Cancer Test Could Allow More Patients to Benefit from Immunotherapy

A research team from Brigham and Women’s Hospital (Boston, MA, USA) conducted an analysis involving 1,655 patients with either colorectal or endometrial cancer. These patients underwent both immunohistochemistry, the prevailing standard test for this genetic state, and next-generation sequencing tests. Immunohistochemistry detects mutations impacting the antigen, while next-generation sequencing provides a more comprehensive mutation analysis. The study discovered that about 6% of endometrial cancer and 1% of colorectal cancer patients exhibiting mismatch repair deficiency were not identified through immunohistochemistry but were detected via next-generation sequencing. This implies that additional patients who could benefit from immunotherapy might be identified through this more sensitive testing method.

Patients identified with mismatch repair deficiency through sequencing responded more favorably to immunotherapy compared to other treatments, with survival and treatment outcomes similar to those diagnosed by both testing methods. Furthermore, the research indicated that patients with the same type and stage of cancer who did not undergo immunotherapy had poorer outcomes than those who received this treatment. The researchers now aim to explore whether these findings are consistent across other sequencing panels and cancer types. Additionally, they intend to examine the role of other genetic deficiencies in the context of mismatch repair deficiency.

“In colorectal cancer and endometrial cancer, which are the two types of cancer where mismatch repair deficiency is most commonly seen, immunotherapy is not the standard treatment unless a patient has this condition,” said first author Elias Bou Farhat, MD, a postdoctoral research fellow in the division of Pulmonary and Clinical Care Medicine at Brigham and Women’s Hospital. “But in patients with this condition, even in late-stage cancer, those who receive immunotherapy can live for years and in some cases be potentially cured. Including next-generation sequencing as a complimentary testing practice could benefit patients in all phases of cancer, from pre-treatment to advanced stages.”

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