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Erschienen in: Medical Oncology 3/2021

01.03.2021 | Original Paper

De novo neuroendocrine transdifferentiation in primary prostate cancer–a phenotype associated with advanced clinico-pathologic features and aggressive outcome

verfasst von: Eman Abdulfatah, Zachery R. Reichert, Matthew S. Davenport, Arul M. Chinnaiyan, Vipulkumar Dadhania, Xiaoming Wang, Rahul Mannan, Lakshmi P. Kunju, Brent K. Hollenbeck, Jeffrey S. Montgomery, Samuel D. Kaffenberger, Todd M. Morgan, Ajjai S. Alva, Ganesh S. Palapattu, Ulka N. Vaishampayan, Joshi J. Alumkal, Daniel E. Spratt, Aaron M. Udager, Rohit Mehra

Erschienen in: Medical Oncology | Ausgabe 3/2021

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Abstract

Neuroendocrine transdifferentiation of high-grade prostate cancer (PCA-NT) comprises a morphologic and immunophenotypic transition from conventional adenocarcinoma towards high-grade neuroendocrine/small cell carcinoma. This phenomenon is frequently observed post androgen deprivation and/or radiotherapy, but de novo instances are increasingly recognized. Herein, we report a series of de novo PCA-NT focusing on characteristic morphologic, immunophenotypic and clinical features. Treatment naïve PCA-NT were identified. IHC for PSA, NKX3.1, Chromogranin, Synaptophysin, Cyclin D1, RB and Ki67 were performed. Radiology, treatment and follow-up data were reviewed. Sixteen patients were included. Apart from focal areas of high-grade prostate cancer with acinar features (reminiscent of Grade Group 5 disease), extensive areas with sheets of cells with deep amphophilic/basophilic cytoplasm, enlarged, hyperchromatic nuclei with granular chromatin and inconspicuous to prominent nucleoli with high mitotic activity were identified. Immunohistochemistry showed patchy NKX3.1, patchy PSA, variable Synaptophysin and Chromogranin; RB and CyclinD1 showed loss of expression. Ki67 showed high proliferative index, in most cases. Adverse radiologic findings and metastases were documented in most cases. Two patients died of disease. De novo PCA-NT exhibits high-grade nuclei, high mitotic activity, reduced PSA expression with high Ki67 and functional inactivation of RB1 pathway, suggesting transition from androgen-driven to proliferation-driven phenotype. Most cases presented at advanced stage with adverse radiological findings, metastasis at time of diagnosis, and high mortality. In light of their prognostic and therapeutic implications, pathologists may need to maintain a sensitive threshold for performing immunostains–in particular, Ki67 and CyclinD1–when presented with such cases in their day to day clinical practice.
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Metadaten
Titel
De novo neuroendocrine transdifferentiation in primary prostate cancer–a phenotype associated with advanced clinico-pathologic features and aggressive outcome
verfasst von
Eman Abdulfatah
Zachery R. Reichert
Matthew S. Davenport
Arul M. Chinnaiyan
Vipulkumar Dadhania
Xiaoming Wang
Rahul Mannan
Lakshmi P. Kunju
Brent K. Hollenbeck
Jeffrey S. Montgomery
Samuel D. Kaffenberger
Todd M. Morgan
Ajjai S. Alva
Ganesh S. Palapattu
Ulka N. Vaishampayan
Joshi J. Alumkal
Daniel E. Spratt
Aaron M. Udager
Rohit Mehra
Publikationsdatum
01.03.2021
Verlag
Springer US
Erschienen in
Medical Oncology / Ausgabe 3/2021
Print ISSN: 1357-0560
Elektronische ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-021-01473-2

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