Mass spectrometry to classify non-small-cell lung cancer patients for clinical outcome after treatment with epidermal growth factor receptor tyrosine kinase inhibitors: A multicohort cross-institutional study

被引:231
作者
Taguchi, Fumiko
Solomon, Benjamin
Gregorc, Vanesa
Roder, Heinrich
Gray, Robert
Kasahara, Kazuo
Nishio, Makoto
Brahmer, Julie
Spreafico, Anna
Ludovini, Vienna
Massion, Pierre P.
Dziadziuszko, Rafal
Schiller, Joan
Grigorieva, Julia
Tsypin, Maxim
Hunsucker, Stephen W.
Caprioli, Richard
Duncan, Mark W.
Hirsch, Fred R.
Bunn, Paul A., Jr.
Carbone, David P.
机构
[1] Vanderbilt Univ, Ctr Med, Vanterbilt Ingram Canc Ctr, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Ctr Med, Vanterbilt Ingram Canc Ctr, Div Pulm, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Ctr Med, Vanterbilt Ingram Canc Ctr, Dept Biochem, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Ctr Med, Vanterbilt Ingram Canc Ctr, Dept Canc Biol, Nashville, TN 37232 USA
[5] Univ Colorado, Dept Med Oncol, Denver, CO 80202 USA
[6] Univ Colorado, Dept Pediat, Denver, CO 80202 USA
[7] Hlth Sci Ctr, Aurora, CO USA
[8] Univ Hosp San Raffaele, Inst Sci, Dept Oncol, Milan, Italy
[9] Biodesix, Steamboat Springs, CO USA
[10] ECOG, Biostat Off, Dept Biostat & Computat Biol, Boston, MA USA
[11] Kanazawa Univ, Dept Resp Med, Kanazawa, Ishikawa, Japan
[12] Japanese Fdn Canc Res, Thorac Oncol Ctr, Tokyo, Japan
[13] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD USA
[14] Azienda Osped Perugia, Dept Med Oncol, Perugia, Italy
[15] Med Univ Gdansk, Dept Med Oncol, Gdansk, Poland
[16] Univ Texas, SW Med Ctr, Dept Med, Dallas, TX USA
关键词
D O I
10.1093/jnci/djk195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Some but not all patients with non-small-cell lung cancer (NSCLC) respond to treatment with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). We developed and tested the ability of a predictive algorithm based on matrix-assisted laser desorption ionization (MALDI) mass spectrometry (MS) analysis of pretreatment serum to identify patients who are likely to benefit from treatment with EGFR TKIs. Methods Serum collected from NSCLC patients before treatment with gefitinib or erlotinib were analyzed by MALDI MS. Spectra were acquired independently at two institutions. An algorithm to predict outcomes after treatment with EGFR TKIs was developed from a training set of 139 patients from three cohorts. The algorithm was then tested in two independent validation cohorts of 67 and 96 patients who were treated with gefitinib and erlotinib, respectively, and in three control cohorts of patients who were not treated with EGFR TKIs. The clinical outcomes of survival and time to progression were analyzed. Results An algorithm based on eight distinct m/z features was developed based on outcomes after EGFR TKI therapy in training set patients. Classifications based on spectra acquired at the two institutions had a concordance of 97.1%. For both validation cohorts, the classifier identified patients who showed improved outcomes after EGFR TKI treatment. In one cohort, median survival of patients in the predicted "good" and "poor" groups was 207 and 92 days, respectively (hazard ratio [HR] of death in the good versus poor groups = 0.50, 95% confidence interval [CI] = 0.24 to 0.78). In the other cohort, median survivals were 306 versus 107 days (HR = 0.41, 95% Cl = 0.17 to 0.63). The classifier did not predict outcomes in patients who did not receive EGFR TKI treatment. Conclusion This MALDI MS algorithm was not merely prognostic but could classify NSCLC patients for good or poor outcomes after treatment with EGFR TKIs. This algorithm may thus assist in the pretreatment selection of appropriate subgroups of NSCLC patients for treatment with EGFR TKIs.
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收藏
页码:838 / 846
页数:9
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