Figure 1 from Phase I/II Study of AXL-Specific Antibody–Drug Conjugate Enapotamab Vedotin in Patients with Advanced Solid Tumors
<p>Best change from baseline in sum of target lesions (investigator assessment) in the dose-expansion phase for the NSCLC cohorts (<b>A</b>, <b>C</b>, and <b>E</b>) and baseline tumor H-score levels for AXL positivity by investigator-assessed confirmed best...
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| Kolejni autorzy: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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2025
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| Streszczenie: | <p>Best change from baseline in sum of target lesions (investigator assessment) in the dose-expansion phase for the NSCLC cohorts (<b>A</b>, <b>C</b>, and <b>E</b>) and baseline tumor H-score levels for AXL positivity by investigator-assessed confirmed best overall response (<b>B</b>, <b>D</b>, and <b>F</b>). <b>A</b> and <b>B,</b> Cohort 1 (Q3W): NSCLC with sensitizing <i>EGFR</i> mutations and/or mutations targeted by third-generation TKIs (<i>n</i> = 22). <b>C</b> and <b>D,</b> Cohort 2 (2.2 mg/kg Q3W): NSCLC without activating <i>EGFR</i> mutations or <i>ALK</i> rearrangements (<i>n</i> = 55). <b>E</b> and <b>F,</b> Cohort 8 (3Q4W): NSCLC without activating <i>EGFR</i> mutations or <i>ALK</i> rearrangements (<i>n</i> = 26). NE, not evaluable; PD, progressive disease; PR, partial response.</p> |
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