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1.
Eur J Haematol ; 91(4): 315-21, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23738686

RESUMEN

The outlook for adults with refractory and relapsed acute lymphocytic leukemia (ALL) is poor. CD52 is expressed in most patients with ALL. Alemtuzumab is an anti-CD52 humanized monoclonal antibody. This phase II study assessed the efficacy of alemtuzumab combined with granulocyte-colony stimulating factor (G-CSF) to boost antibody-dependent cell cytotoxicity mediated by neutrophils. Twelve patients with relapsed (n = 11) or refractory (n = 1) ALL, including four relapses postallogeneic stem cell transplantation, were treated and monitored between October 2006 and January 2011. Patients received 1 wk of alemtuzumab every other day at increasing doses of 3, 10, and 30 mg to test tolerance and 30 mg three times a week for 12-18 infusions. If in complete remission (CR), patients received maintenance therapy for 1 wk, every 2 months. G-CSF was administered at 5 µg/kg per day during alemtuzumab administration. The primary endpoint was disappearance of blast cells on a marrow aspirate. CD52 was expressed in all patients. Four patients reached CR. In one additional patient, clearance of blast cells was observed in peripheral blood but not in the marrow. The most frequent adverse events during course 1 of treatment were fever and chills (n = 3), skin rash (n = 3), and bronchospasm (n = 2). Tumor lysis syndrome was observed at treatment initiation in one patient who reached CR. All patients progressed within a few months and all but one died. The surviving patient is still alive after relapse and a second allogeneic stem cell transplantation. This study shows that in relapse/refractory ALL, alemtuzumab with G-CSF can produce good responses of short duration.


Asunto(s)
Anticuerpos Monoclonales Humanizados/uso terapéutico , Antineoplásicos/uso terapéutico , Factor Estimulante de Colonias de Granulocitos/uso terapéutico , Trasplante de Células Madre Hematopoyéticas , Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia , Adulto , Alemtuzumab , Antígenos CD/genética , Antígenos de Neoplasias/genética , Antígeno CD52 , Citotoxicidad Inmunológica , Progresión de la Enfermedad , Esquema de Medicación , Quimioterapia Combinada , Femenino , Expresión Génica , Glicoproteínas/antagonistas & inhibidores , Glicoproteínas/genética , Humanos , Masculino , Persona de Mediana Edad , Neutrófilos/inmunología , Neutrófilos/patología , Leucemia-Linfoma Linfoblástico de Células Precursoras/inmunología , Leucemia-Linfoma Linfoblástico de Células Precursoras/mortalidad , Leucemia-Linfoma Linfoblástico de Células Precursoras/patología , Recurrencia , Análisis de Supervivencia , Trasplante Homólogo
3.
Leuk Lymphoma ; 47(1): 77-80, 2006 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-16321831

RESUMEN

The present study aimed to follow-up variations in plasma Flt3 ligand (FL) concentration after hematopoietic stem cell transplantation and to compare the influence of conditioning regimens on variations in FL concentration. Ten patients undergoing a conditioning regimen, including BEAM, cyclophosphamide (Cy) + total body irradiation or Cy + anti-thymocyte globulins (ATG), which was then followed by hematopoietic stem cell transplantation, were studied. Plasma FL concentrations, white blood cell (WBC) expression of both FL mRNA and the membrane-bound form of FL were carried out at different times post-treatment. The results indicated that plasma FL concentration increased rapidly after the conditioning regimen in all patients, in correlation with the decrease in number of WBCs. The area under the curve of FL according to time was directly correlated with the duration of pancytopenia, except when ATG was included in the conditioning regimen. Although the number of patients was limited in this study, the comparison of ATG-treated patients and other patients suggests that plasma FL concentration is regulated by a complex mechanism partly involving circulating blood cells.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas , Proteínas de la Membrana/metabolismo , Pancitopenia/terapia , Adolescente , Adulto , Suero Antilinfocítico/uso terapéutico , Ciclofosfamida/uso terapéutico , Femenino , Estudios de Seguimiento , Regulación de la Expresión Génica , Humanos , Cinética , Recuento de Linfocitos , Masculino , Proteínas de la Membrana/sangre , Proteínas de la Membrana/genética , Persona de Mediana Edad , Pancitopenia/diagnóstico , Pancitopenia/radioterapia , Valor Predictivo de las Pruebas , ARN Mensajero/genética , ARN Mensajero/metabolismo , Factores de Tiempo , Acondicionamiento Pretrasplante/métodos , Irradiación Corporal Total
4.
Exp Hematol ; 32(4): 397-407, 2004 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15050751

RESUMEN

OBJECTIVE: Optimizing cord blood donor selection based mainly on cell dose and human leukocyte antigen (HLA) disparities may further improve results of unrelated cord blood transplants (UCBT). MATERIALS AND RESULTS: We analyzed 550 UCBTs for hematologic malignancies reported to the Eurocord Registry. Main outcomes and prognostic factors were analyzed in univariable and multivariable analyses incorporating center and period effects and using death and relapse as competitive risks for nonfatal endpoints. Nucleated cell (NC) dose before freezing and number of HLA disparities had a significant influence on outcome. Cumulative incidence (CI) of neutrophil and platelet recovery was associated with the number of HLA mismatches, number of NC before freezing, and use of granulocyte colony-stimulating factor. Coexistence of HLA class I and II disparities and high CD34 cell dose in the graft were associated with graft-vs-host disease grades III-IV. CI of disease relapse was higher in matched transplants showing a graft-vs-leukemia effect increased in HLA-mismatched transplants. Overall 3-year survival was 34.4%. Prognostic factors for survival were recipient age, gender, and disease status. CONCLUSION: Our results provide indications for a better choice of cord blood units according to cord blood cell content and HLA.


Asunto(s)
Recuento de Células Sanguíneas , Trasplante de Células Madre de Sangre del Cordón Umbilical , Neoplasias Hematológicas/terapia , Histocompatibilidad , Donantes de Tejidos , Adolescente , Adulto , Antígenos CD34/análisis , Niño , Preescolar , Trasplante de Células Madre de Sangre del Cordón Umbilical/efectos adversos , Trasplante de Células Madre de Sangre del Cordón Umbilical/normas , Trasplante de Células Madre de Sangre del Cordón Umbilical/estadística & datos numéricos , Supervivencia sin Enfermedad , Femenino , Supervivencia de Injerto , Enfermedad Injerto contra Huésped/epidemiología , Enfermedad Injerto contra Huésped/etiología , Enfermedad Injerto contra Huésped/prevención & control , Efecto Injerto vs Leucemia/inmunología , Factor Estimulante de Colonias de Granulocitos/farmacología , Antígenos HLA/inmunología , Neoplasias Hematológicas/mortalidad , Humanos , Incidencia , Recién Nacido , Tablas de Vida , Masculino , Defectos del Tubo Neural/mortalidad , Defectos del Tubo Neural/terapia , Pronóstico , Modelos de Riesgos Proporcionales , Sistema de Registros/estadística & datos numéricos , Acondicionamiento Pretrasplante/mortalidad , Acondicionamiento Pretrasplante/estadística & datos numéricos , Resultado del Tratamiento
5.
Leuk Lymphoma ; 43(2): 427-8, 2002 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11999581

RESUMEN

Spinal cord compression as an initial manifestation of multiple myeloma is a well-known phenomenon. We report for the first time a patient with spinal cord compression of dual etiology, multiple myeloma and spinal tuberculosis, treated successfully by local radiotherapy, chemotherapy and an antituberculous regimen.


Asunto(s)
Mieloma Múltiple/complicaciones , Compresión de la Médula Espinal/etiología , Tuberculosis de la Columna Vertebral/complicaciones , Terapia Combinada , Femenino , Humanos , Persona de Mediana Edad , Mieloma Múltiple/diagnóstico , Mieloma Múltiple/terapia , Factores de Riesgo , Compresión de la Médula Espinal/diagnóstico , Compresión de la Médula Espinal/terapia , Tuberculosis de la Columna Vertebral/etiología , Tuberculosis de la Columna Vertebral/terapia
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