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Childhood and Adolescent nodular lymphocyte predominant Hodgkin lymphoma - A review of clinical outcome based on the histological variants.
Shankar, Ananth G; Kirkwood, Amy A; Hall, Georgina W; Hayward, Janis; O'Hare, Patricia; Ramsay, Alan D.
Afiliação
  • Shankar AG; Department of Paediatric and Adolescent Oncology, University College London Hospitals NHS Foundation Trust, London, UK.
  • Kirkwood AA; Cancer Research UK & UCL Cancer Trials Centre, University College London, London, UK.
  • Hall GW; Department of Paediatric and Adolescent Oncology, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, London, UK.
  • Hayward J; School of Cancer Sciences, Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
  • O'Hare P; Department of Paediatric and Adolescent Oncology, University College London Hospitals NHS Foundation Trust, London, UK.
  • Ramsay AD; Department of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Br J Haematol ; 171(2): 254-262, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26115355
ABSTRACT
Nodular lymphocyte predominant Hodgkin lymphoma (nLPHL) comprises approximately 10-12% of all childhood Hodgkin lymphoma. As the majority have low stage disease recent years have seen a de-escalation of treatment intensity to avoid treatment-related morbidity. This report evaluates treatment outcome in children with histopathological variants of nLPHL after therapy de-escalation. Biopsies from 60 patients were reviewed and histology categorized as typical (n = 47; 78%) or variant nLPHL (n = 13; 22%). Furthermore, presence of immunoglobulin D (IgD) expression by the lymphocyte predominant (LP) cells was assessed in 41 patients. Treatment outcomes were compared according to treatment received and histopathology of nLPHL. Compared to typical nLPHL, children with variant nLPHL had higher stage disease at diagnosis (stage III 3/13; 23% vs. 3/47; 6%, P = 0·11), lower complete response rates (6/13; 46% vs. 38/47; 81%, P = 0·029) and higher relapse rates (2/13; 15% vs. 2/47; 4%, P = 0·20). Additionally, IgD expression by LP cells was associated with poorer treatment response and was more commonly seen in patients with variant nLPHL. (11/13; 85% vs. 15/28; 54%, P = 0·08). Variant histology appears to be indicative of a poorer prognosis in patients with early stage disease, and may be an important factor to take into account when moving towards reduced intensity treatment for nLPHL.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article