From a surgical point of view, the complexity of patient diseases at Memorial Sloan-Kettering is unmatched. At most institutions, it is impossible for a cancer surgeon to be able to concentrate on just a few diseases and do a high volume of procedures. In a very short time, I gained a vast amount of surgical experience, particularly with liver and pancreas cancer. Our group does more than 250 liver resections and 150 pancreatic resections a year, which makes us an international leader. Doing liver and pancreas surgery is very challenging because both organs are surrounded by major blood vessels. However, the techniques pioneered and improved at the Center help keep the operative risk quite low.
I think the next advance for oncological surgery will be finding ways to improve outcomes by integrating surgery with other treatments. This includes, for example, new radiation techniques, such as intraoperative radiation, which allows treatment to be delivered to patients while they are still in the operating room so they don't need weeks of radiation following surgery. It also includes new chemotherapy drugs that selectively target cancer cells by taking advantage of molecular differences between these cells and normal cells. For example, we've had a landmark success with a targeted molecular therapy called imatinib (Gleevec®) in a large, nationwide clinical trial sponsored by the National Cancer Institute. Patients who received Gleevec following surgery for a rare cancer called a gastrointestinal stromal tumor (GIST) were less likely to have a recurrence of their cancer compared with those who didn't receive it. In 2000, when Gleevec was first applied to GIST, I was working with Murray Brennan [former Chair of Memorial Sloan-Kettering's Department of Surgery] to develop the national trial. Eight years later, we have changed the standard of care in GIST. We're hoping there will be more agents like Gleevec down the road for pancreas and liver cancer.
In addition to surgery, I conduct laboratory research. I learned the basics of immunology research during my residency at Penn and continued gaining expertise in the field after coming to Memorial Sloan-Kettering. Now I conduct research on dendritic cells, which are the master regulators of the immune system throughout the body and which have the potential to generate a strong immune response against cancer. Specifically, we're focusing on the behavior of dendritic cells and other immune cells within the liver. The liver is the most common site for metastatic disease. What could be the reason for this? By analyzing tissue specimens from surgical patients, we found that the dendritic cells within the liver are actually weaker than dendritic cells elsewhere in the same patient.
This discovery has implications for developing therapies that induce dendritic cells to be more active. We've been exploring such therapies in mouse models, and eventually, in collaboration with the Immunology Program at Memorial Sloan-Kettering, we hope to move to human clinical studies.