Palliative Care Oncology in Patients With Relapsed, Refractory, and High-Risk Leukemias or MDS
Launched by UNIVERSITY OF VIRGINIA · Jul 19, 2020
Trial Information
Current as of July 23, 2025
Active, not recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the impact of early and ongoing palliative care for patients with certain types of leukemia and myelodysplastic syndromes (MDS). Palliative care is a specialized type of medical care that focuses on providing relief from symptoms and improving the quality of life for patients with serious illnesses. The goal of this study is to see how this type of care can help patients and their families deal with end-of-life issues, especially for those who are facing relapsed or high-risk forms of these blood cancers.
To be eligible for the study, participants need to be at least 65 years old with a new diagnosis of acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), or high-risk MDS. Alternatively, younger patients aged 18 and older with relapsed or refractory (or hard-to-treat) AML, ALL, or high-risk MDS may also qualify. Participants will be required to give their consent and be available for the study procedures throughout its duration. If you or someone you know might be interested in this trial, it's important to note that patients with a specific type of leukemia called Acute Promyelocytic Leukemia (APL) are not eligible to participate.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Ability to provide informed consent
- • 2. Stated willingness to comply with all study procedures and availability for the duration of the study
- 3. Any of the following:
- • 1. Patients with a new diagnosis of AML, ALL, high risk myelodysplastic syndrome (MDS), or high risk chronic myelomonocytic leukemia (CMML) who are age 65 and older.
- • OR
- • 2. Patients with relapsed AML, ALL, high risk MDS or high risk CMML, ages 18 and older.
- • OR
- • 3. Patients with refractory AML, ALL, high risk MDS or high risk CMML, ages 18 and older.
- • Refractory AML/ALL will be defined as persistent leukemia despite two or more cycles of induction chemotherapy.
- • Refractory MDS will be defined according to the 2006 IWG response criteria Refractory CMML will be based on the assessment of the treating investigator.
- Exclusion Criteria:
- • 1. Participants must not have a diagnosis of Acute Promyelocytic Leukemia (APL)
About University Of Virginia
The University of Virginia (UVA) is a prestigious academic institution renowned for its commitment to advancing medical research and improving patient care through innovative clinical trials. With a focus on interdisciplinary collaboration, UVA leverages its extensive resources and expertise in various fields, including medicine, engineering, and public health, to drive cutting-edge studies that address pressing health challenges. The university's clinical trial programs aim to translate scientific discoveries into effective treatments, ensuring the highest standards of ethical practice and participant safety. Through its strong emphasis on community engagement and education, UVA fosters a culture of research that not only contributes to the scientific community but also enhances the well-being of the populations it serves.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Charlottesville, Virginia, United States
Patients applied
Trial Officials
Karen Ballen, MD
Principal Investigator
University of Virginia
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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