4.8 Article

First-in-human study of PET and optical dual-modality image-guided surgery in glioblastoma using Ga-68-IRDye800CW-BBN

期刊

THERANOSTICS
卷 8, 期 9, 页码 2508-2520

出版社

IVYSPRING INT PUBL
DOI: 10.7150/thno.25599

关键词

glioblastoma; dual-modality imaging; positron emission tomography (PET); near-infrared fluorescence; intraoperative imaging; gastrin-releasing peptide receptor

资金

  1. Intramural Research Program of the National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health
  2. National Key Technology Research and Development Program of the Ministry of Science and Technology of China [2014BAI04B01, 2017YFA0205200]
  3. National Natural Science Foundation of China Projects [81502156]
  4. Beijing Nova Program [xx2017017]
  5. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [ZICEB000087, ZIAEB000073] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Purpose: Despite the use of fluorescence-guided surgery (FGS), maximum safe resection of glioblastoma multiforme (GBM) remains a major challenge. It has restricted surgeons between preoperative diagnosis and intraoperative treatment. Currently, an integrated approach combining preoperative assessment with intraoperative guidance would be a significant step in this direction. Experimental design: We developed a novel Ga-68-IRDye800CW-BBN PET/near-infrared fluorescence (NIRF) dual-modality imaging probe targeting gastrin-releasing peptide receptor (GRPR) in GBM. The preclinical in vivo tumor imaging and FGS were first evaluated using an orthotopic U87MG glioma xenograft model. Subsequently, the first-in-human prospective cohort study (NCT 02910804) of GBM patients were conducted with preoperative PET assessment and intraoperative FGS. Results: The orthotopic tumors in mice could be precisely resected using the near-infrared intraoperative system. Translational cohort research in 14 GBM patients demonstrated an excellent correlation between preoperative positive PET uptake and intraoperative NIRF signal. The tumor fluorescence signals were significantly higher than those from adjacent brain tissue in vivo and ex vivo (p < 0.0001). Compared with pathology, the sensitivity and specificity of fluorescence using 42 loci of fluorescence-guided sampling were 93.9% (95% CI 79.8%-99.3%) and 100% (95% CI 66.4%-100%), respectively. The tracer was safe and the extent of resection was satisfactory without newly developed neurologic deficits. Progression-free survival (PFS) at 6 months was 80% and two newly diagnosed patients achieved long PFS. Conclusions: This initial study has demonstrated that the novel dual-modality imaging technique is feasible for integrated pre- and intraoperative targeted imaging via the same molecular receptor and improved intraoperative GBM visualization and maximum safe resection.

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