Skip to content

Cognitive impairment in patients with lymphoma

A longitudinal feasibility study exploring cancer related cognitive impairment in patients with newly diagnosed aggressive lymphoma undergoing standard chemotherapy with curative intent.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12619001649101
Enrollment
30
Registered
2019-11-26
Start date
2019-11-26
Completion date
2020-09-04
Last updated
2021-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of this study is to assess the feasibility of collecting data on cognition over the course of treatment and recovery in patients with newly diagnosed aggressive lymphoma Who is it for? You may be eligible for this study if you are an adult who has been newly diagnosed with aggressive lymphoma, that is undergoing treatment at Austin Health. Study details All participants in this study will complete their usual treatment as prescribed by their doctor. Participants in this study will be assessed at three timepoints over the course of their treatment and recovery – one before treatment starts, one halfway, and one at the end of the treatment period. The assessment session will involve some tests to assess cognitive function and, in those participants willing to participate, a MRI brain scan and/or a PET/CT brain scan. It is hoped that this research will help determine if a larger study looking at cognitive function during chemotherapy for lymphoma is possible, adding to an underexplored area of cancer research.

Interventions

This longitudinal, feasibility study sets out to explore the pattern of cancer related cognitive impairment in thirty patients with newly diagnosed aggressive lymphoma receiving standard therapy with curative intent, using validated questionnaires, neuropsychological testing, blood-cell inflammatory markers and neuroimaging over a period of eighteen months.

Sponsors

A/Prof Eliza Hawkes
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion criteria: 1. Age greater than or equal to 18 years 2. Newly diagnosed aggressive lymphoma that requires standard chemotherapy treatment with curative intent at Austin Health. Including: • Hodgkin lymphoma • Diffuse large B cell lymphoma • Burkitt lymphoma • Transformed follicular lymphoma • Grade 3b follicular lymphoma 3. Able to read and comprehend English instructions. 4. Eastern Collaborative Oncology Group (ECOG) performance status less than or equal to 2

Exclusion criteria

Exclusion criteria: 1. Central Nervous System (CNS) lymphoma 2. Prior/planned cranial radiotherapy 3. An expected life expectancy < 12 months 4. Medical conditions that may compromise compliance or lead to prolonged hospitalisation 5. Documented history of or current substance abuse 6. Concurrent poorly controlled psychiatric illness.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 21, 2026