A histology-based artificial intelligence (AI) biomarker may help personalize adjuvant chemotherapy selection for patients with resected pancreatic ductal adenocarcinoma, according to the results of a study by Beaufils et al. The investigators developed and validated a deep learning model that analyzes routine histology slides to predict the relative benefit of adjuvant gemcitabine vs modified FOLFIRINOX (mFOLFIRINOX). The resulting biomarker, termed PANCprAId, identified patient subgroups with differential benefit from the two regimens in an external validation cohort from the randomized phase III PRODIGE-24/CCTG PA6 trial. The study is published in the Journal of Clinical Oncology.
A research project funded by the National Institutes of Health (NIH), with collaborators around the country and the world, has generated extensive and diverse collections of patient-derived tumor models. Tumor tissue from patients with cancer contributed to the compendium of tumor models that will enhance the study of tumor biology and be an asset in accelerating the development of cancer therapies, while guiding future research directions.
Pamela Munster, MD, joined the Stanford Cancer Institute as the inaugural Associate Director for Early Detection and Interception Research on August 1, 2026. She also assumed a faculty appointment as a Professor in the Stanford Medicine Division of Oncology.
In a phase Ib study published in the Journal of Clinical Oncology, Zhao et al found that the first-in-class bispecific antibody-drug conjugate (ADC) izalontamab brengitecan (iza-bren, BL-B01D1) demonstrated antitumor activity in patients with relapsed extensive-stage small cell lung cancer, particularly when used as second-line therapy.
Above 80% of cancer care providers globally report a lack of knowledge regarding integrative oncology treatments that prevent them from offering these services to patients, according to survey findings published in Supportive Care in Cancer.
Maura L. Gillison, MD, PhD Maura Gillison did not chase awards. She chased answers, and especially clinically impactful answers. That distinction between the pursuit of recognition and the pursuit of truth defined everything about her as a scientist, a clinician, and a person. She was direct...
In the phase III BOND-003 Cohort C trial, intravesical cretostimogene grenadenorepvec, an oncolytic immunotherapy, produced complete responses in three-quarters of patients with high-risk, bacillus Calmette-Guérin (BCG)-unresponsive, non–muscle-invasive bladder cancer (NMIBC) with carcinoma in...
A panel of ASCO experts voted to approve ASCO’s first guideline on ctDNA testing in patients with solid tumors or lymphoma on November 18, 2025.1 The guideline addresses four overarching clinical questions: when ctDNA testing should (or should not) be used to (1) support cancer diagnosis; (2)...
There is a strong history of breast cancer in my family, and the fact that I have dense breasts adding to my risk of developing the disease, kept me vigilant about getting a yearly mammogram screening since I turned 32. The test never showed any suspicious lesions over the last nearly 2 decades,...
In the 5-year quality-of-life (QOL) analysis of the phase III SUPREMO trial published in The Lancet Oncology, Velikova et al found that women with intermediate-risk breast cancer who received postmastectomy chest wall radiotherapy experienced modestly worse local chest wall symptoms at 5 years, but ...
The Association for Clinical Oncology (ASCO) submitted formal comments (see https://bit.ly/4xYRg1j) to the Centers for Medicare & Medicaid Services (CMS) in response to the 2026 CMS Interoperability Standards and Prior Authorization for Drugs proposed rule. If finalized, this rule will require...
On August 13, the U.S. Food and Drug Administration (FDA) granted accelerated approval to iberdomide (Zenbexus), a cereblon-modulating protein degrader (CELMoD), in combination with daratumumab and hyaluronidase-fihj plus dexamethasone for adults with multiple myeloma who have received at least one ...