Medical research lacks female participants
Medical research lacks female participants
Women should be recruited for clinical trials
Patients who participate in clinical trials not only have access to newer, experimental treatments, they also have access to more routine medical checkups and state-of-the-art technologies.
For people with serious illnesses, and those without access to routine medical care, participation can make a significant difference in their care.
Yet for many women, participation in medical research studies is still not an option. More than a decade after the NIH issued guidelines encouraging the inclusion of women as subjects in clinical research, they still are not fully represented in clinical trials that determine which drugs and treatments get marketed in this country.
Although progress is being made, advocates say, women still have a lot of catching up to do after decades of historical, cultural, and legal barriers that excluded them from both the benefits and risks of participation in medical research.
Many women still are reluctant to participate in clinical trials. And many clinical investigators are reluctant to recruit them, fearing additional complications if a female subject becomes pregnant during the course of treatment or experiences reproductive complications later.
In fact, until 1993, regulations by the FDA prohibited the inclusion of women of childbearing age as subjects in early clinical trials. Those regulations have since been changed and the restriction removed, thus allowing more women to be included in clinical trials, but the results are only now being felt.
"Even though the guidelines changed in 1993, it’s been like turning a battleship," says Sherry Marts, PhD, vice president for scientific affairs for the Society for Women’s Health Research, a Washington, DC-based nonprofit organization that encourages the inclusion of women as research participants and research into gender-linked differences in health and medicine.
"You have to consider trial design and finding ways to recruit and retain women into studies — that took a few years. It is really only in the last few years that some of the data are starting to emerge. That shows you how long it takes to change the system. Data that you collect today will be in front of the FDA in 10 years."
Though more women are being recruited and are participating in clinical trials, there is little evidence that researchers are examining the data to look for any differences in response that might be linked to gender, Marts says.
"That is sort of the follow-up issue to inclusion," she notes. "What’s the point if you are not going to at least look to see if there is a difference?"
Historically, women were excluded from participation as research subjects because of the risk untested agents posed to their future children, says Georgia Sadler, MBA, PhD, clinical professor of surgery in the Cancer Prevention and Control Program at the University of California-San Diego, and director of the center’s community outreach program. Even today, investigators must take painstaking steps to ensure that participants are not pregnant when a trial starts and they understand the importance of not becoming pregnant during the course of the trial.
"There is always the concern about doing harm. You want to weigh the risks and benefits," Sadler says. "You want more benefit than risk — that is the goal, especially when there could be another person involved, namely the child."
Prior to the change in regulation, women of "childbearing potential" (i.e., those who had not yet reached menopause or not undergone a sterilization procedure) were excluded from early trials of drugs that had not been tested for the potential to cause birth defects.
Exceptions were made in instances in which a patient had a life-threatening condition and no other source of treatment was available, Marts adds. "It meant that there were some women in cancer clinical trials, but it did keep them out of trials of most drugs, and it certainly kept them out of the early phase trials," she says.
For many years, the medical community assumed that what worked in men would work — and work in the same way — for women, and vice versa. Drugs not proven effective in male subjects were assumed to have no value for women either.
"For a long time in medicine, we had this thing called the male norm,’" Marts continues. "I say this in my talks and it always gets a laugh, but it is true. It was just assumed that the male was normal’ and women were just small men with different plumbing and a hormone problem. Come to find out, we are not. Our biologies are very different, and that has an impact on our health."
Recent experience has borne this out. For example, the only two drugs currently marketed specifically to treat irritable bowel syndrome seem to be more effective in women. And there are drugs that metabolize differently in men and women.
"There are some drugs that women break down faster than men, so they may need a higher dose or more frequent dosing, and there are some where it is the other way around," Marts says. "It is very challenging to kind of break the data out and figure out exactly what is going on."
Pharmaceutical manufacturers have an understandable disincentive to discover the need for different doses for different populations, she adds. It is great if one dose works for everyone, but that’s not always the case.
And although more women are being included in clinical trials, there is some residual perception that trials are easier with men as subjects.
"We understand perfectly that manufacturers have a profit disincentive to doing this because if they look for a difference, and they find one, then they are going to have to label the drug to say, These people should take it,’ or, These people should not,’" Marts says. "When Drug Company X is looking for the next blockbuster everybody’s-gonna-take-this’ drug, then some advocacy group comes along and says, But does this work differently in women than in men?’ The reaction we get is, We don’t want to know.’"
Pregnancy always a concern
There also is the risk of pregnancy. What happens if a subject is in the early stages of pregnancy and doesn’t know it? Equally dangerous is the potential of a subject becoming pregnant during the course of the trial.
However, both Sadler and Marts say this potential complication is overblown in the minds of some researchers.
"You can ask a woman, Is there any chance you might become pregnant?’ By definition, that means, Have you missed your period?" says Sadler. "Once you have determined that she is not pregnant right now, the next question would be, Are you trying to get pregnant, or do you have any plans to get pregnant? If you have someone who says they are, then you could exclude them because of the potential to do more harm than good."
The riskier the product being tested, the more solid assurance the investigators will want that subjects are not going to become pregnant, she continues. "If you are doing things that are relatively safe, you might say, Well, being on birth control is probably adequate; but if you are testing a new drug for the first time in humans, and [the drug] was highly toxic in animal models, you might say that, unless the person has had her tubes tied or some other procedure, you might not want to take the chance."
During the informed consent process, it also is important to emphasize this risk, the importance of not becoming pregnant, and — should an unplanned pregnancy occur — stress that the investigators need to be notified immediately.
Even with the change in the guidelines and attempts by many investigators to recruit female participants, women are not exactly knocking down clinic doors to get into trials.
Almost any conference involving research professionals will feature a session on recruiting women and minorities — and usually, it’s a single session titled "Recruiting Women and Minorities," as if they were one population, Marts notes.
"You still tend to hear investigators say, Oh, but it is so hard to recruit and retain women," she says. "I always ask them, first of all, Are you listening to your site staff?’ Maybe they have some ideas about how to do this better."
There are some recent examples of large-scale clinical trials involving women and other populations who were thought difficult to recruit that can provide helpful lessons about how to recruit and retain study subjects.
The first, says Marts, is the Women’s Health Initiative, which recruited many older women and followed them for several years. "People said it could never be done. You could never recruit that many older women and keep them in the trial," she points out. "But, as we know, they did."
Other examples can be found in the HIV prevention trials that involve women who are either drug users, partners of drug users, or are professional sex workers.
There are some study sites that have had 98% retention rates over two-year periods with these populations, she says. The sites developed unique ways of maintaining contact with these women, even though the subjects may have been moving frequently, sometimes in and out of homeless shelters, or work in dangerous and illegal conditions — not exactly conducive to regular follow-up visits.
"What they are finding is that it takes more than just herding people into the clinic, performing the visit, writing the next appointment on a note card, patting them on the head, and sending them out," Marts says.
Because women typically shoulder the lion’s share of responsibility for child care and household maintenance, clinics that offer weekend and evening hours, and those that combine multiple services (blood draws, X-rays, other monitoring) at a single visit are often more amenable to female participants, she adds.
They also may be concerned about the safety of the clinic’s location, and whether security is provided.
Obviously, this is not a sole concern for female participants, Marts adds, and researchers may find that concessions they make to attract female participants may recruit more participants overall as well.
Working on a contract with one of the HIV vaccine trials, Marts helped produce a video featuring the subjects talking about the benefits of participating in the study. "There was one interview with a drug addict — who, in this instance, happened to be a man — and the interviewer asked, Why are you doing this? Why agree to be in the trial?’" she relates. "The guy looked at her and said, Lady, I’m a junkie. No one has ever asked me for nothing. These people came, and they asked me to do something for other people. How could I say no?’"
Because clinical trials have, in the past, focused exclusively on men, it’s possible that many women simply don’t recognize this as something that is possible for them — they don’t realize they are able to contribute, Marts notes.
"It is sort of a truism in the not-for-profit world that people don’t volunteer unless they are asked. One of the things that occurred to us early on after they changed the guidelines was that half the population had been reading about medical research and seeing reports in the news, and it was always about men," she says. "Heart disease in men; men should take aspirin, etc. We imagined that women simply don’t feel asked. They don’t feel welcome to participate in these studies."
To help remedy that problem, the society initiated its "Some Things Only a Woman Can Do" campaign, which included a web site, brochures, and other educational materials that encourage women to consider participating in clinical trials.
"It emphasizes that you don’t necessarily have to have a disease or condition to participate, and women are really intrigued to find this out," Marts says.
Conducting clinical research on essentially one population — white men — has handicapped medical research in a number of ways. Studies that include diverse groups of people can yield better information, faster, notes Sadler, whose research focuses on improving recruitment of both women and minorities. "It is important, for example, to have women of childbearing age represented in clinical trials. Let’s say you are looking at blood pressure medication for hypertension. You would not want to exclude women between the ages of 18 and 50 [because] that is a large segment of the population that will eventually take this medication," she says. "Would you want them to take it without it ever having been tested in that population? That is essentially what happens now. If you have a study, and you don’t have a large enough representation of African Americans, Hispanics, or Asians, it is the same thing."
The issues go beyond just genetics and gender, she continues. For example, say a particular drug does really well in subjects who are Asian women, but none of the other participants. Researchers would then look to see why. Perhaps it is something in the diet that these women all had that enhances the drug’s efficacy? Once that is determined, that information could be included in the drug’s labeling.
Conversely, say a certain group does poorly in a trial. For example, all of the Hispanic men don’t respond. Perhaps there is a reason there. Once the likely cause is found, then researchers can recommend a possible solution.
However, if these people are never represented in clinical trials, this information is likely to never be found. For example, say the drug that worked so well for Asian women only is tested in groups of Caucasian men, is found to not work well, and is dropped. Researchers would never know its true potential.
Or suppose a drug that has significant complications for people with certain dietary habits or genetic differences makes it to market. Patients who do not respond to the drug, or worse, experience a poor reaction, are rarely noted.
Outside a clinical trial, Sadler says, individual complications or adverse events occur too far apart for their significance to be noted.
Sadler and her colleagues at the University of California-San Diego have initiated several projects attempting to improve the recruitment of women as clinical research participants.
First, they have written articles in several different professional journals advocating the benefits to patients who participate.
"The media has given clinical trials a bad public reputation," Sadler says. "There are a lot of good things you can say about clinical trials, but you don’t hear about it in the media. You only hear about the bad cases, where someone is injured or a participant dies."
The public, at large, has no idea that development of new drugs and treatments would not happen if patients did not sometimes agree to be subjects. "You may read an article about a new exciting drug that has now been found to reduce cancer mortality by 10%, but you never hear about the clinical trial that yielded this information," she continues. "It looks like it just appeared out of the clear blue sky — someone figured it out, and it worked. No, it was actually 10 different studies and 895 people took part in those various studies. They were Phase 1, Phase 2, and Phase 3 studies; and now, eight years later, here are the results [that] they are very excited to bring that to you. You never see that information in a newspaper article or TV report."
Sadler has written articles for nurses, physical therapists, chaplains, and even nurse-midwives.
"We wanted to reach people, in addition to physicians — who may not have enough time to talk with patients at length about clinical trials in general — [and whom] patients might seek advice from," Sadler says. "We want those professionals to know about clinical trials so that they can pass on reliable information."
Sadler’s group also works to enroll women in small research studies that are very low risk, such as opinion surveys, to acquaint them with the informed consent process. At a later time, some of these people may have a chance to be a trial subject, and will hopefully find the process less intimidating.
"One of the reasons we spend so much time educating health professionals and the public is to try to help communities understand that no participation’ is really no voice,’" Sadler says. "Someone has to step up to the plate. Obviously, we are not saying everyone should do everything, but keep your eyes and ears open, and don’t have a knee-jerk negative response."
Patients who participate in clinical trials not only have access to newer, experimental treatments, they also have access to more routine medical checkups and state-of-the-art technologies. For people with serious illnesses, and those without access to routine medical care, participation can make a significant difference in their care. Yet for many women, participation in medical research studies is still not an option.Subscribe Now for Access
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