echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > JNCI: Comparison of three PD-L1 immunohistochemical analysis methods and their correlation with the prognosis of triple-negative breast cancer patients

    JNCI: Comparison of three PD-L1 immunohistochemical analysis methods and their correlation with the prognosis of triple-negative breast cancer patients

    • Last Update: 2021-06-16
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    In the phase 3 IMpassion130 study, atezolizumab combined with nab-paclitaxel (A+nP) was positive for PD-L1 (tumor infiltrating immune cells [IC] ≥ 1%; SP142 immunohistochemistry [IHC]) late/metastatic Clinical benefits have been demonstrated in patients with triple negative breast cancer (TNBC)
    .

    Immune breast cancer

    This study aims to evaluate whether the other two PD-L1 detection methods are consistent with SP142 and the clinical prognosis of patients
    .

    IHC was used to detect the PD-L1 status (VENTANA SP142, SP263, Dako 22C3) of IC in samples of 614 patients (68.
    1% of the patients were the intent-to-treat population) or as a combined positive score (CPS; 22C3)
    .

    The positive rate of the three detection methods

    The positive rate of the three detection methods

    Using SP142, SP263 and 22C3 experiments, the probability of PD-L1 IC≥1% is 46.
    4% (95% CI 42.
    5-50.
    4%), 74.
    9% (71.
    5-78.
    3%) and 73.
    1% (69/6-76.
    6%), respectively ; 80.
    9% of the samples 22C3 experiment CPS≥1
    .


    When IC≥1% (+), the analytical agreement between SP142 and SP263 and 22C3 is 69.


    Using SP142, SP263 and 22C3 experiments, the probability of PD-L1 IC ≥ 1% is 46.


    PFS and OS in SP142+ and 22C3+ patients treated with A+nP vs P+nP

    PFS and OS in SP142+ and 22C3+ patients treated with A+nP vs P+nP

    PFS and OS in SP142+ and SP263+ patients treated with A+nP vs P+nP

    PFS and OS in SP142+ and SP263+ patients treated with A+nP vs P+nP

    In SP263+ and 22C3+ patients, the clinical activity of A+nP vs.
    placebo+nP (PFS hazard ratio [HR] 0.
    64-0.
    68; overall survival rate [OS]HR: 0.
    75-0.
    79) was determined by double positive (PFS HR 0.
    60–0.
    61) ; OS HR = 0.
    71-0.
    75) rather than a single positive (PFS HR = 0.
    68-0.
    81; OS HR = 0.
    87-0.
    95) is driven
    .


    The consistency of the coordination threshold between SP263 (IC≥4%) and 22C3 (CPS≥10) and SP142 IC≥1% is lower than the standard (about 75%)


    And the SP263 + 22C3 + patients, A + nP clinical activity vs Placebo + nP by double positive rather than a single positive drive

    In conclusion, 22C3 and SP263 tests can identify more PD-L1 positive (IC≥1%) patients than SP142
    .


    No analytical equivalence between different detection methods was observed


    22C3 and SP263 tests can identify more PD-L1 positive (IC≥1%) patients than SP142 22C3 and SP263 tests can identify more PD-L1 positive (IC≥1%) patients than SP142

    Original source:

    Original source:

    Rugo Hope S,Loi Sherene,Adams Sylvia et al.


    PD-L1 Immunohistochemistry Assay Comparison in Atezolizumab plus nab-Paclitaxel-Treated Advanced Triple-Negative Breast Cancer in this message
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.