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UrduIn a recently published Nature Cancer paper, UChicago Medicine researchers have identified the first biomarker that predicts response to the RT and ICB treatment combination. Aneuploidy is a condition where tumor cells exhibit either missing or extra chromosomes. In the current study, mNSCLC patients with high tumor aneuploidy were found to have significantly better survival if RT was added to ICB. By contrast, there was no survival benefit for patients with low aneuploidy when adding RT to ICB treatment. Moreover, the researchers demonstrated that radiotherapy to metastatic sites concomitant with, but not before or after, ICB improves survival in patients with high aneuploidy tumors, according to Sean Pitroda, MD, Assistant Professor of Radiation and Cellular Oncology at UChicago Medicine and the senior author of the paper.
To evaluate the differences in clinical and genomic parameters between sequential (radiation therapy followed by ICB therapy) and concurrent (radiation therapy while ICB is on-board) therapies, 37 patients with mNSCLC were enrolled in a randomized phase 1 clinical trial. Tumor tissue samples that were analyzed before and during treatment showed radiation therapy alone is less effective in tumor cell elimination as compared to simultaneous radiation and immunotherapy.
“A key observation was that radiation therapy alone caused depletion of important immune cells within the tumor, however, with concurrent therapy there was enrichment of immune cells and improved elimination of tumor cells that led to positive survival outcomes in mNSCLC patients,” Pitroda said.
He described that in concurrent treatment, immunotherapy takes the brakes off of the immune cells that would not normally recognize the cancer because cancer has ways to hide from the immune system. Essentially, immunotherapy is unmasking cancer cells and helping those immune cells hone in on the tumor to fight the cancer.
“By giving immunotherapy with radiation, we believe that radiation becomes more effective at killing tumor cells by helping immune cells find the damaged tumor that’s dying off,” he said. “Our findings highlight that radiation therapy alone is not enough to trigger a localized immune response in mNSCLC and the timing of radiation and immunotherapy is critical to this process,” said Pitroda.
The concept of tumor aneuploidy has been of increasing interest to researchers and other work has shown a connection between aneuploidy and the immune system, but exactly how it can be used to improve cancer treatments had not been identified. Liam Spurr, a current medical student at the University of Chicago Pritzker School of Medicine and first author of these studies, had previously developed an algorithm that quantifies the degree of aneuploidy in patients’ tumors when they undergo DNA sequencing. Together, the investigators came up with the hypothesis that perhaps aneuploidy could be useful in determining which tumors might respond better to immunotherapy.
Based on their findings in the Nature Cancer study, the team further tested whether aneuploidy could have utility as a biomarker for predicting survival in another study published in Nature Genetics, where a larger cohort consisting of 1,660 patients with a wide range of cancer types who have been treated with immune checkpoint blockers were re-analyzed. Tumors with a high degree of aneuploidy had a worse prognosis because these patients did not respond to immunotherapy alone. In addition, tumor aneuploidy complemented tumor mutational burden (TMB) – an established biomarker across many cancers for immunotherapy response. Patients with high TMB often respond well to immunotherapy, and patients with low TMB usually do not.
“For low TMB tumors, you look for another biomarker, like aneuploidy, to improve your prediction of immunotherapy response. The ones that have the worst survival after immunotherapy are the ones that have low TMB and high aneuploidy scores and those are probably the patients that need something more than immunotherapy, like radiation, to improve their treatment response and outcomes,” Sean Pitroda said.
Immunotherapy has completely revolutionized how we treat many types of cancer. Some cancers are fatal, especially when they become metastatic, but now people can live for a long time and a fraction can even be cured with immunotherapy. Many patients, however, do not respond to immunotherapy and better strategies are required to improve outcomes, potentially by combining immunotherapies with other cancer treatments like radiation or chemotherapy. The current study identified a completely new way to predicts patients’ response to immunotherapy and proposed that adding radiation to those who do not respond to immunotherapy alone can improve outcomes.
Pitroda said, “We have the first method to personalize therapy—to choose the right therapy for the right patient at the right time—employing radiation and immunotherapy.”
Citations:
Highly aneuploid non-small cell lung cancer shows enhanced responsiveness to concurrent radiation and immune checkpoint blockade: Nature Cancer
Liam F. Spurr, Carlos A. Martinez, Wenjun Kang, Mengjie Chen, Yuanyuan Zha, Robyn Hseu, Stanley I. Gutiontov, William T. Turchan, Connor M. Lynch, Kelli B. Pointer, Paul Chang, Septimiu Murgu, Aliya N. Husain, Brittany Cody, Everett E. Vokes, Christine M. Bestvina, Thomas F. Gajewski, Ralph R. Weichselbaum, Steven J. Chmura, and Sean P. Pitroda from The University of Chicago; Jyoti D. Patel from Northwestern University; Maximilian Diehn from Standford University.
Funding: Ludwig Cancer Research Foundation, a Career Development Award from the LUNGevity Foundation, an Ullman Scholarship in Translational Cancer Immunology from the University of Chicago Comprehensive Cancer Center (UCCCC), a Cancer Spotlight Grant from the UCCCC, a Fight Against Cancer Grant from the United-4 A Cure Foundation, an NIH NCI-SOAR Grant 1R25CA240134-01, NSF2016307, R01 grants GM126553 and HG011883, a Sloan Research Foundation fellowship, and an NCI CCSG grant.
Tumor aneuploidy predicts survival following immunotherapy across multiple cancers: Nature Genetics
Liam F. Spurr, Ralph R. Weichselbaum, and Sean P. Pitroda from The University of Chicago
Funding: Ludwig Cancer Research Foundation, a Career Development Award from the LUNGevity Foundation, an Ullman Scholarship in Translational Cancer Immunology from the University of Chicago Comprehensive Cancer Center (UCCCC), a Cancer Spotlight Grant from the UCCCC, a Fight Against Cancer Grant from the United-4 A Cure Foundation, an NIH NCI-SOAR Grant 1R25CA240134-01.
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About the University of Chicago Medicine & Biological Sciences
The University of Chicago Medicine, with a history dating back to 1927, is one of the nation’s leading academic health systems. It unites the missions of the University of Chicago Medical Center, Pritzker School of Medicine and the Biological Sciences Division. Twelve Nobel Prize winners in physiology or medicine have been affiliated with the University of Chicago Medicine. Its main Hyde Park campus is home to the Center for Care and Discovery, Bernard Mitchell Hospital, Comer Children’s Hospital and the Duchossois Center for Advanced Medicine. It also has ambulatory facilities in Orland Park, South Loop, Homewood and River East as well as affiliations and partnerships that create a regional network of care. UChicago Medicine offers a full range of specialty-care services for adults and children through more than 40 institutes and centers including an NCI-designated Comprehensive Cancer Center. Together with Harvey-based Ingalls Memorial, UChicago Medicine has 1,296 licensed beds, nearly 1,300 attending physicians, over 2,800 nurses and about 970 residents and fellows.
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