Prognosis of recurrence after complete resection in early-stage lung adenocarcinoma based on molecular alterations: a systematic review and meta-analysis

被引:4
作者
Zhou, Chu [1 ]
Jing, Zhongying [2 ]
Liu, Wei [2 ]
Ma, Zihuan [2 ]
Liu, Siyao [2 ]
Fang, Yueyu [3 ]
机构
[1] Nanjing Univ, Sch Med, Nanjing Drum Tower Hosp, Dept Thorac Surg, Nanjing 210008, Peoples R China
[2] Beijing ChosenMed Clin Lab Co Ltd, Beijing 100176, Peoples R China
[3] Nanjing PuKou Peoples Hosp, Dept Med Oncol, Nanjing 211800, Peoples R China
关键词
FACTOR RECEPTOR MUTATION; PATHOLOGICAL STAGE; EGFR MUTATION; CANCER; SURVIVAL; RISK; KRAS; IMPACT; DNA;
D O I
10.1038/s41598-023-42851-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular biomarkers have the potential to predict the recurrence risk of early-stage lung adenocarcinoma (LUAD) after complete resection, but the study results are controversial. We aimed to clarify the association of molecular alterations with disease-free survival (DFS) and recurrence-free survival (RFS) in early-stage LUAD with R0 resection. Comprehensive searches were conducted in PubMed/MEDLINE, Web of Science, and Cochrane Library for this systematic review and meta-analysis with date restrictions from 2012 to 2022. In the 18 included studies, data from a total of 7417 participants in 11 studies and 4167 participants in 9 studies were collected for the EGFR and KRAS meta-analyses, respectively. Two studies were assessed as having a moderate risk of bias, and the others were all assessed as having a high individual risk of bias. The molecular alterations in KRAS rather than EGFR, were associated with a high risk of recurrence for early-stage LUAD patients suffering from R0 resection, especially for those in pStage I, the pooled hazard ratios (HRs) of KRAS were 2.71 (95% CI, 1.81-4.06; I-2=22%; P<0.00001) and 1.95 (95% CI, 1.25-3.20; I-2=57%; P=0.003) with small interstudy heterogeneity in univariate and multivariate analyses, respectively. This finding suggests that molecular alterations in KRAS that could be detected by polymerase chain reaction techniques would provide new insight into stratifying risk and personalizing patient postoperative follow-up.
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页数:11
相关论文
共 44 条
  • [1] Prognostic influence of epidermal growth factor receptor mutation and radiological ground glass appearance in patients with early-stage lung adenocarcinoma
    Aokage, Keiju
    Miyoshi, Tomohiro
    Wakabayashi, Masashi
    Ikeno, Takashi
    Suzuki, Jun
    Tane, Kenta
    Samejima, Joji
    Tsuboi, Masahiro
    [J]. LUNG CANCER, 2021, 160 : 8 - 16
  • [2] Brierley JD., 2017, TNM CLASSIFICATION M
  • [3] Molecular biomarkers for lung adenocarcinoma
    Calvayrac, Olivier
    Pradines, Anne
    Pons, Elvire
    Mazieres, Julien
    Guibert, Nicolas
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2017, 49 (04)
  • [4] Prognostic value of KRAS G12C mutation in lung adenocarcinoma stratified by stages and radiological features
    Cao, Hang
    Ma, Zelin
    Li, Yuan
    Zhang, Yang
    Chen, Haiquan
    [J]. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2023, 166 (06) : E479 - E499
  • [5] Perioperative Dynamic Changes in Circulating Tumor DNA in Patients with Lung Cancer (DYNAMIC)
    Chen, Kezhong
    Zhao, Heng
    Shi, Yanbin
    Yang, Fan
    Wang, Lien Tu
    Kang, Guannan
    Nie, Yuntao
    Wang, Jun
    [J]. CLINICAL CANCER RESEARCH, 2019, 25 (23) : 7058 - 7067
  • [6] Adjuvant EGFR-TKIs for Patients With Resected EGFR-Mutant Non-Small Cell Lung Cancer: A Meta-Analysis of 1,283 Patients
    Chen, Rui-Lian
    Sun, Ling-Ling
    Cao, Yang
    Chen, Han-Rui
    Zhou, Jing-Xu
    Gu, Chu-Ying
    Zhang, Ying
    Wang, Si-Yu
    Hou, Wei
    Lin, Li-Zhu
    [J]. FRONTIERS IN ONCOLOGY, 2021, 11
  • [7] Profiling lung adenocarcinoma by liquid biopsy: can one size fit all?
    Clifford H.W.
    Cassidy A.P.
    Vaughn C.
    Tsai E.S.
    Seres B.
    Patel N.
    O’Neill H.L.
    Hewage E.
    Cassidy J.W.
    [J]. Cancer Nanotechnology, 2016, 7 (1)
  • [8] Prognostic value of epidermal growth factor receptor gene mutation in resected lung adenocarcinoma
    Deng, Chaoqiang
    Zhang, Yang
    Ma, Zelin
    Fu, Fangqiu
    Deng, Lin
    Li, Yuan
    Chen, Haiquan
    [J]. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2021, 162 (03) : 664 - +
  • [9] Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal cancer: a retrospective, pooled biomarker study
    Domingo, Enric
    Freeman-Mills, Luke
    Rayner, Emily
    Glaire, Mark
    Briggs, Sarah
    Vermeulen, Louis
    Fessler, Evelyn
    Medema, Jan Paul
    Boot, Arnoud
    Morreau, Hans
    van Wezel, Tom
    Liefers, Gerrit-Jan
    Lothe, Ragnhild A.
    Danielsen, Stine A.
    Sveen, Anita
    Nesbakken, Arild
    Zlobec, Inti
    Lugli, Alessandro
    Koelzer, Viktor H.
    Berger, Martin D.
    Casteilvi-Bel, Sergi
    Munoz, Jenifer
    de Bruyn, Marco
    Nijman, Hans W.
    Novelli, Marco
    Lawson, Kay
    Oukrif, Dahtnane
    Frangou, Eleni
    Dutton, Peter
    Tejpar, Sabine
    Delorenzi, Mauro
    Kerr, Rachel
    Kerr, David
    Tomlinson, Ian
    Church, David N.
    [J]. LANCET GASTROENTEROLOGY & HEPATOLOGY, 2016, 1 (03) : 207 - 216
  • [10] NOTUM from Apc-mutant cells biases clonal competition to initiate cancer
    Flanagan, Dustin J.
    Pentinmikko, Nalle
    Luopajarvi, Kalle
    Willis, Nicky J.
    Gilroy, Kathryn
    Raven, Alexander P.
    Mcgarry, Lynn
    Englund, Johanna, I
    Webb, Anna T.
    Scharaw, Sandra
    Nasreddin, Nadia
    Hodder, Michael C.
    Ridgway, Rachel A.
    Minnee, Emma
    Sphyris, Nathalie
    Gilchrist, Ella
    Najumudeen, Arafath K.
    Romagnolo, Beatrice
    Perret, Christine
    Williams, Ann C.
    Clevers, Hans
    Nummela, Pirjo
    Lahde, Marianne
    Alitalo, Kari
    Hietakangas, Ville
    Hedley, Ann
    Clark, William
    Nixon, Colin
    Kirschner, Kristina
    Jones, E. Yvonne
    Ristimaki, Ari
    Leedham, Simon J.
    Fish, Paul, V
    Vincent, Jean-Paul
    Katajisto, Pekka
    Sansom, Owen J.
    [J]. NATURE, 2021, 594 (7863) : 430 - +