EMA Recommends Extension of Therapeutic Indications for Durvalumab
New indication concerns the first-line treatment of biliary tract cancer
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1586 results
Geriatric Assessment Intervention Reduces Patient-Reported Symptomatic Toxicities in Older Patients with Advanced Cancer
Findings from the secondary analysis of the GAP70+ study
Duration of Bevacizumab Maintenance of 15 Months Remains the Standard in Front-Line Treatment for Newly Diagnosed Stage IIB-IV Epithelial Ovarian Cancer
Findings from the AGO-OVAR 17 BOOST study
FDA Approves Tremelimumab in Combination with Durvalumab and Platinum-Based Chemotherapy for Metastatic NSCLC
Evidence for efficacy is based on the results from the POSEIDON study
Adding Tremelimumab to Durvalumab and Chemotherapy Provides Survival Benefit for Patients with Metastatic NSCLC
Findings from the POSEIDON study
EMA Recommends Extension of Therapeutic Indications for Trastuzumab Deruxtecan
New indication concerns the treatment of adult patients with advanced HER2-positive gastric or gastroesophageal junction adenocarcinoma who have received a prior trastuzumab-based regimen
High Frequency of Germline ATM Variants in CLL
Chronic lymphocytic leukaemia that develops in patients with rare germline ATM variants is more likely to have 11q deletion
EMA Recommends Granting a Marketing Authorisation for Plerixafor Accord
It is a generic of Mozobil which has been authorised in the EU since 2009
Nivolumab/Ipilimumab Combination Should Precede Dual BRAF/MEK Inhibition in Patients with BRAF-Mutated Unresectable Melanoma
Findings from the DREAMseq study
Pembrolizumab Concurrent with Radiotherapy Does Not Improve the Tumour Control and Survival in Locally Advanced Squamous Cell Carcinoma of Head and Neck Unfit for Cisplatin
PembroRad shows less toxicity from standard of care regimen in unfit patients
FLT3 Internal Tandem Duplication Measurable Residual Disease in Complete Remission Identifies Patients with AML with Profound Risk for Relapse and Death
Impact of NGS-based detection of FLT3 internal tandem duplication measurable residual disease on treatment outcome in newly diagnosed acute myeloid leukaemia
FDA Approves Teclistamab-cqyv for Relapsed or Refractory Multiple Myeloma
Evidence for efficacy is based on the results from the MajesTEC-1 study