Abstract

Simple SummaryPatients diagnosed with pancreatic cancer have a poor prognosis at time of diagnosis, with a 5-year survival rate of merely 10%. The only treatment with curative intent is surgical resection of the tumor and adjacent tumor-containing lymph nodes. To improve surgical outcome and survival, additional (imaging) tools are needed that support complete surgical tumor resection. Firstly, more accurate monitoring of tumor response to neoadjuvant treatment and subsequent determination of resectability is needed. Secondly, an imaging tool is needed for intraoperative guidance allowing accurate identification, delineation, and complete resection of the tumor and suspected lymph nodes. Therefore, both tumor-targeted PET/CT before surgery and real time fluorescence-guidance during surgery could be helpful to improve patient outcome. This review focusses on literature considering tumor-targeted PET/CT and near-infrared fluorescence (NIRF) imaging. Several tumor-targeted agents are under clinical evaluation, and several other promising agents are currently tested preclinically, both with promising results. Their additional diagnostic value and feasibility for future implementation in standard clinical care of PDAC has yet to be established in phase III clinical trials.Background: Despite recent advances in the multimodal treatment of pancreatic ductal adenocarcinoma (PDAC), overall survival remains poor with a 5-year cumulative survival of approximately 10%. Neoadjuvant (chemo- and/or radio-) therapy is increasingly incorporated in treatment strategies for patients with (borderline) resectable and locally advanced disease. Neoadjuvant therapy aims to improve radical resection rates by reducing tumor mass and (partial) encasement of important vascular structures, as well as eradicating occult micrometastases. Results from recent multicenter clinical trials evaluating this approach demonstrate prolonged survival and increased complete surgical resection rates (R0). Currently, tumor response to neoadjuvant therapy is monitored using computed tomography (CT) following the RECIST 1.1 criteria. Accurate assessment of neoadjuvant treatment response and tumor resectability is considered a major challenge, as current conventional imaging modalities provide limited accuracy and specificity for discrimination between necrosis, fibrosis, and remaining vital tumor tissue. As a consequence, resections with tumor-positive margins and subsequent early locoregional tumor recurrences are observed in a substantial number of patients following surgical resection with curative intent. Of these patients, up to 80% are diagnosed with recurrent disease after a median disease-free interval of merely 8 months. These numbers underline the urgent need to improve imaging modalities for more accurate assessment of therapy response and subsequent re-staging of disease, thereby aiming to optimize individual patient’s treatment strategy. In cases of curative intent resection, additional intra-operative real-time guidance could aid surgeons during complex procedures and potentially reduce the rate of incomplete resections and early (locoregional) tumor recurrences. In recent years intraoperative imaging in cancer has made a shift towards tumor-specific molecular targeting. Several important molecular targets have been identified that show overexpression in PDAC, for example: CA19.9, CEA, EGFR, VEGFR/VEGF-A, uPA/uPAR, and various integrins. Tumor-targeted PET/CT combined with intraoperative fluorescence imaging, could provide valuable information for tumor detection and staging, therapy response evaluation with re-staging of disease and intraoperative guidance during surgical resection of PDAC. Methods: A literature search in the PubMed database and (inter)national trial registers was conducted, focusing on studies published over the last 15 years. Data and information of eligible articles regarding PET/CT as well as fluorescence imaging in PDAC were reviewed. Areas covered: This review covers the current strategies, obstacles, challenges, and developments in targeted tumor imaging, focusing on the feasibility and value of PET/CT and fluorescence imaging for integration in the work-up and treatment of PDAC. An overview is given of identified targets and their characteristics, as well as the available literature of conducted and ongoing clinical and preclinical trials evaluating PDAC-targeted nuclear and fluorescent tracers.

Highlights

  • Pancreatic cancer is one of the most lethal cancer types and is the third leading cause of cancer-related death in Europe, which is expected to rise even further within the decades [1,2]

  • Glucose-Regulated Protein-78 (GRP78) expression is upregulated on the cell membrane of pancreatic ductal adenocarcinoma (PDAC) cells and to a lesser extent in precursor lesions, while it is located in the endoplasmic reticulum in normal pancreatic parenchyma, which makes it an interesting target for targeted Positron Emission Tomography (PET)/computed tomography (CT), since the translocation of this protein from the ER to the cell membrane is solely seen on malignant pancreatic cells

  • Yoshioka et al, showed that 18 F-FDG-Positron Emission Tomography—Computed Tomography (PET/CT) could add valuable diagnostic information by demonstrating that a decrease in tumoral metabolic FDG uptake after NT tends to precede anatomic changes in tumor size as seen on ce-CT and magnetic resonance imaging (MRI) [159]. These results suggest that response to treatment might be visualized earlier using 18 F-FDG-PET/CT than ce-CT

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Summary

Introduction

Pancreatic cancer is one of the most lethal cancer types and is the third leading cause of cancer-related death in Europe, which is expected to rise even further within the decades [1,2]. Aiming to increase the number of patients eligible for curative-intent resection and to further optimize surgical outcome, the combination of neoadjuvant induction therapy and adjuvant treatment has been under clinical investigation in the past years [4,17,18,19,20]. The advantages of NT are underlined by the results of the recently published PREOPANC-1 trial This trial compared clinical outcome and survival data of postoperative patients with resectable and borderline resectable disease who had received neoadjuvant or adjuvant therapy. Ferrone et al showed similar results, stating that ce-CT after FOLFIRINOX treatment no longer adequately predicts resectability of the tumor [33] These results underline the need for improved imaging methods for assessment of therapy response, since this is pivotal for accurate (re)staging and determination of tumor resectability [31,34,35]. Internalization of the target-tracer complex, which could facilitate intracellular tracer accumulation is a characteristic of interest as it could result in selective tumor cell uptake and enhanced signals

Overview of PDAC-Associated Molecular Targets for Imaging Purposes
Cathepsin-E
CDCP-1
Endoglin
Fibronectin
2.2.11. Integrins
2.2.12. Mesothelin
2.2.14. Mucin-1
Summary
Primary Diagnostic Work-Up and Monitoring Response to Neoadjuvant Treatment
Clinically Available PET-Tracers for PDAC Imaging
PDAC-Targeted PET-Tracers in Clinical Early Clinical Trials
Integrin αvβ6
Preclinical Evaluation and Development of PDAC-Targeted PET-Tracers
NIR-Fluorescence Imaging and Fluorescence-Guided Surgery
Clinically Tested PDAC Targeted NIRF-Tracers
VEGF-A
Preclinical Evaluation and Development of PDAC-Targeted NIRF-Tracers
Future Perspectives
Conclusions
Results
Ovarian
21 Benign pancreatic lesions
MBq: mild

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