Impact of Targeted Therapy on Cancer-Related Cognitive Impairment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Rochester NCORP Research Base

About this trial

This study examines whether there are differences in brain health or well-being in patients receiving TKI therapy for leukemia compared to individuals who do not receive TKI therapy.

Eligibility criteria

Qualifiers

TKI RECIPIENTS: Participants must have a diagnosis of CML or CLL

TKI RECIPIENTS: Participants must be scheduled to receive their first dose of TKI therapy for CML or CLL within 30 days or have received their first dose of TKI therapy for CML or CLL within the previous 30 days

TKI RECIPIENTS: Participants must be ≥ 18 years of age

TKI RECIPIENTS: Participants must be able to speak and read English

Disqualifiers

Participants must have no history of metastatic cancer, primary brain tumor, or brain irradiation

Participants must have no history of TKI therapy

Participants must have no history of cytotoxic chemotherapy, immune checkpoint inhibitor therapy, hormonal therapy, biologic therapy, radiotherapy within the past 5 years. However, permitted treatments include prior use of hydroxyurea for the treatment of CML or CLL as well as treatment with obinutuzumab or rituximab concurrent with TKI therapy for CLL

Participants must have no history of stroke within the past year and no remaining cognitive symptoms from any stroke prior to the past year

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

400 Participants
are grouped into 2 trial groups

Sponsors and collaborators

University of Rochester NCORP Research Base

Lead sponsor

National Cancer Institute (NCI)

Collaborator