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Hematologic/Blood Cancers

Study of the Biology and Natural History of Disease Outcomes in Patients Treated With Allogeneic Hematopoietic Stem Cell Transplantation for Hematologic Malignancies

NCI-11-C-0125, NCT01326728

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Investigator(s):

Nancy M. Hardy, M.D.
Principal Investigator
Phone: 301-451-1406
hardyn@mail.nih.gov

Referral Contact(s):

Zetta Blacklock, R.N., B.S., B.S.N.
Transplant Coordinator
Phone: 301-594-2056
Fax: 301-451-5578
bblacklock@mail.nih.gov

Sheila Phang, R.N., M.S.
Transplant Coordinator
Phone: 301-435-9379
Fax: 301-451-5578
sphang@mail.nih.gov

 

Key Eligibility Criteria:

  • Individuals from one of the following groups:
    • Have received an allotransplant for hematologic malignancies (blood system cancer) and have disease progression or recurrence
    • Have received an allotransplant for hematologic malignancies (blood system cancer) and in remission 100 days or more after receiving allotransplant treatment
    • Individuals who are candidates for allotransplant therapy for hematologic malignancies and are being evaluated at the Clinical Center for planned allotransplantation
    • Related stem-cell donors of eligible allotransplant recipients
  • Age 0–99 years of age

Study Outline:

  • Recipient/participants with relapse will have clinical and research evaluations at baseline and at 6, 12 and 24 months post-allotransplant, then yearly; evaluation after relapse treatment response and for new protocol options is permitted
  • Recipient/participants in remission will have clinical and research evaluations at baseline and 6, 12 and 24 months post-allotransplant; evaluation for new protocol options, e.g., for relapse, is permitted
  • Pre-transplant participants will have clinical and research evaluations at baseline and at three months post-allotransplant, thereafter per cohort assignment
  • Donor/participants will undergo a clinical evaluation and cell collection for recipient/participant therapy and research; return evaluation for additional clinical product collection is permitted

Additional Information:

  • This trial will be conducted at the NIH Clinical Center in Bethesda, MD. It is open to patients who meet the eligibility requirements, regardless of where they live in the United States.
  • There is no charge for medical care received at NIH Clinical Center.
  • FAQs about this study - provides information for patients about the trial such as frequency and duration of visits, costs, how to enroll, and study outline.
  • PDQ (Physicians Data Query) - provides additional details about this study for health care providers.


Reviewed: 9/6/12
Updated: 10/1/12

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