Clinical Responses to Sotorasib Could Vary by Co-Mutational Status in NSCLC

Article

Progression-free survival lengths were different among patients with non-small cell lung cancer receiving sotorasib when stratified by genomic profile.

Results suggest responses to treatment with sotorasib (Lumakras) might vary via co-mutational status for patients with KRAS p.G12C-mutant non-small cell lung cancer (NSCLC), according to initial results from an exploratory analysis of the phase II CodeBreaK100 clinical trial.1

Sotorasib is a KRAS inhibitor that was first approved in May 2021 for heavily pretreated KRAS p.G12C-mutant NSCLC based on findings from CodeBreaK100 trial, which showed that the first-in-class small molecule elicited an objective response rate of 37.1%, median progression-free survival of 6.8 months and median overall survival of 12.5 months.

“Recently, diverse and frequently coexisting mechanisms of acquired resistance to KRAS inhibitors were reported, including secondary alterations in KRAS itself, as well as other components of the RT kinase MAP kinase pathways,” said Ferdinandos Skoulidis, MD, PHD, department of Thoracic and Head and Neck Medical Oncology at The University of Texas MD Anderson Cancer Center.

Skoulidis presented his team’s findings at the 2021 World Congress on Lung Cancer.2

Researchers conducted tissue analysis and looked at the following genomic profiles in 65 patients, who had baseline tissue samples and at least 3 months follow-up: KEAP1 (n=11); STRK11 (n=13); cell cycle genes (n=27); DNA damage response (DDR) genes (n=50); RAS/MAPK pathway (n=23), PI3K/AKT/mTOR pathway genes (n=24), RTK genes (n=39), WNT pathway genes (n=24).

A total of 33.8% (n=22) patients were early progressors, meaning that their disease progressed before 3 months; 35.4% (n=23) were late progressors (event of progressive disease at or after 3 months; and 30.8% (n=20) had ongoing disease control. However, the results varied by co-mutational subgroups.

Notably, KEAP1 mutational status was associated with early progression (63.6%; n=7), which is consistent with the poor prognosis often seen for these patients. Conversely, the majority of patients with cell cycle (51.9%; n=14) and WNT pathway 50%; n=12) experienced late progression, highlighting an opportunity for combination therapy in this subgroup.

“In view of these results, we hypothesize that baseline tumor genomic profiles may affect clinical response in patterns of resistance to sotorasib,” Skoulidis said.

Further investigation into co-mutational status and sotorasib response is needed, Skoulidis added, emphasizing that the results should be interpreted with caution and should be considered hypothesis-generating.

“RTK genes still [had] no association with either early or late progression, and this warrants further investigation, in larger studies, of course,” he said. “The small sample size of each of the subgroups represents a limitation of the study nonetheless, groupings of permutations into functional pathways may help determine patters of response and resistance.”

References

  1. A Phase 1/2, Study Evaluating the Safety, Tolerability, PK, and Efficacy of AMG 510 in Subjects With Solid Tumors With a Specific KRAS Mutation (CodeBreaK 100). ClinicalTrials.gov. Updated September 2, 2021. Accessed September 14, 2021. https://clinicaltrials.gov/ct2/show/NCT03600883
  2. Skoulidis F, Schuler M, Wolf J, et. Al. Genomic profiles and potential determinants of response and resistance in KRAS p/G12C-mutated NSCLC treated with sotorasib. Presented at: 2021 World Conference on Lung Cancer. Sept. 8-14, 2021; virtual. Abstract MA14.03.
Related Videos
Barbara Smith, MD, PhD, spoke about the potential use of pegulicianine-guided breast cancer surgery based on reports from the phase 3 INSITE trial.
Patient-reported symptoms following surgery appear to improve with the use of perioperative telemonitoring, says Kelly M. Mahuron, MD.
Treatment options in the refractory setting must improve for patients with resected colorectal cancer peritoneal metastasis, says Muhammad Talha Waheed, MD.
Although immature, overall survival data from the KEYNOTE-868 trial may support the use of pembrolizumab plus chemotherapy in patients with endometrial cancer.
Dostarlimab plus chemotherapy appears to yield favorable overall survival in patients with mismatch repair proficient endometrial cancer.
Some patients with large B-cell lymphoma may have to travel a great distance for an initial evaluation for CAR T-cell therapy.
Brian Slomovitz, MD, MS, FACOG discusses the use of new antibody drug conjugates for treating patients with various gynecologic cancers.
Education is essential to referring oncologists manage toxicities associated with CAR T-cell therapy for patients with large B-cell lymphoma.
There is no absolute age cutoff where CAR T cells are contraindicated for those with large B-cell lymphoma, says David L. Porter, MD.
David L. Porter, MD, emphasizes referring patients with large B-cell lymphoma early for CAR T-cell therapy consultation.
Related Content