Patients’ considerations of time toxicity when assessing cancer treatments with marginal benefit

Author:

Gupta Arjun1ORCID,Brundage Michael D2,Galica Jacqueline2,Karim Safiya3,Koven Rachel4,Ng Terry L5,O’Donnell Jennifer2,tenHove Julia2,Robinson Andrew6,Booth Christopher M2ORCID

Affiliation:

1. Division of Hematology, Oncology, and Transplantation, University of Minnesota , Minneapolis, MN , United States

2. Cancer Research Institute, Queen’s University Cancer Care and Epidemiology, Sinclair  , Kingston, ON K7L3N6 , Canada

3. Tom Baker Cancer Centre , Calgary, AB T2N4N2 , Canada

4. Cancer Research Institute, Queen’s University Patient Advocate on behalf of Cancer Care and Epidemiology, Sinclair  , Kingston, ON K7L3N6 , Canada

5. University of Ottawa Division of Medical Oncology, , Ottawa ON K1H8L6 , Canada

6. Cancer Centre of Southeastern Ontario, Kingston General Hospital , Kingston, ON K7L2V7, Canada

Abstract

Abstract Background Effective techniques for eliciting patients’ preferences regarding their own care, when treatment options offer marginal gains and different risks, is an important clinical need. We sought to evaluate the association between patients’ considerations of the time burdens of care (“time toxicity”) with decisions about hypothetical treatment options. Methods We conducted a secondary analysis of a multicenter, mixed-methods study that evaluated patients’ attitudes and preferences toward palliative-intent cancer treatments that delayed imaging progression-free survival (PFS) but did not improve overall survival (OS). We classified participants based on if they spontaneously volunteered one or more consideration of time burdens during qualitative interviews after treatment trade-off exercises. We compared the percentage of participants who opted for treatments with no PFS gain, some PFS gain, or who declined treatment regardless of PFS gain (in the absence of OS benefit). We conducted narrative analysis of themes related to time burdens. Results The study cohort included 100 participants with advanced cancer (55% women, 63% age > 60 years, 38% with gastrointestinal cancer, and 80% currently receiving cancer-directed treatment. Forty-six percent (46/100) spontaneously described time burdens as a factor they considered in making treatment decisions. Participants who mentioned time (vs not) had higher thresholds for PFS gains required for choosing additional treatments (P value .004). Participants who mentioned time were more likely to decline treatments with no OS benefit irrespective of the magnitude of PFS benefit (65%, vs 31%). On qualitative analysis, we found that time burdens are influenced by several treatment-related factors and have broad-ranging impact, and illustrate how patients’ experiences with time burdens and their preferences regarding time influence their decisions. Conclusions Almost half of participating patients spontaneously raised the issue of time burdens of cancer care when making hypothetical treatment decisions. These patients had notable differences in treatment preferences compared to those who did not mention considerations of time. Decision science researchers and clinicians should consider time burdens as an important attribute in research and in clinic.

Funder

Canadian Institutes of Health Research

Pancreatic Cancer Action Network and Institutional Research

Publisher

Oxford University Press (OUP)

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