sTILs Warrant Research as Response Biomarker in Metastatic Breast Cancer

Video

Daniel G. Stover, MD, suggests that stromal tumor infiltrating lymphocytes may serve as a biomarker of immune activation and can potentially help optimize therapy with microtubule-targeting agents for patients with metastatic breast cancer.

At the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting, Daniel G. Stover, MD, spoke with CancerNetwork® about findings from the phase 3 CALGB 40502 (Alliance) trial (NCT00785291). In particular, he discussed how immune activation measured by stromal tumor infiltrating lymphocytes (TILs) may correlate with responses to microtubule-targeting agents among patients with metastatic breast cancer.1

Stover, associate professor of medicine and director of Translational Breast Cancer Research at The Ohio State University Comprehensive Cancer Center, stated that results from the AURORA study may also suggest a relationship between stromal TILs and patient outcomes in the metastatic setting, especially in those with triple-negative breast cancer (TNBC).2 However, he emphasized that additional trials are necessary for validating this association in other settings.

Transcript:

We performed multivariable analyses with additional factors and stromal TILs continued [to] trend towards association with outcomes. But there are multiple factors that influence a patient's response to these targeted therapies. Stromal TILs as a marker of immune activation should be one biomarker that could be incorporated as we think about optimizing therapy for patients. The [benefit] of stromal TILs is that it's such an accessible biomarker easily enumerated off routine slides.

This study certainly warrants further validation among additional samples in the metastatic setting. As we saw from the AURORA study presented in the same session, there is evidence that stromal TILs may have an association with outcomes in the metastatic setting, particularly among [TNBCs]. But the next step, beyond validating this in additional settings or situations, is to design those trials that can impact therapy decisions based on the stromal TIL number.

References

  1. Stover DG, Salgado R, Savenkov O, et al. Association of tumor infiltrating lymphocyte quantity with survival in patients (pts) with metastatic breast cancer (MBC) receiving microtubule-targeting agents: post hoc analysis CALGB 40502 (Alliance). J Clin Oncol. 2023;41(suppl 16):1010. doi:10.1200/JCO.2023.41.16_suppl.1010
  2. Hilbers F, Venet D, Agostinetto E, et al. Characterization of the immune microenvironment in matched primary and metastatic breast cancer lesions from the AURORA study: BIG 14-01. J Clin Oncol. 2023;41(suppl 16):1009. doi:10.1200/JCO.2023.41.16_suppl.1009
Recent Videos
The FirstLook liquid biopsy, when used as an adjunct to low-dose CT, may help to address the unmet need of low lung cancer screening utilization.
An 80% sensitivity for lung cancer was observed with the liquid biopsy, with high sensitivity observed for early-stage disease, as well.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Patients who face smoking stigma, perceive a lack of insurance, or have other low-dose CT related concerns may benefit from blood testing for lung cancer.
Establishment of an AYA Lymphoma Consortium has facilitated a process to better understand and address gaps in knowledge for this patient group.
Adult and pediatric oncology collaboration in assessing nivolumab in advanced Hodgkin lymphoma facilitated the phase 3 SWOG S1826 findings.
Treatment paradigms differ between adult and pediatric oncologists when treating young adults with lymphoma.
Differences in pancreatic cancer responses to treatment elicits a need to better educate patients on expectations in treatment, particularly chemotherapy.
Increasing patient awareness of modifiable risk factors for pancreatic cancer may help mitigate incidence of pancreatic cancers.
It may be crucial to test every patient for markers such as BRAF V600E mutations, NRG1 fusions, and KRAS G12C mutations to help manage pancreatic cancers.
Related Content