Lara Kujtan, MD
Based on recent data, there are well-defined frontline options for patients with non¬–small cell lung cancer (NSCLC) who harbor EGFR
mutations, as well as rarer drivers such as ROS1
. However, more data are needed to understand how to best sequence these therapies, said Lara Kujtan, MD.
State of the Science Summit™ on Advanced Non–Small Cell Lung Cancer, Kujtan, an assistant professor at the University of Missouri–Kansas City School of Medicine, shed light on how to navigate the complex paradigm of oncogene-driven NSCLC and stressed the importance of patient preferences when deciding on optimal treatment approaches.
OncLive: What is the optimal frontline option for EGFR-positive NSCLC?
: Based on the FLAURA study, I would argue that [osimertinib] is what we should use in the frontline setting for our patients for different reasons. There is improved PFS [with this TKI], but the OS data are not mature yet from this study. There is also central nervous system (CNS) activity with osimertinib. In the ARCHER 1050 study, which looked at the use of dacomitinib (Vizimpro), a second-generation EGFR TKI, compared with other common regimens such as erlotinib and bevacizumab (Avastin) or gefitinib and chemotherapy. We [learned that] these drugs can improve survival, but we don't see a benefit in terms of CNS activity.
The FLAURA study compared the use of third-generation EGFR TKIs with first-generation EGFR TKIs. Patients were randomized to receive either osimertinib or gefitinib/erlotinib. The primary endpoint was PFS; the trial met its primary endpoint with a statistically significant increase in PFS at 18 months with osimertinib versus 10 months in the control arm. It was essentially almost a doubling in PFS. Interestingly, they also did several subgroup analyses, and every one of them showed favorable advantage for osimertinib. This was especially the case for CNS metastases, which is not something we had previously seen.
What advances have been made in the frontline treatment for patients with ALK-positive NSCLC?
We have 4 agents approved in the frontline setting for ALK
-driven disease. The National Comprehensive Cancer Network guidelines still have alectinib as the preferred agent, but recently, we have seen encouraging data with brigatinib. We still need longer-term data for brigatinib before we can compare the PFS and CNS activity [with the preferred agent]. This is something we will be eagerly awaiting.
What are the available agents for patients who harbor the rarer mutations?
In patients with BRAF
mutations, there have been some recent trials with single-agent vemurafenib (Zelboraf) that unfortunately seem to show a lot of toxicity for patients. Combination therapies with dabrafenib (Tafinlar) and trametinib (Mekinist) seem to be the best that we have so far.
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