Dr. Matthias Gromeier is a Professor in the Department of Neurosurgery at Duke University Medical Center, [1] [2] who has developed a way to re-engineer a poliovirus to inspire the human immune system to kill cancer cells in a specific set of cancers. The re-engineered virus, called PVSRIPO, cannot replicate itself in normal cells, but can replicate itself in cancer cells that have an overabundance of the protein marker that the poliovirus targets. [3]
PVSRIPO, which Gromeier engineered himself as a postdoc in the 1990s [4] is thought to induce an anti-tumor immune response against the tumor. Phase I trials in glioblastoma (GBM, one of the most deadly brain cancers) results have been very promising. The traditional treatment against GBM, surgical resection followed by chemo usually gives rise to only a 12-month survival in patients; some patients treated with PVSRIPO are still alive, symptomless, 3.5 years after treatment. Only the worst cases of GBM that did not respond to any other treatments were enrolled in the trial. The lab is now testing the virus in other tumors, including breast, pancreas, and many others.
Other research has experimented with cancer treatments using viruses including HIV, smallpox, and measles. However, Dr. Gromeier noted that polio was the most ideal choice due to its ability to seep out and attach itself to a receptor that is found on the surface of the cells that make up nearly every kind of solid tumor. As Gromeier noted, "It’s almost as if polio had evolved for the purpose". [3] Gromeier re-engineered the polio virus by removing a key genetic sequence. The virus can't survive this way, so he repaired the damaged with a harmless bit of cold virus. The new, modified virus, could no longer cause paralysis or death because it couldn't reproduce in normal cells. However, in a cancerous environment, this is still possible. In the process of replicating, the virus releases toxins that poison the cells, indicating cancer cells could be killed. Gromeier performed seven years of safety studies, which included tests on 39 monkeys, to show that the virus does not, in fact, cause polio. In 2011, the FDA approved a trial in humans.
Due in part to Dr. Gromeier's work, more than ten drugs that trigger the immune system have been approved, and they are significantly extending the lives of patients with cancers, including lung cancer and melanoma.
Gromeier was born in Germany. During Gromeier's compulsory military service, prior to attending university, he worked at a large breast-cancer center. Says Gromeier, "Breast cancer, back then especially, was a losing battle... It wouldn’t fulfill my life to prescribe chemotherapy so patients suffered and it didn’t work." [4] Gromeier originally intended to study HIV. In the late 1980s, protease inhibitors were not yet saving lives, and the disease was still considered a death sentence. However, in a twist of fate, Gromeier was unable to find a physician with an HIV lab who would welcome him as a student. On the subject, Gromeier notes “The only lab that would take me was a tired, not very successful polio lab.” [4] He earned his medical degree from the University of Hamburg in 1992, [5] with the intentions of becoming a leading cancer researcher. [4]
After medical school, Gromeier completed a postdoctoral fellowship at New York’s Stony Brook University from 1993 to 1996, [5] as well as a postdoctoral associate position from 1996 to 1999. [5] There he worked in the lab of Eckard Wimmer, one of the world’s leading virologists and a polio specialist. Gromeier spent much of this time studying polio pathogenesis, which is how the virus causes the infectious disease associated with iron lungs and Franklin D. Roosevelt. Although a polio vaccine was developed in the 1950s that nearly ended the disease, it still exists in a handful of developing countries.
While at Stony Brook, in 1993, Gromeier engineered the virus he’d later use in the Duke cancer trials, swapping out a critical part of the structure with the equivalent part of the human rhinovirus, which causes the common cold. Gromeier also studied receptors, proteins on the surface of cells that viruses evolve to recognize. Gromeier discovered that the poliovirus binds to a receptor called CD155, which is found on many solid tumor cells. Through a succession of experiments, starting in the mid-’90s, Gromeier concluded that the modified poliovirus could potentially target cancer. “This was an ignorance-is-bliss type situation,” he says. “I didn’t have preconceived notions of what cancer was and how to fight it. Sometimes for researchers, if you’re very, very well read, very exposed to current opinion, it can mean that you’re biased and have a closed mind.” [4]
Gromeier's early thinking focused on what he now calls a “simple paradigm”: the ability of his modified poliovirus to infect and kill tumor cells. “That’s relatively rare,” he says. “Viruses have evolved over millennia to do certain things, and killing tumors is not generally part of their natural program.” [4]
In 1999, Gromeier accepted a position in the Department of Neurosurgery at the Duke University Medical Center, to which he was drawn in large part by the strength of its brain-tumor research. He had always seen brain cancer as a prospective target for his work. “Poliovirus is the virus that’s most capable of causing the most damage in the brain,” he says. It invades the central nervous system and can paralyze the muscles we need to walk, swallow, and even breathe. “It may sound counterintuitive,” he says, “but I saw this as a sign that it might be a good agent to be used in the brain.” [4] Gromeier currently serves as Professor of Neurosurgery, a Professor in Molecular Genetics and Microbiology, a Professor in Medicine, and a Member of the Duke Cancer Institute. [5]
In 2011, 20-year-old nursing student Stephanie Lipscomb was diagnosed with glioblastoma, as doctors found a tennis-ball-sized tumor in her brain. After unsuccessful attempts at radiation and chemotherapy, 98% of Lipscomb's tumor was surgically removed However, her glioblastoma diagnosis returned in 2012. With recurrent glioblastoma, Lipscomb became the first patient in Gromeier's phase 1 clinical trial in May 2012. After an MRI revealed that the tumor had inflamed in October, indicating that the immune system had awakened and had begun to fight the cancerous cells, Lipscomb became the first successful patient in the trial.
Doctors have concluded that the polio virus initiates the killing, but the immune system possesses sole responsibility, once activated. Upon her enrollment in the trial, Lipscomb's tumor shrank consistently for 21 months, until it eventually disappeared completely. She is cancer-free; the only thing that remains is a hole, an artifact of early surgery.
With the early success, the team raised the dose in the next few patients in hope of an even better result. Donna Clegg, a 60-year-old social worker from Idaho, was the 14th patient in the trial (also facing a glioblastoma diagnosis). In an attempt to hasten the eradication of glioblastoma tumors, doctors opted to use Clegg to test an increased dose. Clegg's polio infusion was three times more potent than the one that worked for Lipscomb. In Clegg, doctors saw the expected inflammation as her immune system attacked the tumor. But the higher dose caused an immune response that was much too powerful: the inflammation put so much pressure on her brain, she became partially paralyzed. This caused Clegg to drop out of the trial.
As of March 2015, there had been 22 patients in the polio trial: 11 died, with 6 of those having been served the higher dose. The other 11 continued to improve: four were in remission.
When asked about the first two patients in the trial, Dr. Darell Bigner, head of the study and of Duke's brain tumor center, provided, “Oh absolutely...[it’s fair to say they are] in remission and I think they would tell you that they consider themselves normal again...I’m very reluctant to use the ‘cure’ word...because we don't know how long it takes to say that a glioblastoma has been cured, but I am beginning to think about it”. [3]
Dr. Gromeier, the creator of the virus, has been testing this therapy against a number of other cancers in a laboratory setting. Similar studies have been (or are imminently being) done for lung cancers, breast cancers, colorectal cancers, prostate cancers, pancreatic cancers, liver cancers, and renal cancers.
In May 2016, Gromier's therapy was granted "breakthrough therapy designation" by the Food and Drug Administration, indicating that the treatment may offer a substantial improvement over available standard therapy. [6]
A brain tumor occurs when abnormal cells form within the brain. There are two main types of tumors: malignant tumors and benign (non-cancerous) tumors. These can be further classified as primary tumors, which start within the brain, and secondary tumors, which most commonly have spread from tumors located outside the brain, known as brain metastasis tumors. All types of brain tumors may produce symptoms that vary depending on the size of the tumor and the part of the brain that is involved. Where symptoms exist, they may include headaches, seizures, problems with vision, vomiting and mental changes. Other symptoms may include difficulty walking, speaking, with sensations, or unconsciousness.
Polio vaccines are vaccines used to prevent poliomyelitis (polio). Two types are used: an inactivated poliovirus given by injection (IPV) and a weakened poliovirus given by mouth (OPV). The World Health Organization (WHO) recommends all children be fully vaccinated against polio. The two vaccines have eliminated polio from most of the world, and reduced the number of cases reported each year from an estimated 350,000 in 1988 to 33 in 2018.
Glioblastoma, previously known as glioblastoma multiforme (GBM), is the most aggressive and most common type of cancer that originates in the brain, and has very poor prognosis for survival. Initial signs and symptoms of glioblastoma are nonspecific. They may include headaches, personality changes, nausea, and symptoms similar to those of a stroke. Symptoms often worsen rapidly and may progress to unconsciousness.
An oncolytic virus is a virus that preferentially infects and kills cancer cells. As the infected cancer cells are destroyed by oncolysis, they release new infectious virus particles or virions to help destroy the remaining tumour. Oncolytic viruses are thought not only to cause direct destruction of the tumour cells, but also to stimulate host anti-tumour immune system responses. Oncolytic viruses also have the ability to affect the tumor micro-environment in multiples ways.
Virotherapy is a treatment using biotechnology to convert viruses into therapeutic agents by reprogramming viruses to treat diseases. There are three main branches of virotherapy: anti-cancer oncolytic viruses, viral vectors for gene therapy and viral immunotherapy. These branches use three different types of treatment methods: gene overexpression, gene knockout, and suicide gene delivery. Gene overexpression adds genetic sequences that compensate for low to zero levels of needed gene expression. Gene knockout uses RNA methods to silence or reduce expression of disease-causing genes. Suicide gene delivery introduces genetic sequences that induce an apoptotic response in cells, usually to kill cancerous growths. In a slightly different context, virotherapy can also refer more broadly to the use of viruses to treat certain medical conditions by killing pathogens.
Northwest Biotherapeutics is a development-stage American pharmaceutical company headquartered in Maryland that focuses on developing immunotherapies against different types of cancer. It was founded in 1996 by Alton L. Boynton.
A radiosensitizer is an agent that makes tumor cells more sensitive to radiation therapy. It is sometimes also known as a radiation sensitizer or radio-enhancer.
The Duke Cancer Institute (DCI) is a National Cancer Institute-designated Comprehensive Cancer Center, research facility, and hospital. Founded in 1971, the center is part of the Duke University School of Medicine and Duke University Health System located in Durham, North Carolina, United States.
Plus Therapeutics, Inc. is a clinical-stage pharmaceutical company developing innovative, targeted radiotherapeutics for adults and children with rare and difficult-to-treat cancers. The company is headquartered in Austin, Texas, United States.
Temozolomide (TMZ), sold under the brand name Temodar among others, is a medication used to treat brain tumors such as glioblastoma and anaplastic astrocytoma. It is taken by mouth or via intravenous infusion.
Vocimagene amiretrorepvec/flucytosine is an experimental combination drug involving a gene therapy agent and a prodrug. It is a candidate drug to treat brain cancers.
Alternating electric field therapy, sometimes called tumor treating fields (TTFields), is a type of electromagnetic field therapy using low-intensity, intermediate frequency electrical fields to treat cancer. A TTField-generating device manufactured by the Israeli company Novocure is approved in the United States and Europe for the treatment of newly diagnosed and recurrent glioblastoma multiforme (GBM), and is undergoing clinical trials for several other tumor types. Despite earning regulatory approval, the efficacy of this technology remains controversial among medical experts.
The Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine is a cancer treatment, research and education institution with six locations in the St. Louis area. Siteman is the only cancer center in Missouri and within 240 miles of St. Louis to be designated a Comprehensive Cancer Center by the National Cancer Institute (NCI). Siteman is also the only area member of the National Comprehensive Cancer Network, a nonprofit alliance of 32 cancer centers dedicated to improving the quality and effectiveness of cancer care.
PVSRIPO, or PVS-RIPO, is the name of a modified polio virus that has recently shown promise for treating cancer. It is the focus of clinical trials being conducted at Duke University.
John Howard Sampson, M.D., Ph.D, M.B.A, M.H.S.c, is the former chief of the department of neurosurgery at Duke University where he serves as a professor of surgery, biomedical engineering, immunology, and pathology.
Sheila K. Singh MD, PhD, FRCSC is a chief pediatric neurosurgeon at McMaster Children's Hospital in Ontario, Canada. She is also Professor of Surgery and Biochemistry, the Division Head of Neurosurgery at Hamilton Health Sciences, the Research Director for McMaster's Division of Neurosurgery, and a scientist/principal investigator appointed to the Stem Cell and Cancer Research Institute at McMaster University.
Peter Edward Fecci is an American neurosurgeon, professor and researcher. He is an Associate Professor of Neurosurgery, Pathology and Immunology at Duke University School of Medicine. He also serves as Director of the Duke Center for Brain and Spine Metastasis, Director of the Brain Tumor Immunotherapy Program, Residency Program Director, and Associate Deputy Director of the Preston Robert Tisch Brain Tumor Center at Duke.
Donald M. O'Rourke is an American neurosurgeon and the John Templeton, Jr., MD Professor of Neurosurgery at the Perelman School of Medicine at the University of Pennsylvania. He graduated from Harvard University with an A.B. in Biochemistry and Molecular Biology in 1983, and attended medical school at the University of Pennsylvania where he also completed neurosurgical residency training. He established the institution's human brain tumor tissue bank in 2001. An elected member of the American Academy of Neurological Surgery, his research at the Translational Center of Excellence in the Abramson Cancer Center focuses on Glioblastoma Multiforme, especially the design and investigation of Chimeric Antigen Receptor immune therapies.
Duane A. Mitchell, M.D., Ph.D. is an American physician-scientist and university professor. He is currently employed at the University of Florida College of Medicine, in Gainesville, Florida as the Assistant Vice President for Research, Associate Dean for Translational Science and Clinical Research, and Director of the University of Florida (UF) Clinical and Translational Science Institute. He is the Phyllis Kottler Friedman Professor in the Lillian S. Wells Department of Neurosurgery. and Co-Director of the Preston A. Wells, Jr. Center for Brain Tumor Therapy. Dr. Mitchell is also the Founder, President, and Chairman of iOncologi, Inc., a biotechnology company in Gainesville, FL specializing in immuno-oncology.
Epitopoietic Research Corporation (ERC) is a Belgian Pharmaceutical company developing ERC1671, which specialise in treatment for Glioblastoma multiforme which is the most aggressive form of brain cancer. In 2019, ERC became the first pharmaceutical company to provide treatment under the US Federal Right-to-try law.