A recent clinical trial suggests that we may be one step closer to preventing multiple myeloma — but there's still a long way to go. The research, which will be presented at this year's annual conference of the American Society of Clinical Oncology, gave the drug Revlimid (lenalidomide) to patients who had a higher than average chance of developing multiple myeloma.
Revlimid is currently used throughout various stages of treatment for multiple myeloma, with enormous benefits for many patients. The patients in this study had a precursor condition known as “smoldering multiple myeloma” (SMM), which can often turn into full blown multiple myeloma. The trial found Revlimid significantly reduces the risk of SMM from becoming cancer in patients at moderate or high risk. After three years, 91 percent of people with SMM and taking lenalidomide still hadn't progressed to multiple myeloma, compared with 66 percent of people who weren't given the drug.
Read More"The benefit to patients with an intermediate risk is very interesting," Dr Sagar Lonial, one of the lead authors, told SurvivorNet. "If we can prove benefit to those patients that's a big deal, because no one is really looking at that group.
For high risk this is practice changing, for intermediate risk, it's provocative, and could well change practice in the long term as well."
This could be big news for the estimated 4,400 people that are diagnosed with smoldering multiple myeloma in the United States each year. Around 10 percent of those people will go on to develop full multiple myeloma annually. Those with high risk have a 50 percent chance of progressing to the active disease in two years. While survival rates for multiple myeloma have steadily increased over the last few years thanks to the availability of several new therapies, there still remains no cure, and it's considered a chronic condition to which most patients will eventually succumb. Revlimid, the study suggests, while not being a cure, could provide a way to significantly slow down this chain of events. "This isn't putting people into remission," Dr Lonial points out, “but is stalling progression." This could give patients additional years of progression-free, and overall, survival.
Despite this encouraging news, the practicalities of taking lenalidomide continuously should be considered, and a proportion of the trial's patients had to stop taking the drug as the side effects — such as diarrhea and constipation — became too much for them to tolerate. It should also be noted that Revlimid isn't cheap, and it's far too early to say whether insurance companies would pay for its continuous use as a preventative measure. But Dr Lonial points out that patients were taken off the drug after two years, and still had increased survival rates after five years, suggesting that perhaps it still might be possible to significantly slow down progression to multiple myeloma without patients having to take a pill for the rest of their lives.
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