Salma Jabbour, MD, on Future Trials in Stage III NSCLC

Video

CancerNetwork® sat down with Salma Jabbour, MD, of Rutgers Cancer Institute, at 2021 ASCO to talk about what she believed was the most interesting and impactful study to come out of the meeting.

At the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, CancerNetwork® spoke with Salma Jabbour, MD, to discuss her thoughts about the phase 2 KEYNOTE-799 trial (NCT03631784). This study examined pembrolizumab (Keytruda) in combination with platinum-doublet chemotherapy and radiation in patients with unresectable, stage III non–small cell lung cancer (NSCLC).

Results of the trial indicated that the treatment regimen for this population of patients demonstrated promising antitumor activity across patient subgroups regardless of PD-L1 expression and tumor histology. In a group of patients with mixed histology who were treated with pembrolizumab plus carboplatin/paclitaxel, the overall response rate was 70.5% (95% CI, 61.2%-78.8%), with more than three-quarters of patients having a response duration longer than 1 year.

Transcript:

I’m, excited about KEYNOTE-799. I do think that this will open the door for many future trials, and much excitement in the stage III setting. I am excited to continue to hear further results about stage III lung cancers.

Reference

Jabbour SK, KEYNOTE-799: Phase 2 trial of pembrolizumab plus platinum chemotherapy and radiotherapy for unresectable, locally advanced, stage 3 NSCLC.

Recent Videos
Educating community practices on CAR T referral and sequencing treatment strategies may help increase CAR T utilization.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Although accuracy remains a focus in whole-body MRI testing in patients with Li-Fraumeni syndrome, comfortable testing experiences may ease anxiety.
Subsequent testing among patients in a prospective study may affirm the ability of cfDNA sequencing to detect cancers in those with Li-Fraumeni syndrome.
cfDNA sequencing may allow for more accessible, frequent, and sensitive testing compared with standard surveillance in Li-Fraumeni syndrome.
STX-478 showed efficacy in patients with advanced solid tumors regardless of whether they had kinase domain or helical PI3K mutations.
STX-478 may avoid adverse effects associated with prior PI3K inhibitors that lack selectivity for the mutated protein vs the wild-type protein.
Phase 1 data may show the possibility of rationally designing agents that can preferentially target PI3K mutations in solid tumors.
Funding a clinical trial to further assess liquid biopsy in patients with Li-Fraumeni syndrome may help with detecting cancers early across the board.
Related Content