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    Home > Active Ingredient News > Antitumor Therapy > Lancet Oncol: Efficacy and safety of the ADC drug Anetumab ravtansine in the treatment of malignant pleural mesothelioma

    Lancet Oncol: Efficacy and safety of the ADC drug Anetumab ravtansine in the treatment of malignant pleural mesothelioma

    • Last Update: 2022-04-24
    • Source: Internet
    • Author: User
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    Before the approval of ipilimumab and nivolumab as first-line combination immunotherapy for malignant pleural mesothelioma in October 2020 , pemetrexed and platinum-based chemotherapy were the only first-line treatment options
    .
    To date, there are few second-line treatment options for malignant pleural mesothelioma


    .


    immunity

    This study is an international, multicenter, randomized, open-label phase 2 trial to evaluate the antibody-drug conjugate Anetumab ravtansine, a fully human anti-mesothelin antibody composed of the toxic group DM4.
    ADC drug) compared with vinorelbine in patients with malignant pleural mesothelioma
    .

    Patients 18 years of age and older with unresectable locally advanced or metastatic mesothelin-overexpressing malignant pleural mesothelioma who progressed on first-line platinum + pemetrexed ± bevacizumab therapy were recruited, randomized 2:1 The group received intravenous Anetumab ravtansine (6.
    5 mg/kg, day 1 of every 21-day cycle) or intravenous vinorelbine (30 mg/m2 weekly) until disease progression, unacceptable toxicity, or death
    .
    The primary endpoint was progression-free survival


    .



    Progression-free survival and overall survival in the two groups


    Progression-free survival and overall survival in the two groups

    Between December 3, 2015, and May 31, 2017, a total of 589 patients were enrolled, of which 248 patients with mesothelin overexpression were randomized into two groups: 155 in the anetumab ravtansine group and 82 in the vinorelbine group bit
    .
    Disease progression occurred in 105 (63%) and 43 (52%) patients in the anetumab ravtansine and vinorelbine groups, respectively, at a median follow-up of 4.
    0 months and 3.
    9 months in the anetumab ravtansine and vinorelbine groups, respectively.
    or death, the median progression-free survival was 4.


    3 months and 4.
    5 months, respectively (hazard ratio 1.
    22, p=0.
    86)


    Progression or death occurred in 105 (63%) and 43 (52%) patients in the anetumab ravtansine and vinorelbine groups, respectively, with a median progression-free survival of 4.



    In conclusion, although Anetumab ravtansine showed a manageable safety profile in patients with malignant pleural mesothelioma, it was not superior to vinorelbine
    .

    Although Anetumab ravtansine showed a manageable safety profile in patients with malignant pleural mesothelioma, it was not superior to vinorelbine no better than vinorelbine

    Original source:

    Original source:

    Hedy L Kindler, et al.
    A netumab ravtansine versus vinorelbine in patients with relapsed, mesothelin-positive malignant pleural mesothelioma (ARCS-M): a randomised, open-label phase 2 trial .
    The Lancet Oncology.


    April, 2022.
    https:/ /doi.


    netumab ravtansine versus vinorelbine in patients with relapsed, mesothelin-positive malignant pleural mesothelioma (ARCS-M): a randomised, open-label phase 2 trial
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