Source: Brigham and Women’s Hospital
Recent clinical trials have indicated that immune checkpoint blockade (ICB) therapy, which is designed to unleash a patient’s immune system to attack cancer, has been revolutionary in its implications for breast cancer treatment, especially for its potential to treat patients with triple negative breast cancer (TNBC). Despite the fact that most breast cancer patients are over the age of 60, most clinical trials enroll patients under the age of 60. Age may be an important consideration with respect to ICB, given that aging is associated with profound changes to the immune system, so whether ICB will benefit patients of all age groups is still unknown. In order to understand the influence of aging on the effectiveness of ICB therapy, researchers from Brigham and Women’s Hospital, the Dana Farber Cancer Institute, and Harvard Medical School conducted preclinical studies using younger and older mice with TNBC, finding that age affects the efficacy of ICB therapy. The results of this study are published in Cancer Discovery.
“Your immune system changes dramatically as you age, but no one has looked at how age affects the efficacy of this new class of drugs in breast cancer,” said co-first author Greg Goreczny, PhD, a postdoctoral fellow in the Brigham’s Hematology Division. “Because there are so few older patients enrolled in clinical trials, not enough is known about the effect of age on ICB therapy. Our initial question was whether ICB therapy would benefit all ages equally or have a greater benefit to some ages than others.”
The team injected TNBC cell lines into young mice, aged 8 to 12 weeks, and old mice, aged 12 to 15 months. Once the mice formed palpable tumors, the researchers gave them four doses of one of two ICB drugs — anti-PD-L1 or anti-CTLA-4 antibodies. They also injected a group with control antibodies. They then measured the tumor growth over time.
The study revealed that age had a huge effect on response to immunotherapy. The young mice experienced significant reduction in tumor growth and better overall survival rates in response to treatment than those who did not receive the treatment. Immunotherapy treatment did not significantly benefit the aged mice compared to those injected with the control.
The investigators also interrogated the METABRIC database, which includes data on tumor samples from patients with TNBC. Gene markers that predicted responsiveness to ICB in the young mice were prevalent in younger patients, but not in older ones. They also found signs indicative of failure of the innate immune system in the tumors of both aged mice and in samples from older patients with TNBC, implying that this study could be relevant to the treatment of people as well. Those findings led the authors to test a new combination therapy. By combining ICB with a STING agonist, a drug that has immune activation properties, they found that tumors in aged mice now responded to ICB and the mice had improved survival.
“Assessing the immune changes that occur with age could be a new way to think about immunotherapy,” said corresponding author Sandra McAllister, PhD, an associate scientist in the Brigham’s Hematology Division. “Immunological age might not be the same as chronological age. We’re beginning to understand the markers of immunological age, and this opens up the possibility of using it to guide treatment decisions in the clinic.”
Other authors of this paper include Jaclyn Sceneay, Kristin Wilson, Sara Morrow, Molly J. DeCristo, Jessalyn M. Ubellacker, Yuanbo Qin, Tyler Laszewski, Daniel G. Stover, Victor Barrera, John N. Hutchinson, Rachel A. Freedman, and Elizabeth A. Mittendorf.
This work was also supported by funds from the National Institute of Health’s National Cancer Institute (NCI R21CA182614) and the Department of Defense BCMRP Era of Hope Scholar Award (W81XWH-14-1-0191) E.A.M. has received remuneration for participation on advisory boards for Astra-Zeneca, Genetech, Merck, Taplmmune, Sellas Lifebioscience, Peregrine pharmaceuticals and EMD Seroro. EAM has served as the principal investigator on investigator-initiated trials that her previous institution, the University of Texas MD Anderson Cancer Center, received support for from Astra-Zeneca and Genentech. No potential conflicts of interest were reported from the other authors.
Paper cited: Sceneay J et al. “Interferon Signaling is Diminished with Age and is Associated with Immune Checkpoint Blockade Efficacy in Triple-Negative Breast Cancer” Cancer Discovery DOI:10.1158/2159-8290.CD-18-1454
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