Etanercept for treatment of idiopathic pneumonia syndrome after allogeneic hematopoietic stem cell transplantation.
نویسندگان
چکیده
marker because of reported hypermethylation in childhood MDS.3 Our patient initially showed 55.4% CALCA methylation in the peripheral blood, which decreased to 4.5% before the eighth cycle of AC. Importantly, reduction in methylation was not only due to clearance of malignant cells, but was evident in the clone itself.4 Before the third cycle, 58% of cells still carried monosomy 7, but completely methylated alleles were no longer detected (Figure 1). Here we report the first patient with JMML and monosomy 7 treated with AC. The favorable response fits well with previous studies1,2 but has additional remarkable aspects. Thrombocytopenia and HbF at diagnosis indicated that this was a rather aggressive case of JMML.5 Using conventional cytostatic therapy, remissions are rare in these cases6 and disappearance of the monosomy 7 clone in JMML without HSCT has never been reported before. In summary, our results suggest that AC therapy may be a viable option for JMML/monosomy 7 patients, either as a pretransplant window or in the absence of a suitable HSCT donor.
منابع مشابه
CLINICAL TRIALS AND OBSERVATIONS The impact of soluble tumor necrosis factor receptor etanercept on the treatment of idiopathic pneumonia syndrome after allogeneic hematopoietic stem cell transplantation
Idiopathic pneumonia syndrome (IPS) refers to a diffuse, noninfectious, acute lung injury after hematopoietic stem cell transplantation. Historically, IPS is associated with respiratory failure and mortality rates exceeding 50%. Preclinical studies have implicated tumor necrosis factoras an important effector molecule in the development of disease. We studied the tumor necrosis factorinhibitor,...
متن کاملThe impact of soluble tumor necrosis factor receptor etanercept on the treatment of idiopathic pneumonia syndrome after allogeneic hematopoietic stem cell transplantation.
Idiopathic pneumonia syndrome (IPS) refers to a diffuse, noninfectious, acute lung injury after hematopoietic stem cell transplantation. Historically, IPS is associated with respiratory failure and mortality rates exceeding 50%. Preclinical studies have implicated tumor necrosis factor-alpha as an important effector molecule in the development of disease. We studied the tumor necrosis factor-al...
متن کاملConcurrent treatment with a tumor necrosis factor-alpha inhibitor and veno-venous extracorporeal membrane oxygenation in a post-hematopoietic stem cell transplant patient with idiopathic pneumonia syndrome: a case report
Idiopathic pneumonia syndrome (IPS) is a fatal non-infectious respiratory complication that develops after hematopoietic stem cell transplantation (HSCT). Because of the poor prognosis of post-HSCT patients with IPS requiring mechanical ventilatory support, performing extracorporeal membrane oxygenation (ECMO) has been regarded as relatively contraindicated in these patients. A tumor necrosis f...
متن کاملAn official American Thoracic Society research statement: noninfectious lung injury after hematopoietic stem cell transplantation: idiopathic pneumonia syndrome.
RATIONALE Acute lung dysfunction of noninfectious etiology, known as idiopathic pneumonia syndrome (IPS), is a severe complication following hematopoietic stem cell transplantation (HSCT). Several mouse models have been recently developed to determine the underlying causes of IPS. A cohesive interpretation of experimental data and their relationship to the findings of clinical research studies ...
متن کاملCT Findings of Pulmonary Complications after Hematopoietic Stem Cell Transplantation
HSCT: Hematopoietic Stem Cell Transplantation; GVHD: GraftVersus-Host-Disease; DAH: Diffuse Alveolar Hemorrhage; ARDS: Acute Respiratory Distress Syndrome; RSV: Respiratory Syncytial Virus; CMV: Cytomegalovirus; HLA: Human Leucocyte Antigen; PCR: Polymerase Chain Reaction; IPS: Idiopathic Pneumonia Syndrome; OP: Organizing Pneumonia; BOOP: Bronchiolitis Obliterans Organizing Pneumonia; COP: Cry...
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ورودعنوان ژورنال:
- Blood
دوره 113 12 شماره
صفحات -
تاریخ انتشار 2009