PAX6 is a useful marker for pancreatic origin of neuroendocrine neoplasms: A tissue microarray study evaluating more than 19,000 tumors from 150 different tumor types
PAX6 immunohistochemistry (IHC) was proposed as a tool to identify a pancreatic origin of neuroendocrine neoplasms (NENs). To evaluate the diagnostic utility of PAX6 IHC, a tissue microarray containing 19,214 samples from 150 tumor types was analyzed. Data on progesterone receptor (PR) and glutamate decarboxylase 2 (GAD2) expression were available from previous studies. PAX6 staining occurred in 2.6% of 17,224 analyzable tumors and 60 tumor categories showed PAX6 positivity in at least one case. The highest rates of PAX6 positivity occurred in pancreatic (42.9-70.8%) and other NENs (up to 50.0%), testicular tumors (up to 58.3%), basal cell carcinomas of the skin (51.9%), squamous cell carcinomas of different organs (1.5-11.8%), and in gynecological tumors (up to 30%). For detection of pancreatic origin of NENs, sensitivity was highest for PAX6 (68.7%) followed by GAD2 (62.6%) and PR (52.5%) while specificity was highest for GAD2 (95.2%), followed by PR (91.3%), and PAX6 (91.1%). Of the analyzed combinations, the highest sensitivity (53.8%) and specificity (100%) was found for PAX6/GAD2, although combinations of PAX6/PR (49.5%/99.3%), PR/GAD2 (40.7%/98.9%), and PAX6/PR/GAD2 (40.6%/100%) did also result in high specificity. Only 14% of the 118 NENs with negativity for all three antibodies were of pancreatic origin. It is concluded that PAX6 IHC is useful to identify a pancreatic origin in case of NEN metastases of unknown origin. The combination with GAD2 and PR further increase the diagnostic performance of PAX6 and results in a >98% specificity in case of positivity for at least 2 of these markers.
Authors
- Katharina Möller (ORCID: https://orcid.org/0000-0002-9739-4274)
- Maximilian Lennartz (ORCID: https://orcid.org/0000-0002-1572-8200)
- Guido Sauter (ORCID: https://orcid.org/0000-0002-9024-4978)
- Anne Menz (ORCID: https://orcid.org/0000-0002-4364-6464)
- Florian Lutz (ORCID: https://orcid.org/0000-0002-3778-3286)
- Eike Burandt (ORCID: https://orcid.org/0000-0002-5705-9084)
- Stefan Steurer (ORCID: https://orcid.org/0000-0002-7199-3615)
- Natalia Gorbokon (ORCID: https://orcid.org/0009-0001-6680-8788)
- Christoph Fraune (ORCID: https://orcid.org/0000-0002-0833-9549)
- Christian Bernreuther
- Till Krech
- Andreas M. Luebke (ORCID: https://orcid.org/0000-0003-1464-6964)
- Sarah Jane Pauline Minner (ORCID: https://orcid.org/0000-0003-0765-3568)
- Claudia Hube‐Magg (ORCID: https://orcid.org/0000-0001-7542-4340)
- Sören Weidemann (ORCID: https://orcid.org/0000-0001-7037-3265)
- Patrick Lebok (ORCID: https://orcid.org/0000-0003-3652-532X)
- Frank Jacobsen (ORCID: https://orcid.org/0009-0009-8047-580X)
- Florian Viehweger
- Till Sebastian Clauditz (ORCID: https://orcid.org/0000-0002-4257-856X)
- Ronald Simon (ORCID: https://orcid.org/0000-0003-0158-4258)
- Andrea Hinsch (ORCID: https://orcid.org/0000-0001-5868-1185)
- Martina Kluth (ORCID: https://orcid.org/0000-0003-4782-4616)
- David Dum (ORCID: https://orcid.org/0000-0002-7884-4313)
- Ria Schlichter
- Andreas Holger Marx (ORCID: https://orcid.org/0000-0002-5182-8364)
- Sophie-Marie Hornburg
Institutions
- Universität Hamburg (DE)
- University Medical Center Hamburg-Eppendorf (DE)
- Klinikum Fulda (DE)
Publication Details
- Journal
- Human Pathology
- Published
- 2024-11-19
- DOI
- https://doi.org/10.1016/j.humpath.2024.105695
- Citations
- 6
- Primary Topic
- Neuroendocrine Tumor Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 2.32