New Clinical Tool Predicts Cancer Risk in Patients with Clonal Hematopoiesis
Findings may drive clinical trials for potential treatment options for CH patients with high blood cancer risk
BOSTON, MA — A new clinical tool developed by a team of researchers led by the Dana-Farber Cancer Institute (Dana-Farber) pinpoints which clonal hematopoiesis (CH) patients are at highest risk for cancer progression. Their work was published this week in The New England Journal of Medicine Evidence.
“We’ve been able to detect clonal hematopoiesis in patients for years now,” said Dana-Farber hematologist–oncologist and lead author Lachelle D. Weeks, MD, PhD. “But this diagnosis often exposes patients to stress and anxiety because it’s unclear who is at highest risk of developing blood cancer. Our tool can help change that.”
Weeks and her colleagues, led by senior author Benjamin Ebert, MD, PhD, chair of medical oncology at Dana-Farber, analyzed data from nearly 200,000 healthy participants in the UK Biobank. They examined exome sequencing data to determine specific genetic mutations associated with CH and combined genetic data with other demographic and laboratory parameters.
From this information, they identified several measures that were highly predictive of blood cancer risk in CH patients. These measures include
a patient’s age
type and number of genetic mutations present in blood cells
fraction of cells in the blood with the CH mutation
low blood counts, and
factors related to red blood cell volume
Computational tool for clonal hematopoiesis risk prediction
The researchers combined these measures together into a computational algorithm, creating a tool that calculates a clonal hematopoiesis risk score (CHRS), which predicts an individual’s future risk of developing blood cancer. CHRS values define three distinct groups of patients according to the likelihood of cancer progression:
low risk (a score less than or equal to 9.5)
intermediate risk (a score ranging from 10 to 12), and
high risk (a score of 12.5 or greater).
While the 10-year risk of blood cancer is less than 1 percent in the low-risk group, the risk of developing a blood cancer such as myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML) is over 50 percent for the high-risk group.
The team validated their tool using three additional cohorts: a second cohort of roughly 250,000 healthy UK Biobank participants as well as two CH patient cohorts evaluated for hematological conditions at the Dana-Farber and the University of Pavia in Italy.
“This tool allows us to detect the minority of patients with clonal hematopoiesis who are at high-risk for developing blood cancer,” said Weeks. “That’s really exciting for two reasons—now we can not only estimate patients’ risk and help reduce some of their anxiety and uncertainty, but also take another critical step forward in building out this new field of early detection for blood cancers.”
How will the tool impact CH diagnosis and treatment?
Clonal hematopoiesis (CH) is a recently characterized condition in which the genetic mutations associated with leukemia and other blood cancers are found in the blood of individuals without cancer. This precancerous state is fairly common—for example, it’s present in roughly 15 percent of people over age 65—but only a small percentage, around 4 percent, will go on to develop blood cancer. Because there is no robust, rigorous way to assess risk, clinicians have struggled to advise CH patients on what the future could hold.
The ability to now stratify CH patients according to their risk of cancer progression will also help propel clinical trials for potential therapeutic interventions that prevent cancer in high-risk CH patients. With the new tool for scoring CH risk that Weeks and her colleagues developed, it will be possible to target experimental treatments to those patients who are most likely to benefit from them during a clinical study
- This press release was originally published on the Dana-Farber Cancer Institute website