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André Bosly

Researcher at Université catholique de Louvain

Publications -  212
Citations -  13388

André Bosly is an academic researcher from Université catholique de Louvain. The author has contributed to research in topics: Diffuse large B-cell lymphoma & International Prognostic Index. The author has an hindex of 51, co-authored 209 publications receiving 12569 citations. Previous affiliations of André Bosly include Catholic University of Leuven.

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Long-Term Results of the R-CHOP Study in the Treatment of Elderly Patients With Diffuse Large B-Cell Lymphoma: A Study by the Groupe d'Etude des Lymphomes de l'Adulte

TL;DR: Using the combination of R-CHOP leads to significant improvement of the outcome of elderly patients with diffuse large B-cell lymphoma, with significant survival benefit maintained during a 5-year follow-up.
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Salvage Regimens With Autologous Transplantation for Relapsed Large B-Cell Lymphoma in the Rituximab Era

TL;DR: It is found that patients with early relapses after rituximab-containing first-line therapy have a poor prognosis, with no difference between the effects of R-ICE and R-DHAP.
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Low-Dose 5-Aza-2′-Deoxycytidine, a DNA Hypomethylating Agent, for the Treatment of High-Risk Myelodysplastic Syndrome: A Multicenter Phase II Study in Elderly Patients

TL;DR: It is confirmed that DAC therapy was effective in half of the studied patients with high-risk myelodysplastic syndrome and is especially active in the patients with the worst prognoses.
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Rituximab plus CHOP (R-CHOP) overcomes bcl-2--associated resistance to chemotherapy in elderly patients with diffuse large B-cell lymphoma (DLBCL).

TL;DR: Rituximab is able to prevent chemotherapy failure in patients with bcl-2 protein overexpression, and is associated with a better overall survival and event-free survival than R-CHOP in b cl-2+ patients.
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Prognostic Significance of T-Cell Phenotype in Aggressive Non-Hodgkin's Lymphomas

TL;DR: Although the poor prognosis of non-ALCL PTCL could be due in part to the presence of adverse prognostic factors at diagnosis, this study shows that the T-cell phenotype is an independent significant factor, which should be incorporated into the definition of prognostic groups.