Articles

  • 1 month ago | onclive.com | Darlene Dobkowski

    Enfortumab vedotin (Padcev) demonstrated a manageable safety profile and no unexpected toxicities in patients aged 80 years and older with urothelial carcinoma, according to findings from a real-word study presented at the 2025 American Society of Clinical Oncology Genitourinary Cancers Symposium. More patients aged 85 years and older received upfront Padcev dose reduction. There were fewer grade 2/3 (moderate to severe) treatment-related side effects with lower starting doses of Padcev.

  • 1 month ago | curetoday.com | Darlene Dobkowski |Alex Biese

    As an expert explained in an interview with CURE, we may be in the midst of a “new era” for small cell lung cancer research. This optimism comes in the wake of the Food and Drug Administration’s (FDA’s) approval of Imdelltra (tarlatamab-dlle) in May 2024 for the treatment of patients with extensive-stage small cell lung cancer (SCLC).

  • 1 month ago | curetoday.com | Alex Biese |Darlene Dobkowski

    Ensacove (ensartinib) has been approved by the Food and Drug Administration (FDA) for adults with anaplastic lymphoma kinase (ALK)-positive locally advanced or metastatic non-small cell lung cancer (NSCLC) who have not previously received an ALK-inhibitor. Ensacove’s efficacy was displayed in the phase 3 eXALT3 clinical trial of 290 patients with locally advanced or metastatic ALK-positive NSCLC who were naïve to prior ALK-targeted therapy.

  • 1 month ago | curetoday.com | Alex Biese |Darlene Dobkowski

    The Food and Drug Administration (FDA) has approved Imfinzi (durvalumab) for adults with limited-stage small cell lung cancer (SCLC) whose disease did not progress after concurrent platinum-based chemotherapy and radiation therapy. The late 2024 approval was based on findings form the ADRIATIC trial of 730 patients with limited-stage SCLC.

  • 1 month ago | curetoday.com | Alex Biese |Darlene Dobkowski

    The Food and Drug Administration (FDA) has granted its first approval for a systemic therapy for patients with non-small cell lung cancer (NSCLC) with an Neuregulin 1 (NRG1) gene fusion, with the accelerated approval of Bizengri (zenocutuzumab-zbco). The FDA approved Bizengri in late 2024 for the treatment of advanced, unresectable or metastatic NSCLC with a NRG1 gene fusion with disease progression on or after prior systemic therapy.

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