PERSONALIZED CANCER TREATMENTS BASED ON TESTING DRUGS QUICKLY LEADS TO FASTER TREATMENT, BETTER OUTCOMES
Personalized Cancer Treatments Based on Testing Drugs Quickly Leads to Faster Treatment, Better Outcomes
April 11th, 13PM April 11th, 13PM(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.)
Diana Azzam,
Florida International University
(THE CONVERSATION) Despite many efforts to find better, more effective ways to treat cancer, it remains a
leading cause of death by diseaseamong children in the U.S.
Cancer patients are also getting younger. Cancer diagnoses among those under 50 has risen by
about 80% worldwideover the past 30 years. As of 2023, cancer is the
second-leading cause of deathboth in the U.S. and around the world. While death rates from cancer have decreased over the past few decades,
about 1 in 3 patients in the U.S.and
1 in 2 patients worldwidestill die from cancer.
Despite advances in standard cancer treatments, many cancer patients still face uncertain outcomes when these treatments prove ineffective. Depending on the stage and location of the cancer and the patient's medical history, most cancer types are treated with a mix of radiation, surgery and drugs. But if those standard treatments fail, patients and doctors enter a trial-and-error maze where effective treatments become difficult to predict because of limited information on the patient's cancer.
My mission as a
cancer researcheris to build a personalized guide of the most effective drugs for every cancer patient. My team and I do this by testing different medications on a patient's own cancer cells before administering treatment, tailoring therapies that are most likely to selectively kill tumors while minimizing toxic effects.
In our newly published results of the first clinical trial combining drug sensitivity testing with DNA testing to identify effective treatments in children with cancer, an approach called
functional precision medicine, we found this approach
can help match patientswith more FDA-approved treatment options and significantly improve outcomes.
What is functional precision medicine?
Even though two people with the same cancer might get the same medicine, they can have very different outcomes. Because
each patient's tumor is unique, it can be challenging to know which treatment works best.
To solve this problem, doctors analyze DNA mutations in the patient's tumor,
bloodor saliva to match cancer medicines to patients. This approach is called
precision medicine. However, the relationship between cancer DNA and how effective medicines will be against them is very complex. Matching medications to patients based on a single mutation overlooks other genetic and nongenetic mechanisms that influence how cells respond to drugs.
How to best match medicines to patients through DNA is still a major challenge. Overall,
only 10% of cancer patientsexperience a clinical benefitfrom treatments matched to tumor DNA mutations.
Functional precision medicine takes a different approach to personalizing treatments. My team and I take a sample of a patient's cancer cells from a biopsy, grow the cells in the lab and expose them to over 100 drugs approved by the Food and Drug Administration. In this process, called
drug sensitivity testing, we look for the medications that kill the cancer cells.
New clinical trial results
Providing functional precision medicine to cancer patients
in real lifeis very challenging.
Off-label use of drugsand financial restrictions are key barriers. The health of cancer patients can also deteriorate rapidly, and physicians may be hesitant to try new methods.
But this is starting to change. Two teams in Europe recently showed that functional precision medicine could match effective treatments to
about 55% ofadult patientswith blood cancers such as leukemia and lymphoma that did not respond to standard treatments.
Most recently, my team's clinical trial
focused on childhood cancer patientswhose cancer came back or didn't respond to treatment. We applied our functional precision medicine approach to 25 patients with different types of cancer.
Our trial showed that we could provide treatment options for almost all patients in less than two weeks. My colleague
Arlet Maria Acanda de la Rochawas instrumental in helping return drug sensitivity data to patients as fast as possible. We were able to provide test results within 10 days of receiving a sample, compared with the roughly 30 days that standard genomic testing results that focus on identifying specific cancer mutations typically take to process.
Most importantly, our study showed that
83% of cancer patientswho received treatments guided by our approach had clinical benefit, including improved response and survival.
Expanding into the real world
Functional precision medicine opens new paths to understanding how cancer drugs can be better matched to patients. Although doctors can read any patient's DNA today, interpreting the results to understand how a patient will respond to cancer treatment is much more challenging. Combining drug sensitivity testing with DNA analysis can help personalize cancer treatments for each patient.
I, along with colleague
Noah E. Berlow, have started to add artificial intelligence to our functional precision medicine program. AI enables us to analyze each patient's data to better match them with tailored treatments and drug combinations. AI also allows us to understand the complex relationships between DNA mutations within tumors and how different treatments will affect them.
My team and I have
started twoclinical trialsto expand the results of our previous studies on providing treatment recommendations through functional precision medicine. We're recruiting a larger cohort of adults and children with cancers that have come back or are resistant to treatment.
The more data we have, the easier it will become to understand how to best treat cancer and ultimately help more patients access personalized cancer treatments.
This article is republished from The Conversation under a Creative Commons license. Read the original article here:
2024-04-11T10:17:00Z dg43tfdfdgfd