EUCTR2007-005563-10-IT进行中(未招募)不适用
Allogeneic Hematopoietic Cell Transplantation Using a Non-myeloablative Preparative Regimen of Total Lymphoid Irradiation and Anti-Thymocyte Globulin for Patients with Hematologic Malignancies - ND
FONDAZIONE NEOPLASIE SANGUE ONLUS0 个研究点开始时间: 2007年12月10日最近更新:
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相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •-Any patient with one of the following hematolymphoid malignancies or syndromes in whom allogeneic NST is warranted. Specific disease categories include: indolent advanced stage Non-Hodgkin Lymphomas, Mantle Cell Lymphoma, Chronic Lymphocytic Leukemia, Hodgkin Disease, Acute Leukemias in any complete remission, Aplastic Anemia, Paroxsymal Nocturnal Hemoglobinuria, Myelodysplastic and Chronic Myeloproliferative Syndromes, Multiple Myeloma. Patients with other selected malignancies/disorders may also be considered but must be approved by the transplant team and the Principal Investigator.
- •-Elderly patients age > 50 < 70 years, or for patients <50 years of age but because of pre-existing medical conditions or prior therapy are considered to be at high risk for regimen-related toxicity associated with conventional myeloablative transplants, or because of refusal to undergo conventional myeloablative regimes.
- •-A fully HLA-identical sibling or matched unrelated donor is available. Patients with one antigen mismatched donors can be considered but only after discussion with the transplant team and the Principal Investigator.
- •-Patient must be competent to give consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-Patients with progressive hematolymphoid malignancies despite conventional therapies, or acute leukemias not in complete remission.
- •-Uncontrolled CNS involvement with disease
- •-Fertile men or women unwilling to use contraceptive techniques during and for 12 months following treatment
- •-Females who are pregnant
- •-Organ dysfunction defined as follows:
- •Cardiac function: ejection fraction <30% or uncontrolled cardiac failure
- •Pulmonary: DLCO <40% predicted
- •Liver function abnormalities: elevation of bilirubin to > 3 mg/dl and/or transaminases >4x the upper limit of normal
- •Renal: creatinine clearance <50 cc/min (24 hour urine collection)
- •-Karnofsky performance score < 60%
- •-Patients with poorly controlled hypertension on multiple antihypertensives
- •-Documented fungal disease that is progressive despite treatment
- •-Viral infections: HIV positive patients. Hepatitis B and C positive patients will be evaluated on a case by case basis
- •-Psychiatric disorders or psychosocial problems which in the opinion of the primary physician or Principal Investigator would place the patient at unacceptable risk from this regimen.
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