For patients with newly diagnosed multiple myeloma not undergoing an autologous stem cell transplant, indefinite lenalidomide maintenance resulted in more toxicity with no survival benefit from continuing treatment until disease progression compared with stopping after 2 years. Results from the randomized phase III ENDURANCE clinical trial by the ECOG-ACRIN Cancer Research Group (ECOG-ACRIN) were published today in The New England Journal of Medicine.
As reported in The Lancet by Lu et al, an interim analysis of the Chinese phase III HARMONi-6 trial showed that ivonescimab plus chemotherapy was associated with significantly improved overall survival vs tislelizumab plus chemotherapy in patients with previously untreated advanced squamous non–small cell lung cancer (NSCLC). A prior report from the trial showed that progression-free survival, the primary endpoint, was significantly better with ivonescimab plus chemotherapy.
An investigational targeted therapy designed to block one of the most common genetic drivers of pancreatic cancer has shown promising early results when combined with standard first-line chemotherapy, according to research presented at the ESMO Gastrointestinal Cancers Congress 2026 (Abstract 340O).
On July 14, the U.S. Food and Drug Administration (FDA) granted traditional approval to selpercatinib (Retevmo), an oral RET inhibitor, for adult and pediatric patients aged 2 years and older with locally advanced or metastatic solid tumors with a RET gene fusion, as detected by an FDA-approved test, whose disease has progressed on or following prior systemic treatment or who have no satisfactory alternative treatment options. Selpercatinib received accelerated approval for this indication for adult patients in 2022 and for pediatric patients aged 2 years and older in 2024.
New findings in a report led by the American Cancer Society (ACS) reveal an urgent picture of a growing global cancer burden and underscore the life-saving potential of stronger prevention and equitable access to care. According to Global Cancer Statistics, 2026, nearly 21 million people were diagnosed with cancer and 9.8 million died from the disease globally in 2024. The estimates show about 1 in 5 people worldwide will develop cancer during their lifetime; 1 in 9 men and 1 in 13 women will die from the disease. The number of cancer cases is projected to reach 34 million by 2050—a 67% increase from 2024—solely based on population aging and growth.
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...
As reported in the Journal of Cancer Education by Kim et al, parallel surveys of cancer survivors and cancer care providers showed gaps in risk awareness and communication about cannabis use. underscoring the need for open, nonjudgmental dialogue and clinical guidance. Although attitudes toward...
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,...
Patients with small cell lung cancer (SCLC) and type 1 antineuronal nuclear or “Hu” antibody (ANNA1/Hu-IgG)–related paraneoplastic neurological syndromes (PNS) may experience longer survival, according to the results of a study published in Journal of Neurology. Additionally, in those with...
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 July 22, the U.S. Food and Drug Administration (FDA) approved zidesamtinib (Jideytro), a ROS1 selective inhibitor, for the treatment of adult patients with locally advanced or metastatic ROS1-positive non–small cell lung cancer (NSCLC) who received a prior ROS1 kinase inhibitor. The approval...