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Derville O'Shea

Researcher at Imperial College London

Publications -  4
Citations -  226

Derville O'Shea is an academic researcher from Imperial College London. The author has contributed to research in topics: Transplantation & Autologous stem-cell transplantation. The author has an hindex of 4, co-authored 4 publications receiving 216 citations. Previous affiliations of Derville O'Shea include Hammersmith Hospital.

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Predictive factors for survival in myeloma patients who undergo autologous stem cell transplantation: a single-centre experience in 211 patients

TL;DR: It is concluded that ASCT is safe and effective and the outcome is independent of age, time from diagnosis, previous treatment and conditioning regimen and the international prognostic index at transplant.
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Posttransplantation imatinib as a strategy to postpone the requirement for immunotherapy in patients undergoing reduced-intensity allografts for chronic myeloid leukemia.

TL;DR: Adjunctive targeted therapy allows the kinetics of disease relapse after a reduced-intensity allograft to be manipulated and represents a novel strategy by which outcome may be improved in patients who undergo transplantation for CML and other leukemias.
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LACE-conditioned autologous stem cell transplantation for relapsed or refractory Hodgkin's lymphoma: treatment outcome and risk factor analysis in 67 patients from a single centre

TL;DR: Mixed cellularity classical or lymphocyte-depleted classical histology subtype and haemoglobin level of 10 g/dl or less at the time of ASCT were identified as risk factors for worse OS, whereas stage III or IV disease at diagnosis and disease status at ASCT predicted inferior PFS.
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Impact of HLA class I and class II DNA high-resolution HLA typing on clinical outcome in adult unrelated stem cell transplantation after in vivo T-cell depletion with alemtuzumab.

TL;DR: In univariate analysis the disease risk group and CMV seronegativity of recipient and donor were the only significant predictors for survival, with 3-year survival probabilities of 71.2% for CML-CP1 and 28% for poor risk diseases.