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Xiuning Le MD PhD

@LeXiuning

Associate Professor Thoracic Head and Neck Medical Oncology
MD Anderson Cancer Center
Houston, TX faculty.mdanderson.org/profiles/xiuni… Joined March 2020
385 Following 2.2K Followers 313 Posts

Latest posts 5

Xiuning Le MD PhD @LeXiuning
πŸ“– πŸ”₯ New online #firmonertinib in EGFR #PACC-mut NSCLC. @Cancer_Cell
πŸ‘‰ Firmonertinib has a trifluoroethoxy group, which enhances its potency against EGFR PACC mutation
πŸ‘‰ 68% response rate with firmonertinib 240 mg daily.
Median progression-free survival of 16.0 months at 240 mg.
πŸ‘‰ 47% intracranial response rate among patients with baseline brain metastases.
@EGFRResisters @Exon20Group @lungoncdoc @riess_md
UT MD Anderson Verified account @UTMDAnderson Oct 16
Results from the Phase 1b FURTHER trial found a targeted therapy that achieved achieved durable antitumor activity for patients with EGFR PACC-mutated non-small cell lung cancer. @LeXiuning #EndCancer spr.ly/6014BHMzuy
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Xiuning Le MD PhD @LeXiuning
😜 Are we ready for the era of #PD1Γ—VEGF #bispecific immunotherapy? πŸ“– Now online in #LancetOncology: #HARMONi β€” #ivonescimab plus chemotherapy in patients with #EGFR-mutant #NSCLC after progression on EGFR TKI therapy.
πŸ‘‰ First global randomized phase 3 study of a PD1Γ—VEGF bispecific antibody
N = 438, with 23% of patients enrolled in the United States
πŸ‘‰ Progression-free survival: 6.8 vs 4.4 months, HR 0.52
πŸ‘‰ Overall survival: 16.8 vs 14.0 months, HR 0.79
πŸ‘‰ Encouraging evidence of protection against CNS progression
πŸ’‘ HARMONi represents an important step in evaluating the potential of simultaneously targeting PD-(L1)1 and VEGF. I hope this will be the first of many positive global studies exploring PD-(L)1 Γ— VEGF approaches for patients with lung cancer and other solid tumors. lnkd.in/gUbwUxTb
❀️ my global col-investigators, @Tony_Calles @delvysra @MNagasaka @DrSanjayPopat @nicogirardcurie, Drs. Passaro, Cappuzzo, Zhang, and many others ❀️
2 replies 18 reposts 78 likes 4.5K views View on X
Xiuning Le MD PhD @LeXiuning
πŸ“– Now online @CD_AACR πŸ”₯
πŸ‘‰ The oncogenic #EGFR–SHC1 #fusion drives hashtag#lungcancer through dual activation of the N-terminal EGFR kinase domain and C-terminal SHC1 phosphorylation sites. This biology requires combined inhibition of both EGFR and SRC-family kinases to achieve effective clinical control.
πŸ‘‰ Most importantly, this represents a novel fusion activation mechanism: SHC1 acts not merely as a facilitating #fusion partner, but as a true #collaborating partner in oncogenesis: a previously unrecognized mechanism with direct therapeutic implications.
πŸ‘‰ Could similar cooperative signaling by fusion partners help explain de novo or early resistance in other fusion-driven cancers? 😜
doi.org/10.1158/2159-8…
@ElizSMcKenna and Jurgen Wolf (University Hospital Cologne, Germany)
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Xiuning Le MD PhD @LeXiuning
πŸ“– πŸ”₯New online from our group at @UTMDAnderson on ultra-precision oncology in #lungcancer
πŸ‘‰ Analysis from over 22,000 #EGFR-mutant tumor samples identified #PACC mutations in 12% of cases (A)
πŸ‘‰ While classical and #Ex20 mutations more commonly occur as single mutations, PACC mutations are more frequently (66%) observed as compound mutations (B).
πŸ‘‰ PACC/PACC and PACC/classical-like compound mutations function biologically similar to single PACC mutations, NOT classical mutations (C)
πŸ‘‰ Compound PACC mutations demonstrate greater sensitivity to EGFR TKIs than single PACC mutations (D)

⚑ πŸ’‘ Largest #EGFR mutation landscape in a Western population.
⚑ πŸ’‘ #Compound EGFR PACC Eare biologically analogous to #single PACC.
⚑ πŸ’‘ Important insights for drug development of next-generation EGFR TKIs.