SUNDAY, May 31 (HealthDay News) -- In a new study, patients with follicular non-Hodgkin lymphoma who received a vaccine made from their own cancer cells went more than 44 months before relapsing, compared to only 30.6 months for those who didn't get the vaccine.
The vaccine trial was one of several studies from the new frontier of "personalized medicine" presented Sunday at the American Society of Clinical Oncology (ASCO) annual meeting, in Orlando, Fla.
The approach aims to hit cancer hard by tailoring treatments to the patient's own genetics or disease, among other factors.
The lymphoma study differs from other vaccine trials in that the tool was patient-specific, study author Dr. Stephen Schuster, an associate professor at the University of Pennsylvania School of Medicine, explained at a Sunday news conference.
The findings could signal a whole new direction in how vaccines are used against cancer, experts said.
"The novelty of the vaccines is that they were individualized to each patient, and that they were directed against a cancer-specific target," said Dr. Louis Weiner, director of Georgetown's Lombardi Comprehensive Cancer Center in Washington, D.C. "Many vaccines are directed against cancer-associated targets and always run the risk of damage to normal cells."
But the lymphoma vaccine is "almost like an immune-system 'smart bomb,'" Weiner noted. "It only goes after malignant cells, and that's very attractive."
For this phase III trial, 76 patients who had been in remission for at least six months following chemotherapy were injected with BiovaxID, a vaccine engineered from cancerous tissues drawn from each individual patient. The mixture also contained compounds designed to heighten the effect of the vaccine.
These individualized vaccines took about three months to develop. Each patient received five injections over six months.
"The vaccine targets the 'idiotype' protein on the cell surface [of cancerous B cells in follicular lymphoma]. The protein is unique to cancer cells and varies from patient to patient," Schuster explained. "The idiotype vaccine with the immune stimulatory molecules improved disease-free survival following chemo."
However, in contrast to other phase III trials involving cancer vaccines, "remission before receiving the vaccine might be a prerequisite for deriving benefit, or at least statistically significant benefit," he added.
Another phase III trial for another cancer vaccine -- this one for advanced melanoma -- also produced promising results, marking the first evidence of clinical benefit of vaccination in patients with melanoma.
This time, researchers added a new cancer vaccine, called gp100:209-217(210M) peptide, to conventional therapy.
"In the past, what we've tried to do in the cancer immunology field is to attack tumors one agent at a time. Now we're starting to combine agents together for effective therapy," said study senior author Dr. Patrick Hwu, melanoma chief at the University of Texas M.D. Anderson Cancer Center in Houston. "Our approach here was to combine the vaccine with interleukin 2 to get immune cells to attack the tumor. All immune approaches try to get killer T-cells to attack the tumor. The vaccine allows the 'soldiers' to go through boot camp, [it] initiates the training of soldiers. The soldiers then multiply into a large army that can then attack tumors to kill them."