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    Home > Active Ingredient News > Antitumor Therapy > J Clin Oncol: Efficacy of temozolomide in combination with low-dose ipilimumab and nivolumab in MSS and MGMT-deficient metastatic colorectal cancer (mCRC)

    J Clin Oncol: Efficacy of temozolomide in combination with low-dose ipilimumab and nivolumab in MSS and MGMT-deficient metastatic colorectal cancer (mCRC)

    • Last Update: 2022-04-22
    • Source: Internet
    • Author: User
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    Recently, the Journal of Clinical Oncology published the results of a single-arm phase II study (MAYA) of temozolomide sensitization in previously treated metastatic colorectal cancer (mCRC) patients with MSS and MGMT loss.
    Efficacy and safety of a follow-up combination of low-dose ipilimumab (ipilimumab) and nivolumab (nivolumab)
    .

    Recently, the Journal of Clinical Oncology published the results of a single-arm phase II study (MAYA) of temozolomide sensitization in previously treated metastatic colorectal cancer (mCRC) patients with MSS and MGMT loss.
    Efficacy and safety of a follow-up combination of low-dose ipilimumab (ipilimumab) and nivolumab (nivolumab)
    .


    Primarily in previously treated patients with metastatic colorectal cancer (mCRC) with MSS and MGMT deletion, sensitization with temozolomide and subsequent combination with low-dose ipilimumab and nivolumab Efficacy and safety


    The study included previously treated metastatic colorectal cancer (mCRC) with MSS status and MGMT loss on examination
    .


    The patients were treated with the first part of the treatment first: temozolomide 150mg/sqm, qd, d1-d5, once every 4 weeks, for a total of 2 cycles; patients who were controlled after 2 cycles entered the second part of the treatment: temozolomide combined with low-dose ipilimumab (1 mg/kg/time, 1 course every 8 weeks) and nivolumab (480 mg/time, 1 course every 4 weeks)


    The study included previously treated metastatic colorectal cancer (mCRC) with MSS status and MGMT loss on examination


    Of the 716 prescreened patients, 204 patients (29%) were molecularly profiled, of whom 135 patients started the first part of treatment
    .


    Of these, 102 (76%) discontinued treatment due to death or disease progression after temozolomide initiation, while 33 (24%) patients who achieved disease control initiated a second portion of treatment and represented the final study population


    Of the 716 prescreened patients, 204 patients (29%) were molecularly profiled, of whom 135 patients started the first part of treatment


    After a median follow-up of 23.


    According to RECIST1.
    1, the ORR for the entire treatment strategy was 45% (95% CI, 29 to 62), with 15 PRs and 0 CRs
    .


    Of the 33 patients, tumor shrinkage of any extent was observed in 26 (79%)


    According to RECIST1.


    Grade 3-4 immune-related adverse events were rash (6%), colitis (3%), and hypophysitis (3%)
    .


    No unexpected adverse events or treatment-related deaths were reported


    Grade 3-4 immune-related adverse events were rash (6%), colitis (3%), and hypophysitis (3%)


    Taken together, the MAYA study suggests that priming with temozolomide followed by a combination of low-dose ipilimumab and nivolumab may result in durable clinical benefit in MSS and MGMT-deficient mCRC
    .

    Taken together, the MAYA study suggests that priming with temozolomide followed by a combination of low-dose ipilimumab and nivolumab may result in durable clinical benefit in MSS and MGMT-deficient mCRC
    .


    The MAYA study suggests that priming with temozolomide followed by low-dose ipilimumab and nivolumab may result in durable clinical benefit in MSS and MGMT-deficient mCRC
    .
    The MAYA study suggests that priming with temozolomide followed by low-dose ipilimumab and nivolumab may result in durable clinical benefit in MSS and MGMT-deficient mCRC
    .

     

    Original source:

    Original source:

    Morano F, Raimondi A, Pagani F, et al .
    Temozolomide Followed by Combination With Low-Dose Ipilimumab and Nivolumab in Patients With Microsatellite-Stable, O 6 -Methylguanine-DNA Methyltransferase-Silenced Metastatic Colorectal Cancer: The MAYA Trial.
    J Clin Oncol .
    2022 Mar 8: JCO2102583.
    doi: 10.
    1200/JCO.
    21.
    02583.
    Epub ahead of print.
    PMID: 35258987.

    Morano F, Raimondi A, Pagani F, et al .
    Temozolomide Followed by Combination With Low-Dose Ipilimumab and Nivolumab in Patients With Microsatellite-Stable, O 6 -Methylguanine-DNA Methyltransferase-Silenced Metastatic Colorectal Cancer: The MAYA Trial.
    J Clin Oncol .
    2022 Mar 8: JCO2102583.
    doi: 10.
    1200/JCO.
    21.
    02583.
    Epub ahead of print.
    PMID: 35258987.
    Morano F, Raimondi A, Pagani F, et al .
    Temozolomide Followed by Combination With Low-Dose Ipilimumab and Nivolumab in Patients With Microsatellite-Stable, O 6 -Methylguanine-DNA Methyltransferase-Silenced Metastatic Colorectal Cancer: The MAYA Trial.
    J Clin Oncol.
    2022 Mar 8:JCO2102583.
    doi: 10.
    1200/JCO.
    21.
    02583.
    Epub ahead of print.
    PMID: 35258987.
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