Panhypopituitarism and diabetus insipidus in a patient with primary central nervous system lymphomaMalaise, Olivier ; FRUSCH, Nicolas ; BECK, Emmanuel et alin Leukemia & Lymphoma (2012), 53(12), 2515-16 Detailed reference viewed: 19 (5 ULg) Prise en charge du lymphome B diffus à grandes cellules en 2012Bonnet, Christophe ; DE PRIJCK, Bernard ; LEJEUNE, Marie et alin Revue Médicale Suisse (2012), 8 Diffuse Large B Cells Lymphoma (DLBCLI is the mast comman non-Hodgkin Iymphoma and comprises a large numberof different entities with different clinico-pathological characteristics. The role of positron ... [more ▼] Diffuse Large B Cells Lymphoma (DLBCLI is the mast comman non-Hodgkin Iymphoma and comprises a large numberof different entities with different clinico-pathological characteristics. The role of positron emission tomography is essential dudog the Ini tial staging and post treatment assessment, and potentially at early or mid-treatmentevaluation of response. First-line therapy comprises immuno-chemotherapy with rituximab and different cytotox ic agents that differforcomponents, dosages and frequency of administration taking worldwlderecognized pre-treatment prognostic variables into account. After relapse, peripheral blood stem cells transplantation remains the only chance of cu re. This review attempts to summarize the current state of our knowledge by highlighting the leads pursued to further improve current therapeutic results. [less ▲] Detailed reference viewed: 9 (2 ULg) Primary central nervous system lymphoma in a patient treated with Natalizumab.Phan-Ba, Rémy ; Bisig, Bettina ; Deprez, Manuel et alin Annals of Neurology (2011), 69(6), 1060-1 Detailed reference viewed: 32 (12 ULg) Lymphome du manteau : prise en charge 2011Bonnet, Christophe ; CAERS, Jo ; DE PRIJCK, Bernard et alin Revue Médicale Suisse (2011), 7 Le lymphome du manteau (LM) représente 6% des lymphomes non hodgkiniens (LNH). Le diagnostic repose sur l'immunophénotypage et la démonstration de la présence de la location entre les chromosomes 11 et 14 ... [more ▼] Le lymphome du manteau (LM) représente 6% des lymphomes non hodgkiniens (LNH). Le diagnostic repose sur l'immunophénotypage et la démonstration de la présence de la location entre les chromosomes 11 et 14, avec surexpression de la cycline D1. Le traitement de première ligne du sujet jeune associe trois cures de R-CHOP21 alternées avec trois cures de R-DHAP21, suivies d'une autogreffe conditionnée par irradiation corporelle totale, cyclophosphamide et aracytine. Le sujet de plus de 65 ans peut bénéficier de huit cures de R-CHOP21. L'intérêt du traitement de maintenance est en cours d'évaluation. L'allogreffe de cellules souches hématopoïétiques offre une chance de guérison aux patients en rechute en bon état général. Les traitements ciblés permettront une amélioration du pronostic de cette maladie. [less ▲] Detailed reference viewed: 42 (4 ULg) Prise en charge actuelle des syndromes myélodysplasiquesCAERS, Jo ; BONNET, Christophe ; et alin Revue Médicale Suisse (2011), 7 Detailed reference viewed: 12 (6 ULg) Enteroviral meningoencephalitis as complication of Rituximab therapy in a patient treated for diffuse large B-cell lymphomaServais, Sophie ; Caers, Jo ; et alin British Journal of Haematology (2010), 150(3), 379-381 Detailed reference viewed: 18 (6 ULg) Le lymphome du manteauJaspers, Aurélie ; Baron, Frédéric ; Bonnet, Christophe et alin Revue Médicale de Liège (2010), 65 Mantle cell lymphoma comprises 3 to 10% of non-Hodgkin's lymphomas. Cyclin D1 expression due to t(11;14) (q13;32) is considered as a hallmark of this lymphoma and plays a pivotal role in the ... [more ▼] Mantle cell lymphoma comprises 3 to 10% of non-Hodgkin's lymphomas. Cyclin D1 expression due to t(11;14) (q13;32) is considered as a hallmark of this lymphoma and plays a pivotal role in the pathophysiology of lymphoma transformation. Median age at diagnosis ranges from 60 to 70 years, and diagnosis is often made at an advances stage with widespread lymphadenopathy and extranodular (particularly bone marrow and gastrointestinal) infiltration. First line treatment consists of combination chemotherapy followed with autologous hematopoietic cell transplantation (HCT) in younger patients, while allogeneic HCT following non-myeloablative conditioning might have a role inpatients relapsing after autologous HCT. [less ▲] Detailed reference viewed: 67 (6 ULg) Toxoplasmore cérébrale compliquant une mini-allogreffe de cellules souches hématopoïétiques du sang périphérique; ; Willems, Evelyne et alin Revue Médicale de Liège (2009), 64(7-8), 366-369 We report the occurrence of a cerebral toxoplasmosis 52 days after a non-myeloablative allogeneic stem cell transplantation as treatment for acute myeloid leukemia. Detailed reference viewed: 76 (6 ULg) Les anticorps monoclonaux en hématologie en 2009Bonnet, Christophe ; Beguin, Yves ; De Prijck, Bernard et alin Revue Médicale de Liège (2009), 64 Directed against the CD20 antigen on B lymphocytes, rituximab (MabThera) is now incorporated in the first line therapy of symptomatic follicular as well as diffuse large B cell non-Hodgkin's lymphoma and ... [more ▼] Directed against the CD20 antigen on B lymphocytes, rituximab (MabThera) is now incorporated in the first line therapy of symptomatic follicular as well as diffuse large B cell non-Hodgkin's lymphoma and offers superior response and survival rates. 90Y ibritumomab tiuxetan (Zevalin) combines the specificity of rituximab for the CD20 antigen and the therapeutic effect of β irradiation. Given in monotherapy, it constitutes an interesting alternative therapy for follicular lymphomas in second relapse. Alemtuzumab (MabCampath) recognizes the CD52 antigen and offers encouraging results in chronic lymphocytic leukemia resistant to classical chemotherapy. [less ▲] Detailed reference viewed: 153 (14 ULg) Traitements actuels du lymphome folliculaireBonnet, Christophe ; Beguin, Yves ; De Prijck, Bernard et alin Revue Médicale Suisse (2009), 5 After diffuse large B-cell lymphoma, follicular lymphoma is the most frequent non-Hodgkin's lymphoma. It remains incurable, except for localized diseases. Advanced disease has to be treated only in the ... [more ▼] After diffuse large B-cell lymphoma, follicular lymphoma is the most frequent non-Hodgkin's lymphoma. It remains incurable, except for localized diseases. Advanced disease has to be treated only in the presence of clinical and/or biology aggressiveness. These patients should be treated by rituximab (Mab-Thera) associated to polychemotherapy comprising cyclophosphamide, vincristine and prednisone. After this therapy, the benefit of rituximab in maintenance has to be confirmed. Autologous stem cell transplantation is also an interesting option. The other therapeutic options comprise radio-immunotherapy with 90Y ibritumomab tiuxetan (Zevalin) and bortezomib (Velcade). [less ▲] Detailed reference viewed: 408 (4 ULg) Tomographie à émission de positons et lymphomesHustinx, Roland ; Jerusalem, Guy ; De Prijck, Bernard ![]() in Médecine Nucléaire : Imagerie Fonctionnelle et Métabolique (2008), 32 Detailed reference viewed: 15 (3 ULg) Indications cliniques de la radiotherapie metabolique dans les tymphomes.Witvrouw, Nancy ; De Prijck, Bernard ; Hustinx, Roland ![]() in Revue Médicale Suisse (2008), 4(168), 1818-22 In their later stages low grade lymphoma are incurable. These lymphomas being radio-sensitive, a treatment of metabolic radioimmunotherapy, using monoclonal antibodies (anti-CD20) as the carrier has been ... [more ▼] In their later stages low grade lymphoma are incurable. These lymphomas being radio-sensitive, a treatment of metabolic radioimmunotherapy, using monoclonal antibodies (anti-CD20) as the carrier has been developed. The aim of this treatment is to use these antibodies to target radiation to tumor tissues while limiting toxicity to normal cells. Ibritumomab tiuxetan (Zevalin) is currently prescribed for patients with relapsed or refractory low-grade follicular lymphoma after rituximab treatment. This outpatient treatment has a high level of overall response rate including complete response and that for a long period. The side effects are essentially hematological and reversible. In the near future many more indications should become apparent and Zevalin should become an important tool in the B-cell lymphoma (low and high grade). [less ▲] Detailed reference viewed: 62 (2 ULg) Comment je traite...La leucémie myéloblastique aiguë (LMA) du sujet age en bon état général.Lejeune, Marie ; Beguin, Yves ; De Prijck, Bernard et alin Revue Médicale de Liège (2008), 63(2), 59-63 This article describes the treatment of acute myeloid leukemia in older patients with good performance status, and then discusses briefly some future therapeutic perspectives. Detailed reference viewed: 153 (6 ULg) Actualités thérapeutiques en hématologie.De Prijck, Bernard ; Baron, Frédéric ; Beguin, Yves et alin Revue Médicale de Liège (2007), 62(5-6), 384-90 This article focuses on recent advances in four important areas of hematology: aggressive lymphomas, allogeneic hematopoietic stem cell transplantation, multiple myeloma, and molecular therapy of cancer. Detailed reference viewed: 83 (8 ULg) Low T-cell chimerism is not followed by graft rejection after nonmyeloablative stem cell transplantation (NMSCT) with CD34-selected PBSC.Baron, Frédéric ; Baudoux, Etienne ; Frere, Pascale et alin Bone Marrow Transplantation (2003), 32(8), 829-34 We investigate the feasibility of CD34-selected peripheral blood stem cell (PBSC) transplantation followed by pre-emptive CD8-depleted donor lymphocyte infusions (DLI) after a minimal conditioning regimen ... [more ▼] We investigate the feasibility of CD34-selected peripheral blood stem cell (PBSC) transplantation followed by pre-emptive CD8-depleted donor lymphocyte infusions (DLI) after a minimal conditioning regimen. Six patients with advanced hematological malignancies ineligible for a conventional myeloablative transplant (n=5) or metastatic renal cell carcinoma (n=1), and with an HLA-identical (n=4) or alternative (n=2) donor were included. The nonmyeloablative conditioning regimen consisted in 2 Gy TBI alone (n=4), 2 Gy TBI and fludarabine (RCC patient, n=1) or cyclophosphamide and fludarabine (patient who had previously received 12 Gy TBI, n=1). Post transplant immunosuppression was carried out with cyclosporin (CyA) and mycophenolate mofetil (MMF). Initial engraftment was achieved in all patients. One out of six patients (17%) experienced grade > or =2 acute GVHD only after abrupt cyclosporin discontinuation and alpha interferon therapy for life-threatening tumor progression. T-cell chimerism was 23% (19-30) on day 28, 32% (10-35) on day 100, 78% (49-95) on day 180 and 99.5% (99-100) on day 365. Three out of four patients who had measurable disease before the transplant experienced a complete response. We conclude that CD34-selected NMSCT followed by CD8-depleted DLI is feasible and preserves engraftment and apparently also the graft-versus-leukemia (GVL) effect. Further studies are needed to confirm this encouraging preliminary report. [less ▲] Detailed reference viewed: 46 (3 ULg) |
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