The University of Texas (UT) MD Anderson Cancer Center is recognizing the leadership of President Peter WT Pisters, MD, following his announced plan to retire from MD Anderson to focus on the next chapter of his career. The UT System Board of Regents and Chancellor John M. Zerwas, MD, have named Jeffrey E. Lee, MD, Interim President, effective immediately. Dr. Pisters will work with Dr. Lee on a thoughtful transition through the end of September.
The addition of spartalizumab to dabrafenib and trametinib demonstrated a long-term survival benefit in patients with BRAF V600–mutant metastatic melanoma, according to the final overall survival analysis from the phase III COMBI-I trial published in the Journal of Clinical Oncology.
For more than a decade, geriatric oncology has evolved from a niche discipline into an evidence-based component of high-quality cancer care. Landmark randomized trials, including the Geriatric Assessment for Patients 70 Years and Older Starting Cancer Treatment (GAP70+) trial,1 the Geriatric Assessment-Driven Intervention (GAIN) trial,2 the Integrated Geriatric Assessment and Treatment Effectiveness (INTEGERATE) study,3 and the Geriatric Intervention in Frail Older Patients With Cancer Receiving Chemotherapy (GERICO) trial,4 have consistently demonstrated that geriatric assessment–guided interventions can reduce treatment toxicity, improve communication and patient-centered care, and support treatment decision-making for older adults with cancer.
First-line treatment with the antibody-drug conjugate sacituzumab govitecan-hziy plus pembrolizumab led to a longer progression-free survival after next line of treatment—ie, progression-free survival–2 (PFS2)—than chemotherapy plus pembrolizumab in patients with previously untreated, PD-L1–positive advanced triple-negative breast cancer, according to an exploratory post hoc analysis of the phase III ASCENT-04/KEYNOTE-D19 trial1 presented at the 2026 ASCO Annual Meeting by Kevin Kalinsky, MD, MS, FASCO, Professor and Director in the Division of Medical Oncology and Co-Director of the Glenn Family Breast Center at Winship Cancer Institute of Emory University School of Medicine, Atlanta.
I was just 24 and in seemingly perfect health when I began experiencing unexplained abdominal pain so excruciating, even daily doses of pain medication failed to provide relief. I was a senior in college and had enrolled in a summer internship program at the University of California, Davis, when my ...
Adjuvant alectinib was associated with early improvements in health-related quality of life that were maintained over 2 years of treatment in patients with resected ALK-positive non–small cell lung cancer (NSCLC). The new analysis of the phase III ALINA trial, reported by Dziadziuszko et al in The...
ASCO members are leading the way to make sure Congress understands the critical importance of federal cancer research funding before the September 30 federal funding deadline. “The People Behind the Progress,” an ASCO social media series, features members sharing how federal cancer research has...
The Personalized Medicine Coalition (PMC), a nonprofit organization dedicated to advancing personalized medicine, recently announced that physician-scientist Norman E. “Ned” Sharpless, MD, has been selected as the recipient of the 20th Annual Award for Leadership in Personalized Medicine,...
Extended-interval dosing of intravenous tarlatamab, at 20 mg every 3 weeks or 30 mg every 4 weeks, demonstrated efficacy and safety that was consistent with the approved tarlatamab dosing regimen in patients with small cell lung cancer (SCLC), according to findings from the phase II DeLLphi-309...
Adding the subcutaneous PD-L1 blocker envafolimab to short-course radiotherapy and CAPEOX (capecitabine and oxaliplatin) improved pathologic complete response (pCR) without a clear safety or surgical feasibility penalty in patients with microsatellite-stable (MSS) locally advanced rectal cancer,...
Subcutaneous administration of tarlatamab was well tolerated in patients with extensive-stage small cell lung cancer (ES-SCLC) in the phase IB DeLLphi-308 trial. Investigators were able to eliminate the preplanned post-dose monitoring in the second part of the study due to the safety of the...