echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > Front Oncol: The efficacy of trastuzumab biosimilar CT-P6 in HER2-positive early stage (EBC) and metastatic breast cancer (MBC) patients in the real world

    Front Oncol: The efficacy of trastuzumab biosimilar CT-P6 in HER2-positive early stage (EBC) and metastatic breast cancer (MBC) patients in the real world

    • Last Update: 2021-11-02
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Breast cancer is a heterogeneous disease with multiple subtypes
    .
    Human epidermal growth factor receptor 2 (HER2) is amplified in approximately 25% of breast cancers, resulting in a more aggressive phenotype and a poor prognosis


    .


    Breast cancer is a heterogeneous disease with multiple subtypes


    The study retrospectively investigated the medical records of the South Korean Severance Breast Cancer Registry


    .


    The study retrospectively investigated the medical records of the South Korean Severance Breast Cancer Registry


    254 patients with HER2-positive EBC were analyzed


    103 patients with HER2-positive MBC were analyzed


    For EBC patients, there was no difference in the percentage of pCR obtained between the two groups


    pCR

    pCR

    The median follow-up time (range) of MBC patients treated with CT-P6 and RTZ was 23.


    0 (3.


    The median follow-up time (range) of MBC patients treated with CT-P6 and RTZ was 23.


    Prognosis of MBC patients

    The prognosis of MBC patients The prognosis of MBC patients The prognosis of MBC patients

    There was no significant difference in ORR and DCR between the two groups (ORR: CT-P6 vs RTZ 78.


    9% vs 83.


    There was no significant difference in ORR and DCR between the two groups (ORR: CT-P6 vs RTZ 78.


    Evaluation of the efficacy of MBC

    Evaluation of the efficacy of MBC

    In the EBC cohort, there was no difference in the LVEF rate before treatment between the two groups (mean [95% CI] LVEF: CT-P6: 68.


    1 [60.
    7-69.
    1] vs RTZ: 68.
    1% [67.
    1-69.
    1]; P = 0.
    983) or neoadjuvant There was no difference after treatment (CT-P6: 65.
    9% [65.
    0-66.
    8] vs RTZ: 66.
    5% [65.
    3-67.
    7]; P=0.
    424)
    .
    After neoadjuvant chemotherapy, 23/104 patients (22.
    1%) in the CT-P6 group had a LVEF decrease of ≥10% from baseline, while it was 13/90 (14.
    4%) in the RTZ group (P=0.
    171)
    .
    The LVEF of the two groups of patients did not drop below 50% at any time
    .

    In the EBC cohort, there was no difference in the LVEF rate before treatment between the two groups (mean [95% CI] LVEF: CT-P6: 68.
    1 [60.
    7-69.
    1] vs RTZ: 68.
    1% [67.
    1-69.
    1]; P = 0.
    983) or neoadjuvant There was no difference after treatment (CT-P6: 65.
    9% [65.
    0-66.
    8] vs RTZ: 66.
    5% [65.
    3-67.
    7]; P=0.
    424)
    .
    After neoadjuvant chemotherapy, 23/104 patients (22.
    1%) in the CT-P6 group had a LVEF decrease of ≥10% from baseline, while it was 13/90 (14.
    4%) in the RTZ group (P=0.
    171)
    .
    The LVEF of the two groups of patients did not drop below 50% at any time
    .
    In the EBC cohort, there was no difference in the LVEF rate before treatment between the two groups (mean [95% CI] LVEF: CT-P6: 68.
    1 [60.
    7-69.
    1] vs RTZ: 68.
    1% [67.
    1-69.
    1]; P = 0.
    983) or neoadjuvant There was no difference after treatment (CT-P6: 65.
    9% [65.
    0-66.
    8] vs RTZ: 66.
    5% [65.
    3-67.
    7]; P=0.
    424)
    .
    After neoadjuvant chemotherapy, 23/104 patients (22.
    1%) in the CT-P6 group had a LVEF decrease of ≥10% from baseline, while it was 13/90 (14.
    4%) in the RTZ group (P=0.
    171)
    .
    The LVEF of the two groups of patients did not drop below 50% at any time
    .

    In the MBC cohort, both CT-P6 and RTZ showed manageable cardiac safety, which was assessed by LVEF
    .
    Of the 38 patients in the CT-P6 group, 19 (50.
    0%) had a LVEF decrease of ≥10% from baseline, while the RTZ group was 27/63 (42.
    9%) (P=0.
    695)
    .
    Among patients treated with CT-P6, 3/38 (7.
    9%) of patients had LVEF dropped to less than 50% at any time
    .
    One of the patients stopped CT-P6 for 1 month and then restarted; the rest of the patients continued the treatment, and the treatment was stopped after 3 months due to the progress of the disease
    .
    Among patients treated with RTZ, 4/65 (6.
    2%) had LVEF dropped to less than 50% at any time
    .
    Two of the patients discontinued RTZ treatment, one patient resumed treatment after one month of discontinuation, and the other continued to use RTZ treatment
    .

    In the MBC cohort, both CT-P6 and RTZ showed manageable cardiac safety, which was assessed by LVEF
    .
    Of the 38 patients in the CT-P6 group, 19 (50.
    0%) had a LVEF decrease of ≥10% from baseline, while the RTZ group was 27/63 (42.
    9%) (P=0.
    695)
    .
    Among patients treated with CT-P6, 3/38 (7.
    9%) of patients had LVEF dropped to less than 50% at any time
    .
    One of the patients stopped CT-P6 for 1 month and then restarted; the rest of the patients continued the treatment, and the treatment was stopped after 3 months due to the progress of the disease
    .
    Among patients treated with RTZ, 4/65 (6.
    2%) had LVEF dropped to less than 50% at any time
    .
    Two of the patients discontinued RTZ treatment, one patient restarted treatment after one month of discontinuation, and the other continued to use RTZ treatment
    .
    In the MBC cohort, both CT-P6 and RTZ showed manageable cardiac safety, which was assessed by LVEF
    .
    Of the 38 patients in the CT-P6 group, 19 (50.
    0%) had a LVEF decrease of ≥10% from the baseline, while the RTZ group was 27/63 (42.
    9%) (P=0.
    695)
    .

    In summary, real-world data show that trastuzumab biosimilar CT-P6 has similar effectiveness and cardiac safety to RTZ in HER2-positive EBC and MBC patients
    .

    In summary, real-world data show that trastuzumab biosimilar CT-P6 has similar effectiveness and cardiac safety to RTZ in HER2-positive EBC and MBC patients
    .
    Real-world data indicate that the trastuzumab biosimilar CT-P6 has similar effectiveness and cardiac safety to RTZ in HER2-positive EBC and MBC patients
    .
    Real-world data indicate that the trastuzumab biosimilar CT-P6 has similar effectiveness and cardiac safety to RTZ in HER2-positive EBC and MBC patients
    .

    Original source:

    Original source:

    Bae SJ, Kim JH, Ahn SG, Jeung HC, Sohn J, Kim GM, Kim MH, Kim SI, Park S, Park HS, Kim JY and Jeong J (2021) Real-World Clinical Outcomes of Biosimilar Trastuzumab (CT-P6 ) in HER2-Positive Early-Stage and Metastatic Breast Cancer.
    Front.
    Oncol.
    11:689587.
    doi: 10.
    3389/fonc.
    2021.
    689587

    Bae SJ, Kim JH, Ahn SG, Jeung HC, Sohn J, Kim GM, Kim MH, Kim SI, Park S, Park HS, Kim JY and Jeong J (2021) Real-World Clinical Outcomes of Biosimilar Trastuzumab (CT-P6 ) in HER2-Positive Early-Stage and Metastatic Breast Cancer.
    Front.
    Oncol.
    11:689587.
    doi: 10.
    3389/fonc.
    2021.
    689587 Leave a message here
    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.