While important, getting all these tests done can be logistically
challenging, expensive and sometimes uncomfortable for patients. But what if a
single blood test could screen for most common cancer types all at once?
This is the promise of multicancer early detection tests, or
MCEDs. This year, President Joe Biden identified developing MCED tests as a
priority for the Cancer Moonshot, a US$1.8 billion federal
effort to reduce the cancer death rate and improve the quality of life of
cancer survivors and those living with cancer.
As a laboratory medicine physician
and researcher who develops molecular tests for cancer, I
believe MCED tests are likely to transform cancer screening in the near future,
particularly if they receive strong federal support to enable rapid innovation.
How MCED tests work
All cells in the body,
including tumor cells, shed
DNA into the bloodstream when they die. MCED tests look for the
trace amounts of tumor DNA in the bloodstream. This circulating “cell-free” DNA
contains information about what type of tissue it came from and whether it is
normal or cancerous.
Testing to look for
circulating tumor DNA in the blood is not new. These liquid biopsies – a fancy way of saying
blood tests – are already widely used for patients with advanced-stage cancer.
Doctors use these blood tests to look for mutations in the tumor DNA that help
guide treatment. Because patients with late-stage cancer tend to have a large
amount of tumor DNA circulating in the blood, it’s relatively easy to detect
the presence of these genetic changes.
MCED tests are different from existing liquid biopsies because
they are trying to detect early-stage cancer, when there aren’t that many tumor
cells yet. Detecting these cancer cells can be challenging early on because
noncancer cells also shed DNA into the bloodstream. Since most of the circulating
DNA in the bloodstream comes from noncancer cells, detecting the presence of a
few molecules of cancer DNA is like finding a needle in a haystack.
Making things even more difficult, blood cells shed abnormal DNA
naturally with aging, and these strands can be confused for circulating cancer
DNA. This phenomenon, known as clonal
hematopoiesis, confounded early attempts at developing MCED tests,
with too many false positive results.
Fortunately, newer tests are able to avoid
blood cell interference by focusing on a type of “molecular
barcode” embedded in the cancer DNA that identifies the tissue it came from.
These barcodes are a result of DNA
methylation, naturally existing modifications to the surface of DNA
that vary for each type of tissue in the body. For example, lung tissue has a
different DNA methylation pattern than breast tissue. Furthermore, cancer cells
have abnormal DNA methylation patterns that correlate with cancer type. By
cataloging different DNA methylation patterns, MCED tests can focus on the
sections of DNA that distinguish between cancerous and normal tissue and pinpoint
the cancer’s origin site.
Testing options
There are currently several MCED tests in development and in
clinical trials. No MCED test is currently FDA-approved or
recommended by medical societies.
In 2021, the biotech company GRAIL launched the first commercially
available MCED test in the U.S. Its Galleri test claims to detect over 50
different types of cancers. At least two other U.S.-based companies, Exact
Sciences and Freenome, and one Chinese company, Singlera
Genomics, have tests in development. Some of these tests use
different cancer detection methods in addition to circulating tumor DNA, such
as looking for cancer-associated proteins in blood.
MCED tests are not yet typically covered by insurance. GRAIL’s
Galleri test is currently priced
at $949, and the company offers a payment plan for people who have
to pay out of pocket. Legislators have introduced a bill in Congress to provide
Medicare coverage for MCED tests that obtain FDA approval. It is unusual for
Congress to consider legislation devoted to a single lab test, and this
highlights both the scale of the medical market for MCED and concerns about
disparities in access without coverage for these expensive tests.
How should MCED tests be
used?
Figuring out how MCED tests should be implemented in the clinic
will take many years. Researchers and clinicians are just beginning to address
questions on who should be tested, at what age, and how past medical and family
history should be taken into account. Setting guidelines for how doctors will
further evaluate positive MCED results is just as important.
There is also concern that MCED tests may result in overdiagnoses
of low-risk, asymptomatic cancers better
left undetected. This happened with prostate cancer screening. Previously,
guidelines recommended that all men ages 55 to 69 regularly get blood tests to
determine their levels of PSA, a protein produced by cancerous and noncancerous
prostate tissue. But now the recommendation is more nuanced, with screening
suggested on an individual basis that takes into account personal preferences.
Another concern is that further testing to confirm positive MCED
results will be costly and a burden to the medical system, particularly if a
full-body scan is required. The out-of-pocket cost for an MRI, for example,
can run up to thousands of dollars. And patients
who get a positive MCED result but are unable to confirm the presence of cancer
after extensive imaging and other follow-up tests may develop lifelong anxiety
about a potentially missed diagnosis and continue to take expensive tests in
fruitless search for a tumor.
Despite these concerns, early clinical studies show promise.
A 2020 study of over 10,000 previously
undiagnosed women found 26 of 134 women with a positive MCED test were
confirmed to have cancer. A 2021
study sponsored by GRAIL found that half of the over 2,800
patients with a known cancer diagnosis had a positive MCED test and only 0.5%
of people confirmed to not have cancer had a false positive test. The test
performed best for patients with more advanced cancers but did detect about 17%
of the patients who had very-early-stage disease.
MCED tests may soon revolutionize the way clinicians approach
cancer screening. The question is whether the health care system is ready for
them.
-The Conversation, Colin Pritchard, Professor of Laboratory
Medicine and Pathology, University of Washington