High tumor mutational burden (TMB) was useful for predicting clinical responses to immune checkpoint inhibitors only in a subset of cancer types, according to a study published by McGrail et al in Annals of Oncology.
The findings suggest that TMB status may not be reliably used as a universal biomarker for predicting immunotherapy response. While TMB status was capable of successfully predicting response to checkpoint blockade in certain cancers, such as melanoma, lung cancer, and bladder cancer, there was no association with improved outcomes in other malignancies, including breast, prostate, and brain cancers.
“This study represents the most comprehensive analysis to date of TMB as a biomarker for response to immune checkpoint blockade,” said lead study author Daniel J. McGrail, PhD, a postdoctoral fellow in Systems Biology at The University of Texas MD Anderson Cancer Center. “Our results do not support applying high TMB status as a universal biomarker for immunotherapy response, suggesting that additional tumor type–specific studies are needed to clarify how best to apply TMB status in cancer types where it does not appear to be associated with outcomes.”
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TMB as a Biomarker
Genetic mutations within a tumor lead to the production of mutant proteins, or neoantigens, which can be recognized as abnormal by the immune system. It follows that a high TMB would render tumors more immunogenic, which is why TMB status has become a leading candidate biomarker for predicting immunotherapy response, explained Dr. McGrail.
In June 2020, the U.S. Food and Drug Administration approved the anti–PD-1 therapy pembrolizumab for patients with advanced and refractory cancers with a high TMB, as indicated by a defined threshold level of mutations. The approval was based on results from the phase II KEYNOTE-158 study, which found improved overall responses in patients with a high TMB. However, the trial did not include several cancer types, such as breast, prostate, and brain cancers, which have not typically responded to immune checkpoint blockade therapy.
“The FDA approval of pembrolizumab for patients with high TMB certainly provides an important option for many patients,” said senior study author Shiaw-Yih Lin, PhD, Professor of Systems Biology at MD Anderson. “However, we felt that it was important to look more closely at TMB status in a broader group of cancer types and establish approaches to harmonize TMB across various assays to enable clinicians to best utilize the recent FDA approval.”
Methodology
The researchers analyzed over 10,000 tumors across 31 cancer types from The Cancer Genome Atlas to study the relationship between TMB status and tumor immunogenicity, measured by the infiltration of immune cells (CD8-positive T cells) into the tumor. They identified two classes of tumors: those with and without a strong correlation between TMB status and T-cell infiltration.
The authors hypothesized that TMB status would not be able to predict immunotherapy response equally in these two groups. They evaluated this using previously published studies and MD Anderson patient cohorts.
Results
For cancers with a strong correlation between TMB status and T-cell infiltration, patients with a high TMB had improved clinical outcomes. Across all cancer types in this category, patients with a high TMB had a 39.8% overall response rate to checkpoint inhibitors, which was significantly higher than those with a low TMB.
In contrast, TMB status was not predictive of outcome in the second class of tumors. Within this category, patients with a high TMB had a 15.3% overall response rate, which was actually lower than the response rate for patients with low TMB.
“While TMB status does show value in predicting response to immune checkpoint blockade in several cancer types, this was not generalizable across all cancers,” said Dr. McGrail. “For those cancer types where a high TMB does not appear to increase immunogenicity, additional prospective studies are needed to determine if TMB status can be an effective clinical biomarker and at what threshold.”
Additionally, the researchers found that evaluating TMB status by sequencing a targeted panel of cancer-related genes may overestimate TMB when compared to whole-exome sequencing, which offers an unbiased approach. While whole-exome sequencing is not feasible in a clinical setting, the threshold for defining high TMB status may need to be evaluated in a cancer type–specific manner, Dr. McGrail explained.
The authors noted that this study is limited by retrospective analyses across various DNA sequencing approaches, as well as variations in the immune checkpoint inhibitors and clinical outcomes reported across the different cohorts included.
Disclosure: This study was supported by the National Cancer Institute, the George and Barbara Bush Endowment for Innovative Cancer Research, the Kidney Cancer Association Young Investigator Award, the Prostate Cancer Foundation Young Investigator Award, the Cancer Prevention & Research Institute of Texas, and the Breast Cancer Moon Shot®, part of MD Anderson’s Moon Shots Program®. For full disclosures of the study authors, visit annalsofoncology.org.
