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Relapsed or poorly responsive nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents - a report from the United Kingdom's Children's Cancer and Leukaemia Study Group.
Shankar, Ananth G; Kirkwood, Amy A; Depani, Sarita; Bianchi, Eleonora; Hayward, Janis; Ramsay, Alan D; Hall, Georgina W.
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.
  • Depani S; Department of Paediatric and Adolescent Oncology, University College London Hospitals NHS Foundation Trust, London, UK.
  • Bianchi E; Department of Paediatric and Adolescent Oncology, University College London Hospitals NHS Foundation Trust, London, UK.
  • Hayward J; Cancer Research UK Clinical Trials Unit, School of Cancer Sciences, University of Birmingham, Birmingham, UK.
  • Ramsay AD; Department of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
  • Hall GW; Department of Paediatric Oncology and Haematology, Children's Services, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Br J Haematol ; 173(3): 421-31, 2016 05.
Article em En | MEDLINE | ID: mdl-26996288
ABSTRACT
There is a paucity of data on the treatment outcome in children with relapsed or poorly responsive nodular lymphocyte predominant Hodgkin lymphoma (nLPHL). This retrospective report evaluates the treatment outcome in a national cohort of children with relapsed or poorly responsive nLPHL. A total of 37 patients, 22 with relapsed and 15 with poorly responding disease, are the subjects of this report. Of the 22 patients with relapsed nLPHL, 11 had relapsed after primary excision biopsy, 10 after chemotherapy and 1 after chemotherapy and involved field radiotherapy. The majority had localized disease at relapse. The median time to relapse was 8 months after chemotherapy and 11 months after excision biopsy. Seven of the 15 patients with poorly responding nLPHL had variant histology. Three patients with initial poor response did not receive any further treatment and have had no disease progression. Transformation to diffuse large B cell lymphoma, in addition to evolution from typical to variant nLPHL occurred in one patient each. Thirty-four patients have been successfully re-treated with second chemotherapy or radiotherapy. Multiple relapses were uncommon but treatable. Relapse or poorly responsive nLPHL is fully salvageable with either additional chemotherapy and or radiotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radioterapia / Doença de Hodgkin / Terapia de Salvação / Antineoplásicos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Humans / Infant / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radioterapia / Doença de Hodgkin / Terapia de Salvação / Antineoplásicos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Humans / Infant / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article