News Release

Researchers capture first images of oxygen in cancer tumors during radiation therapy

Using specialty cameras and an oxygen probe drug injection, researchers at Dartmouth's Norris Cotton Cancer Center can now image oxygen from within cancer tumors during radiation while the probe is excited by Cherenkov light, a byproduct of radiation.

Peer-Reviewed Publication

Dartmouth Health

Oxygen Map

image: An oxygen map image recovered from a mouse undergoing radiation therapy. The luminescent oxygen probe PtG4 is injected during the week of radiation treatment and localizes between the cells of the tumor as illustrated by microscopy (red). view more 

Credit: Brian Pogue, PhD

LEBANON, NH - Oxygen in cancer tumors is known to be a major factor that helps radiation therapy be successful. Hypoxia, or starvation of oxygen, in solid tumors is also thought to be an important factor in resistance to therapy. However, it is difficult to monitor tumor oxygenation without invasive sampling of oxygen distributions throughout the tissue, or without averaging across the whole tumor, whereas oxygen is highly heterogenous within a tumor. A research team at Dartmouth's and Dartmouth-Hitchcock's Norris Cotton Cancer Center led by Brian Pogue, PhD, has developed the first non-invasive way to directly monitor oxygen distributions within the tumor right at the time when radiation therapy is happening. With injection of an oxygen probe drug, PtG4, they are able to image the distribution of oxygen from within the tumor. The method measures the luminescence lifetimes of PtG4 while it is excited by the Cherenkov light emitted by the radiation therapy. The drug, PtG4, stays in the tumor for at least a week, and works for imaging repeatedly.

"The imaging is all done without any additional radiation, simply by using a camera to monitor the emissions during radiotherapy treatment," explains Pogue. "Following two tumor lines, one which is known to be responsive to radiation and one which is known to be resistant, we could see differences in the oxygenation of the tumor which are reflective of their differences in response." The team's findings, "Tissue pO2 Distributions in Xenograft Tumors Dynamically Imaged by Cherenkov-Excited Phosphorescence during Fractionated Radiation Therapy," are newly published in Nature Communications, by lead author, Xu Cao.

Pogue's team is able to capture oxygenation imaging through special technology. "We have a unique set of time-gated cameras in our radiation therapy department that were designed for Cherenkov-based radiation dosimetry, but we have used them for this additional purpose of monitoring oxygen in the tumors under treatment," says Pogue. "So access to these specialized Cherenkov cameras made the measurements possible." Pogue's team also collaborated with Professor Sergei Vinogradov and his team at the University of Pennsylvania Perelman School of Medicine, who produced the PtG4 and supported the work with drug characterization and co-supervision of the study.

Pogue hopes to develop this tumor monitoring ability into a useful clinical aid used to track tumor response to radiation therapy, especially tumors that are known to be hypoxic. Having such information available at the time of treatment could be helpful in influencing treatment decisions such as giving a radiation boost where needed. "When a patient gets radiation therapy, the treatment should be designed to directly utilize as much information about the patient's tumor as possible," says Pogue. "Today, we use the shape of the tumor and the tissue around it. But, we need to also think about using measurements of the tumor metabolism because this affects the success of treatment as well. Future radiation therapy treatments should ideally incorporate metabolic features such as oxygenation of the tumor when the treatment is planned or delivered."

The next steps toward this future are already underway. Pogue's team is looking to characterize how small of a region they can track the oxygenation from, and how fast they can take measurements. "Our goal is to produce oxygen images at video rate, with a spatial resolution that allows us to see radiobiologically relevant hypoxia nodules in the tumor of humans," explains Pogue.

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Brian W. Pogue, PhD, is Co-Director of the Translational Engineering in Cancer Research Program at Dartmouth's and Dartmouth-Hitchcock's Norris Cotton Cancer Center, MacLean Professor of Engineering at Dartmouth's Thayer School of Engineering, and Professor of Surgery at the Geisel School of Medicine at Dartmouth, and President and Co-Founder of DoseOptics, which develops camera systems and software for radiotherapy imaging of Cherenkov light for dosimetry. His research interests include optics in medicine, biomedical imaging to guide cancer therapy, molecular-guided surgery, dose imaging in radiation therapy, Cherenkov light imaging, image-guided spectroscopy of cancer, photodynamic therapy, and modeling of tumor pathophysiology and contrast.

About Norris Cotton Cancer Center at Dartmouth-Hitchcock

Norris Cotton Cancer Center combines advanced cancer research at Dartmouth's Geisel School of Medicine with patient-centered cancer care provided at Dartmouth-Hitchcock Medical Center in Lebanon, NH, at Dartmouth-Hitchcock regional locations in Manchester, Nashua and Keene, NH, and St. Johnsbury, VT, and at partner hospitals throughout New Hampshire and Vermont. It is one of 51 centers nationwide to earn the National Cancer Institute's "Comprehensive Cancer Center" designation. Learn more about Norris Cotton Cancer Center research, programs, and clinical trials online at cancer.dartmouth.edu.


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