Biagio Ricciuti, MD, Discusses Correlative Analysis of PD-L1 Expression in NSCLC Treated With Pembrolizumab Monotherapy

Video

Biagio Ricciuti, MD, spoke about results of pembrolizumab monotherapy administration in patients with non–small cell lung cancer who had a PD-L1 tumor proportion score of 90% or more.

Biagio Ricciuti, MD, of the Lowe Center for Thoracic Oncology at Dana-Farber Cancer Institute, spoke with CancerNetwork® at the 2022 American Society of Clinical Oncology Annual Meeting, about topline results of a study in patients with non–small cell lung cancer (NSCLC) with a PD-L1 tumor proportion score (TPS) of 90% or more. The investigators observed an increased amount of CD8-positive and PD-1–positive T cells in those with TPS 90% or greater. Additionally, patients who had a PD-L1 TPS of 50% to 89% had increased mutations of STK11, KEAP1, FBXW7, and CTNNB1.

Transcript:

We were interested to identify patients with NSCLC whose tumors underwent immunofluorescence, which allowed us to explore the proportion of immune cells in the tumor. While those patients with PD-L1 expression of 90% to 100% had an increased number of CD8-positive and PD-1–positive T cells in the tumor, this enrichment was significantly higher compared with the population of 50% to 89%. This suggests that these tumors may reach immune cells and therefore can potentially elicit a strong antitumor immune response. In addition to looking at the immunophenotype [in these tumors], we also performed comprehensive genomic profiling. We compared the genomic features of tumors with a PD-L1 expression of 50% to 89% and 90% to 100%. From this comparison, we learned that tumors with the PD-L1 expression of 90% to 100% were significantly less likely to harbor mutations in genes that have been shown previously to correlate with resistance to immunotherapy such as STK11, KEAP1, FBXW7, and others. Overall, this suggested that these tumors with very high PD-L1 expressions may have unique immunophenotypic features, in addition to the biomarker itself, and may continue to explain why these patients derive benefit from immunotherapies.

Reference

Ricciuti B, Elkrief A, Alessi J, et al. Three-year outcomes and correlative analyses in patients with non–small cell lung cancer (NSCLC) and a very high PD-L1 tumor proportion score (TPS) ≥ 90% treated with first-line pembrolizumab. J Clin Oncol. 2022;40 (suppl 16):9043. doi: 10.1200/JCO.2022.40.16_suppl.9043

Recent Videos
A third of patients had a response [to lifileucel], and of the patients who have a response, half of them were alive at the 4-year follow-up.
We are seeing that, in those patients who have relapsed/refractory melanoma with survival measured as a few weeks and no effective treatments, about a third of these patients will have a response.
We have the current CAR [T-cell therapies], which target CD19; however, we need others.
“Every patient [with multiple myeloma] should be offered CAR T before they’re offered a bispecific, with some rare exceptions,” said Barry Paul, MD.
Barry Paul, MD, listed cilta-cel, anito-cel, and arlo-cel as 3 of the CAR T-cell therapies with the most promising efficacy in patients with multiple myeloma.
Jose Sandoval Sus, MD, discussed standard CAR T-cell therapies in patients across multiple high-risk lymphoma indications.
4 experts in this video
Elucidating nonresponses to bispecific T-cell engagers may be an important research consideration in the multiple myeloma field.
Barriers to access and financial toxicities are challenges that must be addressed for CAR T-cell therapies in LBCL, according to Jose Sandoval Sus, MD.
Fixed treatment durations with bispecific antibodies followed by observation may help in mitigating infection-related AEs, according to Shebli Atrash, MD.
Related Content