1. EGFR: Osimertinib, dacomitinib 1L
2. Afatinib (1L) with or without cetuximab ( after progression on Osimertinib)
3. ALK :Alectinib, Brigatinib, Lorlatinib all 1L, Lorlatinib can be 2L
4. Dabrafenib Trametinib can do 1L in BRAF V600E mutated
5. 2nd line EGFR exon 20- amivantamab, mobocertinib
6. KRAS G12 C 2L Sotorasib/ adagrasib
7. MET exon 14: 1L ok tepotinib, capmatinib, crizotinib
8. ROS 1: 1L Entrectenib ( better if brain mets) crizotinib, ceritinib. Lorlatinib can be used 2L.
9. NTRK- 1L entrectenib, larotrectinib
10. HER 2 mutated- TDxd 2L
11. RET-1 L selpercatinib/ pralsetinib
Stage 4 lung cancer and IO
Cemiplimab monotherapy PDL1 50% or higher- median OS 26 m vs 13 months
Cemiplimab with chemotherapy median OS 22 m vs 13 m.
Both are category 1.
Cemiplimab with chemo: The most common (≥15%) adverse reactions were alopecia, musculoskeletal pain, nausea, fatigue, peripheral neuropathy, and decreased appetite.
The recommended cemiplimab-rwlc dose is 350 mg IV every 3 weeks.
What subgroup of patients did the cemiplimab not benefit even though the overall population benefited? PDL1< 1%, women and non smokers. Underpowered to test the benefits.
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