Loss to follow-up of minorities, adolescents, and young adults on clinical trials: A report from the Children's Oncology Group.
Vidya PuthenpuraLingyun JiXinxin XuMichael E RothDavid R FreyerA Lindsay FrazierAsher M MarksFarzana D PashankarPublished in: Cancer (2023)
Little is known about disparities in loss to follow-up for pediatric cancer clinical trial participants. In this study, we found that participants who were adolescents and young adults when treated, those who identified as a racial and/or ethnic minority, or those residing in areas with lower socioeconomic status at diagnosis were associated with higher rates of loss to follow-up. As a result, the ability to assess their long-term survival, treatment-related health conditions, and quality of life is hindered. These findings suggest the need for targeted interventions to improve long-term follow-up among disadvantaged pediatric clinical trial participants.
Keyphrases
- clinical trial
- phase ii
- open label
- public health
- healthcare
- double blind
- palliative care
- papillary thyroid
- young adults
- physical activity
- mental health
- cancer therapy
- randomized controlled trial
- squamous cell carcinoma
- childhood cancer
- squamous cell
- risk assessment
- drug delivery
- lymph node metastasis
- social media
- human health