Published online by JCI Insight, it is the first report of “clinical implementation of tumor profiling in an enterprise-wide, unselected cancer patient population,” according to the authors. The report contains data on 3,727 patients whose samples were analyzed during the first year of the Profile program at Dana-Farber/Brigham and Women’s Cancer Center and Boston Children’s Hospital. Unlike most other genomic testing programs, Profile tumor analysis is offered to all patients regardless of age, cancer type, or stage of the cancer.
While determining the genetic makeup of a patient’s tumor is a critical tool for precision cancer medicine, the report’s authors noted several challenges and unanswered questions about large-scale clinical application of the methods. Just over half of patients in the study who gave consent and had tumor profiling ordered by a physician actually received results, due to a variety of technical and logistical factors. For example, a patient’s cancer sample might not have had sufficient material for study or for DNA sequencing.
And in only a minority of cases – about 10 percent across the cohort, the researchers estimated – was the test information used in caring for the patient, although in some cancer types genomic results were used in a much higher percent of cases. Reasons for the attrition rate included absence of effective drugs, timing of genomic testing in the course of a patient’s disease, less-than-optimal access to targeted drugs or clinical trials, and patient and provider preferences. Identifying these barriers allows researchers to develop and implement new solutions, with the goal of improving the rate of use of the genomic results, the authors said.
Overall, the turnaround time from receiving the sample to issuing a report of the findings was 5.3 weeks – a timespan the researchers said they have since shortened to less than three weeks.
Profile tumor genotyping, which started in 2011, uses a platform called OncoPanel that comprehensively sequences hundreds of known cancer-related genes in a patient sample to look for mutations or other genetic alterations that drive tumors and which might be “actionable” – that is, potentially helpful in guiding the choice of a precision treatment or in enrolling the patient in appropriate clinical drug trials. Although 3,727 cases were reported in this paper, more than 15,000 individual tumors have been analyzed to date.
“A widespread genomic profiling initiative is expensive, and this cost has been borne by our institutions,” said Laura MacConaill, PhD, of Dana-Farber Cancer Institute and Brigham and Women’s Hospital (BWH), the scientific director of the Profile program and corresponding author of the publication. First author of the report is Lynette M. Sholl, MD, of BWH.
MacConaill noted that the results of Profile genomic testing are being used to further research within the institutions and are being shared more widely with initiatives like Project GENIE of the American Association for Cancer Research (AACR), which will help advance the field of precision medicine.
The study wasn’t designed to measure whether tumor profiling made a difference in how patients fared, but “it nonetheless lays the groundwork for more systematic study of the impact of genomics on clinical practice and patient outcomes,” the report said.
According to the report, at least one actionable mutation was discovered in about two-thirds of patient samples. In 20 percent of cases, such mutations could inform treatment decisions, such as matching a patient’s tumor profile to a targeted drug or improving the original diagnosis. In the remaining cases, the information could lead to referring the patient to clinical trials of approved or investigational drugs. Tumor profiling can also reveal rare mutations and other changes that make some cancers unusually responsive to targeted drugs – knowledge that can be applied to patients with a variety of cancer types.
The report gave some examples of how genomic testing clarified or changed a patient’s diagnosis, which in turn altered treatment and prognosis.
• A patient with blood cancer who had received several diagnoses was found, through testing, to have an unusual form of acute myeloid leukemia (AML), which predicted responsiveness to imatinib. He was treated with that drug and experienced a “dramatic and sustained clinical response.”
• Testing revealed an ALK gene rearrangement when a sample of a patient’s uterine leiomyosarcoma was profiled. Although she needed no further treatment, doctors would be prepared to give her an ALK inhibitor drug if needed later on.
• A patient’s undifferentiated small bowel sarcoma was found to contain a KIT gene deletion, resulting in a revised diagnosis of GIST (gastrointestinal stromal tumor) that was successfully treated with imatinib.
The authors concluded that “Genomic results may alter management in diverse scenarios; however, additional barriers must be overcome to enable precision cancer medicine on a large scale.”
This work was supported by Dana-Farber, Brigham and Women’s Hospital, and grant support from the National Cancer Institute (5R33CA155554 and 5K23CA157631).
About Dana-Farber Cancer InstituteFrom achieving the first remissions in childhood cancer with chemotherapy in 1948, to developing the very latest new therapies, Dana-Farber Cancer Institute is one of the world’s leading centers of cancer research and treatment. It is the only center ranked in the top 4 of U.S. News and World Report’s Best Hospitals for both adult and pediatric cancer care. Dana-Farber sits at the center of a wide range of collaborative efforts to reduce the burden of cancer through scientific inquiry, clinical care, education, community engagement, and advocacy. Dana-Farber/Brigham and Women’s Cancer Center provides the latest in cancer care for adults; Dana-Farber/Boston Children's Cancer and Blood Disorders Center for children. The Dana-Farber/Harvard Cancer Center unites the cancer research efforts of five Harvard academic medical centers and two graduate schools, while Dana-Farber Community Cancer Care provides high quality cancer treatment in communities outside Boston’s Longwood Medical Area.
Dana-Farber is dedicated to a unique, 50/50 balance between cancer research and care, and much of the Institute’s work is dedicated to translating the results of its discovery into new treatments for patients locally and around the world.
About Brigham and Women’s Hospital
Brigham and Women's Hospital (BWH) is a 793-bed nonprofit teaching affiliate of Harvard Medical School and a founding member of Partners HealthCare. BWH has more than 4.2 million annual patient visits and nearly 46,000 inpatient stays, is the largest birthing center in Massachusetts and employs nearly 16,000 people. The Brigham’s medical preeminence dates back to 1832, and today that rich history in clinical care is coupled with its national leadership in patient care, quality improvement and patient safety initiatives, and its dedication toresearch, innovation, community engagement and educating and training the next generation of health care professionals. Through investigation and discovery conducted at its Brigham Research Institute (BRI), BWH is an international leader in basic, clinical and translational research on human diseases, more than 3,000 researchers, including physician-investigators and renowned biomedical scientists and faculty supported by nearly $666 million in funding. For the last 25 years, BWH ranked second in research funding from the National Institutes of Health (NIH) among independent hospitals. BWH is also home to major landmark epidemiologic population studies, including the Nurses' and Physicians' Health Studies and the Women's Health Initiative as well as the TIMI Study Group, one of the premier cardiovascular clinical trials groups. For more information, resources and to follow us on social media, please visit BWH’s online newsroom.
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