Somatostatin receptor expression and clinical outcome of multilineage pituitary tumours expressing PIT1 and SF1

被引:6
|
作者
Fookeerah, Prishila [1 ,2 ]
Varikatt, Winny [3 ,4 ]
Shingde, Meena [3 ,4 ]
Dexter, Mark A. J. [4 ,5 ]
Mclean, Mark [1 ,2 ]
机构
[1] Westmead Hosp, Dept Diabet & Endocrinol, Sydney, Australia
[2] Western Sydney Univ, Sch Med, Sydney, Australia
[3] Westmead Hosp, Dept Tissue Pathol & Diag Oncol, Sydney, Australia
[4] Univ Sydney, Westmead Clin Sch, Sydney, Australia
[5] Westmead Hosp, Dept Neurosurg, Sydney, Australia
关键词
multilineage PIT1 and SF1; pituitary neuroendocrine tumours; pituitary adenomas; acromegaly; somatostatin receptor; transcription factor; plurihormonal; SURGERY; SSTR2A;
D O I
10.1530/EC-23-0328
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The application of transcription factor immunohistochemistry to pituitary neuroendocrine tumour (PitNET) assessment has allowed identification of tumours that do not conform to a single lineage. Multilineage pituitary transcription factor 1 (PIT1) and steroidogenic factor 1 (SF1) PitNETs are a rare and relatively newly described tumour subtype. These tumours express both transcription factors and may also express combinations of hormones corresponding to both lineages. Histological and clinical characteristics can vary, and overall clinical behaviour and prognosis is not known. We describe the clinical outcomes and somatostatin receptor status (SSTR) of a series of nine cases identified from our cohort of pituitary tumours at Westmead Hospital. Eight PitNETs (88.9%) expressed growth hormone and caused acromegaly at presentation. Of the seven macrotumours that caused acromegaly, one had cavernous sinus invasion. The Ki-67 labeling index score ranged from 0.6% to 3.6%. About 88% of tumours that secreted excess growth hormone exhibited strong immunostaining for SSTR 2 and all tumours displayed weak immunoreactivity for SSTR5. In 62.5% of patients with acromegaly, cure was achieved after surgical resection. Somatostatin receptor ligands resulted in clinical remission in cases where medical treatment was initiated. There was no new tumour recurrence or regrowth over an overall mean follow-up period of 62.5 months.
引用
收藏
页数:5
相关论文
共 6 条
  • [1] Multilineage Pituitary Neuroendocrine Tumors (PitNETs) Expressing PIT1 and SF1
    Sylvia L. Asa
    Ozgur Mete
    Nicole D. Riddle
    Arie Perry
    Endocrine Pathology, 2023, 34 : 273 - 278
  • [2] Multilineage Pituitary Neuroendocrine Tumors (PitNETs) Expressing PIT1 and SF1
    Asa, Sylvia L.
    Mete, Ozgur
    Riddle, Nicole D.
    Perry, Arie
    ENDOCRINE PATHOLOGY, 2023, 34 (03) : 273 - 278
  • [3] Multilineage Pituitary Neuroendocrine Tumors Expressing TPIT and SF1: A Clinicopathological Series of Six Tumors
    Asa, Sylvia L.
    Faiman, Gregg H.
    Mohamed, Amr
    Mete, Ozgur
    ENDOCRINE PATHOLOGY, 2024, 35 (04) : 349 - 353
  • [4] Somatostatin receptor biology in neuroendocrine and pituitary tumours: part 1-molecular pathways
    Cakir, Mehtap
    Dworakowska, Dorota
    Grossman, Ashley
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2010, 14 (11) : 2570 - 2584
  • [5] Differential somatostatin receptor (SSTR) 1-5 expression and downstream effectors in histologic subtypes of growth hormone pituitary tumors
    Kiseljak-Vassiliades, Katja
    Xu, Mei
    Mills, Taylor S.
    Smith, Elizabeth E.
    Silveira, Lori J.
    Lillehei, Kevin O.
    Kerr, Janice M.
    Kleinschmidt-DeMasters, B. K.
    Wierman, Margaret E.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2015, 417 (0C) : 73 - 83
  • [6] Expression and function of somatostatin receptor subtype 1 in human growth hormone secreting pituitary tumors deriving from patients partially responsive or resistant to long-term treatment with somatostatin analogs
    Matrone, C
    Pivonello, R
    Colao, A
    Cappabianca, P
    Cavallo, LM
    De Caro, MLD
    Taylor, JE
    Culler, MD
    Lombardi, G
    Di Renzo, GF
    Annunziato, L
    NEUROENDOCRINOLOGY, 2004, 79 (03) : 142 - 148