Publications by authors named "Ananth G Shankar"

Article Synopsis
  • The study explores the immune microenvironment of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) and its similarities with T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL), focusing on the variations in immune cell types present in different histological patterns.
  • Researchers used advanced imaging techniques to examine how certain immune cells were expanded or depleted in NLPHL cases with various histological features compared to THRLBCL cases.
  • The results revealed significant depletion of T-regulatory cells in NLPHL and an increase in cytotoxic immune cells as the disease progressed, suggesting a connection between NLPHL and THRLBCL and highlighting potential new biomarkers for targeting immune checkpoints in treatment.
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Advanced stage nodular lymphocyte predominant Hodgkin lymphoma (nLPHL) is extremely rare in children and as a consequence, optimal treatment for this group of patients has not been established. Here we retrospectively evaluated the treatments and treatment outcomes of 41 of our patients from the UK and France with advanced stage nLPHL. Most patients received chemotherapy, some with the addition of the anti CD20 antibody rituximab or radiotherapy.

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Article Synopsis
  • There is limited information on the outcomes of treatments for children with relapsed or poorly responsive nodular lymphocyte predominant Hodgkin lymphoma (nLPHL), prompting a study on a national cohort of 37 patients.
  • Of the 22 patients with relapsed nLPHL, over half had localized disease at relapse, with a median relapse time of 8 months post-chemotherapy and 11 months post-surgery.
  • The study found that most patients were successfully re-treated with additional chemotherapy or radiotherapy, indicating that relapse or poorly responsive nLPHL can be effectively managed and treated.
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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.

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Anemia in children with cancer is not an uncommon complication and is usually multifactorial in etiology. In numerous trials in adult cancer patients, treatment with recombinant erythropoietin has been shown to increase hemoglobin levels, reduce red blood cell transfusion requirements, and improve quality of life. Much less has been published of its use in the prevention or treatment of cancer-associated anemia (CAA) in children, in whom chemotherapy is usually more intensive and likely to result in greater myelosuppression.

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Objectives: To determine the clinical outcome and prognostic factors for overall survival in children with recurrent and/or primary refractory Hodgkin disease (HD) after high-dose therapy and autologous hemopoietic stem cell transplantation (AHSCT). The survival outcome of this treatment was compared with conventional salvage therapy without stem cell transplantation.

Methods: Clinical records of 51 patients with relapsed or refractory HD who underwent AHSCT were reviewed.

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Acquired hyperthyroidism is most commonly autoimmune in etiology. In the setting of allogeneic bone marrow transplantation (BMT), the use of radiotherapy (total body irradiation) as part of the regimen prior to BMT is known to cause endocrine dysfunction, especially hypopituitarism and hypothyroidism, but hyperthyroidism is rare. The authors report this unusual and late complication in a young boy after BMT for relapsed childhood lymphoblastic leukemia and discuss the possible etiologies.

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