Evidence map›Paper›PMID 35578031›Full record

ArticleJournal of cancer research and clinical oncology2023

Allele frequency and proportion defined by circulating tumor DNA profiling predict tyrosine kinase inhibitors' therapeutic outcomes for non-small cell lung cancer.

Jiajia Song, Ling Bai, Jianzhao Zhai, Zhaodan Xin, Liting You, Yi Zhou, Juan Zhou, Binwu Ying

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jiajia Song *Department of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Ling Bai *Department of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Jianzhao ZhaiDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Zhaodan XinDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Liting YouDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Yi ZhouDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China.
Juan ZhouDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China. zhoujuan39@qq.com.
Binwu YingDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chendu, Sichuan, China. yingbinwu@scu.edu.cn.ORCID http://orcid.org/0000-0001-8077-3908

Funding

Applied Basic Research Program of Sichuan Province 2020YJ0106Innovative Research Group Project of the National Natural Science Foundation of China U20A20394Sichuan Province Science and Technology Support Program 2020YFS0214Sichuan Province Science and Technology Support Program 2020YFS0511
6 · The paper itself

Abstract

purposeCirculating tumor DNA is more and more accessible for patients who cannot undergo biopsy. No consistent conclusion has been reached on whether frequency and proportion of mutations defined by ctDNA profiling can predict therapeutic outcomes.

methodsOne hundred patients with non-small cell lung cancer harboring activating EGFR mutations (exon 19 deletion, L858R and T790M mutation) were collected in West China hospital from December 18, 2017 to December 31, 2019. We retrospectively analyzed the frequency and proportion distribution of ctDNA mutations and its relationship with tyrosine kinase inhibitors therapeutic outcomes.

resultsPatients with lower frequency of sensitizing EGFR mutations (< 3%) had a longer progression-free survival (PFS) time than those with higher frequency (15 months vs. 10 months, p = 0.028). Moreover, patients with the lower ratio of T790M mutation frequency and the maximum-somatic-allele-frequency (T790M/MSAF < 30%) had a less prolonged PFS than those with higher T790M/MSAF (7 months vs. 15 months, p = 0.013).

conclusionThe frequency and proportion of ctDNA mutations are worth clinical attention in the prediction of therapeutic outcomes.

Indexed as

Carcinoma, Non-Small-Cell LungCirculating Tumor DNALung NeoplasmsErbB ReceptorsGene FrequencyHumansMutationProgression-Free SurvivalProtein Kinase InhibitorsRetrospective StudiesTyrosine Kinase InhibitorsCirculating Tumor DNAErbB ReceptorsProtein Kinase InhibitorsTyrosine Kinase InhibitorsBiomarkerEGFRMutationPrognosisTargeting therapy

Identifiers

PMID35578031
PMCPMC11797840

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