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Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma

BACKGROUND: A high Ki-67 proliferation index (PI) in neoplastic cells is associated with poor survival in mantle cell lymphoma (MCL). We aimed to determine the cut-off values for the Ki-67 PI as a prognostic factor in MCL according to bone marrow findings. METHODS: Immunohistochemical (IHC) staining...

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Autores principales: Jeong, Tae-Dong, Chi, Hyun-Sook, Kim, Min-Sun, Jang, Seongsoo, Park, Chan-Jeoung, Huh, Joo Ryung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931931/
https://www.ncbi.nlm.nih.gov/pubmed/27382558
http://dx.doi.org/10.5045/br.2016.51.2.127
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author Jeong, Tae-Dong
Chi, Hyun-Sook
Kim, Min-Sun
Jang, Seongsoo
Park, Chan-Jeoung
Huh, Joo Ryung
author_facet Jeong, Tae-Dong
Chi, Hyun-Sook
Kim, Min-Sun
Jang, Seongsoo
Park, Chan-Jeoung
Huh, Joo Ryung
author_sort Jeong, Tae-Dong
collection PubMed
description BACKGROUND: A high Ki-67 proliferation index (PI) in neoplastic cells is associated with poor survival in mantle cell lymphoma (MCL). We aimed to determine the cut-off values for the Ki-67 PI as a prognostic factor in MCL according to bone marrow findings. METHODS: Immunohistochemical (IHC) staining for Ki-67 was performed on formalin-fixed paraffin-embedded biopsy tissues from 56 patients with MCL. Patients were grouped based on their Ki-67 PI values. Survival analyses were carried out and the cut-off value for the Ki-67 PI was determined. RESULTS: Of the 56 patients, 39 (69.6%) showed bone marrow involvement of MCL; 21 of these patients had leukemic manifestations at the time of diagnosis. The results of the Ki-67 IHC staining were as follows: ≤10% in 22 patients, 11–20% in 14 patients, 21–30% in 3 patients, 31–40% in 4 patients, 41–50% in 4 patients, and >50% in 9 patients. A cut-off value of 20% revealed significantly different survival rates with mean survival times of 69.8 months (Ki-67 PI≤20%) and 47.9 months (Ki-67 PI>20%), irrespective of bone marrow findings (P=0.034). Clinical outcomes did not differ, regardless of bone marrow findings. However, in cases with bone marrow involvement, the Ki-67 cut-off value of 30% for overall survival was required to yield statistical significance (P=0.033). CONCLUSION: The 20% cut-off value for the Ki-67 PI was clinically meaningful, regardless of bone marrow involvement of MCL. For patients with bone marrow involvement, the statistically significant cut-off value increased to 30%.
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spelling pubmed-49319312016-07-05 Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma Jeong, Tae-Dong Chi, Hyun-Sook Kim, Min-Sun Jang, Seongsoo Park, Chan-Jeoung Huh, Joo Ryung Blood Res Original Article BACKGROUND: A high Ki-67 proliferation index (PI) in neoplastic cells is associated with poor survival in mantle cell lymphoma (MCL). We aimed to determine the cut-off values for the Ki-67 PI as a prognostic factor in MCL according to bone marrow findings. METHODS: Immunohistochemical (IHC) staining for Ki-67 was performed on formalin-fixed paraffin-embedded biopsy tissues from 56 patients with MCL. Patients were grouped based on their Ki-67 PI values. Survival analyses were carried out and the cut-off value for the Ki-67 PI was determined. RESULTS: Of the 56 patients, 39 (69.6%) showed bone marrow involvement of MCL; 21 of these patients had leukemic manifestations at the time of diagnosis. The results of the Ki-67 IHC staining were as follows: ≤10% in 22 patients, 11–20% in 14 patients, 21–30% in 3 patients, 31–40% in 4 patients, 41–50% in 4 patients, and >50% in 9 patients. A cut-off value of 20% revealed significantly different survival rates with mean survival times of 69.8 months (Ki-67 PI≤20%) and 47.9 months (Ki-67 PI>20%), irrespective of bone marrow findings (P=0.034). Clinical outcomes did not differ, regardless of bone marrow findings. However, in cases with bone marrow involvement, the Ki-67 cut-off value of 30% for overall survival was required to yield statistical significance (P=0.033). CONCLUSION: The 20% cut-off value for the Ki-67 PI was clinically meaningful, regardless of bone marrow involvement of MCL. For patients with bone marrow involvement, the statistically significant cut-off value increased to 30%. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016-06 2016-06-23 /pmc/articles/PMC4931931/ /pubmed/27382558 http://dx.doi.org/10.5045/br.2016.51.2.127 Text en © 2016 Korean Society of Hematology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jeong, Tae-Dong
Chi, Hyun-Sook
Kim, Min-Sun
Jang, Seongsoo
Park, Chan-Jeoung
Huh, Joo Ryung
Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title_full Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title_fullStr Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title_full_unstemmed Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title_short Prognostic relevance of the Ki-67 proliferation index in patients with mantle cell lymphoma
title_sort prognostic relevance of the ki-67 proliferation index in patients with mantle cell lymphoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931931/
https://www.ncbi.nlm.nih.gov/pubmed/27382558
http://dx.doi.org/10.5045/br.2016.51.2.127
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