Star Tribune (Minneapolis, MN)
The cancer, which had spread widely through her body, went into complete remission and was undetectable in Erholtz's body after just one dose of the measles vaccine, which has an uncanny affinity for certain kinds of tumors.
Erholtz was one of just two subjects in the experiment and the only one to achieve complete remission. But the experiment provides the "proof of concept" that a single, massive does of intravenous viral therapy can kill cancer by overwhelming its natural defenses, according to Dr.
"It's a landmark," Russell said in an interview last week. "We've known for a long time that we can give a virus intravenously and destroy metastatic cancer in mice. Nobody's shown that you can do that in people before."
The research, published online Wednesday in the journal Mayo Clinic Proceedings, represents a "benchmark to strive for and improve upon," according to an accompanying editorial by Dr.
"Without trying to hype it too much, it is a very significant discovery," Bell said in an interview.
The next step is a bigger trial to see if the measles blitzkrieg works in a larger number of patients -- a trial that Mayo expects to launch no later than September.
Researchers have known for decades that viruses can be used to destroy cancer. They bind to tumors and use them as hosts to replicate their own genetic material; the cancer cells eventually explode and release the virus. Antiviral vaccines that have been rendered safe can produce the same effects and can also be modified to carry radioactive molecules to help destroy cancer cells without causing widespread damage to healthy cells around the tumors. The body's immune system then attacks any remaining cancer that carries remnants of the vaccine's genetic imprint.
Researchers worldwide are working with a variety of cancer-killing viruses, including herpes and poxvirus, and they have produced long-lasting cures in rodent studies, Bell noted in his editorial. "Many have been tried in humans but no one has shown this type of systemic activity [seen in the Mayo study]," he said.
The Mayo research could also help solve a related puzzle. Researchers have suspected for some time that there is a threshold level of virus that is required to defeat the defense mechanisms in cancerous tumors, Bell said, and the Mayo study helps set the bar.
In addition, various viruses show an affinity for particular organs, Russell said. Pneumonia and influenza, for example, damage the lungs. Hepatitis damages the liver.
"We have a virus that can do that selectively to a tumor without at the same time causing damage to normal tissues in the body," Russell said.
The strain that Russell used was isolated in 1954 from the throat of an 11-year-old boy named
Most people have been inoculated with the vaccine, rendering it vulnerable to their immune systems. But patients with multiple myeloma often have suppressed immune systems, which can allow the virus to do its work.
The normal dose of vaccine contains 10,000 infectious units of the measles virus, Russell said. Mayo started out giving patients 1 million infectious units and gradually cranked up the dosage -- but it didn't work until Erholtz and another patient were injected with 100 billion infectious units, he said.
While the treatment worked in Erholtz, whose tumors were primarily in her bone marrow, the results weren't sustained in the second patient, whose tumors were largely confined to her leg muscles. Russell said researchers need to study how the nature of the tumor affects the lethality of the virus.
"I think if we had been able to give bigger dose, we might have got a better outcome in that second patient," he said.
But at least for now, there's no second chance. Once the vaccine has been delivered, the body's immune system will recognize it and attack it. Russell said breaking down the immune system before the treatment will be part of another upcoming clinical trial.
Researchers also may be able to bypass the immune system by taking a patient's cells and converting them into Trojan horses. The virus is loaded into the cells, and they are injected back into the bloodstream. "That way it doesn't get destroyed before it reaches its target," Russell said.
Close to success
Researchers, he said, have two primary approaches: Inject the virus directly into tumors to get passed their defenses or inject it into the bloodstream and hope it will seek out tumors and overwhelm them, as was done in the Mayo study.
Saab said he expects one of these virus "platforms" is likely to become standard treatment for a cancer such as myeloma or pancreatic cancer within three to four years.
After reading a draft of the Mayo study, Saab called it "an incredibly innovative way to actually attack the cancer and perhaps even offer a better chance at complete remission," especially in combination with radioactive molecules and immune system therapy.
He cautioned that the study still must be confirmed in large randomized clinical trials -- the point where many hopes get dashed.
"Unless we get to the third stage of development, we are only cautiously optimistic," Saab said.
For her part, Erholtz has no regrets about participating in the study and remains optimistic that she will remain cancer-free at her annual checkup next month in
"We don't let the cancer cloud hang over our house, let's put it that way, or we would have lived in the dark the last 10 years," Erholtz said.
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