Identification and Application of Emerging Biomarkers in Treatment of Non-Small-Cell Lung Cancer: Systematic Review

被引:5
|
作者
Restrepo, Juan Carlos [1 ]
Guevara, Darly Martinez [1 ]
Lopez, Andres Pareja [2 ]
Palacios, John Fernando Montenegro [3 ]
Liscano, Yamil [1 ]
机构
[1] Univ Santiago Cali, Dept Fac Salud, Grp Invest Salud Integral GISI, Cali 760035, Colombia
[2] Univ CES, Fac Ciencias, Unidad Tox Vitro UTi, Grp Invest, Medellin 050021, Colombia
[3] Univ Santiago Cali, Dept Hlth, Specializat Internal Med, Cali 760035, Colombia
关键词
biomarkers; early diagnosis; personalized treatments; immunotherapy; survival; tumor genetics; non-small-cell lung cancer; CIRCULATING TUMOR DNA; PHASE-II TRIAL; 1ST-LINE TREATMENT; PREDICTIVE BIOMARKERS; MUTATIONAL BURDEN; EFFICACY; PD-L1; CHEMOTHERAPY; GUT; OSIMERTINIB;
D O I
10.3390/cancers16132338
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Lung cancer remains a leading cause of cancer-related mortality globally, requiring new diagnostic and therapeutic approaches. This research arises from the need to improve diagnostic accuracy and treatment effectiveness for patients with non-small cell lung cancer. The authors aim to systematically evaluate the potential of emerging biomarkers, including circulating tumor DNA, microRNAs and mutational load of blood tumors and their relationship with different treatments. The findings of this study could have a significant impact on the research community by providing a basis for integrating these biomarkers into clinical practice, thereby improving personalized treatment strategies and patient outcomes in non-small cell lung cancer.Abstract Non-small-cell lung cancer (NSCLC) comprises approximately 85% of all lung cancer cases, often diagnosed at advanced stages, which diminishes the effective treatment options and survival rates. This systematic review assesses the utility of emerging biomarkers-circulating tumor DNA (ctDNA), microRNAs (miRNAs), and the blood tumor mutational burden (bTMB)-enhanced by next-generation sequencing (NGS) to improve the diagnostic accuracy, prognostic evaluation, and treatment strategies in NSCLC. Analyzing data from 37 studies involving 10,332 patients from 2020 to 2024, the review highlights how biomarkers like ctDNA and PD-L1 expression critically inform the selection of personalized therapies, particularly beneficial in the advanced stages of NSCLC. These biomarkers are critical for prognostic assessments and in dynamically adapting treatment plans, where high PD-L1 expression and specific genetic mutations (e.g., ALK fusions, EGFR mutations) significantly guide the use of targeted therapies and immunotherapies. The findings recommend integrating these biomarkers into standardized clinical pathways to maximize their potential in enhancing the treatment precision, ultimately fostering significant advancements in oncology and improving patient outcomes and quality of life. This review substantiates the prognostic and predictive value of these biomarkers and emphasizes the need for ongoing innovation in biomarker research.
引用
收藏
页数:37
相关论文
共 50 条
  • [31] Identification of Biomarkers for Non-small-cell Lung Cancer Patients Treated With an Immune Checkpoint Inhibitor
    Kubo, Sousuke
    Kobayashi, Nobuaki
    Somekawa, Kohei
    Hirata, Momo
    Kamimaki, Chisato
    Aiko, Hiroko
    Katakura, Seigo
    Teranishi, Shuhei
    Watanabe, Keisuke
    Hara, Yu
    Yamamoto, Masaki
    Kudo, Makoto
    Kaneko, Takeshi
    ANTICANCER RESEARCH, 2020, 40 (07) : 3889 - 3896
  • [32] Gefitinib for non-small-cell lung cancer treatment
    D'Incecco, Armida
    Cappuzzo, Federico
    EXPERT OPINION ON DRUG SAFETY, 2011, 10 (06) : 987 - 996
  • [33] Surgical treatment of non-small-cell lung cancer
    Schuhan, C.
    Dienemann, H.
    ONKOLOGE, 2011, 17 (08): : 684 - +
  • [34] Crizotinib in the Treatment of Non-Small-Cell Lung Cancer
    Rothschild, Sacha I.
    Gautschi, Oliver
    CLINICAL LUNG CANCER, 2013, 14 (05) : 473 - 480
  • [35] Gefitinib for the treatment of non-small-cell lung cancer
    Campbell, Lynn
    Blackhall, Fiona
    Thatcher, Nicholas
    EXPERT OPINION ON PHARMACOTHERAPY, 2010, 11 (08) : 1343 - 1357
  • [36] Bevacizumab in the treatment of non-small-cell lung cancer
    Stinchcombe, T. E.
    Socinski, M. A.
    ONCOGENE, 2007, 26 (25) : 3691 - 3698
  • [37] Gefitinib for the treatment of non-small-cell lung cancer
    Hida, Toyoaki
    Ogawa, Shizu
    Park, Jang Chul
    Park, Ji Young
    Shimizu, Junichi
    Horio, Yoshitsugu
    Yoshida, Kimihide
    EXPERT REVIEW OF ANTICANCER THERAPY, 2009, 9 (01) : 17 - 35
  • [38] Pembrolizumab for the Treatment of Non-Small-Cell Lung Cancer
    Garon, Edward B.
    Rizvi, Naiyer A.
    Hui, Rina
    Leighl, Natasha
    Balmanoukian, Ani S.
    Eder, Joseph Paul
    Patnaik, Amita
    Aggarwal, Charu
    Gubens, Matthew
    Horn, Leora
    Carcereny, Enric
    Ahn, Myung-Ju
    Felip, Enriqueta
    Lee, Jong-Seok
    Hellmann, Matthew D.
    Hamid, Omid
    Goldman, Jonathan W.
    Soria, Jean-Charles
    Dolled-Filhart, Marisa
    Rutledge, Ruth Z.
    Zhang, Jin
    Lunceford, Jared K.
    Rangwala, Reshma
    Lubiniecki, Gregory M.
    Roach, Charlotte
    Emancipator, Kenneth
    Gandhi, Leena
    NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (21): : 2018 - 2028
  • [39] Selumetinib in the treatment of non-small-cell lung cancer
    Bernabe, Reyes
    Patrao, Ana
    Carter, Louise
    Blackhall, Fiona
    Dean, Emma
    FUTURE ONCOLOGY, 2016, 12 (22) : 2545 - 2560
  • [40] Bevacizumab in the treatment of non-small-cell lung cancer
    T E Stinchcombe
    M A Socinski
    Oncogene, 2007, 26 : 3691 - 3698