|Videos|August 12, 2016
FDA Approval in Head and Neck Cancer, European Approval in NSCLC, Breakthrough Designation in Breast Cancer, and More
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Long-Term Cilta-Cel Data Show Low Rates of PFS Events in Standard-Risk R/R Myeloma
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Nonresponse to Bridging Therapy and Peak ALC After Cilta-Cel Are Associated With Neurotoxicity, NRM in Myeloma
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FDA Updates Axi-Cel Label to Remove Limitation of Use in R/R PCNSL
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FDA Underscores Risks Associated With DPD Deficiency and Capecitabine/5-FU Use in Cancer Care
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