Patients in phase 1 cancer trials: psychological distress and understanding of trial information

Authors

  • Katrine T. Gad Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Ulrik Lassen Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Anne K. Duun-Henriksen Statistics and Data analysis, The Danish Cancer Society Research Center, Copenhagen, Denmark
  • Susanne O. Dalton Survivorship & Inequality in Cancer, The Danish Cancer Society Research Center, Copenhagen, Denmark; Department of Clinical Oncology and Palliative Services, Zealand University Hospital, Naestved, Denmark
  • Morten Mau-Sørensen Late Effect Research Unit (CASTLE), Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Pernille E. Bidstrup Survivorship & Inequality in Cancer, The Danish Cancer Society Research Center, Copenhagen, Denmark
  • Beverley. L. Høeg Statistics and Data analysis, The Danish Cancer Society Research Center, Copenhagen, Denmark
  • Kristoffer S. Rohrberg Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Iben Spanggard Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Annika von Heymann Late Effect Research Unit (CASTLE), Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Christoffer Johansen Late Effect Research Unit (CASTLE), Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

DOI:

https://doi.org/10.1080/0284186X.2021.1993331

Keywords:

Anxiety, clinical trial, phase 1, depression, informed consent, psychological distress

Abstract

Background

Psychological distress may be present among patients who are considering enrollment in phase 1 cancer trials, as they have advanced cancer and no documented treatment options remain. However, the prevalence of psychological distress has not been previously investigated in larger cohorts. In complex phase 1 cancer trials, it is important to ensure adequate understanding of the study premises, such as the undocumented effects and the risk of adverse events.

Materials and methods

In a prospective study, patients completed questionnaires at two time points. We investigated psychological distress, measured as stress, anxiety, and depression, among patients at their first visit to the phase 1 unit (N = 229). Further, we investigated the understanding of trial information among patients who were enrolled in a phase 1 cancer trial (N = 57).

Results

We enrolled 75% of 307 eligible patients. We found a lower mean score of stress in our population compared to population norms, while the mean scores of anxiety and depression were higher. A total of 9% showed moderate to severe symptoms of anxiety and 11% showed moderate to severe symptoms of depression, which indicates higher levels than cancer patients in general. A total of 46 (81% of enrolled patients) completed questionnaires on trial information and consent. The understanding of the information on phase 1 cancer trials in these patients was slightly lower than the level reported for cancer trials in general. Some aspects relating to purpose, benefit, and additional risks were understood by fewer than half of the patients.

Conclusion

Our results suggest that distress is not as prevalent in the population of patients referred to phase 1 cancer trials as in the general cancer population. Although patients’ understanding of trial information was reasonable, some aspects of complex phase 1 cancer trials were not easily understood by enrolled patients.

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Published

2022-03-04

How to Cite

Gad, K. T., Lassen, U., Duun-Henriksen, A. K., Dalton, S. O., Mau-Sørensen, M., Bidstrup, P. E., … Johansen, C. (2022). Patients in phase 1 cancer trials: psychological distress and understanding of trial information. Acta Oncologica, 61(3), 341–348. https://doi.org/10.1080/0284186X.2021.1993331