3 results on '"van Boxtel, Wim"'
Search Results
2. Prognostic value of PSMA, c-MET and E-cadherin in salivary duct carcinoma.
- Author
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van Boxtel W, Uijen MJM, Verhaegh GW, Willems SM, Jonker MA, Schalken JA, van Engen-van Grunsven ICH, and van Herpen CML
- Subjects
- Adult, Aged, Aged, 80 and over, Biomarkers, Tumor, Cadherins metabolism, Carcinoma, Ductal diagnosis, Carcinoma, Ductal mortality, Carcinoma, Ductal therapy, Disease Susceptibility, Female, Gene Expression, Humans, Immunohistochemistry, In Situ Hybridization, Kaplan-Meier Estimate, Male, Middle Aged, Neoplasm Metastasis, Neoplasm Staging, Prognosis, Proportional Hazards Models, Proto-Oncogene Mas, Proto-Oncogene Proteins c-met metabolism, Receptors, Androgen genetics, Receptors, Androgen metabolism, Salivary Gland Neoplasms diagnosis, Salivary Gland Neoplasms mortality, Salivary Gland Neoplasms therapy, Cadherins genetics, Carcinoma, Ductal etiology, Proteasome Endopeptidase Complex metabolism, Proto-Oncogene Proteins c-met genetics, Salivary Gland Neoplasms etiology
- Abstract
Objectives: Salivary duct carcinoma (SDC) is a rare and aggressive subtype of salivary gland cancer. Androgen receptor (AR) (96%) and HER2 (29-46%) expression, and a high propensity for regional lymph node metastases are hallmarks of the disease. We hypothesized that c-MET, E-cadherin, PSMA tumor and PSMA neovascular expression may be prognostic factors in SDC., Materials and Methods: Expression levels of these proteins were established on tissue microarrays containing 165 primary SDC tumor specimens. Association with survival was studied with Kaplan-Meier curves, and univariable and multivariable Cox regression models. Furthermore, association with lymph node status, AR and HER2 expression, and gender was studied., Results: We found that patients with high PSMA tumor expression showed a significantly longer overall survival (OS) (median 83 vs. 43 months, P = 0.022), a trend towards a longer DFS (median 51 vs. 22 months, P = 0.094), and significantly reduced hazard ratio for death in the univariable Cox regression model (HR 0.46, P = 0.034). In the multivariable model only a high number of tumor-positive lymph nodes and high age (>80) at diagnosis were prognostic for poor OS. High PSMA tumor expression was also significantly associated with low N-stage (P = 0.001) and expression was higher in women versus men (P = 0.029). High PSMA tumor expression and E-cadherin loss were significantly associated with strong and weak AR-expression, respectively (P = 0.033 and P = 0.007). None of the factors were significantly associated with HER2 expression., Conclusion: c-MET, E-cadherin, and tumor and neovascular PSMA expression are no independent prognostic factors in SDC., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2020
- Full Text
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3. 68 Ga-PSMA-HBED-CC PET/CT imaging for adenoid cystic carcinoma and salivary duct carcinoma: a phase 2 imaging study.
- Author
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van Boxtel W, Lütje S, van Engen-van Grunsven ICH, Verhaegh GW, Schalken JA, Jonker MA, Nagarajah J, Gotthardt M, and van Herpen CML
- Subjects
- Adult, Aged, Antigens, Surface metabolism, Carcinoma, Ductal therapy, Edetic Acid administration & dosage, Edetic Acid pharmacokinetics, Edetic Acid therapeutic use, Female, Gallium Isotopes, Gallium Radioisotopes, Glutamate Carboxypeptidase II metabolism, Humans, Magnetic Resonance Imaging methods, Male, Middle Aged, Neoplasm Metastasis diagnostic imaging, Neoplasm Metastasis pathology, Neoplasm Recurrence, Local diagnostic imaging, Neoplasm Recurrence, Local pathology, Oligopeptides administration & dosage, Oligopeptides therapeutic use, Prospective Studies, Prostatic Neoplasms metabolism, Prostatic Neoplasms pathology, Radiopharmaceuticals administration & dosage, Radiopharmaceuticals pharmacokinetics, Radiopharmaceuticals therapeutic use, Salivary Ducts pathology, Salivary Gland Neoplasms pathology, Carcinoma, Adenoid Cystic diagnostic imaging, Carcinoma, Ductal metabolism, Edetic Acid analogs & derivatives, Oligopeptides pharmacokinetics, Positron Emission Tomography Computed Tomography methods
- Abstract
Rationale : Treatment options for recurrent and/or metastatic (R/M) adenoid cystic carcinoma (ACC) and salivary duct carcinoma (SDC), major subtypes of salivary gland cancer, are limited. Both tumors often show overexpression of prostate-specific membrane antigen (PSMA). In prostate cancer, PSMA-ligands labeled with
68 Ga or177 Lu are used for imaging and therapy, respectively. Primary aim of this study in R/M ACC and SDC patients was to systematically investigate68 Ga-PSMA-uptake by PET/CT imaging to determine if PSMA radionuclide therapy could be a treatment option. Methods : In a prospective phase II study, PET/CT imaging was performed 1 h post injection of68 Ga-PSMA-HBED-CC in 15 ACC patients and 10 SDC patients. Maximum standardized uptake values (SUV) were determined in tumor lesions. Immunohistochemical PSMA expression was scored in primary tumors and metastatic tissue. Standard imaging (MRI or CT) was performed for comparison. Results : In ACC patients, SUVmax ranged from 1.1 to 30.2 with a tumor/liver-ratio >1 in 13 out of 14 evaluable patients (93%). In SDC patients, SUVmax ranged from 0.3 to 25.9 with a tumor/liver-ratio >1 in 4 out of 10 patients (40%). We found a large intra-patient inter-metastatic variation in uptake of68 Ga-PSMA, and immunohistochemistry did not predict ligand uptake in ACC and SDC. Finally, PSMA-PET detected additional bone metastases compared to CT in 2 ACC patients with unexplained pain. Conclusion : In 93% of ACC patients and 40% of SDC patients we detected relevant PSMA-ligand uptake, which warrants to study PSMA radionuclide therapy in these patients. Additionally, our data provide arguments for patient selection and treatment timing. Finally, PSMA-PET imaging has added diagnostic value compared to CT in selected patients., Competing Interests: Competing Interests: The authors have declared that no competing interest exists., (© The author(s).)- Published
- 2020
- Full Text
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