinium enhancement of brain tumours primarily reflects impairment of the blood-brain barrier. Recent findings Combined chemo-irradiation with temozolomide may induce in 20-30% of cases pseudoprogression, defined as an increase of contrast-enhancement and/or oedema on MRI without true tumour progression. Also, full-blown radiation necrosis may be more frequent after combined chemo-irradiation. After treatment with vascular endothelial growth factor receptor signalling pathway inhibitors pseudoresponse is frequent: a decrease in contrast-enhancement of brain tumours on MRI without a decrease of tumour activity. This to some extent explains the high response rate without a major increase in survival after treatment with these agents for recurrent glioblastoma. Summary Both pseudo-phenomenona confuse the assessment of outcome of brain tumours in clinical practice and in clinical trials. To overcome these issues, alternative endpoints and response criteria are being developed by an international working party [response assessment in neuro-oncology (RANG)]. It is as yet unclear to what extent alternative imaging tools (positron emission tomography and MRI techniques) provide more reliable indicators of outcome.
机构:
Univ Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USA
Clarke, Jennifer L.
;
Chang, Susan
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USA
机构:
Univ Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USA
Clarke, Jennifer L.
;
Chang, Susan
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol Surg, Div Neurooncol, San Francisco, CA 94143 USA