First chimeric antigen receptor (CAR) T cell therapy targeting B cell-activating factor receptor (BAFF-R) eradicates blood cancers that relapsed after CD19 CAR T therapiesSeptember 25, 2019
City of Hope’s research on the new CAR T, published in Science Translational Medicine, offers hope for patients who have relapsed after commercially available CD19 immunotherapy treatments
DUARTE, Calif. — The first CAR T cell therapy targeting the B cell-activating factor receptor on cancerous cells eradicated CD19-targeted therapy-resistant human leukemia and lymphoma cells in animal models, according to City of Hope research published today in Science Translational Medicine. The new therapy will be used in a clinical trial next year for patients who relapsed after CD19 immunotherapy treatments and may potentially be used as a first-line of CAR T cell therapy treatment.
An estimated 20 to 30% of leukemia and lymphoma patients who achieve remission after receiving CD19 CAR T therapy will relapse after a few years. The effectiveness of those CAR T cells, which target the CD19 protein on cancerous B cells, starts to wear off and the cancer returns.
But there new hope for those patients who relapse after receiving axicabtagene ciloleucel (commercial name: Yescarta) or tisagenlecleucel (commercial name: Kymriah), the Food and Drug Administration-approved CD19 CAR T cell therapies, as well as another type of CD19-targeted immunotherapy, blinatumomab (commercial name: Blincyto).
“One major obstacle to current CAR T therapy is that in up to a third of these patients, the tumor is actually smart and comes back because it has learned how to no longer express the target that’s recognized by the original immunotherapy,” said Larry Kwak, M.D., Ph.D., vice president and deputy director of City of Hope’s comprehensive cancer center and the study’s principal author, who leads the research with Hong Qin, Ph.D., a research professor in City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation. “To combat that, City of Hope research has found a new, and potentially more effective, target for CAR T cell therapy against B cell leukemias and lymphomas. We plan to open a clinical trial next year using the BAFF-R CAR T cell therapy.”
“This new treatment could change the face of leukemia and lymphoma treatment in the U.S. and worldwide,” added Kwak, the Dr. Michael Friedman Professor in Translational Medicine.
CAR T cell therapy involves taking a patient’s T cells from the bloodstream. The immune cells are then genetically engineered in a laboratory to recognize and attack a specific cancer-associated protein, such as BAFF-R, and reintroduced into the patient’s bloodstream, where they get to work destroying tumor cells.
For this study, animal models with CD19 therapy-resistant human-tumors (including Burkitt, mantel cell, and other non-Hodgkin’s lymphoma subtypes and acute lymphoblastic leukemia) received BAFF-R CAR T therapy. Remarkable tumor regression and prolonged survival were observed after treatment with these CAR T cells. In animal models with human Burkitt lymphoma, BAFF-R CAR T therapy achieved complete tumor regression with 100% long-term survival.
For another part of the study, the animal models had a mixed population of CD19-positive and negative human tumors. They then received either CD19 CAR T cell therapy or BAFF-R CAR T cell therapy; the BAFF-R CAR T cells were able to eradicate both tumor populations while treatment failed in those receiving CD19 CAR T cells.
Tumor samples from patients who relapsed after receiving CD19-targeted immunotherapy (blinatumomab) were also investigated. The study demonstrated that BAFF-R CAR T cells were consistently active against these tumors, whereas CD19 CAR T cells had greatly diminished responses to each patient’s relapse tumor compared to the pre-therapy samples.
“We did a head-to-head comparison of two new therapies, and our data showed that our BAFF-R CAR T therapy actually did a better job than FDA-approved CD19 CAR T therapies,” Qin said. “If these results continue, we will pursue BAFF-R CAR T therapy as a kind of frontline CAR T therapy treatment for lymphoma and leukemia patients.”
City of Hope plans to open a clinical trial next year using the BAFF-R CAR T cell therapy for B cell leukemia and lymphoma patients who have relapsed after receiving CD19 CAR T cell therapies or blinatumomab.
When the BAFF-R CAR T trial opens, City of Hope will manufacture the CAR T cells using in its own facility, the Cellular Therapy Production Center. This process includes a critical step: collecting patients’ T cells and genetically engineering the T cells with viruses also produced at a City of Hope GMP facility, the Center for Biomedicine & Genetics. These two facilities, coupled with the Chemical GMP Synthesis Facility, make City of Hope one of the few cancer centers in the world with the ability to produce GMP cellular, genetic and drug-based therapies for its patients.
City of Hope licensed the BAFF-R CAR T to PeproMene Bio Inc.
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About City of Hope
City of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin and numerous breakthrough cancer drugs are based on technology developed at the institution. A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is the highest ranked cancer hospital in the West, according to U.S. News & World Report’s Best Hospitals: Specialty Ranking. Its main campus is located near Los Angeles, with additional locations throughout Southern California. For more information about City of Hope, follow us on Facebook, Twitter, YouTube or Instagram.