EMA Recommends Granting a Conditional Marketing Authorisation for Teclistamab
It is indicated as monotherapy in adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies
Oncology News
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Intratumoural Administration of the Oncolytic Herpes Virus Shows Survival Benefit and a Safe Profile in Patients with Residual or Recurrent Glioblastoma
Findings from a pivotal single-arm phase II study
Zero Mutation ctDNA Triage for Selection of Patients with Metastatic Colorectal Cancer for Panitumumab Rechallenge
Findings from the CHRONOS study
FDA Approves Darolutamide Tablets for Metastatic Hormone-Sensitive Prostate Cancer
Evidence for efficacy is based on the results from the ARASENS study
Marginal Benefit in Overall and Progression-Free Survival from New Anticancer Drugs
New anticancer drugs substantially reduce the risk of death and tumour progression, but only marginally extend patient survival
EMA Recommends Granting a Marketing Authorisation for Nivolumab / Relatlimab
It is indicated for the first-line treatment of advanced melanoma in adults and adolescents 12 years of age and older with tumour cell PD-L1 expression < 1%
Neoadjuvant Niraparib Demonstrates Promising Antitumour Activity and Safety in Patients with Localised HER2-negative, BRCA-mutated Breast Cancer
Findings from the single-arm, phase II study
Trastuzumab Deruxtecan Shows High Intracranial Response Rate in Patients with Active Brain Metastases from HER2-positive Breast Cancer
Findings from the TUXEDO-1 study
Molecular Profiling Identifies Targetable Alterations in Majority of Patients with Advanced Rare Gastrointestinal Malignancies
Findings from the ARCAGEN study (EORTC-1843)
Largest Study on Frequent Aspirin Use Supports Reduction in Ovarian Cancer Risk
Findings from an analysis of data from two ovarian cancer consortia
Genetic Risk Score Increases Prediction of Severe Obesity in Adult Survivors of Childhood Cancer
Genetic testing, along with assessment of clinical risk factors, could be used to identify survivors at high risk for severe obesity and associated cardio-metabolic complications
EMA Recommends Granting a Marketing Authorisation for Lutetium (177lu) Chloride
This radiopharmaceutical precursor must be used only for the radiolabelling of carrier medicines that have been specifically developed and authorised for radiolabelling with lutetium chloride