there have been countless scientific discoveries made by women, yet attributed to men. consider biophysicist rosalind franklin’s discovery of the double helix — a double-stranded dna molecule — that was attributed to the work of american biologist james watson and english physicist francis crick. in 1905, dr. nettie stevens challenged conventional beliefs about sex determination, demonstrating that the y chromosome plays a pivotal role in male development. despite stevens’ pivotal findings, her mentor e.b. wilson received credit for the discovery.
the terms ‘sex’ and ‘ gender ’ are not interchangeable. according to the canadian institutes of health research, sex refers to the biological differences between males and females, and encompasses sex organs, endogenous hormones and chromosomes. gender, however, is a sociocultural construction that encompasses the roles, norms and behaviours expected for males and females in society, which may or may not correspond to their sex.
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differences between sexes have far-reaching effects on various aspects of cancer, including its epidemiology, pathophysiology (how and why a cancer starts and grows), clinical manifestations (signs and symptoms), disease progression, and response to treatment. current approaches to cancer care, particularly in precision medicine, often overlook the significance of gender and sex. viewing the patient through a sex and gender lens is a first step toward personalized care. precision medicine is a hot topic in cancer care that focuses on the genomic profile of the tumour. approaches to precision medicine use mutational or other genomic data to assign therapy without considering how the sex of the individual might influence therapeutic efficacy. thus, i t is unclear whether precision medicine will equally benefit all patient populations or if they will have the unintended consequence of exacerbating preexisting health disparities.
still, research has shown that women often do not receive the same level of treatment for cancer as men. this is unsurprising, since women have historically been excluded from clinical trials, leading to a focus on male physiology in research and medical attention. in fact, t he diagnosis, treatment and prevention of disease originates from studies carried out mainly on male cells, male mice and men .
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this underrepresentation of women has created gender-specific gaps in medical and disease knowledge, putting their health at risk, and also perpetuaing disparities in our understanding of drug effects and real world treatment outcomes.
in the context of phase iii clinical trials for new cancer treatments, it is optimal for the study population to closely resemble the demographic that will eventually use these treatments, so when trial populations deviate from the actual disease incidence in society, the reproducibility and generalizability of results become limited. for example, c linical trial data generated in men does not necessarily extrapolate to women , who exhibit a 1.5 to 1.7 times greater risk of experiencing adverse reactions to drugs. they also face higher hospitalization rates due to these reactions, even when accounting for age-related differences.
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