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Assessing Depressive Symptoms in Patients With Cancer Treated With Interleukin-2: A Comparison of 2 Measures
Shawn M McClintock1, Robin B Dail, Laura S Howe-Martin
1Author Affiliations: Division of Psychology, Department of Psychiatry, UT Southwestern Medical Center (Drs McClintock and Howe-Martin), Dallas, Texas; Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine (Dr McClintock), Durham, North Carolina; College of Nursing, University of South Carolina (Dr Dail), Columbia, South Carolina; Moncrief Cancer Institute, UT Southwestern Medical Center (Dr Howe-Martin); Duke Clinical Research Institute (Dr Mann), Durham, North Carolina; and Duke University School of Nursing (Dr Bailey), Durham, North Carolina.
Background:
High-dose interleukin-2 is a therapy available for individuals with renal cell carcinoma; however, it can produce adverse effects, specifically depressive symptoms. There is limited information regarding the trajectory of depressive symptoms and measurement-based care assessment of depressive symptoms.
Objective:
The purpose was to describe the trajectory of depressive symptoms and compare 2 depression measures.
Methods:
A descriptive, mixed-method case study approach was used to describe the longitudinal trajectory of depressive symptoms The qualitative assessment included a journal entry and an interview. The quantitative depression symptom severity measures included the 8-item self-report Patient-Reported Outcomes Measurement Information System Depression and the 30-item Inventory of Depressive Symptomatology-Clinician Rated (IDS-C).
Results:
Ten cases were enrolled. The maximum number of interleukin-2 doses that any patient received within a single hospitalization ranged from 4 to 12. Mean scores on the 8-item Patient-Reported Outcomes Measurement Information System Depression showed no changes in depressive symptoms from pretreatment to posttreatment, nor across hospitalizations. Mean total scores on the IDS-C increased from "normal" to "mild severity" depressive symptom range across all treatment cycles, suggesting transient depressive symptoms within hospitalizations. Qualitative data from the case supported the IDS-C increase, suggesting that the patient developed depressive symptoms pretreatment to posttreatment.
Conclusions:
Understanding the trajectory of depressive symptoms allows for the identification of critical time points when depressive symptoms present and change across treatment. It is critical to use measurement-based care using validated measures to assess for the presence and changes in depressive symptoms.
Implications For Practice:
Validated self-report or clinician-rated depression symptom measures should be used to document the presence or absence of depressive symptoms in this population.
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