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Clinical Trials Search at Vanderbilt-Ingram Cancer Center

Connect® Myeloid Disease Registry

The purpose of the Connect® Myeloid disease registry is to provide unique insights into treatment decisions and treatment patterns as they relate to clinical outcomes of patients with myeloid diseases in routine clinical practice. This disease registry will also evaluate molecular and cellular markers that may provide further prognostic classification which may or may not be predictive of therapy and clinical outcomes.
Leukemia
N/A
Adults
Not Available
Not Available
Mohan, Sanjay
National
Vanderbilt University
11-11-2015
Other
VICCHEM14133
NCT01688011

Eligibility

18 Years
BOTH
NO
Inclusion Criteria:

Patients must be able to provide written informed consent form (ICF)

Must be willing and able to complete baseline and follow-up HRQoL instruments, for which patients must be proficient in either English or Spanish

AML patients must be at least 55 years of age at the time of informed consent.

MF, ICUS, and MDS patients must be at least 18 years of age at the time of informed consent. Idiopathic Cytopenias of Undetermined Significance (ICUS), Myelodysplastic Syndromes (MDS), Acute Myeloid Leukemia (AML) patients:

Newly diagnosed primary or secondary disease. To be considered "newly diagnosed", a patient's confirmed diagnosis must be made no more than 60 days prior to the date of consent signature. (An additional 5-day window [i.e., up to 65 days prior to the date of ICF signature] may be allowed in special circumstance upon sponsor approval)

Cohort assignment confirmed by central eligibility review. Cohort assignment must also be confirmed by the site. Myelofibrosis (MF) patients:

Patients who initiated their first active systemic treatment for MF and/or MF-related cytopenias within 60 days prior to the date of consent signature. This cohort allows the enrollment of subjects with a diagnosis of Myelodysplastic/Myeloproliferative overlap syndromes (MDS/MPN overlap syndrome).

Cohort assignment is confirmed by the site. Central eligibility review is not required.



Exclusion Criteria:

Suspected or proven acute promyelocytic leukemia (APL) (FAB M3 or WHO 2008) based on morphology, immunophenotype, molecular assay or karyotype

Currently enrolled in any interventional clinical trial where the patient is being treated with an investigational product that cannot be identified.

Idiopathic Cytopenias of Undetermined Significance (ICUS), Myelodysplastic Syndromes (MDS) patients who received or are receiving active (disease modifying) therapy for the treatment of MDS prior to the date of informed consent.

Acute Myeloid Leukemia (AML) patients who initiated active (disease modifying treatment for AML more than 2 weeks prior to the date of consent.

Myelodysplastic/Myeloproliferative (MDS/MPN) overlap syndrome patients with suspected or proven excluding juvenile myelomonocytic leukemia.

To learn more about any of our clinical
trials, call 1-800-811-8480 or complete
the online Self-Referral Form here: