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    Home > Active Ingredient News > Antitumor Therapy > Front Oncol: Real-world assessment of the long-term efficacy of first-line pembrolizumab monotherapy in advanced NSCLC patients with PD-L1 ≥ 50%

    Front Oncol: Real-world assessment of the long-term efficacy of first-line pembrolizumab monotherapy in advanced NSCLC patients with PD-L1 ≥ 50%

    • Last Update: 2022-04-23
    • Source: Internet
    • Author: User
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    Recently, Frontiers in Oncology published a real-world study from the United States, mainly evaluating the long-term efficacy of first-line pembrolizumab (pembrolizumab) monotherapy in patients with advanced NSCLC
    with PD-L1 ≥ 50% .

    Recently, Frontiers in Oncology published a real-world study from the United States, mainly evaluating the long-term efficacy of first-line pembrolizumab (pembrolizumab) monotherapy in patients with advanced NSCLC
    with PD-L1 ≥ 50% .


    NSCLC

    The study included two cohorts of patients: the electronic medical record cohort (EHR cohort) and the manual review cohort (spotlight cohort), and assessed overall survival (OS) in the two cohorts, and real-world progression-free survival (rwPFS) in the spotlight cohort and real-world Tumor Response (rwTR)
    .

    The study included two cohorts of patients: the electronic medical record cohort (EHR cohort) and the manual review cohort (spotlight cohort), and assessed overall survival (OS) in the two cohorts, and real-world progression-free survival (rwPFS) in the spotlight cohort and real-world Tumor Response (rwTR)
    .


    The EHR cohort included 566 patients (298 [53%] men); whereas the spotlight cohort included 228 patients (105 [46%] men); the median age of patients in both groups was 71 years
    .

    The EHR cohort included 566 patients (298 [53%] men); whereas the spotlight cohort included 228 patients (105 [46%] men); the median age of patients in both groups was 71 years
    .


    The median follow-up time in the EHR and spotlight cohorts was 35.
    1 months (range 12.
    0-52.
    7) and 38.
    4 months (range 33.
    1-44.
    9), respectively
    .


    The median OS was 19.


    The median follow-up time in the EHR and spotlight cohorts was 35.


    Of the 182 (32%) patients in the EHR cohort who received second-line systemic therapy, most commonly platinum-based chemotherapy or immunotherapy (ICI monotherapy or ICI-chemotherapy), 63 (35%) patients received third-line therapy treatment, and 16/63 (25%) patients received fourth-line therapy
    .


    In the spotlight cohort, 87 (38%) patients received second-line therapy, of which 26 (30%) received third-line therapy; 7 were fourth-line therapy, and 3 were fifth-line therapy


    Of the 182 (32%) patients in the EHR cohort who received second-line systemic therapy, most commonly platinum-based chemotherapy or immunotherapy (ICI monotherapy or ICI-chemotherapy), 63 (35%) patients received third-line therapy treatment, and 16/63 (25%) patients received fourth-line therapy


    For the spotlight cohort, the median rwPFS was 7.
    3 months (95% CI, 5.
    7 9.
    2)
    .

    For the spotlight cohort, the median rwPFS was 7.
    3 months (95% CI, 5.
    7 9.
    2)
    .


    For the spotlight cohort, the median rwPFS was 7.


    In the spotlight cohort, a total of 17 patients (7%) had an rwTR assessment of CR, 71 patients (31%) had a PR assessment of PR, and the rwTRR was 38.
    6% (95% CI, 32.
    2-45.
    2) for a total of 122 patients ( 54%) disease control (CR + PR + stable disease)
    .

    In the spotlight cohort, a total of 17 patients (7%) had an rwTR assessment of CR, 71 patients (31%) had a PR assessment of PR, and the rwTRR was 38.
    6% (95% CI, 32.
    2-45.
    2) for a total of 122 patients ( 54%) disease control (CR + PR + stable disease)
    .


    In the spotlight cohort, a total of 17 patients (7%) had an rwTR assessment of CR, 71 patients (31%) had a PR assessment of PR, and the rwTRR was 38.


    For 151 of 228 patients (66%) who discontinued pembrolizumab, the most common reasons were disease progression (70 [46%]) and treatment-related adverse reactions (35 [23%])
    .


    No serious adverse reactions were found


    For 151 of 228 patients (66%) who discontinued pembrolizumab, the most common reasons were disease progression (70 [46%]) and treatment-related adverse reactions (35 [23%])


    In conclusion, the study shows that for patients with advanced NSCLC with PD-L1≧50%, the real-world efficacy of first-line pembrolizumab (pembrolizumab) monotherapy is consistent with clinical studies, which supports the application of this regimen
    .

    In conclusion, the study shows that for patients with advanced NSCLC with PD-L1≧50%, the real-world efficacy of first-line pembrolizumab (pembrolizumab) monotherapy is consistent with clinical studies, which supports the application of this regimen
    .
    Studies have shown that for patients with advanced NSCLC with PD-L1≧50%, the real-world efficacy of first-line pembrolizumab (pembrolizumab) monotherapy is consistent with clinical studies, supporting the application of this regimen
    .
    Studies have shown that for patients with advanced NSCLC with PD-L1≧50%, the real-world efficacy of first-line pembrolizumab (pembrolizumab) monotherapy is consistent with clinical studies, supporting the application of this regimen
    .

    Original source:

    Original source:

    Velcheti V, Hu X, Yang L, Pietanza MC and Burke T (2022) Long-Term RealWorld Outcomes of First-Line Pembrolizumab Monotherapy for Metastatic Non-Small Cell Lung Cancer With ≥50% Expression of Programmed Cell Death-Ligand 1.
    Front .
    Oncol.
    12:834761.
    doi: 10.
    3389/fonc.
    2022.
    834761

    Velcheti V, Hu X, Yang L, Pietanza MC and Burke T (2022) Long-Term RealWorld Outcomes of First-Line Pembrolizumab Monotherapy for Metastatic Non-Small Cell Lung Cancer With ≥50% Expression of Programmed Cell Death-Ligand 1.
    Front .
    Oncol.
    12:834761.
    doi: 10.
    3389/fonc.
    2022.
    834761

     

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