Assessment of gender representation in clinical trials leading to FDA approval for oncology therapeutics between 2014 and 2019: A systematic review-based cohort study.
Kyle A DymanusMohit ButaneyDiana E MageeAmanda E HirdAmy N LuckenbaughMerry W MaMary E HallHeather L HuelsterAaron A LavianaNancy B DavisMartha K TerrisZachary KlaassenChristopher J D WallisPublished in: Cancer (2021)
This study assesses whether gender disparities exist in clinical trials leading to US Food and Drug Administration (FDA) cancer drug approvals. From January 2014 to April 2019, 149 clinical trials leading to FDA oncology drug approvals showed 60.3% and 39.7% of the enrollees were male and female, respectively. Gender representation varied by specific tumor when compared with the expected incidence rate of cancer in the United States, although women were more often underrepresented. Increased efforts are needed with regard to ensuring equitable representation in oncology clinical trials.
Keyphrases
- clinical trial
- drug administration
- palliative care
- papillary thyroid
- phase ii
- mental health
- squamous cell
- open label
- double blind
- study protocol
- small molecule
- polycystic ovary syndrome
- squamous cell carcinoma
- risk factors
- randomized controlled trial
- healthcare
- childhood cancer
- lymph node metastasis
- neural network
- adipose tissue
- emergency department
- adverse drug
- young adults
- human health
- quality improvement