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Yong-Chen William Lu, PhD, discusses a phase I dose-escalation study investigating the genetically engineered CD4 T cells' ability to target the MAGE-A3 protein.
Yong-Chen William Lu, PhD
Results of a phase I dose-escalation study—the first clinical trial testing an immunotherapy that uses genetically engineered CD4 T-cells, rather than CD8 T-cells—demonstrate that the treatment could have potential in all metastatic tumor types, according to Yong-Chen William Lu, PhD.
In an interview with OncLive, Lu, a fellow in the Surgery Branch of the National Cancer Institute, discusses a phase I dose-escalation study investigating the genetically engineered CD4 T cells' ability to target the MAGE-A3 protein, as well as the treatment's potential toxicities and currently ongoing responses in some patients still enrolled in the trial.Lu: I presented the first CD4 genetically modified T-cell therapy against cancer. In this study, which was a first-line trial, we used different doses for the dose escalation to test different doses for the cell. We had 8 patients on dose escalation and another 6 patients on the highest dose, and for that we found 3 patients who responded to all therapy. One patient is a patient with cervical cancer, 1 patient with esophageal cancer, and another one with urothelial cancer. Those 3 patients are still showing an ongoing response and are doing well.
For this trial, we have 2 major questions. The first question is to test whether the CD4 T cell has the response to the cancer in most therapies, similar to CD8 T-cell therapy. The second question we wanted to ask is volume, because currently the cancer immunotherapy regimen has been to target melanoma, lymphoma, leukemia, and renal cell carcinoma, but the rest of the majority of cancers and those patients did not receive the benefit from that.
What is the mechanism of action for this drug?
What was the safety profile?
This trial tests the hypothesis that T-cell therapy can be applied to any type of cancer. We have been treating patients with melanoma, breast cancer, and cervical cancer. You could potentially apply this to many different types of cancer.Our major focus is in the phase II study. For the phase I study, we were confirming that this trial is safe and that we can use the higher dose to do that. In the phase II study, we are going to initially treat 20 patients, then up to 40 patients, for different cancer types. Our major focus will be in melanoma, cervical cancer, esophageal cancer, and urothelial cancer. Hopefully we will understand the effectiveness of this T cell therapy against different types of cancer.It's a very important, but very difficult question, because as we mentioned this is the first CD4 T cell therapy. We know very little about it. So far what we know is that the CD4 T cell is doing the job of helping the CD8 T cell. Other than that, we don't know much. We definitely have lots of work to do, both in humans and maybe mice studies. We hope that this trial will stimulate scientists to know more about the CD4 T cell and do more basic research toward the question.Thus far, the toxicities have been very mild. It's the same as all the other T-cell therapies; we have to use chemotherapy to clean out all the T cells that are in the patients, and that will create a space for our modified T cells to expand within the patient. Unfortunately, that is the same as other chemotherapies where you get the same side effects as a chemotherapy regimen.
What are some of the biggest questions that you hope to answer?
Other than that, most of the responses have been very mild. The only ones that happened for this particular trial is that 12 of the 14 patients experienced high fever for around 1 to 2 weeks, and that might be the worst thing. This is because, as we all know, the immune system needs to be stimulated to fight the cancer cells. It's the same when we have the flu—we might have a fever to fight the disease. Other than that, we haven't seen much toxicities. Only 1 patient at the end of this trial had acute fever and renal injury, but that might have been from a patient-specific issue because we didn't see that in other patients. We couldn't figure out the cause of that, but other than that it's been very safe.The first question is the whether the CD4 T cell is useful or not, as we mentioned, and the second question is whether we can apply this treatment to different types of cancers. Lastly—and it's our great hope as scientists—we want to apply this therapy to the general population. We hope after the successful phase I study, everything goes well for the phase II and phase III and so on, and we hope people receive the benefit of our cancer research.