Michael W. Young, a biologist who studies the genetic regulation of biological clocks, accepted the Nobel medal and diploma today from King Carl XVI Gustaf of Sweden. Young was announced as a recipient of the 2017 Nobel Prize in Physiology or Medicine, along with Jeffrey C. Hall and Michael Rosbash of Brandeis University, in October.
The Nobel Prize Award Ceremony took place at the Stockholm Concert Hall in Sweden. The awards are presented annually on December 10, the anniversary of Alfred Nobel’s death. As part of Nobel Week leading up the ceremony, Young delivered the Nobel Lecture in Physiology or Medicine Wednesday at the Karolinska Institute.
Young, who is the Richard and Jeanne Fisher Professor and head of the Laboratory of Genetics, was honored for his discoveries of molecular mechanisms controlling the circadian rhythm. He used genetics to identify gene mutations that disrupt the ability of the fruit fly Drosophila melanogaster to appropriately modulate its internal clock in response to a changing environment, and went on to define their biochemical mechanisms. His work has direct implications for understanding human sleep disorders, the mechanisms of jet lag, and the challenges of working on the night shift.
Newswise - PHILADELPHIA - Two investigational immunotherapy approaches, including chimeric antigen receptor (CAR) T cell therapy, have shown encouraging results in the treatment of multiple myeloma patients who had relapsed and were resistant to other therapies. Researchers from the University of Pennsylvania's Abramson Cancer Center administered CAR T cells to patients following chemotherapy, with 64 percent of patients responding in a clinical trial. In a separate study, patients got an infusion of an experimental monoclonal antibody, which resulted in an overall response rate of 60 percent. Both of these investigational approaches targeted a receptor called B-Cell Maturation Antigen (BCMA), which is highly expressed in myeloma and thus a promising target for treatment. These studies will be presented as oral abstracts at the 59th Annual American Society of Hematology Meeting and Exposition in Atlanta.
Multiple myeloma (MM) is a bone marrow cancer that affects plasma cells. Normal plasma cells work as part of the immune system, but in MM these cells become cancerous and grow out of control, leading to multiple painful bone tumors, as well as anemia, kidney failure and recurrent infections. The American Cancer Society estimated there will be more than 30,200 new cases of MM in 2017. Standard treatments include chemotherapy and radiation and can include a stem cell transplant.
The first study (Abstract #505) used CART-BCMA, a specifically engineered type of CAR T cell developed by Penn researchers in collaboration with Novartis as part of a global research and development alliance that began in 2012. The investigational treatment modifies patients' own immune T cells, which are collected and reprogrammed to seek and destroy the patients' cancer cells. After being infused back into patients' bodies, these newly built "hunter" cells both multiply and attack, targeting cells that express BCMA. Patients were given a single dose of chemotherapy before the CART-BCMA infusion to temporarily clear out normal white blood cells and help the hunter cells to expand. Two dose levels of CART-BCMA cells were explored in a population of heavily-pretreated patients. These patients had a median of seven prior lines of therapy.
In the clinical trial, the lower dosage group had five patients, two of whom (40 percent) achieved at least a minor response to the treatment (defined as 25 percent or greater reduction in myeloma protein levels). The higher dosage group had ten patients, and eight of those (80 percent) had a minor response or better, including one complete response. The trial is ongoing, with additional patients being treated at the higher dose group.
Twelve of the 15 patients experienced cytokine-release syndrome, a toxicity that involves varying degrees of flu-like symptoms, with high fevers, nausea, and muscle pain, and can require ICU-level care. All patients recovered, with one requiring tocilizumab, a standard therapy for this side effect, and one receiving siltuximab, a similar cytokine-blocking drug.
Three of the patients in the study experienced neurotoxicity, which resolved on its own. There were no treatment-related deaths.
"This follows up on our previous report that showed that six out of nine patients had clinical benefit to CART-BCMA given alone, without chemotherapy" said the study's lead author Adam D. Cohen, MD, an assistant professor of Hematology and Oncology at Penn and the director of Myeloma Immunotherapy in Penn's Abramson Cancer Center. "All of these data indicate BCMA is an attractive target in refractory myeloma, and our hope is that combining the CAR T cells with chemotherapy will increase the expansion and persistence of the CAR T cells, though longer follow-up is needed to assess this."Ting and his team have performed more than 350 transgender surgeries since March 2016. More recently, they created a fellowship program to help train surgeons in the field. Along the way, Ting has helped pioneer new surgical procedures and techniques. That, he tells us, makes his work exciting and sometimes a little scary: “It’s a unique opportunity to be doing a specialty that is so underdeveloped, to be entering the field really in its infancy.”
Michael C. Milone, MD, PhD, an associate professor of Pathology and Laboratory Medicine at Penn, was the study's senior author. The study was supported by the Penn-Novartis alliance.
Cohen is the senior author on a second study also targeting BCMA in MM (Abstract #741), in this case with an experimental drug called GSK2857916, for which the FDA granted a breakthrough therapy designation in early November to allow for expedited development. It links a chemotherapy drug called MMAF to a monoclonal antibody against BCMA, allowing for targeted delivery of the chemotherapy directly to the myeloma cancer cells in the bone marrow. In this first-in-human, multi-center trial, patients received an infusion every three weeks for up to 16 treatment cycles. The overall response rate was 60 percent (21 out of 35 patients), including 51 percent with very good partial responses - meaning more than a 90 percent reduction in myeloma protein levels. The median progression-free survival was about eight months.
"Response rates that high are really unprecedented for a single agent in relapsed, refractory disease" Cohen said. "It's especially important to this patient population, since they are heavily pre-treated and have limited options for treatment."
Cohen noted 57 percent of patients in this trial had undergone five prior lines of therapy or more.
There was significant eye toxicity associated with this treatment, including dry eye, blurry vision, and light sensitivity in 63 percent of patients. Cohen said these effects were caused by the chemotherapy portion of the drug. They were mild in most patients and improved with eye drops. These patients held treatment and restarted at a lower dose once the toxicity resolved.
Cohen says Penn will continue research related to this compound. There is a larger study planned around the treatment, as well as a study evaluating this drug in combination with other therapies.
This study was supported by GlaxoSmithKline, which is developing GSK2857916.
Editor's Note: The University of Pennsylvania has licensed some technologies involved in these studies to Novartis. Some of the scientists involved in these trials are inventors of these technologies. As a result of the licensing relationship with Novartis, the University of Pennsylvania receives significant financial benefit, and some of these inventors have benefitted financially and/or may benefit financially in the future. Cohen has received consulting honorarium from GlaxoSmithKline.
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