Experiences and perspectives of individuals accessing CAR-T cell therapy: A qualitative analysis of online Reddit discussions.

J Cancer Policy

Canadian Centre for Applied Research in Cancer Control (CC-ARCC), Vancouver, British Columbia, Canada; Cancer Control Research, BC Cancer, Vancouver, British Columbia, Canada; Faculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.

Published: December 2021

AI Article Synopsis

  • Several CAR-T therapies for treating blood cancers are approved, but there is limited understanding among patients and caregivers about these treatments and the uncertainties they bring.
  • Data was collected from Reddit discussions in cancer-related subreddits, leading to the analysis of 87 relevant posts that highlighted themes such as community support, the search for cures, and treatment access challenges.
  • The study emphasizes the need for technology assessments that reflect patient experiences and encourages balanced decision-making between patients and doctors to improve awareness and resource allocation in cancer treatments.

Article Abstract

Introduction: Several chimeric antigen receptor (CAR-T) T-cell therapies have been approved for use for haematological malignancies. Despite known safety, access, and cost issues, little is known about how patients and caregivers understand novel treatments such as CAR-T and their associated uncertainties.

Methods: We gathered data from Reddit, an online public social media site. We performed a keyword search in three relevant subreddit threads: r/cancer, r/lymphoma, r/leukemia. We systematically extracted threads and associated comments and reviewed against our inclusion criteria.

Results: We identified a total of 186 posts and 87 were included in the qualitative analysis from March 1, 2013, to April 15, 2021. Qualitative content analysis was used to identify themes. Of those excluded, 88 contained discussions of other immunotherapies and 11 were scientific profiles. We identified four themes: 1) navigating uncertainty with community, 2) finding a cure, 3) managing treatment-related uncertainties, and 4) overcoming uncertainties related to access. We found patients experience numerous barriers when seeking access to novel therapeutics, such as CAR-T therapies.

Conclusions: The perceptions and struggles of patients and their families are relevant for developing technology assessments that are sensitive to patient experiences, as well as to inform policies for equitable resource allocation.

Policy Summary: Our study underscores the importance of balanced decision making between patients and physicians to ensure patients understand the risk and benefits of cancer treatments. Study investigators might evaluate trial participants based on patient demographics to ensure equitable access to studies for individuals in settings where internet access is less common.

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Source
http://dx.doi.org/10.1016/j.jcpo.2021.100303DOI Listing

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