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Alternate Title Phase II Study of Allogeneic Umbilical Cord and Placental Blood Transplantation in Patients With Chronic Myeloid Leukemia, Acute Leukemia, Lymphoma, Myeloma, Myelodysplasia, Aplastic Anemia, Fanconi's Anemia, Histiocytosis, Hereditary Immunodeficiency, or Storage Disorder
Trial Description Umbilical cord blood or placental blood transplantation may be able to replace immune cells that were destroyed by the chemotherapy or radiation therapy that was used to kill cancer cells. Phase II trial to study the effectiveness of umbilical cord blood and placental blood transplantation in treating patients who have hematologic cancer or aplastic anemia. Eligibility criteria include the following:
Final eligibility for a clinical trial is determined by the health professionals conducting the trial. Patients will receive chemotherapy and/or radiation therapy followed by umbilical cord blood. Patients will receive follow-up evaluations every 1-2 weeks for 6 months. Important: For more details about this trial, refer to the Health Professional version of the trial summary. If you are interested in participating in a clinical trial, contact your doctor for a referral or call a trial contact person listed below. You may see the same contact person listed at more than one site, however, if you call the number listed you can ask to speak to the study coordinator or person involved with the specific trial you are interested in. If you have questions about cancer or clinical trials, call the Cancer Information Service at 1-800-4-CANCER (1-800-422-6237). General information about clinical trials, including risks, benefits, and costs, can be found on NCI's Web site. Trial Lead Organizations Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center
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