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May 28, 2026
Chris Ryan
The FDA has approved durvalumab in combination with BCG for the treatment of adult patients with BCG-naive, high-risk NMIBC.
Courtney Flaherty
The FDA has accepted for review an NDA for bezuclastinib plus sunitinib in imatinib-pretreated GIST, with a PDUFA date of November 30, 2026.
Roswell Park Comprehensive Cancer Center
Roswell Park Comprehensive Cancer Center researchers will share key data at the 2026 ASCO Annual Meeting.
Rising rates of early-onset cancers have prompted shifts in management strategies and new research avenues.
May 27, 2026
OncLive Staff
The zanidatamab triplet significantly improved both PFS and OS vs trastuzumab plus chemotherapy in HER2-positive gastroesophageal cancer.
The FDA has approved pivekimab sunirine-pvzy (Decnupaz) for the treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm.
Kyle Doherty
OncLive spoke with experts in the field of GU oncology to gain their insights on the most notable presentations from the 2026 AUA Annual Meeting.
The FDA priority review of neladalkib for TKI-pretreated ALK-positive NSCLC is supported by data from the phase 1/2 ALKOVE-1 trial.
Sylvester Comprehensive Cancer Center
Researchers found machine learning models using patient-reported outcomes and clinical data could help forecast unplanned health care use after treatment.
Ashling Wahner
The FDA extended the review period for camizestrant plus a CDK4/6 inhibitor in hormone receptor–positive breast cancer with an emergent ESR1 mutation.
RD118 produced an ORR of 94.4% and a median PFS of 18.2 months in heavily pretreated patients with relapsed/refractory multiple myeloma.
May 26, 2026
A DSMB has recommended the continuation of the BRIA-ABC trial evaluating Bria-IMT in patients with metastatic breast cancer, with no safety concerns.
Dana-Farber Cancer Institute
Studies in pancreatic and prostate cancer selected for ASCO’s Plenary Program.
Neil D. Gross, MD, FACS, discusses how anti–PD-1 therapy is changing treatment approaches in advanced CSCC.
The European Medicines Agency’s CHMP has issued a positive opinion for encorafenib plus cetuximab and mFOLFOX6 in first-line BRAF V600E–mutant mCRC.