November 12th, 2026FDA Grants Breakthrough Therapy Designation to 64Cu-SAR-bisPSMA for PSMA PET in Biochemically Recurrent Prostate CancerPhase 2 Co-PSMA data showed higher lesion detection with 64Cu-SAR-bisPSMA vs 68Ga-PSMA-11 in biochemical recurrence after prostatectomy.Read more
November 11th, 2026LITESPARK-022 PRO Data Further Support Adjuvant Belzutifan Plus Pembrolizumab in ccRCCThomas Powles, MBBS, MRCP, MD, discusses LITESPARK-022 QOL findings and patient selection for adjuvant belzutifan plus pembrolizumab in RCC.Read more
November 10th, 2026Genomic Testing, Toxicity, and Sequencing Shape Treatment Decisions in Advanced Prostate CancerExperts weigh genomic testing, treatment intensification, and radioligand sequencing in advanced prostate cancer care.Read more
November 10th, 2026FDA Approves Companion Diagnostic for Pembrolizumab in MSI-H Solid TumorsThe PCR-based OncoMate MSI Dx Analysis System can now identify patients with MSI-H solid tumors who may be eligible for pembrolizumab.Read more
November 9th, 2026Gedatolisib sNDA Accepted by FDA for PIK3CA-Mutated, HR+, HER2– Advanced Breast CancerThe FDA set a June 25, 2027, target action date for gedatolisib plus fulvestrant in PIK3CA-mutated, HR-positive, HER2-negative advanced breast cancer.Read more
November 8th, 2026JNJ-87189401 Plus Pasritamig Drives Deep PSA Responses With Favorable Safety in Pretreated mCRPCA dual antigen–targeted T-cell engager doublet produced durable PSA responses in late-line metastatic castration-resistant prostate cancer.Read more
November 7th, 2026VET3-TGI Generates Responses in Checkpoint Inhibitor–Refractory Cutaneous CancersVET3-TGI produced responses in injected and non-injected lesions without dose-limiting toxicities in the phase 1/1b STEALTH-001 trial.Read more
November 6th, 2026Canakinumab Reduces Nodule Size in High-Risk Lung PrecancersIL-1β blockade with canakinumab was well tolerated and reduced nodule size in patients with high-risk indeterminate pulmonary nodules.Read more