Skip to main content

Patient with melanoma receives tumor-infiltrating lymphocyte therapy

Submitted by vicc_news on

Vanderbilt-Ingram Cancer Center has treated its first patient in a newly launched therapy program that magnifies the power of a person’s natural defense system against tumors. 

Tumor-infiltrating lymphocyte (TIL) therapy involves isolating the white blood cells from a tumor after it is surgically removed, expanding the magnitude of those cells in a laboratory, and then infusing them back into the patient to elicit a more powerful counterattack. The highly personalized treatment is currently approved for patients with advanced stages of melanoma whose tumors have grown despite immunotherapies and/or targeted therapies. 

The patient who received the therapy in late January has melanoma that has spread to the bone, abdomen, liver and brain despite multiple lines of other treatments. A team of clinicians harvested white blood cells from a tumor in the patient’s liver, then shipped them to a laboratory where they were supercharged before being infused back into the patient, who is being monitored. Additional patients are scheduled to receive TIL therapy. Vanderbilt-Ingram launched the program as a standard of care service line after previously treating patients with TIL therapy in clinical trials. 

“The mission of Vanderbilt Health is to get treatments that are cutting-edge to the patients who need them the most,” said Olalekan Oluwole, MBBS, MPH, associate professor of Medicine and a hematologist who specializes in cellular therapies. “Some of these patients have exhausted prior standard of care options.” 

About a third of patients who receive TIL therapy respond to it. 

“On the surface that doesn’t sound like a lot, but the great thing about TIL therapy is when it does work, it can lead to long-term durable response. It can keep right on working for years or even indefinitely,” said Douglas Johnson, MD, MSCI, professor of Medicine and clinical director of melanoma, who holds the Susan and Luke Simons Directorship. 

Establishing the TIL program required assembling a team of multidisciplinary clinicians trained to handle the care needs of patients while simultaneously handling the logistics of getting their white blood cells shipped to a laboratory. 

Sarah Moseley, BSN, RN, the coordinator for immune effector cell and gene therapy patient care, led that process. She described the process of navigating care for patients who receive TIL therapy, which involves surgeons, oncologists, hematologists and specialized nurses. 

“I am with the patient from start to finish,” Moseley said. “Once a patient is identified by Dr. Johnson, he immediately gets me involved. The patient has to be approved by our cell therapy team and our surgery team as well as Dr. Johnson to make sure that they’re a good candidate. The next step is the insurance process, which is probably the hardest part because this is a new and expensive therapy. It is a detailed process involving our financial team, our managed care team and us nurses as well.” 

The nurses serving as patient care coordinators also include Leslie Mader, BSN, RN, OCN, and Brittney Baer, BSN, RN.  

“I or one of my nurse colleagues go to the surgery, and we transport the specimen from the operating room to the processing lab, where a courier picks it up,” Moseley said. “Without the specimen, there is no product for the therapy. It has to be done quickly, and it must be done right every time. Then we get the patients set up for cell infusion after about five to six weeks.” 

The launch of the TIL program is the latest achievement in cellular therapies for Vanderbilt-Ingram, which is an international leader in the field. The cancer center offered clinical trials for therapies, which became standards of care, most notably CAR-T, which is shorthand for chimeric antigen receptor T-cell therapy. Vanderbilt-Ingram established an outpatient protocol for patients to receive CAR-T and treats more patients with this immunotherapy than any other provider in the state. It is offering clinical trials to expand the treatment for additional types of cancer and to make it more easily accessible to patients. 

“The launch of our TIL program represents a natural and important evolution of Vanderbilt-Ingram’s leadership in cellular therapy,” said Ben Ho Park, MD, PhD, the Benjamin F. Byrd Jr. Professor of Oncology, professor of Medicine and director of Vanderbilt-Ingram Cancer Center. “Building on the infrastructure, clinical expertise and multidisciplinary coordination established through our CAR-T program, we are now able to offer another highly personalized immunotherapy to patients with otherwise limited options. Our goal is not only to deliver these complex therapies safely and effectively, but also to continue advancing the science so that more patients, across more cancer types, can benefit in the years ahead.” 

Clinicians with the cellular therapy team built the TIL program on the foundation of the CAR-T program. However, there are major differences between these treatment modalities. With CAR-T, immune cells are reengineered to attack cancer from the T cells in a patient’s blood. With TIL therapy, white blood cells are taken from a patient’s tumor and are then multiplied so they can stage a better counterattack against cancer. 

Currently, CAR-T is approved by the Food and Drug Administration only for certain blood cancers. TIL therapy is approved only for advanced melanoma when patients have not responded to other treatments. However, clinical trials are underway to expand the therapies for other types of cancers.  

The post Patient with melanoma receives tumor-infiltrating lymphocyte therapy appeared first on Vanderbilt Health News.

Vanderbilt-Ingram researchers present cancer advancements at ASH 2025 

Submitted by vicc_news on

Researchers from Vanderbilt-Ingram Cancer Center will present findings from clinical trials, laboratory discoveries and innovations in caring for patients with hematologic cancers and other blood diseases at ASH 2025 in Orlando, Florida, Dec. 6-9. 

ASH 2025 is the American Society of Hematology Annual Meeting and Exposition. Established in 1958, ASH is the world’s largest professional organization for clinicians and scientists who study blood diseases.  

Three of the presentations from Vanderbilt-Ingram researchers will focus on chimeric antigen receptor T-cell (CAR-T) therapies, a form of immunotherapy that involves treating cancer with white blood cells that have been reengineered to attack cancer cells. Vanderbilt-Ingram is an international leader in advancing the efficacy of and expanding access to CAR-T therapies.

Olalekan Oluwole, MBBS, MPH, associate professor of Medicine, who leads the cellular therapy research program at Vanderbilt-Ingram, will present data on health care resource utilizations of the therapies in U.S. patients treated at newly authorized treatment centers. He will also provide an overview of outcomes for inpatient and outpatient CAR-T treatment. Grace Mercadante, MD, will present data on the impact of clonal hematopoiesis on CAR-T therapy. 

Michael DeBaun, MD, MPH, the J.C. Peterson, MD, Professor of Pediatrics and founder and director of the Vanderbilt-Meharry Sickle Cell Disease Center of Excellence, will speak at a special session focusing on ASH’s sickle cell disease initiative. He will present findings from “Sickle Cell Trait Does Not Cause ‘Sickle Cell Crisis’ Leading to Exertion Related Death: A Systematic Review.” 

Other topics researchers will address include acute myeloid leukemia, myelodysplastic syndrome, drug resistance, potential adverse reactions and risk comparisons of treatments, pediatric blood disorders, multiple myeloma, bispecific antibody treatment, and graft-versus-host disease. 

A complete list of presentations from Vanderbilt researchers follows: 

Sally Momoh, MD – Sex-related differences in silent cerebral infarction burden among adults with sickle cell disease 

Jamila Mammadova, MD – Behind the blood-brain barrier: Contemporary screening practice patterns and trends of central nervous system involvement in acute myeloid leukemia treated with intensive regimens and hypomethylating agent/venetoclax 

Alyssa Jarabek – Impact of innate immune memory on myelodysplastic syndrome progression by TET2-driven inflammation 

Raymond Zhang – VISTA contributes to disease progression in high-risk myelodysplastic syndrome 

Mattew Villaume, MD, PhD – EB2023 primes mitochondria for BCL2 dependence and induces pyroptotic cell death via AMPK signaling and the unfolding protein response 

Grace Mercadante, MD – The impact of clonal hematopoiesis on CAR-T cell therapy outcomes: a single-center analysis 

Ghadeer Dawwas, PhD, MSc, MBA – Risk of serious bleeding with concomitant use of apixaban or rivaroxaban with amiodarone compared to flecainide or sotalol in patients with atrial fibrillation  

Olalekan Oluwole, MBBS, MPH – Real-world health care utilization following CAR-T cell therapy in U.S. patients treated in newly authorized treatment centers 

Erin Christensen, MS, DO – A case series of pediatric patients with congenital thrombotic thrombocytopenia purpura treated with recombinant ADAMTS13 

Andrew Jallouk, MD, PhD – Real-world outcomes of mosunetuzumab use in indolent and aggressive lymphomas  

Bhagirathbhai Dholaria, MBBS – Characterization of a population with newly diagnosed standard risk multiple myeloma by 2025 ims/IMWG definition with exceptional long-term outcomes after fixed duration therapy 

Y. Emily Chu – The acute myeloid leukemia microenvironment is defined by ineffective immune surveillance despite the presence of activated, clonally-expanded CD8 T cells with preserved effector function 

Michael DeBaun, MD, MPH – Findings from “Sickle cell trait does not cause ‘sickle cell crisis’ leading to exertion related death: a systematic review ”

Mattew Villaume, MD, PhD – F1 subunit-specific ATP synthase inhibition disrupts AML mitochondrial metabolism distinctly from other electron transport chain inhibitors 

Lauren Klein, MD, – Early weight gain predicts nutritional recovery in children with sickle cell anemia and severe acute malnutrition in Nigeria 

Olalekan Oluwole, MBBS, MPH – U.S. cost consequence and time toxicity model for advanced therapies in the treatment for relapsed/refractory third-line or later diffuse large B-cell lymphoma: a comparison of axicabtagene ciloleucel with bispecific antibodies 

Olalekan Oluwole, MBBS, MPH – Outcomes of inpatient and outpatient CAR-T in newly authorized treatment centers in the United States 

Elizabeth Pollard, MD – Leukapheresis for acute leukemia with hyperleukocytosis: line complications, resource utilization, and early mortality outcomes 

Carrie Kitko, MD – Long-term treatment duration and safety of axatilimab among patients with chronic graft-versus-host disease in AGAVE-201 

The post Vanderbilt-Ingram researchers present cancer advancements at ASH 2025  appeared first on VUMC News.

Subscribe to Olalekan_Oluwole