Diagnoses Disease Clinical Trial
Official title:
Clinical Study on the Efficacy of Amide Proton Transfer Magnetic Resonance Imaging in Predicting the Efficacy of Bevacizumab in Recurrent Malignant Gliomas
Targeted therapy with bevacizumab is the main method to prolong the progression-free
survival of patients with recurrent malignant gliomas in recent years. Using noninvasive
imaging methods to predict which RMG may respond to bevacizumab regimen therapy is a
clinical problem ; on the other hand, repeated gadolinium enhancement may increase the risk
of gadolinium ion deposition of brain tissue. Furthermore,there may be a false response
phenomenon and cause assessment bias.in the evaluation of treatment efficacy,owing to
bevacizumab is only anti-tumor angiogenesis.
Amide Proton Transfer (APT) is a new molecular imaging technique. Our previous studies have
shown that imaging features and signal changes of APT can fully reflect the therapeutic
effect of malignant glioma,without the injection of contrast agent and avoid the side
effects.
RMG patients will be recruited in this study . This project will be designed multi-center,
prospective, observational clinical research. The changes of APT signal intensity before and
after treatment will be compared with those of different types of RMG line. The relationship
between APT imaging characteristics and clinical end point events will be investigated and
compared with conventional MR imaging technique. The sensitivity, specificity and accuracy
of the progression-free survival and median overall survival will be measured after
treatment with bevacizumab.
Recurrent Malignant Gliomas (RMG) have a very short survival time, and re-operation risk is
large and failed to significantly improve the prognosis of patients. At present, targeted
therapy with bevacizumab is effective in prolonging the progression of patients However, a
considerable proportion of recurrent malignant gliomas are insensitive to bevacizumab, and
therefore, using noninvasive imaging methods to predict which RMG is sensitive to
bevacizumab therapy prior to targeted therapy is very important On the other hand, the
current evaluation of bevacizumab is mainly based on the degree of gadolinium enhancement
and tumor volume changes, repeated gadolinium injection may increase the risk of gadolinium
ion deposition of brain tissue, and because of Bevacizumab only acting as an anti-tumor
angiogenesis, and a false response may occur in assessing efficacy, which is a bias in the
overall assessment of bevacizumab.
Amide Proton Transfer (APT) is a new molecular imaging technique for the detection indirect
of free protein and peptide concentrations based on chemical saturation exchange. Our
previous studies have shown that APT signal is independent of gadolinium-enhanced imaging
markers , The signal intensity is closely related to the density of tumor cells, cell
proliferation and angiogenesis. Therefore, the imaging features and signal changes of APT
can fully reflect the therapeutic effect of malignant glioma, and avoid the side effects
caused by contrast injection.
This study will be designed as multi-center, prospective, observational clinical research.
100 cases of RMG patients in Zhujiang Hospital and Nanfang Hospital will be recruited. The
patients will be examined with conventional MRI and APT-MRI imaging of 3.0T high field MRI.
The treatment of different types of RMG line will be scanned with APT protocol. The changes
of signal intensity will be studied. The relationship between APT imaging characteristics
and clinical end point events will be observed and compared with conventional MR imaging
technique. Two techniques will be used to predict the the 6-month progression-free survival
after bevacizumab treatment. The aim of this study is to determine whether APT can predict
the efficacy of bevacizumab in the treatment of RMG, and which RMG is effective and
sensitive to bevacizumab therapy .Also,we will evaluate the feasibility of APT-MR imaging as
a surrogate biomarker for predicting the efficacy of targeted therapy and to establish the
basic criteria for the selection of individualized targeted therapy regimens for RMG.
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