Bi-weekly Teclistamab Dosing Receives FDA Approval for Relapsed/Refractory Multiple Myeloma
February 21st 2024A supplemental Biologics License Application for teclistamab-cqyv (Tecvayli) has been approved by the FDA at a reduced dose of 1.5 mg/kg every 2 weeks for the treatment of patients with relapsed/refractory multiple myeloma who have maintained a complete response or greater for at least 6 months.
SBRT Plus Standard of Care Improves PFS in Oligoprogressive NSCLC
February 19th 2024Stereotactic ablative radiotherapy with standard-of-care therapy improved progression-free survival in patients with oligoprogressive non-small cell lung cancer, although the benefit was not seen in those with oligoprogressive breast cancer.
Tislelizumab Plus Chemo Improves Event-Free Survival in Stage II-IIIA NSCLC
February 17th 2024The use of perioperative tislelizumab plus neoadjuvant chemotherapy has been supported by findings from the phase 3 RATIONALE-315 study as a treatment for resectable stage II to IIIA non–small cell lung cancer.
Osimertinib Receives Approval From FDA for EGFR-Mutated Locally Advanced or Metastatic NSCLC
February 16th 2024The FDA approved osimertinib for use with platinum-based chemotherapy to treat patients with locally advanced or metastatic non-small cell lung cancer that harbor EGFR exon 19 deletions or exon 21 L858R mutations.