In Talk on Personalized Medicine, Life Technologies’ CEO Explains Shift in Corporate Strategy

personalized medicine, Lucier also made some other noteworthy observations:

—“If you have one in five drugs wrong in cancer, and you’re fighting cancer, those of you may have even had that battle, you know that time is of the essence. So the last thing you can have is a mistake, or a trial-and-error approach. Unfortunately, that is the state of medicine today.”

—“Cancer is the right place to start in terms of engineering disease…The way we talk about it today, cancer is a geography, or a location on your body, you know, breast cancer or pancreatic cancer. Actually, the people who are really in the avant-garde of cancer treatment today know that’s not the way you’ve got to be thinking about it in the future. It’s actually by pathway. [For example, in a brain cancer study] it turned out the best drug to deal with the brain cancer was a drug for testicular cancer. It shows that they were actually the exact same cancer. So it’s really about the pathway, or what pathway has been perturbed and mutated, and then you’re trying to do something to impact that…The way we’re going to be thinking about cancer in the future is, what ‘pathway’ cancer do you have—not ‘is it breast cancer?'”

—“The real problem here is the regulatory environment… The FDA is certainly at this point a step or two behind potentially in the science, and certainly has more of a focus on safety and risk mitigation, versus treatment and hopefully advancing therapy. I would love to see a more candid, open debate in society about what risks we’re willing to take for experimental drugs and perhaps give the patients more of a voice in that decision. Today patients don’t have a big enough voice in the ultimate decision. The FDA has no upside. So they’re constantly out to mitigate the downside risk. Obviously the companies only want the upside, so there’s got to be something in between that brings the patient back into this equation.”

—“Our friends down the road at [San Diego-based] Illumina and Life Technologies have certainly been involved in this absolute explosion of knowledge that has taken place in just the last five years. [National Institutes of Health director] Francis Collins likes to say that we’ve learned more about human disease in the last five years than we have in the previous 50 years. I think that trend is actually going to accelerate, not decelerate. The next five years we’ll know more about the association of our genome to the disease than we did in the last 50.”

Author: Bruce V. Bigelow

In Memoriam: Our dear friend Bruce V. Bigelow passed away on June 29, 2018. He was the editor of Xconomy San Diego from 2008 to 2018. Read more about his life and work here. Bruce Bigelow joined Xconomy from the business desk of the San Diego Union-Tribune. He was a member of the team of reporters who were awarded the 2006 Pulitzer Prize in National Reporting for uncovering bribes paid to San Diego Republican Rep. Randy “Duke” Cunningham in exchange for special legislation earmarks. He also shared a 2006 award for enterprise reporting from the Society of Business Editors and Writers for “In Harm’s Way,” an article about the extraordinary casualty rate among employees working in Iraq for San Diego’s Titan Corp. He has written extensively about the 2002 corporate accounting scandal at software goliath Peregrine Systems. He also was a Gerald Loeb Award finalist and National Headline Award winner for “The Toymaker,” a 14-part chronicle of a San Diego start-up company. He takes special satisfaction, though, that the series was included in the library for nonfiction narrative journalism at the Nieman Foundation for Journalism at Harvard University. Bigelow graduated from U.C. Berkeley in 1977 with a degree in English Literature and from the Columbia University Graduate School of Journalism in 1979. Before joining the Union-Tribune in 1990, he worked for the Associated Press in Los Angeles and The Kansas City Times.