Prognostic role of the VeriStrat test in first line patients with non-small cell lung cancer treated with platinum-based chemotherapy

被引:13
作者
Grossi, Francesco [1 ]
Genova, Carlo [1 ]
Rijavec, Erika [1 ]
Barletta, Giulia [1 ]
Biello, Federica [1 ]
Dal Bello, Maria Giovanna [1 ]
Meyer, Krista [2 ]
Roder, Joanna [2 ]
Roder, Heinrich [2 ]
Grigorieva, Julia [2 ]
机构
[1] IRCCS AOU San Martino IST Ist Nazl Ric Canc, Lung Canc Unit, Largo R Benzi 10, I-16132 Genoa, Italy
[2] Biodesix, 2970 Wilderness Pl, Boulder, CO 80301 USA
关键词
Non-small cell lung cancer; VeriStrat; Chemotherapy; Biomarkers; Prognosis; First line therapy; TYROSINE-KINASE INHIBITORS; SERUM AMYLOID-A; MASS-SPECTROMETRY; PHASE-3; TRIAL; DOUBLE-BLIND; ERLOTINIB; STAGE; EXPRESSION; PLACEBO; GEMCITABINE;
D O I
10.1016/j.lungcan.2017.12.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: VeriStrat (R) is a blood-based test that utilizes matrix-assisted laser desorption/ionization time-of-flight (MALDI ToF) mass spectrometry to assign a binary classification of VeriStrat Good or VeriStrat Poor that is associated with treatment outcomes in cancer patients. A number of other studies have shown an association between VeriStrat status and clinical outcomes in second and subsequer t lines of therapy. The prognostic properties of VeriStrat were demonstrated in the placebo arms of two randomized studies in non-small cell lung cancer (NSCLC): TOPICAL and BR.21; the predictive properties of the test were shown in a prospective randomized phase III study PROSE in the second line treatment of NSCLC with erlotinib versus chemotherapy. Motivated by these observations, we sought to extend the clinical utility of VeriStrat to standard first line chemotherapy and evaluated the performance of the test in a number of clinical studies of patients treated with platinum-based regimens. Materials and methods: We examine the performance of VeriStrat in three independent clinical trials where the test classification was acquired for prospectively collected baseline samples from 481 patients treated with platinum-based chemotherapy in first line. Results: Across these trials, 66-70% of patients were classified as VeriStrat Good; patients classified as VeriStrat Good had significantly longer progression-free survival and overall survival than VeriStrat Poor patients, with hazard ratios ranging from 0.36 to 0.72 and 0.26 to 0.51, respectively. These results demonstrated that VeriStrat is a strong prognostic test in NSCLC patients treated with platinum-based regimens in the first line. Conclusion: VeriStrat provides valuable clinical information that may be used to support patient-physician conversations regarding prognosis and treatment options, and to identify a subset of patients who might benefit from other treatment strategies, possibly in the framework of clinical trials.
引用
收藏
页码:64 / 69
页数:6
相关论文
共 39 条
  • [1] Excision repair cross-complementation group 1 predicts progression-free and overall survival in non-small cell lung cancer patients treated with platinum-based chemotherapy
    Azuma, Koichi
    Komohara, Yoshihiro
    Sasada, Tetsuro
    Terazaki, Yasuhiro
    Ikeda, Jiro
    Hoshino, Tomoaki
    Itoh, Kyogo
    Yamada, Akira
    Aizawa, Hisamichi
    [J]. CANCER SCIENCE, 2007, 98 (09) : 1336 - 1343
  • [2] Human SR-BII mediates SAA uptake and contributes to SAA pro-inflammatory signaling in vitro and in vivo
    Baranova, Irina N.
    Souza, Ana C. P.
    Bocharov, Alexander V.
    Vishnyakova, Tatyana G.
    Hue, Xuzhen
    Vaisman, Boris L.
    Amar, Marcelo J.
    Chen, Zhigang
    Remaley, Alan T.
    Patterson, Amy P.
    Yuen, Peter S. T.
    Star, Robert A.
    Eggerman, Thomas L.
    [J]. PLOS ONE, 2017, 12 (04):
  • [3] SERUM AMYLOID-A (SAA) VARIATIONS IN PATIENTS WITH CANCER - CORRELATION WITH DISEASE-ACTIVITY, STAGE, PRIMARY SITE, AND PROGNOSIS
    BIRAN, H
    FRIEDMAN, N
    NEUMANN, L
    PRAS, M
    SHAINKINKESTENBAUM, R
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 1986, 39 (07) : 794 - 797
  • [4] Prognostic and Predictive Role of the VeriStrat Plasma Test in Patients with Advanced Non-Small-Cell Lung Cancer Treated with Erlotinib or Placebo in the NCIC Clinical Trials Group BR.21 Trial
    Carbone, David P.
    Ding, Keyue
    Roder, Heinrich
    Grigorieva, Julia
    Roder, Joanna
    Tsao, Ming-Sound
    Seymour, Lesley
    Shepherd, Frances A.
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (11) : 1653 - 1660
  • [5] VeriStrat® classifier for survival and time to progression in non-small cell lung cancer (NSCLC) patients treated with erlotinib and bevacizumab
    Carbone, David P.
    Salmon, J. Stuart
    Billheimer, Dean
    Chen, Heidi
    Sandler, Alan
    Roder, Heinrich
    Roder, Joanna
    Tsypin, Maxim
    Herbst, Roy S.
    Tsao, Anne S.
    Tran, Hai T.
    Dang, Thao P.
    [J]. LUNG CANCER, 2010, 69 (03) : 337 - 340
  • [6] Hyperprogressive Disease Is a New Pattern of Progression in Cancer Patients Treated by Anti-PD-1/PD-L1
    Champiat, Stephane
    Dercle, Laurent
    Ammari, Samy
    Massard, Christophe
    Hollebecque, Antoine
    Postel-Vinay, Sophie
    Chaput, Nathalie
    Eggermont, Alexander
    Marabelle, Aurelien
    Soria, Jean-Charles
    Ferte, Charles
    [J]. CLINICAL CANCER RESEARCH, 2017, 23 (08) : 1920 - 1928
  • [7] Cho W. C., 2010, BR J CANC, V102
  • [8] Detection of Tumor Epidermal Growth Factor Receptor Pathway Dependence by Serum Mass Spectrometry in Cancer Patients
    Chung, Christine H.
    Seeley, Erin H.
    Roder, Heinrich
    Grigorieva, Julia
    Tsypin, Maxim
    Roder, Joanna
    Burtness, Barbara A.
    Argiris, Athanassios
    Forastiere, Arlene A.
    Gilbert, Jill
    Murphy, Barbara
    Caprioli, Richard M.
    Carbone, David P.
    Cohen, Ezra E. W.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2010, 19 (02) : 358 - 365
  • [9] DeMieke B., 2016, CURR MED CHEM, V23, P1725
  • [10] Serum Amyloid A As a Prognostic Marker in Melanoma Identified by Proteomic Profiling
    Findeisen, Peter
    Zapatka, Marc
    Peccerella, Teresa
    Matzk, Heike
    Neumaier, Michael
    Schadendorf, Dirk
    Ugurel, Selma
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (13) : 2199 - 2208