DOI
https://doi.org/10.47689/2181-1415-vol6-iss11/S-pp1-9Keywords
NFPA , IHC , proliferation markersAbstract
Aim. To perform a comparative analysis of immunohistochemical data in patients with macro- and giant non-functional pituitary adenomas (NFPA).
Materials and methods. Twenty patients with NFPA were studied: group 1 included 10 pituitary macroadenomas and group 2 included 10 giant pituitary adenomas. All patients underwent transnasal pituitary adenomectomy and a standardized diagnostic protocol that included fundus examination, visual-field testing every 3 months, and laboratory assays (STH, IGF-1, LH, FSH, ACTH, TSH, prolactin, free thyroxine, cortisol). Resected specimens were examined immunohistochemically with determination of Ki-67 and p53 expression.
Results. The odds of an aggressive NFPA phenotype were 8.2 times higher (p < 0.001) when invasive growth was present (sensitivity 86%, specificity 53%, Youden index 0.45, accuracy 66%). Per-percentage-point increases in marker expression were strongly associated with aggressiveness: a coefficient of 5.2 per percentage point for the Ki-67–positive tumor-cell nuclei (p < 0.001) and 3.1 per percentage point for p53-immunopositive nuclei (p < 0.001).
Conclusions. Significant threshold values were identified: p53 ≥ 2% (reported CI: 0.94) and a Ki-67 labelling index ≥ 4% (reported CI: 0.98), the latter being the most reliable individual marker for differentiating macro NFPA from giant NFPA. Tumors with immunoexpression of at least two markers were observed in 54% of the cohort and were classified as aggressive adenomas. By marker counts: p53-positive cases—4 in group 1 and 5 in group 2; Ki-67 ≥ 4%—5 in group 1 and 6 in group 2. Overall, 11 of 20 IHC-examined patients were assessed as having a risk of growth recurrence.
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