The U.S. Food and Drug Administration (FDA) has expanded approval for a personalized cellular therapy developed at the University of Pennsylvania’s Abramson Cancer Center, this time for the treatment of adult patients with relapsed or refractory large B-Cell lymphoma after two or more lines of systemic therapy. Today’s approval includes treatment of diffuse large B-cell lymphoma (DLBCL) – the most common form of non-Hodgkin’s lymphoma – as well as high grade B-cell lymphoma and DLBCL arising from follicular lymphoma. The approval was granted today to Novartis for the chimeric antigen receptor (CAR) T-cell therapy Kymriah® (tisagenlecleucel, formerly CTL019), making it the second indication for the nation’s first personalized cellular therapy for cancer.
DLBCL affects approximately 30 percent of patients with NHL, and there are an estimated 27,000 newly diagnosed cases of DLBCL in the U.S. each year. About 6,500 of those patients have relapsed or refractory disease after two or more therapies and may now be eligible for Kymriah.
“This is an exciting event – seeing this lifesaving therapy become available widely to a large patient population with an unmet medical need,” said Stephen J. Schuster, MD, the Robert and Margarita Louis-Dreyfus Professor in Chronic Lymphocytic Leukemia and Lymphoma Clinical Care and Research and director of the Lymphoma Program at Penn’s Abramson Cancer Center. “Many lives may be saved.”
In August 2017, Kymriah became the first therapy based on gene transfer ever approved by the FDA, when it was authorized for children and young adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). The FDA’s action is the latest accomplishment in the alliance between Penn and Novartis, which entered into a global collaboration in 2012 to further research, develop, and commercialize Kymriah and other CAR T-cell therapies for the treatment of cancers.
Investigators at Penn’s Perelman School of Medicine, who led research, development, and clinical trials of CAR T therapy, in collaboration with Novartis, called today’s approval a massive step with potentially life-saving implications for patients.
Schuster led two studies examining CAR T therapy in DLBCL, including research published in the New England Journal of Medicine detailing long-term follow up of the first cohort of these patients treated with the therapy at Pennand the global, multi-center, Novartis-sponsored trial known as JULIET. At the 59th American Society of Hematology (ASH) annual meeting, the data presented from the JULIET trial showed an overall response of 53 percent, with 40 percent of patients achieving a complete response, among the 81 infused patients with three or more months of follow-up or earlier discontinuation. At six-month analysis, the median duration of response was not reached.
“We’re proud to have developed this therapy through all phases of development and clinical trials right here at Penn and in collaboration with Novartis,” said Carl June, MD, the Richard W. Vague Professor in Immunotherapy in the department of Pathology and Laboratory Medicine in the Perelman School of Medicine and director of the Center for Cellular Immunotherapies in the Abramson Cancer Center.
Kymriah will be available through a network of certified treatment centers throughout the United States, including the Hospital of the University of Pennsylvania.
The treatment modifies patients’ own immune T cells, which are collected and reprogrammed at the Novartis manufacturing facility to potentially seek and destroy the patients’ lymphoma cells. Once they are infused back into patients’ bodies, these newly built cells both multiply and attack, targeting cells that express a protein called CD19. Tests reveal the army of hunter cells can grow to more than 10,000 new cells for each single engineered cell patients receive – producing durable remission rates in refractory lymphoma –, and can survive in the body for years.
“Our collaboration with Penn has delivered Kymriah, a transformational therapy and first CAR-T to be approved, initially for pediatric and young adult patients with ALL and today for adult patients with DLBCL,” said Liz Barrett, CEO, Novartis Oncology. “We are grateful to Penn for their leadership and to the courageous patients who participated in the clinical trials that have advanced Kymriah to be one of the most exciting technologies ever developed to fight cancer.”
Kymriah was first tested at Penn in 2010 in adult patients with advanced chronic lymphocytic leukemia (CLL). The first DLBCL trial, including double hit lymphoma, follicular lymphoma, and mantle cell lymphoma, opened at Penn in February 2014.
Many patients in the DLBCL trials experienced a side effect called cytokine release syndrome (CRS). CRS is a toxicity associated with CAR T therapy, which includes varying degrees of flu-like symptoms, with fevers, nausea, and muscle pain, and can require ICU-level care. According to the data presented at ASH, 58 percent of patients in the DLBCL global study experienced CRS, including some who experienced moderate or severe toxicities. Twenty-one of those patients (26 percent) required treatment with tocilizumab, a therapy approved for CAR T cell-induced severe or life-threatening CRS, or corticosteroids. All of those patients recovered from their CRS. Other toxicities included infections (34 percent of patients), cytopenias or low blood count (36 percent), neurologic events (21 percent), febrile neutropenia (13 percent), and a metabolic abnormality called tumor lysis syndrome (one percent). All of the toxicities resolved on their own or with treatment, and there were no treatment-related deaths.
Novartis will create a registry to follow patients for 15 years after being treated to monitor their progress and any potential, future side effects.
The Novartis-Penn Center for Advanced Cellular Therapeutics (CACT) opened in 2016 and hosted Vice President Joe Biden at the launch of his Cancer Moonshot initiative, cementing Penn’s role as international innovator in the development and manufacturing of personalized cellular therapies.