echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > 2022 ESMO Global Perspectives Prof. Siow Ming Lee: Immunologic monotherapy can also bring survival benefits to patients with poor NSCLC

    2022 ESMO Global Perspectives Prof. Siow Ming Lee: Immunologic monotherapy can also bring survival benefits to patients with poor NSCLC

    • Last Update: 2022-10-01
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com


    The European Society for Internal Oncology (ESMO) Annual Meeting is the most prestigious and influential oncology conference
    in Europe.

    The 2022 ESMO Conference will be held from September 9 to 13, 2022 in an offline (Paris, France) combination of online methods, ESMO Conference covers basic research, translational research and the latest clinical research progress, will provide a broad and excellent academic platform
    for clinical practice, multidisciplinary discussion, etc.

    A number of blockbuster studies in the field of lung cancer will be presented at this year's ESMO conference
    .

    In the plenary session III, Professor Siow Ming Lee presented the results
    of the Phase III IPSOS study.

    During the conference, Professor Siow Ming Lee was honored to have Professor Siow Ming Lee interpret the findings
    .

    Details are as follows:


    Professor Siow Ming Lee is in the view

    Professor Siow Ming Lee

    University College London Hospitals

    Patients with poor advanced NSCLC urgently need better regimens

    Virtually all first-line key immunotherapy studies included non-small cell lung cancer (NSCLC) patients with
    a physical status (PS) score of 0 or 1 in the Eastern United States Collaborative Oncology Group (ECOG).



    We know that the PS score status is not specified in the indications for immunomonotherapy PD-L1 expression > 50% of advanced NSCLC, but in fact, there are no prospective randomized controlled studies
    in patients who are not suitable or unable to tolerate standard platinum-containing chemotherapy and PS scores of 2 or 3.



    Therefore, we clinicians do not recommend immunotherapy plus chemotherapy for patients with advanced NSCLC who are in a poor state and have a PS of 2/3, because combination therapy is too
    toxic for this part of the patient.


    New advances or changes in clinical practice: Immunological monodrugs improve the survival of the elderly population and ensure a better quality of life


    This year, our team presented the results of a Phase III IPSOS study at ESMO that showed that altilizumab monotherapy improves overall survival (OS)
    in patients with poor NSCLC, predominantly older adults, regardless of physical status or PD-L1 expression.



    The IPSOS study reached the primary endpoint of OS (HR=0.
    78) and doubled the 2-year survival rate of patients (24.
    3% vs 12.
    4%), with a quarter of patients receiving antilizumab surviving at 2 years while maintaining a good quality of life, and no new adverse events
    were found in this population.

    Immunotherapy alone is effective
    regardless of the patient's PD-L1 expression level.



    The median age of patients included in the study was 75 years, 75% of patients over 70 years of age, and 31% of patients over 80 years of age, compared with the median age of enrollment in other first-line immunotherapy trials generally less than 65 years
    .



    IPSOS studies are likely to alter clinical practice in patients with poor PS scores or elderly patients with advanced NSCLC without driver gene mutations
    .


    Study details

    Professor Siow Ming Lee

    1

    background

    Multiple studies have shown that first-line immunotherapy ± chemotherapy significantly improves patient OS
    compared with chemotherapy.


    method

    Patients with no driver gene mutation, poor PS (≥2), or complications over 70 years of age who are not suitable for locally advanced/metastatic NSCLC with platinum-containing double-agent chemotherapy were included in the study
    .

    Enrolled patients were randomly assigned to attilizumab (every 3 weeks, intravenously, 1200 mg) or monotherapy chemotherapy (vinorebine or gemcitabine) in a 2:1 ratio for 3 or 4 cycles
    .

    The main endpoint is OS
    .

    Key secondary endpoints were objective response rate (ORR), progression-free survival (PFS), and duration of response (DOR) and OS and PFS in PD-L1-positive populations
    .
    Study the design

    3

    outcome

    A total of 453 patients were enrolled in the study and were randomly assigned to the attilizumab group (302 patients) and the chemotherapy group (151 patients
    ).

    The median age was 75 years (range, 33-94), with 31% of patients over 80 years of age, 72% of men, and 83%
    of patients with ECOG PS≥2.

    The median follow-up time of 41.
    0 months at data cut-off on 30 April 2022 significantly improved patient OS compared with chemotherapy (HR=0.
    78; 95% CI: 0.
    63, 0.
    97; P=0.
    028).


    Primary endpoints: Consistent survival benefit was also observed in key subgroups with OS results
    , including PD-L1 expression levels, PS and histology type subgroups
    .

    The OS subgroup analyzed
    the ORR of 16.
    9% and 7.
    9%, respectively, and the median DOR of 14 months and 7.
    8 months, respectively
    , in the Atelizumab monotherapy group and the chemotherapy group, respectively.

    The median PFS in
    both groups was 4.
    2 months and 4.
    0 months (HR = 0.
    87),
    respectively.

    The incidence of treatment-related adverse events (TRAE) in the secondary endpoints PFS
    altilizumab group and the chemotherapy group was 16.
    3% and 33.
    3%, respectively, and the incidence of grade 5 TAE was 1.
    0% and 2.
    7%,
    respectively.


    Safety analysis compared with chemotherapy significantly improved the time to chest pain exacerbation time (TTCD) in patients with chest pain (HR=0.
    51; 95% CI: 0.
    27 to 0.
    97), and found that there was also a significant improvement
    in loss of appetite and cough compared with baseline.

    Patients reported outcome TTCD outcomes

    4

    conclusion

    Regardless of histology type, PD-L1 expression, and ECOG PS score, first-line altelizumab significantly improved OS unsuitable for platinum patients (HR=0.
    78) compared with chemotherapy, and the estimated number of patients surviving at 2 years of attilizumab was twice that
    of chemotherapy.

    Antilizumab is associated with stable health-related quality of life and improved TTCD
    in patients compared with chemotherapy.

    Regardless of the subgroup population, the IPSOS study was the first prospective study to show improvements in OS in patients with poor prognosis, finding no new adverse events while ensuring quality of
    life in patients 。 LBA11-IPSOS: Results from a phase III study of first-line (1L) atezolizumab (atezo) vs single-agent chemotherapy (chemo) in patients (pts) with NSCLC not eligible for a platinumcontaining regimen.
    2022 ESMO.
    Editor: Xiaoyuan Typesetting: Xiaoyuan Execution: Youshi
    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.