Abstract 4593: Molecular and immunohistochemical classification of extrapulmonary small cell neuroendocrine carcinomas: A study of 181 cases

Abstract Extrapulmonary small cell neuroendocrine carcinoma (EP-SCNC) is a rare malignancy with a poor prognosis. Most patients with EP-SCNC have metastatic disease upon presentation, and their average overall survival (OS) is less than 12 months. Our study aimed to conduct a complex analysis of EP-SCNC. One hundred and eighty-one EP-SCNC tissue samples were subjected to a complex analysis. One hundred and fifty-five tumors were pure EP-SCNC, while 26 were combined tumors. Immunohistochemistry for ASCL1, NEUROD1, YAP1, POU2F3, Rb1, p53, cyclin D1, p16, PTEN, DLL3, PD-L1, CD56, synaptophysin, chromogranin A, and INSM1 was performed, and 128 samples were analyzed molecularly using next generation sequencing (NGS), comprising DNA and RNA analysis. Detailed results on immunohistochemical and molecular analyses were provided for each primary origin of EP-SCNC separately. Median survival for the whole cohort of patients was 8.94 months. Patient age (≥ 70 years), tumor mutational burden (TMB) < 15, and TP53 and BRCA2 mutations were negative prognostic factors. High expression of ASCL-1 was associated with shorter OS, whereas high expression of YAP1 was associated with longer OS. Patients with genitourinary tumors had significantly better OS than those with gastrointestinal tract EP-SCNC tumors. Rb1 expression loss was detected more often in genitourinary tract SCNCs. In contrast, p16 overexpression was found more often in genitourinary tract SCNCs. POU2F3 expression was detected more often in combined tumors, whereas NEUROD1 was detected more often in pure EP-SCNC. Regarding “druggable markers, ” DLL3 was expressed in 66% of tumors and PD-L1 in 17.4%.Detailed analyses of different prognostic and predictive markers are needed to better understand EP-SCNC biology and create more personalized therapy to improve patient prognosis. Citation Format: Radoslav Matej, Pavel Dundr, Klara Pavlickova, Marian Svajdler, Jan Hojny, Nikola Hajkova. Molecular and immunohistochemical classification of extrapulmonary small cell neuroendocrine carcinomas: A study of 181 cases [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4593.

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Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-4593
Primary Topic
Neuroendocrine Tumor Research Advances
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article
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article

Abstract 4593: Molecular and immunohistochemical classification of extrapulmonary small cell neuroendocrine carcinomas: A study of 181 cases

Radoslav Matěj, Klára Pavlíčková, Marián Švajdler, Nikola Hájková et al.
Cancer Research
Neuroendocrine Tumor Research Advances
article

Abstract 4593: Molecular and immunohistochemical classification of extrapulmonary small cell neuroendocrine carcinomas: A study of 181 cases

Radoslav Matěj, Klára Pavlíčková, Marián Švajdler, Nikola Hájková, J. Hojný, Pavel Dundr
article en

Abstract

Abstract Extrapulmonary small cell neuroendocrine carcinoma (EP-SCNC) is a rare malignancy with a poor prognosis. Most patients with EP-SCNC have metastatic disease upon presentation, and their average overall survival (OS) is less than 12 months. Our study aimed to conduct a complex analysis of EP-SCNC. One hundred and eighty-one EP-SCNC tissue samples were subjected to a complex analysis. One hundred and fifty-five tumors were pure EP-SCNC, while 26 were combined tumors. Immunohistochemistry for ASCL1, NEUROD1, YAP1, POU2F3, Rb1, p53, cyclin D1, p16, PTEN, DLL3, PD-L1, CD56, synaptophysin, chromogranin A, and INSM1 was performed, and 128 samples were analyzed molecularly using next generation sequencing (NGS), comprising DNA and RNA analysis. Detailed results on immunohistochemical and molecular analyses were provided for each primary origin of EP-SCNC separately. Median survival for the whole cohort of patients was 8.94 months. Patient age (≥ 70 years), tumor mutational burden (TMB) < 15, and TP53 and BRCA2 mutations were negative prognostic factors. High expression of ASCL-1 was associated with shorter OS, whereas high expression of YAP1 was associated with longer OS. Patients with genitourinary tumors had significantly better OS than those with gastrointestinal tract EP-SCNC tumors. Rb1 expression loss was detected more often in genitourinary tract SCNCs. In contrast, p16 overexpression was found more often in genitourinary tract SCNCs. POU2F3 expression was detected more often in combined tumors, whereas NEUROD1 was detected more often in pure EP-SCNC. Regarding “druggable markers, ” DLL3 was expressed in 66% of tumors and PD-L1 in 17.4%.Detailed analyses of different prognostic and predictive markers are needed to better understand EP-SCNC biology and create more personalized therapy to improve patient prognosis. Citation Format: Radoslav Matej, Pavel Dundr, Klara Pavlickova, Marian Svajdler, Jan Hojny, Nikola Hajkova. Molecular and immunohistochemical classification of extrapulmonary small cell neuroendocrine carcinomas: A study of 181 cases [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4593.

Cancer ResearchVol. 85(8_Supplement_1)
General University Hospital in Prague (CZ)
Openalex Percentile: Top 88%
Neuroendocrine Tumor Research Advances
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