More than 100 drugs are approved for cancer treatment, but predicting which ones will help a particular patient is an inexact science at best. A device developed at the Massachusetts Institute of Technology (MIT) may change that. The implantable device, about the size of the grain of rice, can carry small doses of up to 30 different drugs. After implanting it in a tumour and letting the drugs diffuse into the tissue, researchers can measure how effectively each one kills the patient’s cancer cells.
“Such a device could eliminate much of the guesswork now involved in choosing cancer treatments,” says Oliver Jonas, a postdoc at MIT’s Koch Institute for Integrative Cancer Research and lead author of a paper describing the device in Science Translational Medicine. “You can use it to test a patient for a range of available drugs, and pick the one that works best.”
The paper’s senior authors are Robert Langer, the David H. Koch Professor at MIT and a member of the Koch Institute, the Institute for Medical Engineering and Science, and the Department of Chemical Engineering; and Michael Cima, the David H. Koch Professor of Engineering at MIT and a member of the Koch Institute and the Department of Materials Science and Engineering.
Most of the commonly used cancer drugs work by damaging DNA or otherwise interfering with cell function. Recently, scientists have also developed more targeted drugs designed to kill tumour cells that carry a specific genetic mutation. However, it is usually difficult to predict whether a particular drug will be effective in an individual patient.
In some cases, doctors extract tumour cells, grow them in a lab dish, and treat them with different drugs to see which ones are most effective. However, this process removes the cells from their natural environment, which can play an important role in how a tumour responds to drug treatment.
“The approach that we thought would be good to try is to essentially put the lab into the patient,” Jonas says. “It’s safe and you can do all of your sensitivity testing in the native microenvironment.”
The device, made from a stiff, crystalline polymer, can be implanted in a patient’s tumour using a biopsy needle. After implantation, drugs seep 200 to 300μm into the tumour, but do not overlap with each other. Any type of drug can go into the reservoir, and the researchers can formulate the drugs so that the doses that reach the cancer cells are similar to what they would receive if the drug were given by typical delivery methods such as intravenous injection.
After one day of drug exposure, the implant is removed, along with a small sample of the tumour tissue surrounding it, and the researchers analyse the drug effects by slicing up the tissue sample and staining it with antibodies that can detect markers of cell death or proliferation.
To test the device, the researchers implanted it in mice that had been grafted with human prostate, breast, and melanoma tumours. These tumours are known to have varying sensitivity to different cancer drugs, and the MIT team’s results corresponded to those previously seen differences.
The researchers then tested the device with a type of breast cancer known as triple negative, which lacks the three most common breast cancer markers: estrogen receptor, progesterone receptor, and Her2. This form of cancer is particularly aggressive, and none of the drugs used against it are targeted to a specific genetic marker.
Using the device, the researchers found that triple negative tumours responded differently to five of the drugs commonly used to treat them. The most effective was paclitaxel, followed by doxorubicin, cisplatin, gemcitabine, and lapatinib. They found the same results when delivering these drugs by intravenous injection, suggesting that the device is an accurate predictor of drug sensitivity.
“In this study, the researchers compared single drugs to each other, but the device could also be used to test different drug combinations by putting two or three drugs into the same reservoir,” Jonas says.
“This device could help us identify the best chemotherapy agents and combinations for every tumour prior to starting systemic administration of chemotherapy, as opposed to making choices based on population-based statistics. This has been a longstanding pursuit of the oncology community and an important step toward our goal of developing precision-based cancer therapy,” says Jose Baselga, Chief Medical Officer at Memorial Sloan Kettering Cancer Center and an author of the paper.
The researchers are now working on ways to make the device easier to read while it is still inside the patient, allowing them to get results faster. They are also planning to launch a clinical trial in breast cancer patients next year.
“This is a stunning advance in the approach to treating complex cancers,” says Henry Brem, a professor of neurosurgery and oncology at Johns Hopkins School of Medicine who was not involved in the research. “This work is transformative in that it now opens the doors to truly personalised medicine with the right drug or drug combination being utilised for each tumour.”
Another possible application for this device is to guide the development and testing of new cancer drugs. Researchers could create several different variants of a promising compound and test them all at once in a small trial of human patients, allowing them to choose the best one to carry on to a larger clinical trial.
The research was funded by Kibur Medical and the National Cancer Institute. Other authors of the paper are Heather Landry, a graduate student at Harvard University; Jason Fuller, a former MIT graduate student; John Santini, president and CEO of ApoGen Biotechnologies; and Robert Tepper, a partner in Third Rock Ventures.