Cited by 141Adrenal and Paraganglionic TumorsNeuroendocrine Tumor Research AdvancesRenal cell carcinoma treatment

Immunohistochemistry of a proliferation marker Ki67/MIB1 in adrenocortical carcinomas: Ki67/MIB1 labeling index is a predictor for recurrence of adrenocortical carcinomas

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MORIMOTO, Ryo, SATOH, Fumitoshi, MURAKAMI, Osamu, SUZUKI, Takashi, ABE, Takaaki, TANEMOTO, Masayuki, ABE, Michiaki, URUNO, Akira +5 more·2008·Endocrine Journal

Abstract

Adrenocortical carcinoma (ACC) is a rare, highly malignant tumor. The aim of the present study is to evaluate the prognostic relevance of a proliferation marker Ki67/MIB1 by immunohistochemistry in 17 cases who underwent resections of the primary tumors and diagnosed to have ACC at Tohoku University Hospital based on the criteria of Weiss during the period from 1976 to 2005. The follow-up periods ranged from 221 days to 10659 days (about 29 years) with the median of 1895 days. The median age at diagnosis was 46 years old, and the mean size of the primary tumors was 7.1 cm with the minimal of 3.5 cm. Ki67/MIB1 labeling index (Ki67/MIB1LI) ranged from 1% to 26%. Kaplan-Meier analysis revealed that patients with Ki67/MIB1LI of 7% or more were associated with significantly shortened disease-free survival (P = 0.0037). The evaluation with Weiss criteria revealed that the median score of Weiss criteria was five, and 13 patients (76.5%) presented positive findings in the criteria of mitotic rate. The survival analysis with Weiss score showed that patients with the scores of 6 or more had both significantly shortened disease-free survival (P = 0.0001) and overall survival (P = 0.0063). The present study has suggested that Ki67/MIB1LI, as well as Weiss score, is a useful predictor for tumor recurrence after resection of the primary tumors in patients with ACC.

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  • The cutoff at which a Ki67 labeling index confirms the diagnosis of ACC and predicts aggressive disease is debated and ranges from >2.5% to >7%.

    “The cutoff at which a Ki67 labeling index confirms the diagnosis of ACC and predicts aggressive disease is debated and ranges from >2.5% to >7% (113,115-117).”

    From Adrenal incidentaloma (2020) · cites this paper as [116]

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Research works printed but not linked: 2

  1. Allolio B, Fassnacht M (2006) Clinical review: adreno- cortical carcinoma: clinical update. J Clin Endocrinol Metab 91: 2027-2037.
  2. Norton JA (2005) Adrenal tumors. In: DeVita VT Jr, Hellman S, Rosenberg SA (eds) Cancer: principles and practice of oncology. 7th ed. Lippincott Williams & Wilkins, Philadelphia: 1528-1539.

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Authors
MORIMOTO, R., SATOH, F., MURAKAMI, O., SUZUKI, T., ABE, T., TANEMOTO, M., ABE, M., URUNO, A., ISHIDOYA, S., ARAI, Y., TAKAHASHI, K., SASANO, H., & ITO, S.
Affiliations
Tohoku University (JP)
Venue
Endocrine Journal
Published
2008
Volume
55
Issue
1
Pages
49-55
ISSN
  • 0918-8959 (ISSN-L)
  • 1348-4540
OpenAlex
W2045466543
Cited by
141
References
20
Citations by year
2025: 2 · 2024: 4 · 2023: 5 · 2022: 6 · 2021: 8 · 2020: 14 · 2019: 13 · 2018: 11 · 2017: 11 · 2016: 7 · 2015: 10 · 2014: 12 · 2013: 8 · 2012: 7
FWCI
8.08
Type
journal article
Language
en
Open access
Locations
  • Endocrine Journal (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Epidemiology › Neuroendocrine Tumor Research Advances
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Renal cell carcinoma treatment
Keywords
adrenocortical carcinoma, cell proliferation markers, tumor recurrence, mitotic activity, disease-free survival, overall survival, prognostic factors, adrenalectomy
MeSH terms
Adolescent, Adrenal Cortex Neoplasms, Adult, Aged, Female, Follow-Up Studies, Humans, Immunohistochemistry, Male, Middle Aged, Prognosis, Recurrence, Retrospective Studies, Biomarkers, Tumor, Adrenocortical Carcinoma, Ki-67 Antigen, Ubiquitin-Protein Ligases, Cell Proliferation

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