2025 SITC Election | Vice President | At-Large Directors
The 2025 SITC Election will take place May 2–16, 2025. SITC regular or emertius members eligible to vote and help choose the future leaders of the society.
The 2025 SITC Election will take place May 2–16, 2025. SITC regular or emertius members eligible to vote and help choose the future leaders of the society.
In AEGEAN, perioperative durvalumab plus neoadjuvant chemotherapy, versus neoadjuvant chemotherapy alone, significantly improved event-free survival and pathological complete response (primary endpoints; modified ITT [mITT] population,…
Join SITC and a panel of experts for an afternoon of in-depth education on all aspects of cellular therapies, T Cell Engagers and TIL Therapies
Most of the published data with trastuzumab deruxtecan (T-DXd) derive from clinical trials with selected populations and little representation of US patients. Limited real-world data…
Lung cancer (LC) incidence and mortality have changed significantly over the past few decades, yet the disease remains the leading cause of cancer-related deaths worldwide.…
Sugemalimab with chemotherapy showed a superior long-term overall survival benefit compared with placebo with chemotherapy, as a first-line treatment for patients with NSCLC with no…
Invasive mucinous adenocarcinoma (IMA) is a type of primary lung adenocarcinoma characterized by tumor cells that exhibit a goblet or columnar cell morphology and contain…
Canakinumab is a human monoclonal anti–interleukin-1β antibody with the potential to enhance the activity of PD-(L)1 inhibitors by inhibiting protumor inflammation.
The PHAROS primary analysis showed robust antitumor activity and acceptable safety with encorafenib plus binimetinib in patients with BRAF V600E-mutant metastatic NSCLC (mNSCLC). We report…
Virtual webinar featuring presentations & discussions on selected abstracts in lung cancer from ASCO 2025. Chaired by Noemí Reguart Moderated by Stephen Liu, Nicolas Girard…
Microabstract: Osimertinib showed PFS of 20.1 months and OS of 42.0 months in EGFRm+ NSCLC, comparable to those of the FLAURA trial. Adverse events included…