Prediction of outcome of non-small cell lung cancer patients treated with chemotherapy and bortezomib by time-course MALDI-TOF-MS serum peptide profiling.
Prediction of outcome of non-small cell lung cancer patients treated with chemotherapy and bortezomib by time-course MALDI-TOF-MS serum peptide profiling.
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DOI:
10.1186/1477-5956-7-34
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发表时间:
2009-09-03
期刊:
影响因子:
2
通讯作者:
Jimenez CR
中科院分区:
文献类型:
--
作者:
Voortman J;Pham TV;Knol JC;Giaccone G;Jimenez CR
Only a minority of patients with advanced non-small cell lung cancer (NSCLC) benefit from chemotherapy. Serum peptide profiling of NSCLC patients was performed to investigate patterns associated with treatment outcome. Using magnetic bead-assisted serum peptide capture coupled to matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), serum peptide mass profiles of 27 NSCLC patients treated with cisplatin-gemcitabine chemotherapy and bortezomib were obtained. Support vector machine-based algorithms to predict clinical outcome were established based on differential pre-treatment peptide profiles and dynamic changes in peptide abundance during treatment. A 6-peptide ion signature distinguished with 82% accuracy, sensitivity and specificity patients with a relatively short vs. long progression-free survival (PFS) upon treatment. Prediction of long PFS was associated with longer overall survival. Inclusion of 7 peptide ions showing differential changes in abundance during treatment led to a 13-peptide ion signature with 86% accuracy at 100% sensitivity and 73% specificity. A 5-peptide ion signature could separate patients with a partial response vs. non-responders with 89% accuracy at 100% sensitivity and 83% specificity. Differential peptide profiles were also found when comparing the NSCLC serum profiles to those from cancer-free control subjects. This study shows that serum peptidome profiling using MALDI-TOF-MS coupled to pattern diagnostics may aid in prediction of treatment outcome of advanced NSCLC patients treated with chemotherapy.
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影响因子:
6.2
作者:
Ludwig, H;Khayat, D;Facon, T
通讯作者:
Facon, T
影响因子:
9
作者:
Smith, Fraser M.;Gallagher, William M.;Reynolds, John V.
通讯作者:
Reynolds, John V.
DOI:
10.1093/jnci/djk195
发表时间:
2007-06-06
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
Taguchi, Fumiko;Solomon, Benjamin;Carbone, David P.
通讯作者:
Carbone, David P.
DOI:
10.1093/jnci/92.3.205
发表时间:
2000-02-02
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
Therasse, P;Arbuck, SG;Gwyther, SG
通讯作者:
Gwyther, SG
影响因子:
2
作者:
Jimenez, Connie R.;El Filali, Zineb;Li, Ka Wan
通讯作者:
Li, Ka Wan