2019
DOI: 10.1016/j.jtho.2019.06.031
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Combined Model of Frameshift Mutations and Tumor Mutation Burden in Predicting Preliminary Response to Immune Checkpoint Inhibitors in NSCLC

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(4 citation statements)
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“…observed in patients without PD-L1 expression [44,45]. Tumor mutational burden is an index estimating the number of mutations carried out by cancer cells [46][47][48][49][50] and has been proposed as a potential predictive response factor [46][47][48][49][50]. The increased tumor mutational burden leads to the synthesis and secretion of an increased amount of neoantigens stimulating immune-response against cancer [46][47][48][49][50].…”
Section: Ongoing Studies With Immune-checkpoint Inhibitors and Possib...mentioning
confidence: 99%
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“…observed in patients without PD-L1 expression [44,45]. Tumor mutational burden is an index estimating the number of mutations carried out by cancer cells [46][47][48][49][50] and has been proposed as a potential predictive response factor [46][47][48][49][50]. The increased tumor mutational burden leads to the synthesis and secretion of an increased amount of neoantigens stimulating immune-response against cancer [46][47][48][49][50].…”
Section: Ongoing Studies With Immune-checkpoint Inhibitors and Possib...mentioning
confidence: 99%
“…Tumor mutational burden is an index estimating the number of mutations carried out by cancer cells [46][47][48][49][50] and has been proposed as a potential predictive response factor [46][47][48][49][50]. The increased tumor mutational burden leads to the synthesis and secretion of an increased amount of neoantigens stimulating immune-response against cancer [46][47][48][49][50]. Nonetheless, the mutational load may also increase after exposure to agents promoting DNA damage, including alkylating antitumor agents such as temozolomide [51][52][53][54][55].…”
Section: Ongoing Studies With Immune-checkpoint Inhibitors and Possib...mentioning
confidence: 99%
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