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    Home > Active Ingredient News > Antitumor Therapy > J Clin Oncol: Long-term efficacy of Selpercatinib in patients with RET fusion-positive NSCLC

    J Clin Oncol: Long-term efficacy of Selpercatinib in patients with RET fusion-positive NSCLC

    • Last Update: 2022-09-30
    • Source: Internet
    • Author: User
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    Selpercatinib is a first-line highly selective RET kinase inhibitor with potent CNS activity approved for the treatment of non-small cell lung cancer (NSCLC)
    with positive RET fusion.
    In the LIBRETTO-001 trial, Selpercatinib demonstrated long-lasting antitumor activity, including intracranial efficacy
    .

    In this paper, researchers have updated their analysis
    of the long-term efficacy and safety of Selpercatinib in RET fusion-positive NSCLC.

    The LIBRETTO-001 trial was a single-group, open-label, phase I/II trial that enrolled 69 patients with initially treated RET fusion-positive NSCLC and 247 patients with REET-fusion-positive NSCLC who had received platinum-based chemotherapy
    .
    The primary endpoint was the objective response rate
    .
    Secondary endpoints included duration of remission, progression-free survival, overall survival, and safety
    .


    Long-term efficacy of Selpercatinib

    In the initial treatment of patients, the objective response rate is 84%, and 6% of patients have achieved complete remission
    .


    Among patients who had received platinum-based chemotherapy, the objective response rate was 61%, and 7% of patients achieved complete remission
    .


    Among the 26 patients with neurologic metastases at baseline, the objective intracranial response rate was 85%, including 27% of complete response
    .


    Overall, extended follow-up analysis of this large cohort study showed that Selpercatinib consistently demonstrated durable and robust therapeutic activity, including intracranial antitumor activity
    , in previously treated and untreated patients with RET fusion-positive NSCLC.


    Original Source:

    Alexander Drilon, et al.


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