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What is CD4+CD56+ malignancy and how should it be treated?
CD4+CD56+ malignancy is a rare neoplasm with a typical clinical pattern, an aggressive course and high early relapse rate despite good initial response to chemotherapy. In this review, the impact of different therapeutic approaches on clinical outcome has been studied. We evaluated 91 published case...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091947/ https://www.ncbi.nlm.nih.gov/pubmed/13130309 http://dx.doi.org/10.1038/sj.bmt.1704215 |
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author | Reimer, P Rüdiger, T Kraemer, D Kunzmann, V Weissinger, F Zettl, A Konrad Müller-Hermelink, H Wilhelm, M |
author_facet | Reimer, P Rüdiger, T Kraemer, D Kunzmann, V Weissinger, F Zettl, A Konrad Müller-Hermelink, H Wilhelm, M |
author_sort | Reimer, P |
collection | PubMed |
description | CD4+CD56+ malignancy is a rare neoplasm with a typical clinical pattern, an aggressive course and high early relapse rate despite good initial response to chemotherapy. In this review, the impact of different therapeutic approaches on clinical outcome has been studied. We evaluated 91 published cases and our own six patients in terms of clinical features, immunophenotype/cytogenetics and treatment outcome. Treatment was divided into four groups: (A) chemotherapy less intensive than CHOP; (B) CHOP and CHOP-like regimens; (C) therapy for acute leukemia; (D) allogeneic/autologous stem cell transplantation. The median overall survival was only 13 months for all patients. Patients with skin-restricted disease showed no difference in the overall survival from patients with advanced disease (17 and 12 months, respectively). Age ⩾60 years was a negative prognostic factor. Age-adjusted analysis revealed improved survival after high-dose chemo/radiotherapy followed by allogeneic stem cell transplantation when performed in first complete remission. This therapeutic approach should be recommended for eligible patients with CD4+CD56+ malignancy. For older patients the best treatment option is still unknown. |
format | Online Article Text |
id | pubmed-7091947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70919472020-03-24 What is CD4+CD56+ malignancy and how should it be treated? Reimer, P Rüdiger, T Kraemer, D Kunzmann, V Weissinger, F Zettl, A Konrad Müller-Hermelink, H Wilhelm, M Bone Marrow Transplant Article CD4+CD56+ malignancy is a rare neoplasm with a typical clinical pattern, an aggressive course and high early relapse rate despite good initial response to chemotherapy. In this review, the impact of different therapeutic approaches on clinical outcome has been studied. We evaluated 91 published cases and our own six patients in terms of clinical features, immunophenotype/cytogenetics and treatment outcome. Treatment was divided into four groups: (A) chemotherapy less intensive than CHOP; (B) CHOP and CHOP-like regimens; (C) therapy for acute leukemia; (D) allogeneic/autologous stem cell transplantation. The median overall survival was only 13 months for all patients. Patients with skin-restricted disease showed no difference in the overall survival from patients with advanced disease (17 and 12 months, respectively). Age ⩾60 years was a negative prognostic factor. Age-adjusted analysis revealed improved survival after high-dose chemo/radiotherapy followed by allogeneic stem cell transplantation when performed in first complete remission. This therapeutic approach should be recommended for eligible patients with CD4+CD56+ malignancy. For older patients the best treatment option is still unknown. Nature Publishing Group UK 2003-09-16 2003 /pmc/articles/PMC7091947/ /pubmed/13130309 http://dx.doi.org/10.1038/sj.bmt.1704215 Text en © Nature Publishing Group 2003 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Reimer, P Rüdiger, T Kraemer, D Kunzmann, V Weissinger, F Zettl, A Konrad Müller-Hermelink, H Wilhelm, M What is CD4+CD56+ malignancy and how should it be treated? |
title | What is CD4+CD56+ malignancy and how should it be treated? |
title_full | What is CD4+CD56+ malignancy and how should it be treated? |
title_fullStr | What is CD4+CD56+ malignancy and how should it be treated? |
title_full_unstemmed | What is CD4+CD56+ malignancy and how should it be treated? |
title_short | What is CD4+CD56+ malignancy and how should it be treated? |
title_sort | what is cd4+cd56+ malignancy and how should it be treated? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091947/ https://www.ncbi.nlm.nih.gov/pubmed/13130309 http://dx.doi.org/10.1038/sj.bmt.1704215 |
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