Highlights from the Oncology Nursing Society's 10th National Conference on Cancer Nursing Research
Held February 12-14, 2009, Orlando, Fla

ORLANDO, FLA—For the more than 2 million breast cancer survivors in the United States, improved treatments have prolonged life at the cost of some unpleasant side effects. Among them, the cognitive changes known as “chemo brain” may be the most upsetting.

“Cognitive dysfunction is a significant problem,” affirmed Diane Von Ah, PhD, RN, an assistant professor in adult health at the Indiana University School of Nursing, estimating that the problem affects up to 83% of breast cancer patients. “It's prevalent, bothersome to women, and can be potentially debilitating and impact their quality of life.”

Dr Von Ah told meeting attendees that because the etiology of cognitive dysfunction is not known, the condition is difficult to treat. However, she suspects there are a number of underlying factors, and researched the relationship between serotonin and “chemo brain” based on the direct relationship between the neurotransmitter and estrogen. Estrogen withdrawal is a consequence of breast cancer treatment.

The double-blind, placebo-controlled, crossover trial employed acute tryptophan depletion therapy. Because tryptophan is a precursor to serotonin, alterations in tryptophan levels will affect serotonin. The intervention group received a higher dose of an amino acid to deplete tryptophan compared to the control group (100% vs 25%). Participants completed neuropsychological testing 5 hours after administration of the amino acid, at the tryptophan nadir. Women in the intervention group were depleted 85% by hour 5, and the control had a 49% reduction in tryptophan. Twenty women completed the study.

“We did not find a significant impact on short-term memory, but we did in long-term memory,” said Dr Von Ah. The team also found changes in motor function in the dominant and nondominant hands during the tryptophan depletion, but no significant changes to attention, concentration, executive function, or information processing speed.

The responses did not vary for antiestrogen use, antidepressant use, treatment protocols, or genetic factors. There were no significant differences in mood or blood sugar between the groups.

“In our study, we found that serotonin may be involved in memory consolidation and psychomotor ability,” stated Dr Von Ah. “We need to do further research to fully understand the protective role of serotonin in cognitive dysfunction, so we can do more with potentially novel treatment therapies, either pharmacologically or behaviorally through diet.”

Dr Von Ah presented a second study in which she investigated self-reported cognitive dysfunction and quality of life in African-American and Caucasian breast cancer survivors in a descriptive, correlational study of secondary data from a larger quality-of-life study. The sample included 134 women (46% African American and 54% Caucasian) 1-10 years postdiagnosis.

More than 1 in 4 survivors (26%) reported poor attention, indicating that cognitive dysfunction can continue long after treatment. Deficits in capacity to direct attention correlated with poorer quality of life, including more depressive symptoms, lower sense of overall wellbeing, less social support, lower parental satisfaction, poorer physical functioning, and greater fatigue. Younger women had more attention problems, depression, and fatigue. African-American women had decreased social support and decreased levels of physical function. Women with increased comorbidities had increased depression, increased fatigue, and decreased well-being.

“Capacity to direct attention was related to poorer quality-of-life outcomes, suggesting interventions may have a broad impact on quality of life in breast cancer survivors,” summarized Dr Von Ah.

Joyce Thielen, PhD, RN, CS, associate director of undergraduate studies at Elms College in Chicopee, Mass, said women undergoing breast cancer chemotherapy frequently report changes in memory, executive function, organization, and multitasking abilities, yet subjective testing often does not correlate with the degree of severity patients are indicating. She conducted a qualitative study to better understand 13 women's experiences and what it meant to them. She found the cognitive changes often were insidious and the women many times blamed them on menopause, lack of sleep, or early Alzheimer's disease.

“They looked inside for answers to the attention problems they were having,” Dr Thielen explained.

The women reported an inability to read or to “keep their eye on the ball,” or had trouble working. The women also indicated difficulty driving or correctly taking medications. Family support helped them cope. They reported that nurses and doctors dismissed their cognitive complaints.

“It's important to discuss side effects with patients and families,” Dr Thielen said. “The assessment needs to be at time of initial treatment and ongoing to pick up subtle changes that may develop.”

Dr Thielen also encouraged educating nursing students as well as nurses about “chemo brain” and the inclusion of neurocognitive measurements in clinical trials.

Catherine Jansen PhD, RN, OCN, an oncology clinical nurse specialist at Kaiser Permanente Medical Center, San Francisco, investigated cognitive function prior to chemotherapy, whether it changes over time, and its relationship with anxiety, depression, fatigue, anemia, menopausal status, and the patient's perception of cognitive functioning. The prospective trial included 71 women receiving Adriamycin (doxorubicin) and cyclophosphamide (AC) or AC followed by a taxane. Participants completed multiple validated tests.

Preliminary results showed no significant changes in immediate memory, language, attention, executive function, and motor skills. However a significant effect of time was found for visuospatial skill, attention, and delayed memory. Significant changes in cognitive function remained when researchers controlled for anxiety, depression, fatigue, and hemoglobin levels.