Dr. @BrunaPellini deftly discusses pembrolizumab/divarasib, elisrasib, and elisrasib/pembrolizumab in KRAS G12C+ NSCLC. Very promising efficacy but MUST balance against toxicity. Patient selection will be key here.
1stL in KRASG12Cmut NSCLC will be crowded and complex. Elisrasib, another KRASG12Coff inh, reported activityn in 1stL alone and combo with pembro. Next future: how to decide intensification? Based on PDL1, comut, brain met status🤯.Will not be easy!! To icity is a concern #ASCO26
🫁 D3S-001: first-line elisrasib ± pembrolizumab in KRAS G12C-mutant NSCLC #ASCO26
🎯 Elisrasib monotherapy: ORR 78.0%, mPFS 12.4 months, 12-month OS 90%
💥 Elisrasib + pembrolizumab: ORR 81.3%, mPFS not reached, 12-month OS 88.8%
⚡ Responses were rapid, with most responders achieving response by week 6
🚨 Higher grade ≥3 TRAEs with the combination (32.7%)
The response rates are elis-rising…now we wait to see whether phase III data can truly KRAS the finish line 😉 #ASCO26
@OncoAlert@OncoReporte@ASCO@_SEOM@LungCancerRx@Lung_Cancers
Brave study with elisrasib a novel KRAS G12off inhibitor as monotherapy in first line setting regardless of PD-L1. ORR >60% in all PD-L1 categories. PFS promising. G3 tox 7%
Elisrasib active on common mechanisms of resistance to other KRAS inhibitors (such KRAS amp).
#ASCO2026
A next-generation KRAS G12C inhibitor, elisrasib, showed promising first-line activity in advanced KRAS G12C-mutant NSCLC, both alone and with pembrolizumab. Response rates were 78% with monotherapy and 84.6% with the combination, with especially strong activity in tumors with high PD-L1 expression.
These are early results point to a potential new treatment option on the horizon for a common lung cancer driver mutation -- but there is work to be done. Larger studies should aim to confirm the benefit and find ways to improve safety. #ASCO26 #NSCLC #lungcancer #KRAS
#ASCO26 Safety quite reassuring. Monotherapy G3+ TRAE 7% with 9% dose interruption and no discontinuation. Elisrasib + pembro combo shows 10% pembro discontinuation from TRAE. With combo, note LFT elevation but primarily low grade with AST/ALT elevated but not bilirubin.
#ASCO26 1L elisrasib + pembroizumab in KRAS G12C NSCLC with RR 81% with DCR 98%, mDOR NR with 73% at 12m, mPFS NR with 54% at 12m and 12m OS rate 89%. Illustrative cases showing rapid, deep responses including CNS responses.
Dr. Shun Lu #ASCO26: first-line elisrasib (D3S-001) +/- pembrolizumab in KRAS G12C NSCLC, global study. With elirasib monotherapy, RR 78% with early suggestion of durability. Median DOR NR but 53% at 1 year and mPFS 12.4m with 12m OS rate 90%. Impressive early data.
With @AACR 2026 abstracts out, we asked leading AI models to identify the most anticipated trials in oncology, here’s their combined ranking.
Early-phase KRAS-targeted programs like RMC-9805-001 (zoldonrasib) and D3S-001-100 (elisrasib) rise to the top, alongside first-in-human approaches and novel pathway-driven strategies.
The list highlights strong momentum in:
▶️ Next-generation KRAS inhibition (G12D and G12C)
▶️ Cell cycle and synthetic lethality targets (PKMYT1, WEE1, RB pathway)
▶️ Emerging immunotherapy combinations and novel targets like CCR8 and B7-H3
Together, these studies reflect how the field is advancing through early clinical innovation, novel mechanisms, and biomarker-driven strategies heading into AACR 2026.
Which study are you watching most closely?
Explore more insights and data from #AACR26 👉 https://t.co/bMhp9sykLc
#LARVOL #AACR2026 #CancerResearch #CancerData #Oncology #OncologyInsights #ClinicalTrials | @DrJNaidoo | @dr_yakupergun | @HHorinouchi | @MPishvaian
🫁 Elisrasib showed “robust and durable efficacy” in patients with previously treated locally advanced or metastatic KRAS G12C NSCLC, according to results from an ongoing phase 1/2 trial presented at #AACR26 by @cbcbc1971.
➡️ Read more: https://t.co/wMOlsArHKg
#lcsm#NSCLC
Encouraging results from #AACR26 on Elisrasib (D3S-001) for KRAS G12C NSCLC by Dr. Cho 🧬
Key highlights:
✅ 2L+ G12Ci Naïve: 59.5% ORR, mDOR 14.9 months.
✅ 3L+ G12Ci Refractory: 32.3% PR rate, mDOR 15.6 months.
✅ Mechanism: CNS penetrable; overcomes resistance in G12Ci-refractory settings.
✅ Safety: Favorable profile with consistent, manageable results.
With FDA Breakthrough Therapy and Fast Track designations, this next-gen inhibitor is moving to pivotal trials for both monotherapy and combination settings. 🚀📈
@AACR@KRASKickers@cbcbc1971@yonsei_u@OncoAlert
Dr. Byoung Chul Cho presented elisrasib (D3S-001), next gen KRAS G12C inhibitor in NSCLC at #AACR26. Images not posted by request. In 84 pts with no prior G12C inhibitor, RR 59.5%, DCR 98.8%, PFS 9.4m. In pts with prior G12Ci, RR 32.3%, DCR 83.9% DOR 15.6, PFS 8.1m. ctDNA clearance in 80% of pts. In KRAS G12C with STK11/KEAP1 co-mutation, RR 55% (vs 76% in wild type). Safety reassuring: AST/ALT elevations in 10-13%, only 1 case of G3 each.
Byoung Chul Cho shared updated phase I/II clinical trial results evaluating elisrasib in patients with locally advanced or metastatic NSCLC at #AACR26. Learn more in AACR Annual Meeting News: https://t.co/zDWUL0UnRx
A multinational study @NatureMedicine led by CU Medicine proved that D3S-001, a next-generation KRAS-G12C inhibitor developed in mainland China, showed promising results in treating various types of solid tumours in terms of anti-tumour activity, safety and tolerability. https://t.co/iRPyl6cDdL
📖: https://t.co/CgHEyL7hni
@TonyMok9@herbloong