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ASCO 2024 | CheckMate 8HW: nivolumab and ipilimumab in MSI-H/dMMR mCRC

John Strickler, MD, Duke University, Durham, NC, gives an overview of the Phase III CheckMate 8HW trial (NCT04008030), which assessed nivolumab and ipilimumab or chemotherapy in the first-line setting in patients with microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) metastatic colorectal cancer (mCRC). Using checkpoint inhibitors resulted in superior progression-free survival (PFS), but additional research is needed to compare nivolumab and ipilimumab with nivolumab alone to properly personalize treatment in this area. This interview took place during the 2024 American Society of Clinical Oncology (ASCO) Meeting in Chicago, IL.

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Disclosures

Stock and Other Ownership Interests – Triumvira Immunologics, Inc
Consulting or Advisory Role – Abbvie; Amgen; AstraZeneca; Bayer; Beigene; Daiichi Sankyo/Astra Zeneca; GlaxoSmithKline; Janssen Oncology; Jazz Pharmaceuticals; Lilly; Merck; Natera (Inst); Pfizer; Roche/Genentech; Seagen; Taiho Oncology; Takeda
Research Funding – A*STAR (Inst); Abbvie (Inst); Amgen (Inst); AstraZeneca/MedImmune (Inst); Bayer (Inst); BeiGene (Inst); Curegenix (Inst); Daiichi Sankyo/Lilly (Inst); Erasca, Inc (Inst); GlaxoSmithKline (Inst); Leap Therapeutics (Inst); Lilly (Inst); Roche/Genentech (Inst); Seagen (Inst)
Expert Testimony – Seagen
Travel, Accommodations, Expenses – Seagen