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Statin-Specific Effects May Influence Immunotherapy Outcomes in Patients With Head and Neck Squamous Cell Carcinoma
4+ day, 21+ hour ago (358+ words) Allen Khudaverdyan, MD, NYU Grossman School of Medicine, New York, New York, discusses results from a large retrospective analysis evaluating the association between concurrent statin use and overall survival in patients with head and neck squamous cell carcinoma treated with…...
Zanidatamab-Based Regimens Redefine First-Line Treatment of HER2-Positive Gastroesophageal Adenocarcinoma
5+ day, 22+ hour ago (652+ words) Geoffrey Ku, MD, Memorial Sloan Kettering Cancer Center, New York, New York, discusses how findings from the phase 3 HERIZON-GEA-01 trial are reshaping first-line treatment of HER2-positive gastroesophageal adenocarcinoma following the approval of zanidatamab plus chemotherapy, with or without tislelizumab. He…...
FDA Approves Camizestrant Plus CDK4/6 Inhibitor Following Emergence of ESR1 Mutation in Advanced Breast Cancer
6+ day, 1+ hour ago (273+ words) Based on results from the phase 3 SERENA-6 trial, the US Food and Drug Administration (FDA) granted accelerated approval to camizestrant (Etcamah; AstraZeneca) in combination with a CDK4/6 inhibitor for patients with HR-positive, HER2-negative locally advanced or metastatic breast cancer following detection…...
Molecularly Guided Treatment Intensification in Metastatic Prostate Cancer
2+ week, 3+ day ago (839+ words) Andrew Hahn, MD, MD Anderson Cancer Center, Houston, Texas, presents a case of de novo metastatic prostate cancer to illustrate how comprehensive molecular profiling can inform upfront treatment selection. Hi, my name is Andy Hahn, I'm an assistant professor of…...
FDA Approves Zanidatamab-Based Regimens for First-Line HER2-Positive Advanced Gastroesophageal Adenocarcinoma
2+ week, 6+ day ago (192+ words) The approval of zanidatamab plus tislelizumab and chemotherapy applies to patients with HER2 IHC 3+ or IHC 2+/ISH+ tumors, while zanidatamab plus chemotherapy without tislelizumab is approved for patients with HER2 IHC 3+ disease. HER2 positivity must be confirmed using an FDA-approved test. PFS was…...