One obstacle may be the baffling scaffolding scientists erect around their studies. For example, cancer is a disease of aging, but many clinical trials on cancer drugs exclude older people from participating.
One study, in The Journal of Clinical Oncology, found that older patients “are underrepresented in cancer clinical trials relative to their disease burden.”
In another study on the exclusion of large segments of cancer populations, published last year in The Oncologist, researchers argued that “the criteria for participation in some clinical trials may be overly restrictive and limit enrollment.”
But the problem of low enrollment is often attributed to patient resistance. The reluctance of some patients makes perfect sense to me. Fear about unforeseen side effects escalates when consent forms, like the ones I signed, state that a new regimen cannot cure but might kill patients.
People facing a poor prognosis may not want to squander their limited energy on travelling, undergoing invasive scans or inhabiting hospital environments. The location of trials in urban centres poses a challenge for rural populations. Additionally, eligibility requirements make it impossible to enroll when people don’t have a specific genetic mutation or have previously taken a specific drug
Yet other qualms seem to be based on persistent delusions. Quite a few people miss out on free, cutting-edge treatment because of spurious suppositions. The commonly held view that patients will be given nothing but a placebo is rarely the case. In a randomised study, people on one arm may not receive the new medicine, but they will get “the best standard of care available” and their progress will be monitored. Placebos cannot be employed when an effective therapy is available. They may be used to test a supplementary protocol, but patients would be informed. And not all trials are randomised.
Why enroll if most trials result neither in medical breakthroughs nor in extending survival rates? One answer: even negative data extend scientific knowledge. Another: the ethical backbone of research (worth repeating) requires that all participants in trials receive “the best standard of care available” for their specific disease. Did I mention that this care is free?
The worries of patients that they will be reduced to guinea pigs should be put to rest by an important principle underscored by the physician, author and cancer survivor Dr. Wendy Harpham. When clinicians care for patients, she explains, they “abide by their professional oath as physicians to act with their patients’ welfare as their top priority.” Should a regimen prove deleterious, patients would be encouraged to drop out. In any case and for whatever reason, enrolled patients are always free to stop participating.
All these inhibitions retard enrollment; however, low rates of participation should also be attributed to insufficient information. While confronting cancer, a situation fraught with terror about personal survival, most men and women simply do not know our options and we do not have the ability to discover them on our own.
Unless oncologists are themselves researchers, they may not guide patients toward clinical trials. It is not in their self-interest to do so and it would take a considerable amount of time. Despite the government’s effort to make its website user-friendly, finding a suitable clinical trial can be exceptionally difficult. Online help sites may steer some patients to the right trials, but not all.
Only recently did I learn about clinical trial navigators, professionals who may be nurses or lay people, and who work to locate and explain trial options, negotiate complex eligibility issues and offer support as decisions are made. There is some evidence that trial navigators can promote the inclusion of racial and ethnic minorities who have been shockingly underrepresented in clinical trials. They are employed at a number of cancer centres.
The majority of pediatric patients — 60 per cent of babies, children and young adults — are treated in clinical trials. In the past 50 years, the overall survival rate for children has increased from 10 per cent to over 80 per cent, a heartening statistic not totally attributable to clinical trials but surely related to them.
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