The immunohistochemical expression of SSTR2A is an independent prognostic factor in meningioma

• DOI: 10.1007/s10143-021-01651-w
• Publication Date: 2021-10-04T18:39:03Z
• Authors: Christina Fodi; Marco Skardelly; Johann-Martin Hempel; Elgin Hoffmann; Salvador Castaneda; Ghazaleh Tabatabai; Jürgen Honegger; Marcos Tatagiba; Jens Schittenhelm; Felix Behling
• Keywords: 0301 basic medicine; 03 medical and health sciences; Meningeal Neoplasms/pathology [MeSH] ; Immunohistochemistry ; Humans [MeSH] ; SSTR ; Tissue microarray ; Prognosis ; Meningeal Neoplasms/diagnosis [MeSH] ; Immunohistochemistry [MeSH] ; Original Article ; Recurrence-free survival ; Meningioma/pathology [MeSH] ; Somatostatin receptor ; Prognosis [MeSH] ; Meningioma/diagnosis [MeSH] ; Neoplasm Recurrence, Local [MeSH] ; Meningioma ; Receptors, Somatostatin/metabolism [MeSH]; Meningeal Neoplasms; Humans; Original Article; Receptors, Somatostatin; Neoplasm Recurrence, Local; Meningioma; Prognosis; Immunohistochemistry

AbstractThe expression of somatostatin receptors in meningioma is well established. First, suggestions of a prognostic impact of SSTRs in meningioma have been made. However, the knowledge is based on few investigations in small cohorts. We recently analyzed the expression of all five known SSTRs in a large cohort of over 700 meningiomas and demonstrated significant correlations with WHO tumor grade and other clinical characteristics. We therefore expanded our dataset and additionally collected information about radiographic tumor recurrence and progression as well as clinically relevant factors (gender, age, extent of resection, WHO grade, tumor location, adjuvant radiotherapy, neurofibromatosis type 2, primary/recurrent tumor) for a comprehensive prognostic multivariate analysis (n = 666). The immunohistochemical expression scores of SSTR1, 2A, 3, 4, and 5 were scored using an intensity distribution score ranging from 0 to 12. For recurrence-free progression analysis, a cutoff at an intensity distribution score of 6 was used. Univariate analysis demonstrated a higher rate of tumor recurrence for increased expression scores for SSTR2A, SSTR3, and SSTR4 (p = 0.0312, p = 0.0351, and p = 0.0390, respectively), while high expression levels of SSTR1 showed less frequent tumor recurrences (p = 0.0012). In the Kaplan–Meier analysis, a higher intensity distribution score showed a favorable prognosis for SSTR1 (p = 0.0158) and an unfavorable prognosis for SSTR2A (0.0143). The negative prognostic impact of higher SSTR2A expression remained a significant factor in the multivariate analysis (RR 1.69, p = 0.0060). We conclude that the expression of SSTR2A has an independent prognostic value regarding meningioma recurrence.