"It's not enough," she said of the current success rate for treating AML. "We need to take patients to the next level."
Bloomfield's team followed 144 AML patients who had one of two irregular cytogenes: "8;21 translocation" or "inverse 16." Compared to inverse 16, the 8;21 abnormality was linked to earlier deaths overall and less chance of survival if the cancer returned, despite the fact that patients received roughly the same treatment. Non-whites with the 8;21 abnormality were even worse off, but oddly, there was no racial differences seen with inverse 16.
The reason why this one abnormal gene is linked to lower success rates remains unclear. Meanwhile, Bloomfield said that she and others are busy studying whether new treatment combinations can improve survival rates.
She envisions a future where doctors can match specific genetic information to all the therapies that show an effect against leukemia. The information could then be entered into a computer, which would pick the treatment that might work best for an individual patient.
This era of personalized medicine may be far off. Still, Bloomfield said considerable progress has already been made against AML. When she first started treating patients 20 years ago the average survival was only two weeks. Now, about half of all AML patients are cured of their cancer for many years, and the rates continue to improve.
"That's pretty exciting," said Bloomfield.