FDA Approves Larotrectinib for NTRK-Positive Solid Tumors
The FDA has granted full approval to larotrectinib for select patients with solid tumors harboring a NTRK gene fusion.
The FDA has granted full approval to larotrectinib for select patients with solid tumors harboring a NTRK gene fusion.
The FDA has awarded full approval to frontline nivolumab plus ipilimumab for the treatment of adult patients with unresectable hepatocellular carcinoma.
Michael J. Morris, MD, discusses data from the PSMAfore trial that supported the FDA expanded approval of lutetium Lu 177 vipivotide tetraxetan in mCRPC.
Henry M. Kuerer, MD, PhD, FACS, CMQ, discusses a study on selective elimination of breast surgery after exceptional response to neoadjuvant therapy in early breast…
D-VRd has the potential to significantly improve clinical outcomes in transplant-ineligible or -deferred patients with newly diagnosed multiple myeloma.
Here is your snapshot for all therapeutic options that were cleared by the FDA in April 2025 spanning tumor types.
Panelists discuss how they approach the treatment of HER2-positive advanced breast cancer with brain metastases, outlining the criteria for therapy selection, the role of patient-specific…
Stergios J. Moschos, MD, discusses how the use of bridging therapy can enhance the efficacy of adoptive T-cell therapies for patients with melanoma.
Daraxonrasib was safe and active in the pretreated advanced non–small cell lung cancer harboring RAS mutations.
Educating patients and health care providers about BiTE-associated CRS and ICANS increases comfort levels with giving these agents in outpatient settings.
The association between greater hematologic AEs and increased OS necessitates early receipt of G-CSF after NALIRIFOX infusion for patients with PDAC.