image: Stomach cancer cells from a mouse model; PDL1 molecules are stained pink. view more
Credit: Wang lab, Columbia University Irving Medical Center
NEW YORK, NY (Nov. 5, 2020)--Immunotherapy for stomach cancer may work better if the therapy is delivered earlier in the course of disease and in combination with standard chemotherapy, a new study from researchers at Columbia University Vagelos College of Physicians and Surgeons suggests.
The study, in mice, was published online in the journal Gastroenterology.
"Patients with advanced stomach cancer have limited treatment options," says Woosook Kim, PhD, first author of the paper who was an associate research scientist at Columbia when the study was done. "Many are not eligible for surgical resection, and response to radiotherapy or chemotherapy is often low."
Many cancers express proteins that prevent our immune cells from attacking the tumor. Immunotherapies block these proteins, thereby unleashing the immune cells. Immunotherapies that block proteins called PD1 and PDL1 have been approved for patients with advanced stomach cancer as a second- or third-line treatment after chemotherapy, but response rates are low.
To better understand why immunotherapies don't work well in advanced stomach cancer, the Columbia researchers looked closely at the microenvironment around the tumors in mice that develop this disease.
The researchers discovered that mice with more advanced disease had an abundance of myeloid-derived suppressor cells (MDSCs) that also express PDL1 proteins, which appear to overpower the immunotherapy.
When immunotherapy was given to mice with these advanced tumors, the cancer was unaffected. Only when immunotherapy was given to the mice early, before tumors formed and prior to the accumulation of MDSCs, could cancer progression be slowed.
Combining immunotherapy with standard chemotherapy also shrank larger stomach tumors, because the chemotherapy killed many of the MDSCs.
"Our study suggests that adding chemotherapy to immunotherapy may improve responsiveness in part through the targeting of MDSCs," says Timothy Wang, MD, the Dorothy L. and Daniel H. Silberberg Professor of Medicine at Columbia University Vagelos College of Physicians and Surgeons and study leader. "While we do not have enough information to determine if the level of MDSCs may predict response to this dual regimen, our findings show that administering immunotherapy in combination with chemotherapy earlier in the course of the disease, when MDSC levels are much lower, may boost response rates in stomach cancer," says Wang.
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More Information
The paper, titled "PD-1 Signaling Promotes Tumor-Infiltrating Myeloid-Derived Suppressor Cells and Gastric Tumorigenesis in Mice," was published online Oct. 28, 2020, in Gastroenterology.
The other authors are Timothy Chu (Columbia), Henrik Nienhuser (Columbia), Armando Del Portillo (Columbia), Helen Remotti (Columbia), Ruth White (Columbia), Yoko Hayakawa (University of Tokyo), Hiroyuki Tomita (Gifu University School of Medicine), James Fox (Massachusetts Institute of Technology), and Charles Drake (Columbia).
The Columbia authors received support from the National Institutes of Health (P30CA013696, R35CA21088) and the Merck Foundation.
The authors report no financial or other conflicts of interest.
Journal
GASTROENTEROLOGY