"Immunotherapy is the new, hot thing, but sometimes traditional chemotherapy can be a better choice," said Marwan Fakih, M.D., senior author of the new study and co-director of the Gastrointestinal Cancer Program at City of Hope. "Our study suggests tumor genomics could help doctors decide what kind of treatment will benefit each patient most. Taking this kind of personalized medicine approach, we will be able to provide patients with options that yield better outcomes and are more cost-effective."
"Comprehensive genomic profiling is critical to assess the underlying genomic drivers of a tumor, as well as important biomarkers that require broad DNA interrogation like tumor mutational burden (TMB) and microsatellite instability (MSI)," said Alexa Schrock, Ph.D., associate director of clinical development at Foundation Medicine. "In this study, we've seen the importance of evaluating both TMB and MSI when making treatment decisions for metastatic colorectal cancer patients."
"Finding methods to identify the right, personalized treatment for a patient is top-of-mind, especially in today's precision medicine landscape," Fakih said. "This study is the first to use degree of tumor mutation as a predictor of response to immunotherapy in metastatic colorectal cancer patients with MSI. For cancer patients, timely, appropriate treatment is imperative." Fakih and his colleagues retrospectively analyzed the data of 22 patients - all of whom had high MSI, a biomarker that indicates they're a good candidate to receive immune checkpoint inhibitor treatment. The patients received either pembrolizumab or nivolumab, both of which are U.S. Food and Drug Administration-approved for metastatic colorectal cancer patients.
The scientists looked at tumor characteristics, tumor genomics and outcome data and compared those analyses to a database containing 18,140 metastatic colorectal cancer patients.
The patients whose tumor cells had a mutation score less than a cut-off point of 37 were less likely to respond to immunotherapy and more likely to have their disease quickly worsen. Those who had a tumor mutation score above the cut-off point of 41 were more likely to respond to pembrolizumab or nivolumab. Notably, the patients who responded to immunotherapy appeared to have durable responses, with the majority experiencing ongoing major shrinkage beyond 1.5 years (the time of study analysis).
The implication is that patients with MSI and a high tumor mutation score should consider receiving immunotherapy as their first treatment, Fakih said. Those with MSI and a low tumor mutation score (less than 37) should be considered for chemotherapy rather than immunotherapy as their first treatment option, Fakih added. Of course, more research is needed to validate these important findings.
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