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Cited by 342

The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.

Major Prognostic Role of Ki67 in Localized Adrenocortical Carcinoma After Complete Resection

Open access
Beuschlein, Felix, Weigel, Jens, Saeger, Wolfgang, Kroiss, Matthias, Wild, Vanessa, Daffara, Fulvia, Libé, Rosella, Ardito, Arianna, Al Ghuzlan, Abir, Quinkler, Marcus, Oßwald, Andrea, Ronchi, Cristina L., de Krijger, Ronald, Feelders, Richard A., Waldmann, Jens, Willenberg, Holger S., Deutschbein, Timo, Stell, Anthony, Reincke, Martin, Papotti, Mauro, Baudin, Eric, Tissier, Frédérique, Haak, Harm R., Loli, Paola, Terzolo, Massimo, Allolio, Bruno, Müller, Hans-Helge, Fassnacht, Martin·2015·The Journal of Clinical Endocrinology & Metabolism

Abstract

BACKGROUND: Recurrence of adrenocortical carcinoma (ACC) even after complete (R0) resection occurs frequently. OBJECTIVE: The aim of this study was to identify markers with prognostic value for patients in this clinical setting. DESIGN, SETTING, AND PARTICIPANTS: From the German ACC registry, 319 patients with the European Network for the Study of Adrenal Tumors stage I-III were identified. As an independent validation cohort, 250 patients from three European countries were included. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Clinical, histological, and immunohistochemical markers were correlated with recurrence-free (RFS) and overall survival (OS). RESULTS: Although univariable analysis within the German cohort suggested several factors with potential prognostic power, upon multivariable adjustment only a few including age, tumor size, venous tumor thrombus (VTT), and the proliferation marker Ki67 retained significance. Among these, Ki67 provided the single best prognostic value for RFS (hazard ratio [HR] for recurrence, 1.042 per 1% increase; P < .0001) and OS (HR for death, 1.051; P < .0001) which was confirmed in the validation cohort. Accordingly, clinical outcome differed significantly between patients with Ki67 <10%, 10-19%, and ≥20% (for the German cohort: median RFS, 53.2 vs 31.6 vs 9.4 mo; median OS, 180.5 vs 113.5 vs 42.0 mo). Using the combined cohort prognostic scores including tumor size, VTT, and Ki67 were established. Although these scores discriminated slightly better between subgroups, there was no clinically meaningful advantage in comparison with Ki67 alone. CONCLUSION: This largest study on prognostic markers in localized ACC identified Ki67 as the single most important factor predicting recurrence in patients following R0 resection. Thus, evaluation of Ki67 indices should be introduced as standard grading in all pathology reports of patients with ACC.

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Metadata

Authors
Beuschlein, F., Weigel, J., Saeger, W., Kroiss, M., Wild, V., Daffara, F., Libé, R., Ardito, A., Al Ghuzlan, A., Quinkler, M., Oßwald, A., Ronchi, C. L., de Krijger, R., Feelders, R. A., Waldmann, J., Willenberg, H. S., Deutschbein, T., Stell, A., Reincke, M., Papotti, M., Baudin, E., Tissier, F., Haak, H. R., Loli, P., Terzolo, M., Allolio, B., Müller, H.-H., & Fassnacht, M.
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2015-03-01
Volume
100
Issue
3
Pages
841-849
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W1976454566
Cited by
342
References
36
FWCI
27.87
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Major Prognostic Role of Ki67 in Localized Adrenocortical Carcinoma After Complete Resection. https://app.cochat.ai/papers/10.1210/jc.2014-3182
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Beuschlein, F., Weigel, J., Saeger, W., Kroiss, M., Wild, V., Daffara, F., Libé, R., Ardito, A., Al Ghuzlan, A., Quinkler, M., Oßwald, A., Ronchi, C. L., de Krijger, R., Feelders, R. A., Waldmann, J., Willenberg, H. S., Deutschbein, T., Stell, A., Reincke, M., . . . Fassnacht, M. (2015). Major Prognostic Role of Ki67 in Localized Adrenocortical Carcinoma After Complete Resection. The Journal of Clinical Endocrinology & Metabolism. https://doi.org/10.1210/jc.2014-3182

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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