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Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis

BACKGROUND: Secondary myeloid neoplasms comprise a group of diseases arising after chemotherapy, radiation, immunosuppressive therapy or from aplastic anemia. Few studies have addressed prognostic factors in these neoplasms. METHOD: Forty-two patients diagnosed from 1987 to 2008 with secondary myelo...

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Autores principales: Tanizawa, Roberta Sandra da Silva, Zerbini, Maria Claudia Nogueira, Rosenfeld, Ricardo, Kumeda, Cristina Aiko, Azevedo, Raymundo Soares, Siqueira, Sheila Aparecida Coelho, Velloso, Elvira Deolinda Rodrigues Pereira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339394/
https://www.ncbi.nlm.nih.gov/pubmed/28270344
http://dx.doi.org/10.1016/j.bjhh.2016.09.015
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author Tanizawa, Roberta Sandra da Silva
Zerbini, Maria Claudia Nogueira
Rosenfeld, Ricardo
Kumeda, Cristina Aiko
Azevedo, Raymundo Soares
Siqueira, Sheila Aparecida Coelho
Velloso, Elvira Deolinda Rodrigues Pereira
author_facet Tanizawa, Roberta Sandra da Silva
Zerbini, Maria Claudia Nogueira
Rosenfeld, Ricardo
Kumeda, Cristina Aiko
Azevedo, Raymundo Soares
Siqueira, Sheila Aparecida Coelho
Velloso, Elvira Deolinda Rodrigues Pereira
author_sort Tanizawa, Roberta Sandra da Silva
collection PubMed
description BACKGROUND: Secondary myeloid neoplasms comprise a group of diseases arising after chemotherapy, radiation, immunosuppressive therapy or from aplastic anemia. Few studies have addressed prognostic factors in these neoplasms. METHOD: Forty-two patients diagnosed from 1987 to 2008 with secondary myeloid neoplasms were retrospectively evaluated concerning clinical, biochemical, peripheral blood, bone marrow aspirate, biopsy, and immunohistochemistry and cytogenetic features at diagnosis as prognostic factors. The International Prognostic Scoring System was applied. Statistical analysis employed the Kaplan–Meier method, log-rank and Fisher's exact test. RESULTS: Twenty-three patients (54.8%) were male and the median age was 53.5 years (range: 4–88 years) at diagnosis of secondary myeloid neoplasms. Previous diseases included hematologic malignancies, solid tumors, aplastic anemia, autoimmune diseases and conditions requiring solid organ transplantations. One third of patients (33%) were submitted to chemotherapy alone, 2% to radiotherapy, 26% to both modalities and 28% to immunosuppressive agents. Five patients (11.9%) had undergone autologous hematopoietic stem cell transplantation. The median latency between the primary disease and secondary myeloid neoplasms was 85 months (range: 23–221 months). Eight patients were submitted to allogeneic hematopoietic stem cell transplantation to treat secondary myeloid neoplasms. Important changes in bone marrow were detected mainly by biopsy, immunohistochemistry and cytogenetics. The presence of clusters of CD117(+) cells and p53(+) cells were associated with low survival. p53 was associated to a higher risk according to the International Prognostic Scoring System. High prevalence of clonal abnormalities (84.3%) and thrombocytopenia (78.6%) were independent factors for poor survival. CONCLUSION: This study demonstrated that cytogenetics, bone marrow biopsy and immunohistochemistry are very important prognostic tools in secondary myeloid neoplasms.
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spelling pubmed-53393942017-03-13 Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis Tanizawa, Roberta Sandra da Silva Zerbini, Maria Claudia Nogueira Rosenfeld, Ricardo Kumeda, Cristina Aiko Azevedo, Raymundo Soares Siqueira, Sheila Aparecida Coelho Velloso, Elvira Deolinda Rodrigues Pereira Rev Bras Hematol Hemoter Original Article BACKGROUND: Secondary myeloid neoplasms comprise a group of diseases arising after chemotherapy, radiation, immunosuppressive therapy or from aplastic anemia. Few studies have addressed prognostic factors in these neoplasms. METHOD: Forty-two patients diagnosed from 1987 to 2008 with secondary myeloid neoplasms were retrospectively evaluated concerning clinical, biochemical, peripheral blood, bone marrow aspirate, biopsy, and immunohistochemistry and cytogenetic features at diagnosis as prognostic factors. The International Prognostic Scoring System was applied. Statistical analysis employed the Kaplan–Meier method, log-rank and Fisher's exact test. RESULTS: Twenty-three patients (54.8%) were male and the median age was 53.5 years (range: 4–88 years) at diagnosis of secondary myeloid neoplasms. Previous diseases included hematologic malignancies, solid tumors, aplastic anemia, autoimmune diseases and conditions requiring solid organ transplantations. One third of patients (33%) were submitted to chemotherapy alone, 2% to radiotherapy, 26% to both modalities and 28% to immunosuppressive agents. Five patients (11.9%) had undergone autologous hematopoietic stem cell transplantation. The median latency between the primary disease and secondary myeloid neoplasms was 85 months (range: 23–221 months). Eight patients were submitted to allogeneic hematopoietic stem cell transplantation to treat secondary myeloid neoplasms. Important changes in bone marrow were detected mainly by biopsy, immunohistochemistry and cytogenetics. The presence of clusters of CD117(+) cells and p53(+) cells were associated with low survival. p53 was associated to a higher risk according to the International Prognostic Scoring System. High prevalence of clonal abnormalities (84.3%) and thrombocytopenia (78.6%) were independent factors for poor survival. CONCLUSION: This study demonstrated that cytogenetics, bone marrow biopsy and immunohistochemistry are very important prognostic tools in secondary myeloid neoplasms. Sociedade Brasileira de Hematologia e Hemoterapia 2017 2016-12-22 /pmc/articles/PMC5339394/ /pubmed/28270344 http://dx.doi.org/10.1016/j.bjhh.2016.09.015 Text en © 2016 Associaç˜ao Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Tanizawa, Roberta Sandra da Silva
Zerbini, Maria Claudia Nogueira
Rosenfeld, Ricardo
Kumeda, Cristina Aiko
Azevedo, Raymundo Soares
Siqueira, Sheila Aparecida Coelho
Velloso, Elvira Deolinda Rodrigues Pereira
Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title_full Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title_fullStr Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title_full_unstemmed Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title_short Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
title_sort secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339394/
https://www.ncbi.nlm.nih.gov/pubmed/28270344
http://dx.doi.org/10.1016/j.bjhh.2016.09.015
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